1-Phenylpropan-1-ol (1-Phenyl-1-propanol) [C9H12O] by Asch

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3 substances in Reaxys

2018-07-03 16h:52m:01s (UTC)

1. Query

Search as: As drawn ) AND (IDE.XRN=1906759) OR (IDE.XRN=2041556) OR (IDE.XRN=2041555))

1/229

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Reaxys ID 1906759 View in Reaxys

1/3 CAS Registry Number: 93-54-9 Chemical Name: 1-Phenyl-1-propanol; 1-phenyl-1-propanol Linear Structure Formula: C2H5CH(C6H5)OH Molecular Formula: C9H12O Molecular Weight: 136.194 Type of Substance: isocyclic InChI Key: DYUQAZSOFZSPHD-UHFFFAOYSA-N Note:

Substance Label (214) Label References 1a

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14a

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(±)-16

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13b

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b13

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10b

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b20

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b15

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1bd

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16a

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(RS)-1P1P

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c2h

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Zhang, Shi Yuan; Wojtas, Lukasz; Zaworotko, Michael J.; Journal of the American Chemical Society; vol. 137; nb. 37; (2015); p. 12045 - 12049, View in Reaxys; Liu, Juan; Wang, Fei; Ding, Qing-Rong; Zhang, Jian; Inorganic Chemistry; vol. 55; nb. 24; (2016); p. 12520 - 12522, View in Reaxys

Perna; Ricci; Scilimati; Mena; Pisano; Palmieri; Agrimi; Vitale; Journal of Molecular Catalysis B: Enzymatic; vol. 124; (2016); p. 29 - 37, View in Reaxys

Zink-Lorre, Nathalie; Font-Sanchis, Enrique; Sastre-Santos, Ángela; Fernández-Lázaro, Fernando; Dyes and Pigments; vol. 127; (2016); p. 9 - 17, View in Reaxys

Jung, Thais Cordeiro; Argouarch, Gilles; Van De Weghe, Pierre; Catalysis Communications; vol. 78; (2016); p. 52 54, View in Reaxys

rac-2o

Tian, Cheng; Gong, Lei; Meggers, Eric; Chemical Communications; vol. 52; nb. 22; (2016); p. 4207 - 4210, View in Reaxys

rac-1o

Hernández, José G.; Frings, Marcus; Bolm, Carsten; ChemCatChem; vol. 8; nb. 10; (2016); p. 1769 - 1772, View in Reaxys

Liu, Changhui; Pan, Bin; Gu, Yanlong; Chinese Journal of Catalysis; vol. 37; nb. 6; (2016); p. 979 - 986, View in Reaxys

Sahin, Irfan; Emir, Sedat; Ispir, Esin; Karakaya, Idris; Gumus, Selcuk; Ulusoy, Mahmut; Karabuga, Semistan; Catalysis Communications; vol. 85; (2016); p. 30 - 33, View in Reaxys

XIX

Patent; Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences; East China University of Science and Technology; Ding, Kai; Cao, Wei; (9 pag.); CN104710286; (2016); (B) Chinese, View in Reaxys

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Gülcemal, Süleyman; Gülcemal, Derya; Whitehead, George F. S.; Xiao, Jianliang; Chemistry - A European Journal; vol. 22; nb. 30; (2016); p. 10513 - 10522, View in Reaxys

rac-10k

El-Sepelgy, Osama; Alandini, Nurtalya; Rueping, Magnus; Angewandte Chemie - International Edition; vol. 55; nb. 43; (2016); p. 13602 - 13605; Angew. Chem.; vol. 128; nb. 43; (2016); p. 13800 - 13803,4, View in Reaxys

I-21

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys

1&21%

Patent; UNIVERSITAET DES SAARLANDES; HUY, Peter Helmut; (208 pag.); WO2016/202894; (2016); (A1) English, View in Reaxys

Patonay; Hajdu; Jeko; Levai; Micskei; Zucchi; Tetrahedron Letters; vol. 40; nb. 7; (1999); p. 1373 - 1374, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys; Wei, Yu; Rao, Bin; Cong, Xuefeng; Zeng, Xiaoming; Journal of the American Chemical Society; vol. 137; nb. 29; (2015); p. 9250 - 9253, View in Reaxys

Tohma, Hirofumi; Takizawa, Shinobu; Maegawa, Tomohiro; Kita, Yasuyuki; Angewandte Chemie - International Edition; vol. 39; nb. 7; (2000); p. 1306 - 1308, View in Reaxys; Tohma, Hirofumi; Maegawa, Tomohiro; Takizawa, Shinobu; Kita, Yasuyuki; Advanced Synthesis and Catalysis; vol. 344; nb. 3-4; (2002); p. 328 - 337, View in Reaxys; Pascanu, Vlad; Bermejo Gómez, Antonio; Ayats, Carles; Platero-Prats, Ana Eva; Carson, Fabian; Su, Jie; Yao, Qingxia; Pericàs, Miquel À.; Zou, Xiaodong; Martín-Matute, Belén; ACS Catalysis; vol. 5; nb. 2; (2015); p. 472 479, View in Reaxys

Fukuzawa, Shin-Ichi; Nakano, Narihito; Saitoh, Takahide; European Journal of Organic Chemistry; nb. 13; (2004); p. 2863 - 2867, View in Reaxys; Jana, Umasish; Biswas, Srijit; Maiti, Sukhendu; Tetrahedron Letters; vol. 48; nb. 23; (2007); p. 4065 - 4069, View in Reaxys; Wang, Dong; Deraedt, Christophe; Ruiz, Jaime; Astruc, Didier; Journal of Molecular Catalysis A: Chemical; vol. 400; (2015); p. 14 - 21, View in Reaxys

Bhati, Nishi; Sarma, Kuladip; Goswami, Amrit; Chemistry Letters; vol. 37; nb. 5; (2008); p. 496 - 497, View in Reaxys; Wang, Rongzhou; Ma, Juan; Li, Feng; Journal of Organic Chemistry; vol. 80; nb. 21; (2015); p. 10769 - 10776, View in Reaxys

IVo

Khurana, Jitender M.; Dawra, Kiran; Sharma, Purnima; RSC Advances; vol. 5; nb. 16; (2015); p. 12048 - 12051, View in Reaxys

Jiang, He-Yan; Zheng, Xu-Xu; Catalysis Science and Technology; vol. 5; nb. 7; (2015); p. 3728 - 3734, View in Reaxys

Bai, Wei; Lee, Ka-Ho; Tse, Sunny Kai San; Chan, Ka Wing; Lin, Zhenyang; Jia, Guochen; Organometallics; vol. 34; nb. 15; (2015); p. 3686 - 3698, View in Reaxys

Metsänen, Toni T.; Gallego, Daniel; Szilvási, Tibor; Driess, Matthias; Oestreich, Martin; Chemical Science; vol. 6; nb. 12; (2015); p. 7143 - 7149, View in Reaxys

Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys

Enders, Dieter; Haertwig, Andreas; Raabe, Gerhard; Runsink, Jan; European Journal of Organic Chemistry; nb. 9; (1998); p. 1771 - 1792, View in Reaxys; Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 - 6104, View in Reaxys

Nakamura, Kaoru; Inoue, Yuko; Matsuda, Tomoko; Misawa, Ibuki; Journal of the Chemical Society - Perkin Transactions 1; nb. 16; (1999); p. 2397 - 2402, View in Reaxys; Sawama, Yoshinari; Morita, Kosuke; Yamada, Tsuyoshi; Nagata, Saori; Yabe, Yuki; Monguchi, Yasunari; Sajiki, Hironao; Green Chemistry; vol. 16; nb. 7; (2014); p. 3439 3443, View in Reaxys

Khan, Abu T.; Choudhury, Lokman H.; Ghosh, Subrata; European Journal of Organic Chemistry; nb. 13; (2005); p. 2782 - 2787, View in Reaxys; Garg, Bhaskar; Ling, Yong-Chien; Journal of the Chinese Chemical Society; vol. 61; nb. 7; (2014); p. 737 - 742, View in Reaxys; Umeda, Rui; Takahashi, Yuuki; Nishiyama, Yutaka; Tetrahedron Letters; vol. 55; nb. 44; (2014); p. 6113 - 6116, View in Reaxys

Perosa, Alvise; Selva, Maurizio; Tundo, Pietro; Journal of Organic Chemistry; vol. 64; nb. 11; (1999); p. 3934 - 3939, View in Reaxys; Gaertner, Peter; Letschnig, Martin F.; Knollmueller, Max; Voellenkle, Horst; Tetrahedron Asymmetry; vol. 10; nb. 24; (1999); p. 4811 - 4830, View in Reaxys; Moore, David; Pu, Lin; Organic letters; vol. 4; nb. 11; (2002); p. 1855 - 1857, View in Reaxys; Adair, Gareth R. A.; Williams, Jonathan M. J.; Chemical Communications; nb. 25; (2007); p. 2608 - 2609, View in Reaxys; Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys; Orita, Akihiro; Yasui, Yutaka; Otera, Junzo; Organic Process Research and Development; vol. 4; nb. 5; (2000); p. 337 - 341, View in Reaxys; Janeczko, Tomasz; Kostrzewa-Suslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys

rac-2a

Wang, Zheng; Ye, Jinjin; Wu, Rui; Liu, Yang-Zi; Fossey, John S.; Cheng, Jiagao; Deng, Wei-Ping; Catalysis Science and Technology; vol. 4; nb. 7; (2014); p. 1909 - 1913, View in Reaxys

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys

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PPO

Tong, Jinhui; Cai, Xiaodong; Wang, Haiyan; Zhang, Qianping; Materials Research Bulletin; vol. 55; (2014); p. 205 211, View in Reaxys

Karabuga, Semistan; Karakaya, Idris; Ulukanli, Sabri; Tetrahedron Asymmetry; vol. 25; nb. 10-11; (2014); p. 851 855, View in Reaxys

22a

Del Aguila-Sanchez, Miguel A.; Santos-Bastos, Neidemar M.; Ramalho-Freitas, Maria C.; Garcia Lopez, Jesus; Costa De Souza, Marcos; Camargos-Resende, Jackson A. L.; Casimiro, Maria; Alves-Romeiro, Gilberto; Iglesias, Maria Jose; Lopez Ortiz, Fernando; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14079 - 14091, View in Reaxys

Huang, Xiaoqiang; Li, Xinyao; Zou, Miancheng; Song, Song; Tang, Conghui; Yuan, Yizhi; Jiao, Ning; Journal of the American Chemical Society; vol. 136; nb. 42; (2014); p. 14858 - 14865, View in Reaxys

Cao, Hui; Cai, Li-Hua; Wang, Chen-Xi; Zhu, Xiao-Han; Li, Zhi-Ming; Hou, Xiu-Feng; Journal of Organometallic Chemistry; vol. 775; (2014); p. 60 - 66, View in Reaxys

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys

rac-5a

Ma, Gaoyuan; Deng, Jun; Sibi, Mukund P.; Angewandte Chemie - International Edition; vol. 53; nb. 44; (2014); p. 11818 - 11821; Angew. Chem.; vol. 53-126; nb. 44; (2014); p. 12180, View in Reaxys

Galletti, Paola; Pori, Matteo; Funiciello, Federica; Soldati, Roberto; Ballardini, Alberto; Giacomini, Daria; ChemSusChem; vol. 7; nb. 9; (2014); p. 2684 - 2689, View in Reaxys

Martin-Matute, Belen; Edin, Michaela; Bogar, Krisztian; Baeckvall, Jan-E.; Angewandte Chemie - International Edition; vol. 43; nb. 47; (2004); p. 6535 - 6539, View in Reaxys; Harrad, Mohamed Anouar; Boualy, Brahim; El Firdoussi, Larbi; Mehdi, Ahmad; Santi, Claudio; Giovagnoli, Stefano; Nocchetti, Morena; Ait Ali, Mustapha; Catalysis Communications; vol. 32; (2013); p. 92 - 100, View in Reaxys

Musser; Richey Jr.; Journal of Organic Chemistry; vol. 65; nb. 23; (2000); p. 7750 - 7756, View in Reaxys; Iida, Kazuki; Miura, Takashi; Ando, Junki; Saito, Susumu; Organic Letters; vol. 15; nb. 7; (2013); p. 1436 - 1439, View in Reaxys

rac-6a

Tauber, Katharina; Fuchs, Michael; Sattler, Johann H.; Pitzer, Julia; Pressnitz, Desiree; Koszelewski, Dominik; Faber, Kurt; Pfeffer, Jan; Haas, Thomas; Kroutil, Wolfgang; Chemistry - A European Journal; vol. 19; nb. 12; (2013); p. 4030 - 4035, View in Reaxys

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys

Marinova, Maya; Kostova, Kalina; Tzvetkova, Pavleta; Tavlinova-Kirilova, Maya; Chimov, Angel; Nikolova, Rosica; Shivachev, Boris; Dimitrov, Vladimir; Tetrahedron Asymmetry; vol. 24; nb. 23; (2013); p. 1453 - 1466, View in Reaxys

PPA

Li, Zi-Jian; Yao, Jia; Tao, Qian; Jiang, Long; Lu, Tong-Bu; Inorganic Chemistry; vol. 52; nb. 20; (2013); p. 11694 11696, View in Reaxys

Belotti, Damien; Cantagrel, Guillaume; Combellas, Catherine; Cossy, Janine; Kanoufi, Frederic; Nunige, Sandra; New Journal of Chemistry; vol. 29; nb. 6; (2005); p. 761 - 764, View in Reaxys; Silva, Camila R.; Souza, Juliana C.; Araujo, Lidiane S.; Kagohara, Edna; Garcia, Thais P.; Pelizzari, Vivian H.; Andrade, Leandro H.; Journal of Molecular Catalysis B: Enzymatic; vol. 83; (2012); p. 23 - 28, View in Reaxys

(+/-)-3, (+/-)-1

Ilies, Laurean; Yoshida, Takumi; Nakamura, Eiichi; Journal of the American Chemical Society; vol. 134; nb. 41; (2012); p. 16951 - 16954,4, View in Reaxys

(Âą)-10

Kataoka, Noriyuki; Okudomi, Masayuki; Chihara, Naoka; Matsumoto, Kazutsugu; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 615 - 621, View in Reaxys

rac-13b

Hobuss, Dennis; Baro, Angelika; Laschat, Sabine; Frey, Wolfgang; Tetrahedron; vol. 64; nb. 8; (2008); p. 1635 1640, View in Reaxys

PhCH(OH)CH2CH3

Lakouraj, Moslem M.; Tajbakhsh, Mahmood; Mahalli, Majid S.; Monatshefte fur Chemie; vol. 139; nb. 2; (2008); p. 117 - 123, View in Reaxys

1-ol

Whitehouse, Christopher J. C.; Bell, Stephen G.; Tufton, Henry G.; Kenny, Richard J. P.; Ogilvie, Lydia C. I.; Wong, Luet-Lok; Chemical Communications; nb. 8; (2008); p. 966 - 968, View in Reaxys

2, d-g

Yadav; Subba Reddy; Pandurangam; Raghavendra Rao; Praneeth; Narayana Kumar; Madavi; Kunwar; Tetrahedron Letters; vol. 49; nb. 27; (2008); p. 4296 - 4301, View in Reaxys

A34

Cesarini, Sara; Spallarossa, Andrea; Ranise, Angelo; Bruno, Olga; La Colla, Paolo; Secci, Barbara; Collu, Gabriella; Loddo, Roberta; Bioorganic and Medicinal Chemistry; vol. 16; nb. 7; (2008); p. 4173 - 4185, View in Reaxys

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2018-07-03 16:52:46

Demizu, Yosuke; Shiigi, Hirofumi; Oda, Takahisa; Matsumura, Yoshihiro; Onomura, Osamu; Tetrahedron Letters; vol. 49; nb. 1; (2008); p. 48 - 52, View in Reaxys

(+/-)-13a

Machado, Luciana L.; Lemos, Telma L.G.; de Mattos, Marcos Carlos; de Oliveira, Maria da Conceicao F.; de Gonzalo, Gonzalo; Gotor-Fernandez, Vicente; Gotor, Vicente; Tetrahedron Asymmetry; vol. 19; nb. 12; (2008); p. 1418 - 1423, View in Reaxys

tab3, product5

Coyne, Anthony G.; Guiry, Patrick J.; Tetrahedron Letters; vol. 48; nb. 5; (2007); p. 747 - 750, View in Reaxys

Table1, entry10, educt

Zareyee, Daryoush; Karimi, Babak; Tetrahedron Letters; vol. 48; nb. 7; (2007); p. 1277 - 1280, View in Reaxys

Table 1, entry 2

Comte, Virginie; Balan, Cedric; Le Gendre, Pierre; Moise, Claude; Chemical Communications; nb. 7; (2007); p. 713 - 715, View in Reaxys

product tab. 3, entr.3

Yu; Zeng; Sun; Deng; Dong; Chen; Wang; Pei; Journal of Organometallic Chemistry; vol. 692; nb. 11; (2007); p. 2306 - 2313, View in Reaxys

11b

Chen, Tao; Liu, Xu-Guang; Shi, Min; Tetrahedron; vol. 63; nb. 23; (2007); p. 4874 - 4880, View in Reaxys

IVf

Hashemi; Bakhtiari; Karimi-Jaberi; Russian Journal of Organic Chemistry; vol. 43; nb. 4; (2007); p. 621 - 622, View in Reaxys

alcohol, tab 2/11

Matano, Yoshihiro; Suzuki, Takeshi; Shinokura, Tomonori; Imahori, Hiroshi; Tetrahedron Letters; vol. 48; nb. 16; (2007); p. 2885 - 2888, View in Reaxys

run3

Wise, Nicola J.; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 48; nb. 21; (2007); p. 3639 - 3641, View in Reaxys

Martinez, Ricardo; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 10; (2007); p. 1599 1605, View in Reaxys

Tab 2/5 alcohol

Sreedhar; Reddy, P. Surendra; Krishna, V. Rama; Tetrahedron Letters; vol. 48; nb. 33; (2007); p. 5831 - 5834, View in Reaxys

Table 2; Entry 7

Cadierno, Victorio; Francos, Javier; Gimeno, Jose; Nebra, Noel; Chemical Communications; nb. 24; (2007); p. 2536 - 2538, View in Reaxys

(+/-)-9

Birman, Vladimir B.; Jiang, Hui; Li, Ximin; Organic Letters; vol. 9; nb. 17; (2007); p. 3237 - 3240, View in Reaxys

T1, E1-2, P2

Coquerel, Yoann; Bremond, Paul; Rodriguez, Jean; Journal of Organometallic Chemistry; vol. 692; nb. 22; (2007); p. 4805 - 4808, View in Reaxys

(+/-)-47

Driver, Tom G.; Harris, Jason R.; Woerpel; Journal of the American Chemical Society; vol. 129; nb. 13; (2007); p. 3836 - 3837, View in Reaxys

Nishibayashi, Yoshiaki; Yamauchi, Akiyoshi; Onodera, Gen; Uemura, Sakae; Journal of Organic Chemistry; vol. 68; nb. 15; (2003); p. 5875 - 5880, View in Reaxys; Poisson, Thomas; Penhoat, Mael; Papamicael, Cyril; Dupas, Georges; Dalla, Vincent; Marsais, Francis; Levacher, Vincent; Synlett; nb. 15; (2005); p. 2285 - 2288; Art.No: D16605ST, View in Reaxys; Mitsudo, Koichi; Kumagai, Hiroki; Takabatake, Fumiko; Kubota, Jun; Tanaka, Hideo; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 8994 - 8997, View in Reaxys

(+/-)-1

Shiina, Isamu; Nakata, Kenya; Tetrahedron Letters; vol. 48; nb. 47; (2007); p. 8314 - 8317, View in Reaxys

(+/-)-11

Birman, Vladimir B.; Li, Ximin; Jiang, Hui; W. Uffman, Eric; Tetrahedron; vol. 62; nb. 2-3; (2006); p. 285 - 294, View in Reaxys

(+/-)-4b

Spivey, Alan C.; Arseniyadis, Stellios; Fekner, Tomasz; Maddaford, Adrian; Leese, David P.; Tetrahedron; vol. 62; nb. 2-3; (2006); p. 295 - 301, View in Reaxys

Substrate, Tab.2, run 6

Mardani, Hamid R.; Golchoubian, Hamid; Tetrahedron Letters; vol. 47; nb. 14; (2006); p. 2349 - 2352, View in Reaxys

t.1, prod., entry 1

Szakonyi, Zsolt; Balazs, Arpad; Martinek, Tamas A.; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 17; nb. 2; (2006); p. 199 - 204, View in Reaxys

4, Tab. 1, entry 2

Xu, Zhaoqing; Lin, Li; Xu, Jiangke; Yan, Wenjin; Wang, Rui; Advanced Synthesis and Catalysis; vol. 348; nb. 4-5; (2006); p. 506 - 514, View in Reaxys

Substrate,Tab.1/2,run 4

Iranpoor, Nasser; Firouzabadi, Habib; Azadi, Roya; Tetrahedron Letters; vol. 47; nb. 31; (2006); p. 5531 - 5534, View in Reaxys

6.1

Kimura, Masanari; Ezoe, Akihiro; Mori, Masahiko; Iwata, Keisuke; Tamaru, Yoshinao; Journal of the American Chemical Society; vol. 128; nb. 26; (2006); p. 8559 - 8568, View in Reaxys

Product, Tab.4, run 5

Enthaler, Stephan; Erre, Giulia; Tse, Man Kin; Junge, Kathrin; Beller, Matthias; Tetrahedron Letters; vol. 47; nb. 46; (2006); p. 8095 - 8099, View in Reaxys

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2018-07-03 16:52:46

18a

Enthaler, Stephan; Jackstell, Ralf; Hagemann, Bernhard; Junge, Kathrin; Erre, Giulia; Beller, Matthias; Journal of Organometallic Chemistry; vol. 691; nb. 22; (2006); p. 4652 - 4659, View in Reaxys

(+/-)-2b

Li, Yan-Yun; Zhang, Xue-Qin; Dong, Zhen-Rong; Shen, Wei-Yi; Chen, Gui; Gao, Jing-Xing; Organic Letters; vol. 8; nb. 24; (2006); p. 5565 - 5567, View in Reaxys

substrate, tab 3/25

Farhadi, Saeid; Zabardasti, Abedien; Babazadeh, Zaynab; Tetrahedron Letters; vol. 47; nb. 50; (2006); p. 8953 8957, View in Reaxys

Tab. 4, entry 8

Kantam, M. Lakshmi; Rao, B. Purna Chandra; Choudary; Sreedhar; Advanced Synthesis and Catalysis; vol. 348; nb. 14; (2006); p. 1970 - 1976, View in Reaxys

rac-16

Berkessel, Albrecht; Sebastian-Ibarz, M. Luisa; Mueller, Thomas N.; Angewandte Chemie - International Edition; vol. 45; nb. 39; (2006); p. 6567 - 6570, View in Reaxys

Boren, Linnea; Martin-Matute, Belen; Xu, Yongmei; Cordova, Armando; Baeckvall, Jan-E.; Chemistry - A European Journal; vol. 12; nb. 1; (2006); p. 225 - 232, View in Reaxys

Table S2 entry 1

Graves, Christopher R.; Zeng, Bi-Shun; Nguyen, SonBinh T.; Journal of the American Chemical Society; vol. 128; nb. 39; (2006); p. 12596 - 12597, View in Reaxys

Tab. 2, entry 10, subs.

Tajbakhsh, Mahmood; Lakouraj, Moslem Mansour; Ramzanian-Lehmali, Farhad; Synlett; nb. 11; (2006); p. 1724 - 1728, View in Reaxys

11a

Law, Man Chun; Wong, Kwok-Yin; Chan, Tak Hang; Chemical Communications; nb. 23; (2006); p. 2457 - 2459, View in Reaxys

Nagaoka; Kayahara; Wakabayashi; Bioscience, biotechnology, and biochemistry; vol. 65; nb. 3; (2001); p. 634 - 637, View in Reaxys; Naik, Sarala; Gopinath, Rangam; Patel, Bhisma K; Tetrahedron Letters; vol. 42; nb. 43; (2001); p. 7679 - 7681, View in Reaxys; Clay, Julia M.; Vedejs, Edwin; Journal of the American Chemical Society; vol. 127; nb. 16; (2005); p. 5766 - 5767, View in Reaxys

5, Tab. 2, entry 13

Handlon, Anthony L.; Guo, Yu; Synlett; nb. 1; (2005); p. 111 - 114; Art.No: S08204ST, View in Reaxys

Table 3. Ent.4. alkanol

Tan, Duan-Ming; Chan, Kin Shing; Tetrahedron Letters; vol. 46; nb. 3; (2005); p. 503 - 505, View in Reaxys

1, R = Et

Bright, Zack R.; Luyeye, Cedric R.; Morton, Angela Ste. Marie; Sedenko, Marina; Landolt, Robert G.; Bronzi, Matthew J.; Bohovic, Katherine M.; Gonser, M. W. Alex; Lapainis, Theodore E.; Hendrickson, William H.; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 684 - 687, View in Reaxys

5an

Aggarwal, Varinder K.; Guang, Yu Fang; Schmidt, Andreas T.; Journal of the American Chemical Society; vol. 127; nb. 6; (2005); p. 1642 - 1643, View in Reaxys

alcohol, entry 6

Zaccheria, Federica; Ravasio, Nicoletta; Psaro, Rinaldo; Fusi, Achille; Tetrahedron Letters; vol. 46; nb. 21; (2005); p. 3695 - 3697, View in Reaxys

subs., Tab.11, entry 8

Wuyts; De Temmerman; De Vos; Jacobs; Chemistry - A European Journal; vol. 11; nb. 1; (2005); p. 386 - 397, View in Reaxys

tab. 1,entry 8, prod- Karimi, Babak; Zareyee, Daryoush; Tetrahedron Letters; vol. 46; nb. 27; (2005); p. 4661 - 4665, View in Reaxys uct 13

Birman, Vladimir B.; Jiang, Hui; Organic Letters; vol. 7; nb. 16; (2005); p. 3445 - 3447, View in Reaxys

tab2, product, entry2

Krzeminski, Marek P.; Wojtczak, Andrzej; Tetrahedron Letters; vol. 46; nb. 48; (2005); p. 8299 - 8302, View in Reaxys

T.1, 1 (R1=Ph, R2=Me)

Kamochi, Yasuko; Kudo, Tadahiro; Masuda, Toshinobu; Takadate, Akira; Chemical and Pharmaceutical Bulletin; vol. 53; nb. 8; (2005); p. 1017 - 1020, View in Reaxys

Khan, Abu T.; Ghosh, Subrata; Choudhury, Lokman H.; European Journal of Organic Chemistry; nb. 22; (2005); p. 4891 - 4896, View in Reaxys

19a

Farhadi, Saeid; Afshari, Mozhgan; Maleki, Mansoureh; Babazadeh, Zaynab; Tetrahedron Letters; vol. 46; nb. 49; (2005); p. 8483 - 8486, View in Reaxys

2, R1=Ph, R2=Et

Tajbakhsh, Mahmoud; Lakouraj, Moslem-Mansor; Yadoolahzadeh, Khadijeh; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 180; nb. 11; (2005); p. 2431 - 2437, View in Reaxys

prod., Tab. 1, entry 2

Yun, Jaesook; Kim, Daesung; Yun, Hoseop; Chemical Communications; nb. 41; (2005); p. 5181 - 5183, View in Reaxys

Tab.3, entry 25, subst.

Chakraborti, Asit K.; Gulhane, Rajesh; Shivani; Synthesis; nb. 1; (2004); p. 111 - 115, View in Reaxys

alcohol, Tab.1, entry 6

Markert, Morris; Mahrwald, Rainer; Synthesis; nb. 9; (2004); p. 1429 - 1433, View in Reaxys

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subst.,Tab. 1,entry 29

Chakraborti, Asit K.; Gulhane, Rajesh; Synlett; nb. 4; (2004); p. 627 - 630, View in Reaxys

C6H5CH(OH)CH2 CH3

Tajbakhsh; Lakouraj; Fadavi; Synthetic Communications; vol. 34; nb. 7; (2004); p. 1173 - 1181, View in Reaxys

substrate, Tab 3, run 6

Firouzabadi, Habib; Iranpoor, Nasser; Sobhani, Sara; Ghassamipour, Soheila; Journal of Organometallic Chemistry; vol. 689; nb. 20; (2004); p. 3197 - 3202, View in Reaxys

educt to 3r

Mormeneo, David; Llebaria, Amadeu; Delgado, Antonio; Tetrahedron Letters; vol. 45; nb. 37; (2004); p. 6831 6834, View in Reaxys

Product, Tab.1, run 8

Bhar, Sanjay; Guha, Sharmistha; Tetrahedron Letters; vol. 45; nb. 19; (2004); p. 3775 - 3777, View in Reaxys

PhCH(Et)OH

Shaozu, Wu; Tianhui, Ren; Ning, Chen; Yulan, Zhang; Organic Preparations and Procedures International; vol. 23; nb. 4; (1991); p. 427 - 431, View in Reaxys; Lee, Jong Chan; Lee, Ji Young; Lee, Seung Jun; Tetrahedron Letters; vol. 45; nb. 25; (2004); p. 4939 - 4941, View in Reaxys

Tab.1.col.2.run 8

Karimi, Babak; Zamani, Asghar; Zareyee, Daryoush; Tetrahedron Letters; vol. 45; nb. 49; (2004); p. 9139 - 9141, View in Reaxys

PhCH(OH)Et

Lorber, Christian Y.; Smidt, Sebastian P.; Osborn, John A.; European Journal of Inorganic Chemistry; nb. 4; (2000); p. 655 - 658, View in Reaxys; Firouzabadi, Habib; Iranpoor, Nasser; Amani, Kamal; Synthesis; nb. 3; (2003); p. 408 - 412, View in Reaxys

10; R=Ph, R'=Et

Cami-Kobeci, Gerta; Williams, Jonathan M.J.; Synlett; nb. 1; (2003); p. 124 - 126, View in Reaxys

substrate, tab2, row 9

Firouzabadi, Habib; Iranpoor, Nasser; Sobhani, Sara; Ghassamipour, Soheila; Amoozgar, Zohreh; Tetrahedron Letters; vol. 44; nb. 5; (2003); p. 891 - 893, View in Reaxys

14a, R=Ph

Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Tetrahedron Asymmetry; vol. 14; nb. 9; (2003); p. 1103 - 1114, View in Reaxys

ROH to 16

Olsen, Christian A.; Joorgensen, Malene R.; Witt, Matthias; Mellor, Ian R.; Usherwood, Peter N. R.; Jaroszewski, Jerzy W.; Franzyk, Henrik; European Journal of Organic Chemistry; nb. 17; (2003); p. 3288 - 3299, View in Reaxys

alcohol 9

Karimi, Babak; Ma'mani, Leyla; Tetrahedron Letters; vol. 44; nb. 32; (2003); p. 6051 - 6053, View in Reaxys

tab. 2, entry 6, subst.

Kim, Sung Soo; Jung, Hyun Chul; Synthesis; nb. 14; (2003); p. 2135 - 2137, View in Reaxys

Tab.3, subst., entry 25

Chakraborti, Asit K.; Gulhane, Rajesh; Shivani; Synlett; nb. 12; (2003); p. 1805 - 1808, View in Reaxys

substrate(table4 en- Chakraborti, Asit K.; Gulhane, Rajesh; Tetrahedron Letters; vol. 44; nb. 17; (2003); p. 3521 - 3525, View in Reaxys try4 substrate Tab. 2, e. 4

Chakraborti, Asit K.; Gulhane, Rajesh; Tetrahedron Letters; vol. 44; nb. 35; (2003); p. 6749 - 6753, View in Reaxys

T. 2-8, substrate

Kim, Sung Soo; Borisova, Galina; Synthetic Communications; vol. 33; nb. 22; (2003); p. 3961 - 3967, View in Reaxys

35b

Stampfer, Wolfgang; Kosjek, Birgit; Faber, Kurt; Kroutil, Wolfgang; Journal of Organic Chemistry; vol. 68; nb. 2; (2003); p. 402 - 406, View in Reaxys

prod., Tab. 2, entry 2

Yu, Jin-Quan; Wu, Hai-Chen; Ramarao, Chandrashekar; Spencer, Jonathan B; Ley, Steven V; Chemical communications (Cambridge, England); nb. 6; (2003); p. 678 - 679, View in Reaxys

Tab. 5, entry 5

Ten Brink, Gerd-Jan; Arends, Isabel W. C. E.; Hoogenraad, Marcel; Verspui, Goeran; Sheldon, Roger A.; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1341 - 1352, View in Reaxys

PhCH(OH)CH2CH 3

Firouzabadi; Fakoorpour; Hazarkhani; Synthetic Communications; vol. 31; nb. 24; (2001); p. 3859 - 3862, View in Reaxys; Firouzabadi, Habib; Iranpoor, Nasser; Amani, Kamal; Nowrouzi, Farhad; Journal of the Chemical Society. Perkin Transactions 1; nb. 23; (2002); p. 2601 - 2604, View in Reaxys

Shiina, Isamu; Konishi, Katsuhiko; Kuramoto, Yu-suke; Chemistry Letters; nb. 2; (2002); p. 164 - 165, View in Reaxys

rac-3e, R2=H, R3=Et

Kashima, Choji; Mizuhara, Saori; Miwa, Yohei; Yokoyama, Yukihiro; Tetrahedron Asymmetry; vol. 13; nb. 16; (2002); p. 1713 - 1719, View in Reaxys

Substrate, Tab.2,run Ganchegui, Benjamin; Bouquillon, Sandrine; Henin, Francoise; Muzart, Jacques; Tetrahedron Letters; vol. 43; nb. 23 37; (2002); p. 6641 - 6644, View in Reaxys tab. 1, entry 2, alc.

Jeong, Kyu-Sung; Kim, Soong-Hyun; Park, Hyun-Jin; Chang, Kyoung-Jin; Kwan, Soo Kim; Chemistry Letters; nb. 11; (2002); p. 1114 - 1115, View in Reaxys

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Matsugi, Masato; Itoh, Kinuyo; Nojima, Masatomo; Hagimoto, Yuri; Kita, Yasuyuki; Chemistry - A European Journal; vol. 8; nb. 24; (2002); p. 5551 - 5564, View in Reaxys

Clerici, Angelo; Pastori, Nadia; Porta, Ombretta; European Journal of Organic Chemistry; nb. 19; (2002); p. 3326 3335, View in Reaxys

Wipf, Peter; Wang, Xiaodong; Organic Letters; vol. 4; nb. 7; (2002); p. 1197 - 1199, View in Reaxys

product of 6e

Pasto, Mireia; Riera, Antoni; Pericas, Miquel A.; European Journal of Organic Chemistry; nb. 14; (2002); p. 2337 2341, View in Reaxys

H-2

Patent; PHARMACIA and UPJOHN COMPANY; EP1203770; (2002); (A1) English, View in Reaxys

Weik, Steffen; Nicholson, Graeme; Jung, Gnther; Rademann, Jrg; Angewandte Chemie - International Edition; vol. 40; nb. 8; (2001); p. 1436 - 1439, View in Reaxys

racemate

Panev, Stefan; Linden, Anthony; Dimitrov, Vladimir; Tetrahedron Asymmetry; vol. 12; nb. 9; (2001); p. 1313 - 1321, View in Reaxys

Table 1. rac(e.e.=0 percent)

Dimitrov, Vladimir; Dobrikov, Georgi; Genov, Miroslav; Tetrahedron Asymmetry; vol. 12; nb. 9; (2001); p. 1323 1329, View in Reaxys

Uemura; Kakiuchi; Nishimura; Inoue; Bulletin of the Chemical Society of Japan; vol. 74; nb. 1; (2001); p. 165 - 172, View in Reaxys

20c

Hage, Annemarie; Petra, Danielle G.I.; Field, Jim A.; Schipper, Dick; Wijnberg, Joannes B.P.A.; Kamer, Paul C.J.; Reek, Joost N.H.; Van Leeuwen, Piet W.N.M.; Wever, Ron; Schoemaker, Hans E.; Tetrahedron Asymmetry; vol. 12; nb. 7; (2001); p. 1025 - 1034, View in Reaxys

Tab 1 Ent 2 comp. 2

Li, Kang Ying; Zhou, Zheng Hong; Chan, Albert S. C.; Tang, Chu Chi; Heteroatom Chemistry; vol. 13; nb. 1; (2001); p. 93 - 95, View in Reaxys

(+/-)-1f

Matsugi, Masato; Itoh, Kinuyo; Nojima, Masatomo; Hagimoto, Yuri; Kita, Yasuyuki; Tetrahedron Letters; vol. 42; nb. 45; (2001); p. 8019 - 8022, View in Reaxys

3aC

Inoue; Kitagawa; Shinokubo; Oshima; Journal of Organic Chemistry; vol. 66; nb. 12; (2001); p. 4333 - 4339, View in Reaxys

(+/-)-6

Schinnerl, Marina; Seitz, Michael; Kaiser, Anja; Reiser, Oliver; Organic Letters; vol. 3; nb. 26; (2001); p. 4259 4262, View in Reaxys

t.2, alcohol, entry 6

De Luca, Lidia; Giacomelli, Giampaolo; Porcheddu, Andrea; Organic Letters; vol. 3; nb. 19; (2001); p. 3041 - 3043, View in Reaxys

(R/S)-1b

Allan; Carnell; Journal of Organic Chemistry; vol. 66; nb. 19; (2001); p. 6495 - 6497, View in Reaxys

7 (1d)

Yasuda; Onishi; Ueba; Miyai; Baba; Journal of Organic Chemistry; vol. 66; nb. 23; (2001); p. 7741 - 7744, View in Reaxys

prod.9, Table 2

Standfest-Hauser; Slugovc; Mereiter; Schmid; Kirchner; Xiaoc; Weissensteiner; Journal of the Chemical Society, Dalton Transactions; nb. 20; (2001); p. 2989 - 2995, View in Reaxys

Persson, B. Anders; Larsson, Anna L. E.; Le Ray, Mikael; Baeckvall, Jan-E.; Journal of the American Chemical Society; vol. 121; nb. 8; (1999); p. 1645 - 1650, View in Reaxys; Copeland; Miller; Journal of the American Chemical Society; vol. 123; nb. 27; (2001); p. 6496 - 6502, View in Reaxys

Armstrong, Susan K.; Clunas, Scott; Synthesis; nb. 2; (2000); p. 281 - 288, View in Reaxys

(RS)-2

Bakker; Spruijt; Van Rantwijk; Sheldon; Tetrahedron Asymmetry; vol. 11; nb. 8; (2000); p. 1801 - 1808, View in Reaxys

alcohol T2, entry E

Subramanyam; Tetrahedron Letters; vol. 41; nb. 34; (2000); p. 6537 - 6540, View in Reaxys

Product, eq. 1

Tian; Kin Shing Chan; Tetrahedron Letters; vol. 41; nb. 45; (2000); p. 8813 - 8816, View in Reaxys

3, Table 1, entry 6

Kitagawa, Kazuya; Inoue, Atsushi; Shinokubo, Hiroshi; Oshima, Koichiro; Angewandte Chemie - International Edition; vol. 39; nb. 14; (2000); p. 2481 - 2483, View in Reaxys

rac-PhCH(OH)Et

Abramson; Lasperas; Galarneau; Desplantier-Giscard; Brunel; Chemical Communications; nb. 18; (2000); p. 1773 - 1774, View in Reaxys

(+/-)-10d

Kita, Yasuyuki; Takebe, Yasushi; Murata, Kenji; Naka, Tadaatsu; Akai, Shuji; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 83 - 88, View in Reaxys

(+/-)-16c

Spivey, Alan C.; Fekner, Tomasz; Spey, Sharon E.; Journal of Organic Chemistry; vol. 65; nb. 10; (2000); p. 3154 3159, View in Reaxys

Tab 1 Ent 2 substrate

Kashiwagi, Yoshitomo; Kurashima, Futoshi; Kikuchi, Chikara; Anzai, Jun-ichi; Osa, Tetsuo; Bobbitt, James M.; Tetrahedron Letters; vol. 40; nb. 35; (1999); p. 6469 - 6472, View in Reaxys

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Firouzabadi, Habib; Karimi, Babak; Abbassi, Mohammad; Journal of Chemical Research - Part S; nb. 3; (1999); p. 236 - 237, View in Reaxys

Iwasaki, Fumiaki; Onomura, Osamu; Mishima, Katsuhiko; Maki, Toshihide; Matsumura, Yoshihiro; Tetrahedron Letters; vol. 40; nb. 42; (1999); p. 7507 - 7511, View in Reaxys

Table 1, entry 10

Nishimura, Takahiro; Onoue, Tomoaki; Ohe, Kouichi; Uemura, Sakae; Journal of Organic Chemistry; vol. 64; nb. 18; (1999); p. 6750 - 6755, View in Reaxys

tab.1, run 2

Yatagai, Masanobu; Ohnuki, Takashi; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 6; (1990); p. 1826 - 1828, View in Reaxys

(RS)-(2b)

Kanoh, Shigeyoshi; Hongoh, Yukihiko; Katoh, Shingo; Motoi, Masatoshi; Suda, Hiroshi; Journal of the Chemical Society, Chemical Communications; nb. 6; (1988); p. 405 - 406, View in Reaxys

Patent-Specific Data (8) References Patent; Qufu Normal University; Wang, Hua; Wei, Wei; Zhu, Minghui; Cui, Huanhuan; (19 pag.); CN106518663; (2017); (A) Chinese, View in Reaxys Patent; Southwest Chemical Design Yuan Co., Ltd.; Xiao Ying; Li Yi; Huang Chaoming; Li Bo; Ding Liang; (8 pag.); CN107245024; (2017); (A) Chinese, View in Reaxys Patent; ERICA Industry-University Cooperation Foundation of Hanyang University; Lee Hak-jun; Go Seong-hyeon; Ahn Hyeonseok; (14 pag.); KR101790573; (2017); (B1) Korean, View in Reaxys Patent; Changzhou University; Zhou Weiyou; Dai Xuan; He Mingyang; Sun Fuan; Pan Jiugao; (8 pag.); CN107176898; (2017); (A) Chinese, View in Reaxys Patent; Zhejiang University; Zhang, Guofu; Li, Shasha; Ding, Chengrong; Zhang, Guihua; Xie, Xiaoqiang; Lei, Jie; (12 pag.); CN105294413; (2016); (A) Chinese, View in Reaxys Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys Patent; RESEARCH & BUSINESS FOUNDATION SUNGKYUNKWAN UNIVERSITY; SONG, CHOON GEUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114445; (2015); (A) Korean, View in Reaxys Patent; Pfizer Inc; US2009/170886; (2009); (A1) English, View in Reaxys Druglikeness (1) 1 of 1

LogP

2.095

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

20.23

Lipinski Number

Veber Number

Related Structure (2) Related Structure References Tomasik,W.; Belzecki,C.; Journal of the Chemical Society, Chemical Communications; (1977); p. 86 - 87, View in Reaxys; Meyers,A.I.; Kendall,P.M.; Tetrahedron Letters; nb. 14; (1974); p. 1337 - 1340, View in Reaxys; Marshall; Prager; Australian Journal of Chemistry; vol. 30; (1977); p. 141,144. 150, View in Reaxys; Ojima; Chemistry Letters; (1974); p. 223,224, View in Reaxys Configuration.

Derivative (7) Comment (Derivative)

Levene; Marker; Journal of Biological Chemistry; vol. 97; (1932); p. 379,381, View in Reaxys; Brewster; Journal of the American Chemical Society; vol. 81; (1959); p. 5475,5482, View in Reaxys; Cram; McCarty; Journal of the American Chemical Society; vol. 79; (1957); p. 2866,2868, View in Reaxys; Arcus; Journal of the Chemical Society; (1944); p. 236, View in Reaxys; Levene; Rothen; Journal of Biological Chemistry; vol. 127; (1937); p. 237,240, 245, View in Reaxys References

Naphthylurethan: F: 100grad

Gocmen,M. et al.; Bulletin de la Societe Chimique de France; (1973); p. 1310 - 1317, View in Reaxys

4-Nitro-benzoat : F=65-65.5grad

Kropf et al.; Tetrahedron Letters; (1969); p. 3427,3428, View in Reaxys

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3,5-Dinitrobenzoat : F:68.5-69.0grad

Baba; Yuki Gosei Kagaku Kyokaishi; vol. 27; (1969); p. 264,265, 266; Chem.Abstr.; vol. 71; nb. 13166, View in Reaxys

Phenylurethan: F: 79grad

Miginiac-Groizeleau; Annales de Chimie (Cachan, France); vol. 6; nb. 13; (1961); p. 1071,1120, View in Reaxys

α-Naphthylurethan: F: 102grad

Banthorpe,D.V. et al.; Journal of the Chemical Society; (1960); p. 4054 - 4087, View in Reaxys

3,5-dinitro-benzoyl derivative (mp: 66.5-67 degree )

Bost et al.; Journal of Organic Chemistry; vol. 22; (1957); p. 51,54, View in Reaxys

4-nitro-benzoyl derivative (mp: 56.5 degree )

Nessmejanow; Ssasonowa; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1941); p. 499,510; Chem.Abstr.; (1943); p. 2724, View in Reaxys

Purification (1) References Giacomelli,G. et al.; Journal of Organic Chemistry; vol. 43; nb. 9; (1978); p. 1790 - 1793, View in Reaxys Melting Point (1) 1 of 1

Melting Point [°C]

Location

Page/Page column 35

Patent; SHARON LABORATORIES LTD.; GARZON, Aaron; GLIKSBERG, Ariel; (0 pag.); WO2016/84078; (2016); (A1) English, View in Reaxys Boiling Point (60) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

217 - 219

Location

Comment (Boiling Point)

Page/Page column 35

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Maguire, Anita R.; Buckley, N. Rachael; O'Leary, Patrick; Ferguson, George; Journal of the Chemical Society - Perkin Transactions 1; nb. 24; (1998); p. 4077 - 4091, View in Reaxys

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Chen; Zhang; Yuan; Synthetic Communications; vol. 21; nb. 1; (1991); p. 107 - 109, View in Reaxys

97 - 99

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Savoia, Diego; Tagliavini, Emilio; Trombini, Claudio; Umani-Ronchi, Achille; Journal of Organic Chemistry; vol. 46; (1981); p. 5344 - 5348, View in Reaxys

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Felkin et al.; Journal of Organometallic Chemistry; vol. 134; (1977); p. 265,266-270, 274,277-278, View in Reaxys

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100 - 101

Kuchar; Brunova; Rejholec; et al.; Collection of Czechoslovak Chemical Communications; vol. 41; nb. 2; (1976); p. 633 - 646, View in Reaxys

100

Mayeda; Journal of the American Chemical Society; vol. 97; (1975); p. 4012,4013, View in Reaxys

0.3

Ford,W.T.; Pietsek,D.J.J.; Journal of the American Chemical Society; vol. 97; (1975); p. 2194 - 2198, View in Reaxys

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98.5

Cervinka,O.; Fusek,J.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 441 446, View in Reaxys

105 - 106

Gocmen,M. et al.; Bulletin de la Societe Chimique de France; (1973); p. 1310 - 1317, View in Reaxys

75 - 84

0.1

Schulz; Jassmann; Bekker; Die Pharmazie; vol. 26; nb. 8; (1971); p. 477 - 481, View in Reaxys

122

Weinges,K. et al.; Chemische Berichte; vol. 104; (1971); p. 3594 - 3606, View in Reaxys

98 - 99

Shorygina; Elkin; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1970); p. 1052,1055; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1970); p. 1114, View in Reaxys

105 - 106

Kropf et al.; Tetrahedron Letters; (1969); p. 3427,3428, View in Reaxys

210 - 211

750

Desai,V.R. et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1969); p. 30 - 32, View in Reaxys; Davies; Kipping; Journal of the Chemical Society; vol. 99; (1911); p. 298, View in Reaxys

104 - 107

Harnden,M.R. et al.; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2095 - 2096, View in Reaxys

101 - 102

Clark-Lewis; Nair; Australian Journal of Chemistry; vol. 20; (1967); p. 2137,2147, View in Reaxys

211 - 212

Ivanov,K.I. et al.; Zhurnal Organicheskoi Khimii; vol. 3; nb. 12; (1967); p. 2120 - 2122,2069 - 2071, View in Reaxys

106 - 108

Kwart,H.; Hoster,D.P.; Journal of Organic Chemistry; vol. 32; (1967); p. 1867 - 1870, View in Reaxys; Tschelinzew; Chemische Berichte; vol. 37; (1904); p. 4539, View in Reaxys; Huston; Friedemann; Journal of the American Chemical Society; vol. 40; (1918); p. 791, View in Reaxys

120 - 124

Rand,L.; Dolinski,R.J.; Journal of Organic Chemistry; vol. 31; (1966); p. 4061 - 4066, View in Reaxys

92 - 94

Mamalis,P. et al.; Journal of Medicinal Chemistry; vol. 8; (1965); p. 684 - 691, View in Reaxys

Mamedov,S. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2877 - 2881,2910 - 2913, View in Reaxys

100 - 101

Almasi et al.; Revue Roumaine de Chimie; vol. 9; (1964); p. 531,538, View in Reaxys

97 - 98

Gelli et al.; Annali di Chimica (Rome, Italy); vol. 54; (1964); p. 1143,1146, View in Reaxys

90 - 91

Pines; Schappell; Journal of Organic Chemistry; vol. 29; (1964); p. 1503,1507, View in Reaxys

108.5 - 109.5

Stiles et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 3337,3341, View in Reaxys

123

Schostakowskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2620,2641, View in Reaxys

105 - 106

Schostakowskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2620,2641, View in Reaxys

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93 - 95

Achmatowicz; Szychowski; Roczniki Chemii; vol. 37; (1963); p. 963,966, View in Reaxys

110

Line't et al.; Arzneimittel Forschung; vol. 12; (1962); p. 347,348, View in Reaxys

108

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys

73 - 75

Cervinka; Collection of Czechoslovak Chemical Communications; vol. 27; (1962); p. 567,571, 572, View in Reaxys

217 - 219

715

Thakar; Rao; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 583,586, View in Reaxys

116

Miginiac-Groizeleau; Annales de Chimie (Cachan, France); vol. 6; nb. 13; (1961); p. 1071,1120, View in Reaxys

97 - 102

Lange et al.; Roczniki Chemii; vol. 35; (1961); p. 1645,1648, View in Reaxys

98 - 100

Christol et al.; Bulletin de la Societe Chimique de France; (1961); p. 2317, View in Reaxys

92 - 94

Banthorpe,D.V. et al.; Journal of the Chemical Society; (1960); p. 4054 - 4087, View in Reaxys

Cymerman-Craig et al.; Australian Journal of Chemistry; vol. 9; (1956); p. 397,402, View in Reaxys

103

Drumheller; Andrews; Journal of the American Chemical Society; vol. 77; (1955); p. 3290,3292, View in Reaxys

110

Zeiss; Tsutsui; Journal of the American Chemical Society; vol. 75; (1953); p. 897,899, View in Reaxys

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113.5 - 114

Delepine; Horeau; Bulletin de la Societe Chimique de France; vol. <5> 4; (1937); p. 31,41, View in Reaxys

Meerwein et al.; Journal fuer Praktische Chemie (Leipzig); vol. <2> 147; (1936); p. 226,239, View in Reaxys

105.5

Kailan; Schwebel; Monatshefte fuer Chemie; vol. 63; (1933); p. 52,67, View in Reaxys

213 - 215

740

Adkins; Cramer; Journal of the American Chemical Society; vol. 52; (1930); p. 4349,4354, View in Reaxys

105 - 106

Stephens; Journal of the American Chemical Society; vol. 50; (1928); p. 190, View in Reaxys

106 - 108

Norris; Cortese; Journal of the American Chemical Society; vol. 49; (1927); p. 2645, View in Reaxys

103

Vernimmen; Bulletin des Societes Chimiques Belges; vol. 33; (1924); p. 100; Chem. Zentralbl.; vol. 95; nb. II; (1924); p. 1341, View in Reaxys

102 - 103

Lepin; Reich; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 47; (1915); p. 153; Chem. Zentralbl.; vol. 87; nb. I; (1916); p. 787, View in Reaxys

128 - 128.4

Smith; Journal of the Chemical Society; vol. 105; (1914); p. 1709, View in Reaxys

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

15/229

2018-07-03 16:52:46

217 - 221

Kishner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 45; (1913); p. 953; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 2129, View in Reaxys

131 - 132

Davies; Kipping; Journal of the Chemical Society; vol. 99; (1911); p. 298, View in Reaxys

105 - 108

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys

108 - 110

120

Klages; Chemische Berichte; vol. 35; (1902); p. 2263; Chemische Berichte; vol. 38; (1905); p. 913, View in Reaxys

143

Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 322; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys

fluessig.

219 - 220

Decomposition.

212

Klages; Chemische Berichte; vol. 36; (1903); p. 621, View in Reaxys

Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 322; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys Barry; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1874); p. 535, View in Reaxys

Refractive Index (26) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

References

1.52

589

Ivanov,K.I. et al.; Zhurnal Organicheskoi Khimii; vol. 3; nb. 12; (1967); p. 2120 - 2122,2069 - 2071, View in Reaxys; Chen; Zhang; Yuan; Synthetic Communications; vol. 21; nb. 1; (1991); p. 107 - 109, View in Reaxys

1.43

589

Gocmen,M. et al.; Bulletin de la Societe Chimique de France; (1973); p. 1310 - 1317, View in Reaxys

1.5227

589

Schulz; Jassmann; Bekker; Die Pharmazie; vol. 26; nb. 8; (1971); p. 477 481, View in Reaxys

1.52

589

1.5191

589

Kropf et al.; Tetrahedron Letters; (1969); p. 3427,3428, View in Reaxys

1.5202

589

Harnden,M.R. et al.; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2095 - 2096, View in Reaxys

1.5208

589

Kwart,H.; Hoster,D.P.; Journal of Organic Chemistry; vol. 32; (1967); p. 1867 - 1870, View in Reaxys

1.5195

589

Clark-Lewis; Nair; Australian Journal of Chemistry; vol. 20; (1967); p. 2137,2147, View in Reaxys

1.5211

589

Ivanov,K.I. et al.; Zhurnal Organicheskoi Khimii; vol. 3; nb. 12; (1967); p. 2120 - 2122,2069 - 2071, View in Reaxys

1.5204

589

Rand,L.; Dolinski,R.J.; Journal of Organic Chemistry; vol. 31; (1966); p. 4061 - 4066, View in Reaxys

1.5194

589

Mamalis,P. et al.; Journal of Medicinal Chemistry; vol. 8; (1965); p. 684 691, View in Reaxys

1.5132

589

Gelli et al.; Annali di Chimica (Rome, Italy); vol. 54; (1964); p. 1143,1146, View in Reaxys

1.5216

589

Mamedov,S. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2877 - 2881,2910 - 2913, View in Reaxys

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2018-07-03 16:52:46

1.5212

589

Pines; Schappell; Journal of Organic Chemistry; vol. 29; (1964); p. 1503,1507, View in Reaxys

1.5182

589

Schostakowskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2620,2641, View in Reaxys

1.5257

589

Vernimmen; Bulletin des Societes Chimiques Belges; vol. 33; (1924); p. 100; Chem. Zentralbl.; vol. 95; nb. II; (1924); p. 1341, View in Reaxys; Line't et al.; Arzneimittel Forschung; vol. 12; (1962); p. 347,348, View in Reaxys

1.5215

589

Traynelis,V.J. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 2377 - 2383, View in Reaxys

1.5269

589

Lange et al.; Roczniki Chemii; vol. 35; (1961); p. 1645,1648, View in Reaxys

1.5233

589

Miginiac-Groizeleau; Annales de Chimie (Cachan, France); vol. 6; nb. 13; (1961); p. 1071,1120, View in Reaxys

1.5203

589

Banthorpe,D.V. et al.; Journal of the Chemical Society; (1960); p. 4054 4087, View in Reaxys

1.5182

589

Cymerman-Craig et al.; Australian Journal of Chemistry; vol. 9; (1956); p. 397,402, View in Reaxys

1.512

589

Drumheller; Andrews; Journal of the American Chemical Society; vol. 77; (1955); p. 3290,3292, View in Reaxys

1.512

589

Zeiss; Tsutsui; Journal of the American Chemical Society; vol. 75; (1953); p. 897,899, View in Reaxys

1.521

589

Nessmejanow; Ssasonowa; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1941); p. 499,510; Chem.Abstr.; (1943); p. 2724, View in Reaxys

1.5267

589

Glacet; Bulletin de la Societe Chimique de France; vol. <5> 5; (1938); p. 895,898, View in Reaxys

1.5124

589

Norris; Cortese; Journal of the American Chemical Society; vol. 49; (1927); p. 2645, View in Reaxys

Density (14) 1 of 14

Density [g·cm-3]

0.989

Reference Temperature [°C]

Measurement Temperature 22 [°C] Doiuchi; Minoura; Israel Journal of Chemistry; vol. 15; (1976); p. 84,85,87, View in Reaxys 2 of 14

Density [g·cm-3]

0.985

Reference Temperature [°C]

Measurement Temperature 15 [°C] Ivanov,K.I. et al.; Zhurnal Organicheskoi Khimii; vol. 3; nb. 12; (1967); p. 2120 - 2122,2069 - 2071, View in Reaxys 3 of 14

Density [g·cm-3]

0.9983

Reference Temperature [°C]

Measurement Temperature 20 [°C] Mamedov,S. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2877 - 2881,2910 - 2913, View in Reaxys 4 of 14

Density [g·cm-3]

0.996

Reference Temperature [°C]

17/229

2018-07-03 16:52:46

Measurement Temperature 20 [°C] Schostakowskii et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 2620,2641, View in Reaxys 5 of 14

Density [g·cm-3]

1.003

Reference Temperature [°C]

Measurement Temperature 20 [°C] Miginiac-Groizeleau; Annales de Chimie (Cachan, France); vol. 6; nb. 13; (1961); p. 1071,1120, View in Reaxys 6 of 14

Density [g·cm-3]

0.9938

Reference Temperature [°C]

Measurement Temperature 23 [°C] Nessmejanow; Ssasonowa; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1941); p. 499,510; Chem.Abstr.; (1943); p. 2724, View in Reaxys 7 of 14

Density [g·cm-3]

1.009

Reference Temperature [°C]

Measurement Temperature 17 [°C] Glacet; Bulletin de la Societe Chimique de France; vol. <5> 5; (1938); p. 895,898, View in Reaxys 8 of 14

Density [g·cm-3]

0.9915

Reference Temperature [°C]

Measurement Temperature 25 [°C] Norris; Cortese; Journal of the American Chemical Society; vol. 49; (1927); p. 2645, View in Reaxys 9 of 14

Density [g·cm-3]

1.0056

Reference Temperature [°C]

Measurement Temperature 20 [°C] Vernimmen; Bulletin des Societes Chimiques Belges; vol. 33; (1924); p. 100; Chem. Zentralbl.; vol. 95; nb. II; (1924); p. 1341, View in Reaxys 10 of 14

Density [g·cm-3]

1.0068

Reference Temperature [°C]

Measurement Temperature 15 [°C] Vernimmen; Bulletin des Societes Chimiques Belges; vol. 33; (1924); p. 100; Chem. Zentralbl.; vol. 95; nb. II; (1924); p. 1341, View in Reaxys 11 of 14

Density [g·cm-3]

1.0136

Reference Temperature [°C]

Smith; Journal of the Chemical Society; vol. 105; (1914); p. 1709, View in Reaxys 12 of 14

Density [g·cm-3]

0.994

Reference Temperature [°C]

18/229

2018-07-03 16:52:46

Measurement Temperature 23 [°C] Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 322; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys 13 of 14

Density [g·cm-3]

1.016

Reference Temperature [°C]

Measurement Temperature 0 [°C] Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 322; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys 14 of 14

Density [g·cm-3]

0.99

Measurement Temperature 15 [°C] Barry; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1874); p. 535, View in Reaxys Association (MCS) (1) 1 of 1

Description (Association (MCS))

Enthalpy of association

Walden,W. et al.; Tetrahedron; vol. 33; (1977); p. 419 - 421, View in Reaxys Chromatographic Data (6) Chromatographic Location data

References

HPLC (High performance liquid chromatography)

supporting informa- Renom-Carrasco, Marc; Gajewski, Piotr; Pignataro, Luca; De Vries, Johannes G.; Piarulli, tion Umberto; Gennari, Cesare; Lefort, Laurent; Advanced Synthesis and Catalysis; vol. 358; nb. 4; (2016); p. 515 - 519, View in Reaxys; Bornschein, Christoph; Gustafson, Karl P. J.; Verho, Oscar; Beller, Matthias; Bäckvall, Jan-E.; Chemistry - A European Journal; vol. 22; nb. 33; (2016); p. 11583 - 11586, View in Reaxys; Mazloomi, Zahra; Pretorius, René; Pàmies, Oscar; Albrecht, Martin; Diéguez, Montserrat; Inorganic Chemistry; vol. 56; nb. 18; (2017); p. 11282 11298, View in Reaxys; Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys

LC (Liquid chromatography)

supporting informa- Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); tion p. 2278 - 2281, View in Reaxys; Luecke, Marcel-Philip; Porwal, Digvijay; Kostenko, Arseni; Zhou, Yu-Peng; Yao, Shenglai; Keck, Matthias; Limberg, Christian; Oestreich, Martin; Driess, Matthias; Dalton Transactions; vol. 46; nb. 47; (2017); p. 16412 - 16418, View in Reaxys

GC (Gas chromatography)

supporting informa- Goek, Luetfiye; Tuerkmen, Hayati; Tetrahedron; vol. 69; nb. 49; (2013); p. 10669 - 10674, tion View in Reaxys; Rodriguez, Cristina; Borzecka, Wioleta; Sattler, Johann H.; Kroutil, Wolfgang; Lavandera, Ivan; Gotor, Vicente; Organic and Biomolecular Chemistry; vol. 12; nb. 4; (2014); p. 673 - 681, View in Reaxys; Nieto, Ismael; Wooten, Alfred J.; Robinson, Jerome R.; Carroll, Patrick J.; Schelter, Eric J.; Walsh, Patrick J.; Organometallics; vol. 32; nb. 24; (2013); p. 7431 - 7439, View in Reaxys; Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys; Vinson, Andrew R. S.; Davis, Victoria K.; Arunasalam, Arunamarie; Jesse, Kate A.; Hamilton, Rachael E.; Shattuck, Morgan A.; Hu, Allison C.; Iafe, Robert G.; Wenzel, Anna G.; Synlett; vol. 26; nb. 6; (2015); p. 765 - 770, View in Reaxys; Bigler, Raphael; Huber, Raffael; Mezzetti, Antonio; Angewandte Chemie - International Edition; vol. 54; nb. 17; (2014); p. 5171 - 5174; Angew. Chem.; vol. 127; nb. 17; (2014); p. 5260 - 5263,4, View in Reaxys; Rösler, Sina; Obenauf, Johannes; Kempe, Rhett; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 7998 - 8001, View in Reaxys; Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 - 2546, View in Reaxys; Çalik, Hatice Selvi; Ispir, Esin; Karabuga, Şemistan; Aslantas, Mehtet; Journal of Organometallic Chemistry; vol. 801; (2016); p. 122 - 129, View in Reaxys; Martínez-Montero, Lía; Gotor, Vicente; Gotor-Fernández, Vicente; Lavandera, Iván; Green Chemistry; vol. 19; nb. 2; (2017); p. 474 - 480, View in Reaxys

TLC (Thin layer chromatography)

supporting informa- Corre, Yann; Rysak, Vincent; Trivelli, Xavier; Agbossou-Niedercorn, Francine; Michon, tion Christophe; European Journal of Organic Chemistry; vol. 2017; nb. 32; (2017); p. 4820 - 4826, View in Reaxys

TLC (Thin layer chromatography)

Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys

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2018-07-03 16:52:46

GC (Gas chromatography)

Conformation (3) Object of Investiga- References tion Conformation

Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys; Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys

Conformation

Ditter; Luck; Berichte der Bunsen-Gesellschaft; vol. 73; (1969); p. 526,532, View in Reaxys; Laurent et al.; Bulletin de la Societe Chimique de France; (1967); p. 1995, View in Reaxys; Ivanov, Petko M.; Spassov, Stefan L.; Journal of Molecular Structure; vol. 145; (1986); p. 181 - 184, View in Reaxys

Energy difference between the conformers

Ivanov, Petko M.; Spassov, Stefan L.; Journal of Molecular Structure; vol. 145; (1986); p. 181 - 184, View in Reaxys

Crystal Property Description (9) Colour & Other Location Properties colourless

supporting informa- Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); tion p. 2278 - 2281, View in Reaxys; Zanardi, Mara M.; Botta, Mara C.; Surez, Alejandra G.; Tetrahedron Letters; vol. 55; nb. 42; (2014); p. 5832 - 5835, View in Reaxys; Peng, Dongjie; Zhang, Mintao; Huang, Zheng; Chemistry - A European Journal; vol. 21; nb. 42; (2015); p. 14737 14741, View in Reaxys; Wang, Ming-Hui; Chen, Ling-Yan; Tetrahedron Letters; vol. 58; nb. 8; (2017); p. 732 - 735, View in Reaxys; Xuan, Qingqing; Zhao, Cong; Song, Qiuling; Organic and Biomolecular Chemistry; vol. 15; nb. 24; (2017); p. 5140 - 5144, View in Reaxys; BruneauVoisine, Antoine; Wang, Ding; Dorcet, Vincent; Roisnel, Thierry; Darcel, Christophe; Sortais, Jean-Baptiste; Organic Letters; vol. 19; nb. 13; (2017); p. 3656 - 3659, View in Reaxys; Corre, Yann; Rysak, Vincent; Trivelli, Xavier; Agbossou-Niedercorn, Francine; Michon, Christophe; European Journal of Organic Chemistry; vol. 2017; nb. 32; (2017); p. 4820 - 4826, View in Reaxys; Wei, Duo; Bruneau-Voisine, Antoine; Chauvin, Téo; Dorcet, Vincent; Roisnel, Thierry; Valyaev, Dmitry A.; Lugan, Noël; Sortais, Jean-Baptiste; Advanced Synthesis and Catalysis; vol. 360; nb. 4; (2018); p. 676 - 681, View in Reaxys

yellow yellow

References

Wang, Rongzhou; Tang, Yawen; Xu, Meng; Meng, Chong; Li, Feng; Journal of Organic Chemistry; vol. 83; nb. 4; (2018); p. 2274 - 2281, View in Reaxys supporting informa- Liu, Ji-Tian; Yang, Shiyi; Tang, Weiping; Yang, Zhanhui; Xu, Jiaxi; Green Chemistry; vol. tion 20; nb. 9; (2018); p. 2118 - 2124, View in Reaxys

colourless

Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys; Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys; Song, Hai-Tao; Ding, Wei; Zhou, Quan-Quan; Liu, Jing; Lu, Liang-Qiu; Xiao, Wen-Jing; Journal of Organic Chemistry; vol. 81; nb. 16; (2016); p. 7250 - 7255, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys

colourless

supporting informa- Nixon, Tracy D.; Whittlesey, Michael K.; Williams, Jonathan M.J.; Tetrahedron Letters; vol. tion 52; nb. 49; (2011); p. 6652 - 6654, View in Reaxys; Lamani, Manjunath; Guralamata, Ravikumara Siddappa; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 52; (2012); p. 6583 - 6585, View in Reaxys

colourless

Werner, Thomas; Riahi, Abdol Majid; Schramm, Heiko; Synthesis; nb. 21; (2011); p. 3482 3490; Art.No: N59811SS, View in Reaxys

yellow

Bull, Steven D.; Davidson, Matthew G.; Johnson, Andrew L.; Mahon, Mary F.; Robinson, Diane E. J. E.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 612 - 620, View in Reaxys

brown

supporting informa- Maytum, Hannah C.; Francos, Javier; Whatrup, David J.; Williams, Jonathan M. J.; Chemtion istry - An Asian Journal; vol. 5; nb. 3; (2010); p. 538 - 542, View in Reaxys

light-brown Dynamic Viscosity (1) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys References

20/229

2018-07-03 16:52:46

0.1349

Thole; Journal of the Chemical Society; vol. 103; (1913); p. 24, View in Reaxys

Electrical Data (3) 1 of 3

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) frequency dependence. Object(s) of Study: temperature dependence Johari; Kalinovskaya; Vij; Journal of Chemical Physics; vol. 114; nb. 10; (2001); p. 4634 - 4642, View in Reaxys

2 of 3

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) frequency dependence. Object(s) of Study: temperature dependence Johari; Kalinovskaya; Vij; Journal of Chemical Physics; vol. 114; nb. 10; (2001); p. 4634 - 4642, View in Reaxys

3 of 3

Description (Electrical Da- Electrical properties ta) Mayeda; Journal of the American Chemical Society; vol. 97; (1975); p. 4012,4013, View in Reaxys; Dannhauser; Iohari; High Temperatures - High Pressures; vol. 4; (1972); p. 195,196-198, View in Reaxys

Further Information (4) Description (FurReferences ther Information) Further information Koeppel et al.; Tetrahedron; vol. 29; (1973); p. 1735,1741,1742,1743, View in Reaxys Further information Badger et al.; Australian Journal of Chemistry; vol. 20; (1967); p. 1439,1445, View in Reaxys Further information Arai; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 1032, View in Reaxys Further information Williams,J.F.A.; Tetrahedron; vol. 18; (1962); p. 1487 - 1493, View in Reaxys Liquid Phase (1) Description (Liquid References Phase) Supercoolability

Johari; Kalinovskaya; Vij; Journal of Chemical Physics; vol. 114; nb. 10; (2001); p. 4634 - 4642, View in Reaxys

Liquid/Liquid Systems (MCS) (1) 1 of 1

Description (Liquid/Liquid Distribution between solvent 1 and solvent 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Comment (Liquid/Liquid Systems (MCS))

phase 1= hexadecane; phase 2= water; distribution coefficient = 3.153

Partner (Liquid/Liquid Systems (MCS))

Hexadecane; water

Natesan, Senthil; Wang, Zhanbin; Lukacova, Viera; Peng, Ming; Subramaniam, Rajesh; Lynch, Sandra; Balaz, Stefan; Journal of Chemical Information and Modeling; vol. 53; nb. 6; (2013); p. 1424 - 1435, View in Reaxys Mechanical Properties (1) Description (MeReferences chanical Properties) Viscosity

Dannhauser; Iohari; High Temperatures - High Pressures; vol. 4; (1972); p. 195,196-198, View in Reaxys

Optical Rotatory Power (26) 1 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

11.9

Wavelength (Optical Rota- 589 tory Power) [nm] Saigo et al.; Chemistry Letters; (1979); p. 545, View in Reaxys 2 of 26

Type (Optical Rotatory Power)

[alpha]

21/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-0.284

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Noyori et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 3129, View in Reaxys 3 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

17.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Mukaiyama,T. et al.; Journal of the American Chemical Society; vol. 101; nb. 6; (1979); p. 1455 - 1460, View in Reaxys; Mukaiyama et al.; Chemistry Letters; (1978); p. 219,220,221, View in Reaxys 4 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-24.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Mukaiyama,T. et al.; Journal of the American Chemical Society; vol. 101; nb. 6; (1979); p. 1455 - 1460, View in Reaxys 5 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-23.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Asami et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 1869, View in Reaxys 6 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

8.36

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Giacomelli,G. et al.; Journal of Organic Chemistry; vol. 43; nb. 9; (1978); p. 1790 - 1793, View in Reaxys 7 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

17.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

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2018-07-03 16:52:46

Yamaguchi et al.; Journal of Organic Chemistry; vol. 42; (1977); p. 1578, View in Reaxys 8 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

0.13

Wavelength (Optical Rota- 350 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Doiuchi; Minoura; Israel Journal of Chemistry; vol. 15; (1976); p. 84,85,87, View in Reaxys 9 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

0.07

Wavelength (Optical Rota- 450 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Doiuchi; Minoura; Israel Journal of Chemistry; vol. 15; (1976); p. 84,85,87, View in Reaxys 10 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

0.03

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Doiuchi; Minoura; Israel Journal of Chemistry; vol. 15; (1976); p. 84,85,87, View in Reaxys 11 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

59.2

Wavelength (Optical Rota- 589 tory Power) [nm] Okamoto,K. et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1976); p. 1617 - 1627, View in Reaxys 12 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

35.8

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-2.21

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

23/229

2018-07-03 16:52:46

Hayashi,T. et al.; Journal of Organometallic Chemistry; vol. 112; (1976); p. 253 - 262, View in Reaxys 14 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

1.94

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Hayashi,T. et al.; Journal of Organometallic Chemistry; vol. 112; (1976); p. 253 - 262, View in Reaxys 15 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

23.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Vigneron; Jacquet; Tetrahedron; vol. 32; (1976); p. 939,944, View in Reaxys; Jacquet; Vigneron; Tetrahedron Letters; (1974); p. 2065, View in Reaxys 16 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-8.47

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yamamoto et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1555, View in Reaxys 17 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

17.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Meyers,A.I.; Kendall,P.M.; Tetrahedron Letters; nb. 14; (1974); p. 1337 - 1340, View in Reaxys 18 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

22.03

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Jacquet; Vigneron; Tetrahedron Letters; (1974); p. 2065, View in Reaxys 19 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-3.15

24/229

2018-07-03 16:52:46

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Giacomelli,G. et al.; Journal of Organic Chemistry; vol. 38; (1973); p. 2370 - 2376, View in Reaxys 20 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

6.54

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Cervinka,O.; Fusek,J.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 441 - 446, View in Reaxys 21 of 26

Type (Optical Rotatory Power)

[M]

Optical Rotatory Power [deg]

-4.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Battioni; Chodkiewicz; Bulletin de la Societe Chimique de France; (1972); p. 2068, View in Reaxys 22 of 26

Type (Optical Rotatory Power)

[M]

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Battioni; Chodkiewicz; Bulletin de la Societe Chimique de France; (1972); p. 2068, View in Reaxys 23 of 26

Type (Optical Rotatory Power)

[alpha]

Giacomelli et al.; Tetrahedron Letters; (1971); p. 4135, View in Reaxys 24 of 26

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-25.53

Wavelength (Optical Rota- 578 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Oki,M.; Kobayashi,K.; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1223 - 1229, View in Reaxys 25 of 26

Type (Optical Rotatory Power)

alpha

Optical Rotatory Power [deg]

-39.4

Wavelength (Optical Rota- 589 tory Power) [nm]

25/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Kwart,H. et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 5532 - 5540, View in Reaxys 26 of 26

Nasipuri; Sarker; Journal of the Indian Chemical Society; vol. 44; (1967); p. 165, View in Reaxys; Laurent et al.; Bulletin de la Societe Chimique de France; (1967); p. 1995, View in Reaxys

Other Thermochemical Data (2) Description (Other References Thermochemical Data) Entropy

Dannhauser; Iohari; High Temperatures - High Pressures; vol. 4; (1972); p. 195,196-198, View in Reaxys

Enthalpy

Dannhauser; Iohari; High Temperatures - High Pressures; vol. 4; (1972); p. 195,196-198, View in Reaxys

Partition octan-1-ol/water (MCS) (2) 1 of 2

log POW

1.77

Location

Paragraph 0081

Patent; The Procter and Gamble Company; Sturgis, David Arthur; LI, Jianjun Justin; FLICKINGER, Marc Adam; HUTCHINS, Virginia Tzung-Hwei; DIERSING, Steven Louis; WUJEK, Steven Michael; (22 pag.); US2018/64624; (2018); (A1) English, View in Reaxys 2 of 2

log POW

1.77

Location

Page/Page column 16

Patent; THE PROCTER & GAMBLE COMPANY; STURGIS, David, Arthur; LI, Jianjun, Justin; FLICKINGER, Marc, Adam; HUTCHINS, Virginia, Tzung-Hwei; DIERSING, Steven, Louis; WUJEK, Steven, Michael; (37 pag.); WO2018/48717; (2018); (A1) English, View in Reaxys Solubility (MCS) (4) 1 of 4

Comment (Solubility (MCS))

not soluble in water

Glotz, Gabriel; Knoechel, Donald J.; Podmore, Philip; Gruber-Woelfler, Heidrun; Kappe, C. Oliver; Organic Process Research and Development; vol. 21; nb. 5; (2017); p. 763 - 770, View in Reaxys 2 of 4

Comment (Solubility (MCS))

soluble in water

Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys 3 of 4

Comment (Solubility (MCS))

Soluble in acetonitrile

Afshari, Mozhgan; Gorjizadeh, Maryam; Afshar, Ghazal; Oriental Journal of Chemistry; vol. 29; nb. 4; (2013); p. 1675 1681, View in Reaxys 4 of 4

Saturation

in pure solvent

Ruelle, Paul; Kesselring, Ulrich W.; Journal of Pharmaceutical Sciences; vol. 86; nb. 2; (1997); p. 179 - 186, View in Reaxys Solution Behaviour (MCS) (1) 1 of 1

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Be- 20 - 90.5 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Stephenson; Stuart; Journal of Chemical and Engineering Data; vol. 31; nb. 1; (1986); p. 56 - 70, View in Reaxys Surface Tension (1) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C]

References

28.4 - 34.9

Smith; Journal of the Chemical Society; vol. 105; (1914); p. 1709, View in Reaxys

10 - 80

NMR Spectroscopy (97) 1 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

26/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Soares, Letiére C.; Alberto, Eduardo E.; Schwab, Ricardo S.; Taube, Paulo S.; Nascimento, Vanessa; Rodrigues, Oscar E. D.; Braga, Antonio L.; Organic and Biomolecular Chemistry; vol. 10; nb. 32; (2012); p. 6595 - 6599, View in Reaxys; Roy, Sudipta Raha; Sau, Samaresh Chandra; Mandal, Swadhin K.; Journal of Organic Chemistry; vol. 79; nb. 19; (2014); p. 9150 - 9160, View in Reaxys; Li, Ke; Niu, Jun-Long; Yang, Ming-Ze; Li, Zhen; Wu, Li-Yuan; Hao, Xin-Qi; Song, MaoPing; Organometallics; vol. 34; nb. 7; (2015); p. 1170 - 1176, View in Reaxys; Wang, Ming-Hui; Chen, Ling-Yan; Tetrahedron Letters; vol. 58; nb. 8; (2017); p. 732 - 735, View in Reaxys; Ichikawa, Tomohiro; Netsu, Moeko; Mizuno, Masahiro; Mizusaki, Tomoteru; Takagi, Yukio; Sawama, Yoshinari; Monguchi, Yasunari; Sajiki, Hironao; Advanced Synthesis and Catalysis; vol. 359; nb. 13; (2017); p. 2269 - 2279, View in Reaxys; Luecke, Marcel-Philip; Porwal, Digvijay; Kostenko, Arseni; Zhou, Yu-Peng; Yao, Shenglai; Keck, Matthias; Limberg, Christian; Oestreich, Martin; Driess, Matthias; Dalton Transactions; vol. 46; nb. 47; (2017); p. 16412 - 16418, View in Reaxys; Liu, Ji-Tian; Yang, Shiyi; Tang, Weiping; Yang, Zhanhui; Xu, Jiaxi; Green Chemistry; vol. 20; nb. 9; (2018); p. 2118 - 2124, View in Reaxys 2 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Roy, Sudipta Raha; Sau, Samaresh Chandra; Mandal, Swadhin K.; Journal of Organic Chemistry; vol. 79; nb. 19; (2014); p. 9150 - 9160, View in Reaxys; Varjosaari, Sami E.; Skrypai, Vladislav; Suating, Paolo; Hurley, Joseph J. M.; Gilbert, Thomas M.; Adler, Marc J.; European Journal of Organic Chemistry; vol. 2017; nb. 2; (2017); p. 229 - 232, View in Reaxys; Wang, Rongzhou; Tang, Yawen; Xu, Meng; Meng, Chong; Li, Feng; Journal of Organic Chemistry; vol. 83; nb. 4; (2018); p. 2274 - 2281, View in Reaxys 3 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Peng, Dongjie; Zhang, Mintao; Huang, Zheng; Chemistry - A European Journal; vol. 21; nb. 42; (2015); p. 14737 - 14741, View in Reaxys; Luecke, Marcel-Philip; Porwal, Digvijay; Kostenko, Arseni; Zhou, Yu-Peng; Yao, Shenglai; Keck, Matthias; Limberg, Christian; Oestreich, Martin; Driess, Matthias; Dalton Transactions; vol. 46; nb. 47; (2017); p. 16412 16418, View in Reaxys; Liu, Ji-Tian; Yang, Shiyi; Tang, Weiping; Yang, Zhanhui; Xu, Jiaxi; Green Chemistry; vol. 20; nb. 9; (2018); p. 2118 - 2124, View in Reaxys 4 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

27/229

2018-07-03 16:52:46

Varjosaari, Sami E.; Skrypai, Vladislav; Suating, Paolo; Hurley, Joseph J. M.; Gilbert, Thomas M.; Adler, Marc J.; European Journal of Organic Chemistry; vol. 2017; nb. 2; (2017); p. 229 - 232, View in Reaxys; Xuan, Qingqing; Zhao, Cong; Song, Qiuling; Organic and Biomolecular Chemistry; vol. 15; nb. 24; (2017); p. 5140 - 5144, View in Reaxys; Wang, Rongzhou; Tang, Yawen; Xu, Meng; Meng, Chong; Li, Feng; Journal of Organic Chemistry; vol. 83; nb. 4; (2018); p. 2274 - 2281, View in Reaxys 5 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

23.24

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Landaeta, Vanessa R.; Rosa, Abel D. Salazar-La; Rodríguez-Lugo, Rafael E.; Inorganica Chimica Acta; vol. 470; (2018); p. 303 - 311, View in Reaxys 6 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 400.1 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

28/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Dubey, Pooja; Gupta, Sonu; Singh, Ajai K.; Dalton Transactions; vol. 47; nb. 11; (2018); p. 3764 - 3774, View in Reaxys 9 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Dubey, Pooja; Gupta, Sonu; Singh, Ajai K.; Dalton Transactions; vol. 47; nb. 11; (2018); p. 3764 - 3774, View in Reaxys 10 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Bastug, Gulluzar; Dierick, Steve; Lebreux, Frederic; Marko, Istvan E.; Organic Letters; vol. 14; nb. 5; (2012); p. 1306 1309, View in Reaxys; Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys; Borah, Ashwini; Goswami, Limi; Neog, Kashmiri; Gogoi, Pranjal; Journal of Organic Chemistry; vol. 80; nb. 9; (2015); p. 4722 - 4728, View in Reaxys; Corre, Yann; Rysak, Vincent; Trivelli, Xavier; Agbossou-Niedercorn, Francine; Michon, Christophe; European Journal of Organic Chemistry; vol. 2017; nb. 32; (2017); p. 4820 - 4826, View in Reaxys 11 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Soares, Letiére C.; Alberto, Eduardo E.; Schwab, Ricardo S.; Taube, Paulo S.; Nascimento, Vanessa; Rodrigues, Oscar E. D.; Braga, Antonio L.; Organic and Biomolecular Chemistry; vol. 10; nb. 32; (2012); p. 6595 - 6599, View in Reaxys; Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys; Song, Hai-Tao; Ding, Wei; Zhou, Quan-Quan; Liu, Jing; Lu, Liang-Qiu; Xiao, WenJing; Journal of Organic Chemistry; vol. 81; nb. 16; (2016); p. 7250 - 7255, View in Reaxys; Wang, Ming-Hui; Chen, LingYan; Tetrahedron Letters; vol. 58; nb. 8; (2017); p. 732 - 735, View in Reaxys; Ichikawa, Tomohiro; Netsu, Moeko; Mizuno, Masahiro; Mizusaki, Tomoteru; Takagi, Yukio; Sawama, Yoshinari; Monguchi, Yasunari; Sajiki, Hironao; Advanced Synthesis and Catalysis; vol. 359; nb. 13; (2017); p. 2269 - 2279, View in Reaxys 12 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

29/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Zhao, Hua; Sun, Hongjian; Li, Xiaoyan; Organometallics; vol. 33; nb. 13; (2014); p. 3535 - 3539, View in Reaxys; Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys; Borah, Ashwini; Goswami, Limi; Neog, Kashmiri; Gogoi, Pranjal; Journal of Organic Chemistry; vol. 80; nb. 9; (2015); p. 4722 - 4728, View in Reaxys; Corre, Yann; Rysak, Vincent; Trivelli, Xavier; Agbossou-Niedercorn, Francine; Michon, Christophe; European Journal of Organic Chemistry; vol. 2017; nb. 32; (2017); p. 4820 - 4826, View in Reaxys 13 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 126 scopy) [MHz] Location

supporting information

Xuan, Qingqing; Zhao, Cong; Song, Qiuling; Organic and Biomolecular Chemistry; vol. 15; nb. 24; (2017); p. 5140 - 5144, View in Reaxys 14 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Bruneau-Voisine, Antoine; Wang, Ding; Dorcet, Vincent; Roisnel, Thierry; Darcel, Christophe; Sortais, Jean-Baptiste; Organic Letters; vol. 19; nb. 13; (2017); p. 3656 - 3659, View in Reaxys 15 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Bruneau-Voisine, Antoine; Wang, Ding; Dorcet, Vincent; Roisnel, Thierry; Darcel, Christophe; Sortais, Jean-Baptiste; Organic Letters; vol. 19; nb. 13; (2017); p. 3656 - 3659, View in Reaxys 16 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

30/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Boucher, Maria M.; Furigay, Maxwell H.; Quach, Phong K.; Brindle, Cheyenne S.; Organic Process Research and Development; vol. 21; nb. 9; (2017); p. 1394 - 1403, View in Reaxys 17 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Bouhachicha; Ngo Ndimba; Roisnel; Lalli; Argouarch; New Journal of Chemistry; vol. 41; nb. 12; (2017); p. 4767 - 4770, View in Reaxys 18 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Bouhachicha; Ngo Ndimba; Roisnel; Lalli; Argouarch; New Journal of Chemistry; vol. 41; nb. 12; (2017); p. 4767 - 4770, View in Reaxys 19 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Mazloomi, Zahra; Pretorius, René; Pàmies, Oscar; Albrecht, Martin; Diéguez, Montserrat; Inorganic Chemistry; vol. 56; nb. 18; (2017); p. 11282 - 11298, View in Reaxys 20 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys; Peng, Dongjie; Zhang, Mintao; Huang, Zheng; Chemistry - A European Journal; vol. 21; nb. 42; (2015); p. 14737 - 14741, View in Reaxys; Paul, Bhaskar; Chakrabarti, Kaushik; Kundu, Sabuj; Dalton Transactions; vol. 45; nb. 27; (2016); p. 11162 - 11171, View in Reaxys 21 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

31/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Song, Hai-Tao; Ding, Wei; Zhou, Quan-Quan; Liu, Jing; Lu, Liang-Qiu; Xiao, Wen-Jing; Journal of Organic Chemistry; vol. 81; nb. 16; (2016); p. 7250 - 7255, View in Reaxys 22 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Howells, Dean; Robiette, Raphael; Fang, Guang Y.; Knowles, Luke S.; Woodrow, Michael D.; Harvey, Jeremy N.; Aggarwal, Varinder K.; Organic and Biomolecular Chemistry; vol. 6; nb. 7; (2008); p. 1185 - 1189, View in Reaxys; Liu, Lijia; Long, Qing; Aoki, Toshiki; Zhang, Geng; Kaneko, Takashi; Teraguchi, Masahiro; Zhang, Chunhong; Wang, Yudan; Chirality; vol. 27; nb. 8; (2015); p. 454 - 458, View in Reaxys 23 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Murphree, S. Shaun; Mason, Jeremy D.; Bean, Theodore G.; Perry, Michelle C.; Synthetic Communications; vol. 42; nb. 13; (2012); p. 1979 - 1986, View in Reaxys; Prasad, Kavirayani R.; Revu, Omkar; Tetrahedron; vol. 69; nb. 39; (2013); p. 8422 - 8428, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys 24 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Prasad, Kavirayani R.; Revu, Omkar; Tetrahedron; vol. 69; nb. 39; (2013); p. 8422 - 8428, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys 25 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

tetrachloromethane

Frequency (NMR Spectro- 300 scopy) [MHz] Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys; Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys

32/229

2018-07-03 16:52:46

26 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

d(4)-methanol

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

tetrachloromethane

Frequency (NMR Spectro- 75 scopy) [MHz] Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys; Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys 29 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

d(4)-methanol

Frequency (NMR Spectro- 75 scopy) [MHz] Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys

33/229

2018-07-03 16:52:46

31 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Frequency (NMR Spectro- 300 scopy) [MHz] Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys 32 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectro- 75 scopy) [MHz] Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys 33 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

methanol

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethyl sulfoxide

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Shoola, Christopher O.; DelMastro, Thomas; Wu, Ruoqiu; Sowa, John R.; European Journal of Organic Chemistry; vol. 2015; nb. 8; (2015); p. 1670 - 1673, View in Reaxys 36 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

34/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Shoola, Christopher O.; DelMastro, Thomas; Wu, Ruoqiu; Sowa, John R.; European Journal of Organic Chemistry; vol. 2015; nb. 8; (2015); p. 1670 - 1673, View in Reaxys 37 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

[(2)H6]acetone

Location

supporting information

Bai, Wei; Lee, Ka-Ho; Tse, Sunny Kai San; Chan, Ka Wing; Lin, Zhenyang; Jia, Guochen; Organometallics; vol. 34; nb. 15; (2015); p. 3686 - 3698, View in Reaxys 38 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Bull, Steven D.; Davidson, Matthew G.; Johnson, Andrew L.; Mahon, Mary F.; Robinson, Diane E. J. E.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 612 - 620, View in Reaxys; Zanardi, Mara M.; Botta, Mara C.; Surez, Alejandra G.; Tetrahedron Letters; vol. 55; nb. 42; (2014); p. 5832 - 5835, View in Reaxys 39 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Shi, Lei; Wang, Yizhan; Li, Bao; Wu, Lixin; Dalton Transactions; vol. 43; nb. 24; (2014); p. 9177 - 9188, View in Reaxys 40 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Zanardi, Mara M.; Botta, Mara C.; Surez, Alejandra G.; Tetrahedron Letters; vol. 55; nb. 42; (2014); p. 5832 - 5835, View in Reaxys

35/229

2018-07-03 16:52:46

41 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys 42 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys 43 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Nieto, Ismael; Wooten, Alfred J.; Robinson, Jerome R.; Carroll, Patrick J.; Schelter, Eric J.; Walsh, Patrick J.; Organometallics; vol. 32; nb. 24; (2013); p. 7431 - 7439, View in Reaxys 44 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Maytum, Hannah C.; Francos, Javier; Whatrup, David J.; Williams, Jonathan M. J.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 538 - 542, View in Reaxys; Ford, Leigh; Atefi, Farzad; Singer, Robert D.; Scammells, Peter J.; European Journal of Organic Chemistry; nb. 5; (2011); p. 942 - 950, View in Reaxys; Nixon, Tracy D.; Whittlesey, Michael K.; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 52; nb. 49; (2011); p. 6652 - 6654, View in Reaxys; Bastug, Gulluzar; Dierick, Steve; Lebreux, Frederic; Marko, Istvan E.; Organic Letters; vol. 14; nb. 5; (2012); p. 1306 - 1309, View in Reaxys 45 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

36/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Zhou, Xiao-Yu; Wang, Duo-Sheng; Bao, Ming; Zhou, Yong-Gui; Tetrahedron Letters; vol. 52; nb. 22; (2011); p. 2826 - 2829, View in Reaxys; Zhao, Qiwu; Curran, Dennis P.; Malacria, Max; Fensterbank, Louis; Goddard, Jean-Philippe; Lacote, Emmanuel; Synlett; nb. 3; (2012); p. 433 - 437, View in Reaxys; Lamani, Manjunath; Guralamata, Ravikumara Siddappa; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 52; (2012); p. 6583 - 6585, View in Reaxys 46 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 270 scopy) [MHz] Location

supporting information

Kim, Jung Won; Koike, Takeshi; Kotani, Miyuki; Yamaguchi, Kazuya; Mizuno, Noritaka; Chemistry - A European Journal; vol. 14; nb. 13; (2008); p. 4104 - 4109, View in Reaxys; Imada, Yasushi; Iida, Hiroki; Kitagawa, Takahiro; Naota, Takeshi; Chemistry - A European Journal; vol. 17; nb. 21; (2011); p. 5908 - 5920, View in Reaxys 48 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 68 scopy) [MHz] Location

supporting information

Imada, Yasushi; Iida, Hiroki; Kitagawa, Takahiro; Naota, Takeshi; Chemistry - A European Journal; vol. 17; nb. 21; (2011); p. 5908 - 5920, View in Reaxys 49 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

37/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 300 scopy) [MHz] Werner, Thomas; Riahi, Abdol Majid; Schramm, Heiko; Synthesis; nb. 21; (2011); p. 3482 - 3490; Art.No: N59811SS, View in Reaxys 50 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Werner, Thomas; Riahi, Abdol Majid; Schramm, Heiko; Synthesis; nb. 21; (2011); p. 3482 - 3490; Art.No: N59811SS, View in Reaxys 51 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Nixon, Tracy D.; Whittlesey, Michael K.; Williams, Jonathan M.J.; Tetrahedron Letters; vol. 52; nb. 49; (2011); p. 6652 6654, View in Reaxys 52 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 270 scopy) [MHz] Location

supporting information

Imada, Yasushi; Kitagawa, Takahiro; Ohno, Takashi; Iida, Hiroki; Naota, Takeshi; Organic Letters; vol. 12; nb. 1; (2010); p. 32 - 35, View in Reaxys 53 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 68 scopy) [MHz] Location

supporting information

Imada, Yasushi; Kitagawa, Takahiro; Ohno, Takashi; Iida, Hiroki; Naota, Takeshi; Organic Letters; vol. 12; nb. 1; (2010); p. 32 - 35, View in Reaxys 54 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

38/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Bull, Steven D.; Davidson, Matthew G.; Johnson, Andrew L.; Mahon, Mary F.; Robinson, Diane E. J. E.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 612 - 620, View in Reaxys 55 of 97

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.4 scopy) [MHz] Location

supporting information

Maytum, Hannah C.; Francos, Javier; Whatrup, David J.; Williams, Jonathan M. J.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 538 - 542, View in Reaxys 56 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Sedelmeier, Joerg; Ley, Steven V.; Baxendale, Ian R.; Green Chemistry; vol. 11; nb. 5; (2009); p. 683 - 685, View in Reaxys 57 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Sedelmeier, Joerg; Ley, Steven V.; Baxendale, Ian R.; Green Chemistry; vol. 11; nb. 5; (2009); p. 683 - 685, View in Reaxys 58 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Yoshida; Miura; Nojima; Kusabayashi; Journal of the American Chemical Society; vol. 105; nb. 20; (1983); p. 6279 - 6285, View in Reaxys; Scheideman, Matthew; Wang, Guoqiang; Vedejs, Edwin; Journal of the American Chemical Society; vol. 130; nb. 27; (2008); p. 8669 - 8676, View in Reaxys 59 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

39/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 67.8 scopy) [MHz] Location

supporting information

Kim, Jung Won; Koike, Takeshi; Kotani, Miyuki; Yamaguchi, Kazuya; Mizuno, Noritaka; Chemistry - A European Journal; vol. 14; nb. 13; (2008); p. 4104 - 4109, View in Reaxys 61 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Gopinath, Rangam; Patel, Bhisma K.; Organic Letters; vol. 2; nb. 26; (2000); p. 4177 - 4180, View in Reaxys; Rist; Begtrup; Journal of the Chemical Society. Perkin Transactions 1; nb. 13; (2001); p. 1566 - 1568, View in Reaxys; Wipf, Peter; Wang, Xiaodong; Organic Letters; vol. 4; nb. 7; (2002); p. 1197 - 1199, View in Reaxys; Ahern, Theresa; Mueller-Bunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 71; nb. 20; (2006); p. 7596 - 7602, View in Reaxys; Chen, Tao; Liu, XuGuang; Shi, Min; Tetrahedron; vol. 63; nb. 23; (2007); p. 4874 - 4880, View in Reaxys 62 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Chen, Tao; Liu, Xu-Guang; Shi, Min; Tetrahedron; vol. 63; nb. 23; (2007); p. 4874 - 4880, View in Reaxys 63 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 300 scopy) [MHz] Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys 64 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

40/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 300 scopy) [MHz] Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys 65 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75 scopy) [MHz] Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys 66 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75 scopy) [MHz] Maytum, Hannah C.; Tavassoli, Bahareh; Williams, Jonathan M.J.; Organic Letters; vol. 9; nb. 21; (2007); p. 4387 - 4389, View in Reaxys 67 of 97

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spec- 1H NMR (CDCI3, 300 MHz, ppm): α 7.34-7.20 (m, 5H), 4.54 (t, J = 6.0 Hz, 1 H), 2.54 (brs, 1 H), troscopy) 1.86-1.64 (m, 2H), 0.88 (t, J = 6.0 Hz, 3H). Comment (NMR Spectroscopy)

Signals given

Patent; LI, Chao-Jun; WO2007/98608; (2007); (A1) English, View in Reaxys 68 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Brown, Herbert C.; Narasimhan, S.; Somayaji, Vishwanatha; Journal of Organic Chemistry; vol. 48; nb. 18; (1983); p. 3091 - 3096, View in Reaxys; Hayashi; Matsumoto; Ito; Tetrahedron Asymmetry; vol. 2; nb. 7; (1991); p. 601 - 612, View in Reaxys; Savoia, Diego; Tagliavini, Emilio; Trombini, Claudio; Umani-Ronchi, Achille; Journal of Organic Chemistry; vol. 46; (1981); p. 5344 - 5348, View in Reaxys; Guijarro, David; Guillena, Gabricia; Mancheno, Balbino; Yus, Miguel; Tetrahedron; vol. 50; nb. 11; (1994); p. 3427 - 3436, View in Reaxys; Suzuki, Noriyuki; Rousset, Christophe J.; Aoyagi, Koichiro; Kotora, Martin; Takahashi, Tamotsu; et al.; Journal of Organometallic Chemistry; vol. 473; nb. 1-2; (1994); p. 117 128, View in Reaxys; Iovel'; Rubina; Popelis; Gaukhman; Lukevits; Chemistry of Heterocyclic Compounds; vol. 32; nb. 3; (1996); p. 294 - 307, View in Reaxys; Uchiyama, Masanobu; Kameda, Mitsuyoshi; Mishima, Osamu; Yokoyama, Nobuko; Koike, Minako; Kondo, Yoshinori; Sakamoto, Takao; Journal of the American Chemical Society; vol. 120; nb. 20; (1998); p. 4934 - 4946, View in Reaxys; Maguire, Anita R.; Buckley, N. Rachael; O'Leary, Patrick; Ferguson, George; Journal of the

41/229

2018-07-03 16:52:46

Chemical Society - Perkin Transactions 1; nb. 24; (1998); p. 4077 - 4091, View in Reaxys; Kobayashi, Juta; Mori, Yuichiro; Kobayashi, Shu; Chemical Communications; nb. 40; (2006); p. 4227 - 4229, View in Reaxys 69 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Hatano, Manabu; Suzuki, Shinji; Ishihara, Kazuaki; Journal of the American Chemical Society; vol. 128; nb. 31; (2006); p. 9998 - 9999, View in Reaxys 70 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Suzuki, Shinji; Ishihara, Kazuaki; Journal of the American Chemical Society; vol. 128; nb. 31; (2006); p. 9998 - 9999, View in Reaxys 71 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Suzuki, Shinji; Ishihara, Kazuaki; Journal of the American Chemical Society; vol. 128; nb. 31; (2006); p. 9998 - 9999, View in Reaxys 72 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Kobayashi, Juta; Mori, Yuichiro; Kobayashi, Shu; Chemical Communications; nb. 40; (2006); p. 4227 - 4229, View in Reaxys 73 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Rist; Begtrup; Journal of the Chemical Society. Perkin Transactions 1; nb. 13; (2001); p. 1566 - 1568, View in Reaxys; Wipf, Peter; Wang, Xiaodong; Organic Letters; vol. 4; nb. 7; (2002); p. 1197 - 1199, View in Reaxys; Ahern, Theresa; MuellerBunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 71; nb. 20; (2006); p. 7596 - 7602, View in Reaxys

42/229

2018-07-03 16:52:46

74 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Horibe, Isao; Seo, Shujiro; Yoshimura, Yohko; Tori, Kazuo; Organic Magnetic Resonance; vol. 22; nb. 7; (1984); p. 428 430, View in Reaxys; Guijarro, David; Guillena, Gabricia; Mancheno, Balbino; Yus, Miguel; Tetrahedron; vol. 50; nb. 11; (1994); p. 3427 - 3436, View in Reaxys; Suzuki, Noriyuki; Rousset, Christophe J.; Aoyagi, Koichiro; Kotora, Martin; Takahashi, Tamotsu; et al.; Journal of Organometallic Chemistry; vol. 473; nb. 1-2; (1994); p. 117 - 128, View in Reaxys; Bloodworth, A. J.; Courtneidge, J. L.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 8; (1982); p. 1807 - 1810, View in Reaxys; Soloshonok; Tang; Hruby; Van Meervelt; Organic letters; vol. 3; nb. 3; (2001); p. 341 - 343, View in Reaxys; Hatzakis, Nikos S.; Smonou, Ioulia; Bioorganic Chemistry; vol. 33; nb. 4; (2005); p. 325 - 337, View in Reaxys; Kobayashi, Juta; Mori, Yuichiro; Kobayashi, Shu; Chemical Communications; nb. 40; (2006); p. 4227 - 4229, View in Reaxys 75 of 97

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spectroscopy)

Comment (NMR Spectroscopy)

Signals given

NMR (300 MHz, CDC13) 8 0.90 (t, 3H), 1.80 (m, 2H), 4.60 (m, 1H), 7.35 (m, 5H).

Patent; MONASH UNIVERSITY; WO2006/2470; (2006); (A1) English, View in Reaxys 76 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 499.739 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Law, Man Chun; Wong, Kwok-Yin; Chan, Tak Hang; Journal of Organic Chemistry; vol. 70; nb. 25; (2005); p. 10434 10439, View in Reaxys 77 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Hirano, Koji; Yorimitsu, Hideki; Oshima, Koichiro; Organic Letters; vol. 7; nb. 21; (2005); p. 4689 - 4691, View in Reaxys 78 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

43/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 500 scopy) [MHz] Hatzakis, Nikos S.; Smonou, Ioulia; Bioorganic Chemistry; vol. 33; nb. 4; (2005); p. 325 - 337, View in Reaxys 79 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Hatzakis, Nikos S.; Smonou, Ioulia; Bioorganic Chemistry; vol. 33; nb. 4; (2005); p. 325 - 337, View in Reaxys 80 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Yang, Xiao-Wu; Sheng, Jian-Heng; Da, Chao-Shan; Wang, Heng-Shan; Su, Wu; Wang, Rui; Chan, Albert S. C.; Journal of Organic Chemistry; vol. 65; nb. 2; (2000); p. 295 - 296, View in Reaxys; Dahmen, Stefan; Braese, Stefan; Chemical Communications; nb. 1; (2002); p. 26 - 27, View in Reaxys; Hu, Aiguo; Ngo, Helen L.; Lin, Wenbin; Organic Letters; vol. 6; nb. 17; (2004); p. 2937 - 2940, View in Reaxys; Rahman, Mohammed S.; Oliana, Marco; Hii, King Kuok; Tetrahedron Asymmetry; vol. 15; nb. 12; (2004); p. 1835 - 1840, View in Reaxys; Aggarwal, Varinder K.; Guang, Yu Fang; Schmidt, Andreas T.; Journal of the American Chemical Society; vol. 127; nb. 6; (2005); p. 1642 - 1643, View in Reaxys; Yun, Jaesook; Kim, Daesung; Yun, Hoseop; Chemical Communications; nb. 41; (2005); p. 5181 - 5183, View in Reaxys 81 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Original Text (NMR Spec- 1H NMR (CDCl3): α 7.31 (m, 5H), 4.55 (t, 3JH-H=6.6 Hz, 1H), 1.76 (m, 2H), 0.88 (t, 3JH-H=7.4 troscopy) Hz, 3H). Comment (NMR Spectroscopy)

Signals given

Patent; Lin, Wenbin; Hu, Aiguo; Ngo, Helen L.; US2004/192543; (2004); (A1) English, View in Reaxys 83 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

44/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Dahmen, Stefan; Braese, Stefan; Chemical Communications; nb. 1; (2002); p. 26 - 27, View in Reaxys 84 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Armstrong, Susan K.; Clunas, Scott; Synthesis; nb. 2; (2000); p. 281 - 288, View in Reaxys; Schinnerl, Marina; Seitz, Michael; Kaiser, Anja; Reiser, Oliver; Organic Letters; vol. 3; nb. 26; (2001); p. 4259 - 4262, View in Reaxys 85 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500.03 scopy) [MHz] Soloshonok; Tang; Hruby; Van Meervelt; Organic letters; vol. 3; nb. 3; (2001); p. 341 - 343, View in Reaxys 87 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500.03 scopy) [MHz] Soloshonok; Tang; Hruby; Van Meervelt; Organic letters; vol. 3; nb. 3; (2001); p. 341 - 343, View in Reaxys 88 of 97

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

45/229

2018-07-03 16:52:46

89 of 97

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Hayashi; Matsumoto; Ito; Tetrahedron Asymmetry; vol. 2; nb. 7; (1991); p. 601 - 612, View in Reaxys; Guijarro, David; Guillena, Gabricia; Mancheno, Balbino; Yus, Miguel; Tetrahedron; vol. 50; nb. 11; (1994); p. 3427 - 3436, View in Reaxys; Suzuki, Noriyuki; Rousset, Christophe J.; Aoyagi, Koichiro; Kotora, Martin; Takahashi, Tamotsu; et al.; Journal of Organometallic Chemistry; vol. 473; nb. 1-2; (1994); p. 117 - 128, View in Reaxys; Iovel'; Rubina; Popelis; Gaukhman; Lukevits; Chemistry of Heterocyclic Compounds; vol. 32; nb. 3; (1996); p. 294 - 307, View in Reaxys; Uchiyama, Masanobu; Kameda, Mitsuyoshi; Mishima, Osamu; Yokoyama, Nobuko; Koike, Minako; Kondo, Yoshinori; Sakamoto, Takao; Journal of the American Chemical Society; vol. 120; nb. 20; (1998); p. 4934 - 4946, View in Reaxys; Maguire, Anita R.; Buckley, N. Rachael; O'Leary, Patrick; Ferguson, George; Journal of the Chemical Society - Perkin Transactions 1; nb. 24; (1998); p. 4077 4091, View in Reaxys 90 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270.05 scopy) [MHz] Kataoka, Yasutaka; Makihira, Isamu; Utsunomiya, Masaru; Tani, Kazuhide; Journal of Organic Chemistry; vol. 62; nb. 24; (1997); p. 8540 - 8543, View in Reaxys 91 of 97

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Dao, Le Thi Anh; Blau, Karla; Pritzkow, Wilhelm; Schmidt-Renner, Wolfgang; Voerckel, Volkmar; Willecke, Lothar; Journal fuer Praktische Chemie (Leipzig); vol. 326; nb. 1; (1984); p. 73 - 80, View in Reaxys 93 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

pyridine-d5

Horibe, Isao; Seo, Shujiro; Yoshimura, Yohko; Tori, Kazuo; Organic Magnetic Resonance; vol. 22; nb. 7; (1984); p. 428 430, View in Reaxys 94 of 97

Description (NMR Spectroscopy)

Spin-spin coupling constants

Comment (NMR Spectroscopy)

1H-1H

Yoshida; Miura; Nojima; Kusabayashi; Journal of the American Chemical Society; vol. 105; nb. 20; (1983); p. 6279 - 6285, View in Reaxys

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95 of 97

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CCl4

Medlik-Balan, A.; Klein, J.; Tetrahedron; vol. 36; nb. 2; (1980); p. 299 - 304, View in Reaxys; Bourgain-Commercon, Monique; Normant, Jean F.; Bulletin de la Societe Chimique de France; vol. 2; nb. 5-6; (1980); p. 289 - 294, View in Reaxys 96 of 97

Description (NMR Spectroscopy)

NMR

Harnden,M.R. et al.; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2095 - 2096, View in Reaxys; Wenkert et al.; Phytochemistry (Elsevier); vol. 15; (1976); p. 1548, View in Reaxys; Nishiguchi et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 2803,2804, View in Reaxys; Dimmel et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 3092, View in Reaxys; Pepin et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 41,43, View in Reaxys 97 of 97

Description (NMR Spectroscopy)

NMR with shift reagents

Yamamoto et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1555, View in Reaxys IR Spectroscopy (15) 1 of 15

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Song, Hai-Tao; Ding, Wei; Zhou, Quan-Quan; Liu, Jing; Lu, Liang-Qiu; Xiao, Wen-Jing; Journal of Organic Chemistry; vol. 81; nb. 16; (2016); p. 7250 - 7255, View in Reaxys 3 of 15

Description (IR Spectroscopy)

Intensity of IR bands; Bands; Spectrum

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

chloroform

Borah, Ashwini; Goswami, Limi; Neog, Kashmiri; Gogoi, Pranjal; Journal of Organic Chemistry; vol. 80; nb. 9; (2015); p. 4722 - 4728, View in Reaxys 5 of 15

Description (IR Spectroscopy)

Bands; Spectrum

Location

supporting information

Shoola, Christopher O.; DelMastro, Thomas; Wu, Ruoqiu; Sowa, John R.; European Journal of Organic Chemistry; vol. 2015; nb. 8; (2015); p. 1670 - 1673, View in Reaxys 6 of 15

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys 7 of 15

Description (IR Spectroscopy)

Bands

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Tang, Yibo; Li, Zenghua; Ma, Dongjuan; Liu, Zhen; Asian Journal of Chemistry; vol. 25; nb. 15; (2013); p. 8677 - 8680, View in Reaxys 8 of 15

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat liquid

Maytum, Hannah C.; Francos, Javier; Whatrup, David J.; Williams, Jonathan M. J.; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 538 - 542, View in Reaxys; Lamani, Manjunath; Guralamata, Ravikumara Siddappa; Prabhu, Kandikere Ramaiah; Chemical Communications; vol. 48; nb. 52; (2012); p. 6583 - 6585, View in Reaxys 9 of 15

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent)

Imada, Yasushi; Iida, Hiroki; Kitagawa, Takahiro; Naota, Takeshi; Chemistry - A European Journal; vol. 17; nb. 21; (2011); p. 5908 - 5920, View in Reaxys 10 of 15

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Gopinath, Rangam; Patel, Bhisma K.; Organic Letters; vol. 2; nb. 26; (2000); p. 4177 - 4180, View in Reaxys 11 of 15

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3360 - 1453 cm**(-1)

Maguire, Anita R.; Buckley, N. Rachael; O'Leary, Patrick; Ferguson, George; Journal of the Chemical Society - Perkin Transactions 1; nb. 24; (1998); p. 4077 - 4091, View in Reaxys 12 of 15

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3350 - 1490 cm**(-1)

Guijarro, David; Guillena, Gabricia; Mancheno, Balbino; Yus, Miguel; Tetrahedron; vol. 50; nb. 11; (1994); p. 3427 - 3436, View in Reaxys 13 of 15

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3390 - 700 cm**(-1)

Savoia, Diego; Tagliavini, Emilio; Trombini, Claudio; Umani-Ronchi, Achille; Journal of Organic Chemistry; vol. 46; (1981); p. 5344 - 5348, View in Reaxys 14 of 15

Description (IR Spectroscopy)

Weitkamp,H.; Korte,F.; Tetrahedron; vol. 20; (1964); p. 2125 - 2135, View in Reaxys; Walden,W. et al.; Tetrahedron; vol. 33; (1977); p. 419 - 421, View in Reaxys; Ditter; Luck; Berichte der Bunsen-Gesellschaft; vol. 73; (1969); p. 526,532, View in Reaxys; Kirchner; Richter; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 81; (1972); p. 274, View in Reaxys; Kirchner; Richter; Berichte der Bunsen-Gesellschaft; vol. 81; (1977); p. 1250,1257, 1259, View in Reaxys 15 of 15

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1020 - 952 cm**(-1)

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Winstein; Trifan; Journal of the American Chemical Society; vol. 74; (1952); p. 1154,1159; Journal of the American Chemical Society; vol. 71; (1949); p. 2953, View in Reaxys Mass Spectrometry (16) Description (Mass Location Spectrometry) electron impact (EI); spectrum

Comment (Mass Spectrometry)

supporting information

References Ichikawa, Tomohiro; Netsu, Moeko; Mizuno, Masahiro; Mizusaki, Tomoteru; Takagi, Yukio; Sawama, Yoshinari; Monguchi, Yasunari; Sajiki, Hironao; Advanced Synthesis and Catalysis; vol. 359; nb. 13; (2017); p. 2269 - 2279, View in Reaxys

electron impact (EI); spectrum

Werner, Thomas; Bauer, Matthias; Riahi, Abdol Majid; Schramm, Heiko; European Journal of Organic Chemistry; vol. 2014; nb. 22; (2014); p. 4876 - 4883, View in Reaxys; Song, Hai-Tao; Ding, Wei; Zhou, QuanQuan; Liu, Jing; Lu, Liang-Qiu; Xiao, Wen-Jing; Journal of Organic Chemistry; vol. 81; nb. 16; (2016); p. 7250 - 7255, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); spectrum

Osako, Takao; Uozumi, Yasuhiro; Chemistry Letters; vol. 38; nb. 9; (2009); p. 902 - 903, View in Reaxys; Shoola, Christopher O.; DelMastro, Thomas; Wu, Ruoqiu; Sowa, John R.; European Journal of Organic Chemistry; vol. 2015; nb. 8; (2015); p. 1670 - 1673, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); spectrum

supporting information

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys

liquid chromatograsupporting informaphy mass spectrom- tion etry (LCMS); spectrum

Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 9; (2013); p. 2278 - 2281, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

Landwehr, Anne; Dudle, Balz; Fox, Thomas; Blacque, Olivier; Berke, Heinz; Chemistry - A European Journal; vol. 18; nb. 18; (2012); p. 5701 5714, View in Reaxys

GCMS (Gas chromatography mass spectrometry); EI (Electron impact)

Page/Page column 91

Patent; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA; BERGMAN, Robert; ELLMAN, Jonathan; NICHOLS, Jason; BISHOP, Lee; VOLKMAN, Jerome; TOSTE, Dean; SON, Sunghee; HARTWIG, John; SERGEEV, Alexey; WO2011/3029; (2011); (A2) English, View in Reaxys

EI (Electron impact); Spectrum

Werner, Thomas; Riahi, Abdol Majid; Schramm, Heiko; Synthesis; nb. 21; (2011); p. 3482 - 3490; Art.No: N59811SS, View in Reaxys

HRMS (High resolution mass spectrometry); ESI (Electrospray ionisation); Spectrum

Werner, Thomas; Riahi, Abdol Majid; Schramm, Heiko; Synthesis; nb. 21; (2011); p. 3482 - 3490; Art.No: N59811SS, View in Reaxys

spectrum

Fowley, Lissa A.; Lee, Jesse C.; Crabtree, Robert H.; Siegbahn, Per E. M.; Journal of Organometallic Chemistry; vol. 504; nb. 1-2; (1995); p. 57 68, View in Reaxys; Iovel'; Rubina; Popelis; Gaukhman; Lukevits; Chemistry of Heterocyclic Compounds; vol. 32; nb. 3; (1996); p. 294 - 307, View in Reaxys; Enthaler, Stephan; Jackstell, Ralf; Hagemann, Bernhard; Junge, Kathrin; Erre, Giulia; Beller, Matthias; Journal of Organometallic Chemistry; vol. 691; nb. 22; (2006); p. 4652 - 4659, View in Reaxys; Wiles, Charlotte; Watts, Paul; Haswell, Stephen J.; Tetrahedron Letters; vol. 47; nb. 30; (2006); p. 5261 - 5264, View in Reaxys

spectrum; electron impact (EI)

Guijarro, David; Guillena, Gabricia; Mancheno, Balbino; Yus, Miguel; Tetrahedron; vol. 50; nb. 11; (1994); p. 3427 - 3436, View in Reaxys; Marques, Carlos Alberto; Selva, Maurizio; Tundo, Pietro; Journal of Organic Chemistry; vol. 60; nb. 8; (1995); p. 2430 - 2435, View in Reaxys; Ursini, Cleber V.; Dias, Gilson H.M.; Rodrigues, J. Augusto R.; Journal of Organometallic Chemistry; vol. 690; nb. 13; (2005); p. 3176 - 3186, View in Reaxys

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metastable ions; IKE(S) (ion kinetic energy (spectrum)) spectrum; chemical ionization (CI)

My, Nguyen kieu; Schilling, Marita; Schwarz, Helmut; Organic Mass Spectrometry; vol. 22; (1987); p. 254 - 258, View in Reaxys Eichinger, Peter C. H.; Bowie, John H.; Blumenthal Thomas; Journal of Organic Chemistry; vol. 51; nb. 26; (1986); p. 5078 - 5082, View in Reaxys

spectrum

collisional activation; MIKE (mass ion kinetic energy)

Liehr, Joachim G.; Caprioli, Richard M.; Beynon, John H.; Morgan, Roger P.; Richter, Wilhelm J.; Organic Mass Spectrometry; vol. 15; nb. 3; (1980); p. 157 - 160, View in Reaxys Schwarz; Bohlmann; Tetrahedron Letters; (1972); p. 1899,1900, 1901, View in Reaxys; Koeppel et al.; Tetrahedron; vol. 29; (1973); p. 1735,1741,1742,1743, View in Reaxys

appearance potentials

Schwarz; Bohlmann; Tetrahedron Letters; (1972); p. 1899,1900, 1901, View in Reaxys

Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Rotational spectrum

Giuliano, Barbara M.; Ottaviani, Paolo; Favero, Laura B.; Caminati, Walther; Grabow, Jens-Uwe; Giardini, Anna; Satta, Mauro; Physical Chemistry Chemical Physics; vol. 9; nb. 32; (2007); p. 4460 - 4464, View in Reaxys

Raman Spectroscopy (2) Description (Ram- References an Spectroscopy) Bands; Spectrum

Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys

Spectrum; Bands

Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys

Use (9) Use Pattern Flavoring additive to biocidal compositions

References Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys to bactericidal compositions Flavoring additive to fungicidal compositions

Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys to anti-viral compositions Flavoring additive to sporicidal compositions

Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive to microbicidal compositions

Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive to pesticidal compositions

Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive to larvicidal compositions

Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys

Flavoring additive Patent; Schuer, Joerg; EP1206184; (2005); (B1) German, View in Reaxys to insecticidal compositions Quantum Chemical Calculations (3)

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Calculated Properties

Method (Quantum Chemical Calculations)

References

Atom distances, an- DFT - density func- Xavier; Periandy; Ramalingam; Spectrochimica Acta - Part A: Molecular and Biomolecular gles; IR bands, intional methods Spectroscopy; vol. 137; nb. 1; (2015); p. 306 - 320, View in Reaxys tensities, transition moments; Molecular orbitals; Electronic energy levels; Oscillator strength, transition probability; Dipole moment, dipole moment derivative; Heat capacity cp, cv IR bands, intensiHF - Hartree-Fock ties, transition mo- (calcns.) ments; Raman bands, intensities, transition moments; Atom distances, angles

Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys

IR bands, intensiDFT - density func- Xavier, S.; Periandy, S.; Ramalingam, S.; Spectrochimica Acta, Part A: Molecular and Biomoties, transition mo- tional methods lecular Spectroscopy; vol. 137; (2015); p. 306 - 320, View in Reaxys ments; Raman bands, intensities, transition moments; Atom distances, angles; NMR shifts, signals, intensities, transition moments; Molecular orbitals; Electronic energy levels; Electronegativity; Population analysis, charge distribution; Oscillator strength, transition probability; Dipole moment, dipole moment derivative; Polarizability, polarizability derivatives; Heat capacity cp, cv; Band structure Medchem (3) 1 of 3

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1906759View in Reaxys

Substance Name

1453634

Qualitative Results

sheep liver esterase inhibition pC = 5.30

Measurement Parameter

qualitative

Kier; Journal of Pharmaceutical Sciences; vol. 69; nb. 7; (1980); p. 807 - 810, View in Reaxys 2 of 3

Target Name

cpA [Aedes aegypti]

Target Synonyms

cpa

Target, Subunit, Species

cpA [Aedes aegypti]

Target Mutant/Chimera Details

cpA [Aedes aegypti]:Wild

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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3 of 3

Target Species (Bioactivity)

Aedes aegypti

Target Transfection

Non Transfected

Bioassay Category

In Vivo (Animal models)

Biological Species/NCBI ID

Aedes aegypti

Substance RN

1906759View in Reaxys

Substance Name

1-phenylpropan-1-ol

Measurement Parameter

activation spikes

Unit

s-1

Measurement Object

of cPA receptor

Quantitative value

-3.5

Target Name

cpA [Aedes aegypti]

Target Synonyms

cpa

Target, Subunit, Species

cpA [Aedes aegypti]

Target Mutant/Chimera Details

cpA [Aedes aegypti]:Wild

Target Species (Bioactivity)

Aedes aegypti

Target Transfection

Non Transfected

Substance Effect

Anti-Mosquito

Bioassay Category

In Vivo (Animal models)

Biological Species/NCBI ID

Aedes aegypti

Substance RN

1906759View in Reaxys

Substance Name

1-phenylpropan-1-ol

Measurement Parameter

inhibition rate

Unit

Measurement Object

cPA receptor activation

Quantitative value

5.7

Reaxys ID 2041556 View in Reaxys

2/3 CAS Registry Number: 613-87-6 Chemical Name: (S)-1-phenyl-1-propanol; 1-(S)-phenylpropanol Linear Structure Formula: C6H5CH(OH)CH2CH3 Molecular Formula: C9H12O Molecular Weight: 136.194 Type of Substance: isocyclic InChI Key: DYUQAZSOFZSPHD-VIFPVBQESA-N Note:

Substance Label (265) Label References 14a

Jimeno, Ciril; Pasto, Mireia; Riera, Antoni; Pericas, Miquel A.; Journal of Organic Chemistry; vol. 68; nb. 8; (2003); p. 3130 - 3138, View in Reaxys; Jarzyski, Szymon; Lesniak, Stanislaw; Pieczonka, Adam M.; Rachwalski, Michal; Tetrahedron Asymmetry; vol. 26; nb. 1; (2015); p. 35 - 40, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys

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Hayashi; Hirate; Kitayama; Tsuji; Torii; Uozumi; Journal of Organic Chemistry; vol. 66; nb. 4; (2001); p. 1441 1449, View in Reaxys; Hara, Nanami; Fujisawa, Shu; Fujita, Mizuki; Miyazawa, Mikako; Ochiai, Kazuma; Katsuda, Satoshi; Fujimoto, Tetsuya; Tetrahedron; vol. 74; nb. 2; (2018); p. 296 - 302, View in Reaxys

Bica, Katharina; Leder, Sonja; Mereiter, Kurt; Gaertner, Peter; Monatshefte fur Chemie; vol. 144; nb. 4; (2013); p. 447 - 453, View in Reaxys; Gonda, Tímea; Bérdi, Péter; Zupkó, István; Fülöp, Ferenc; Szakonyi, Zsolt; International Journal of Molecular Sciences; vol. 19; nb. 1; (2018); Art.No: 81, View in Reaxys

Paul, Caroline E.; Lavandera, Ivan; Gotor-Fernandez, Vicente; Kroutil, Wolfgang; Gotor, Vicente; ChemCatChem; vol. 5; nb. 12; (2013); p. 3875 - 3881, View in Reaxys; Popłoński, Jarosław; Reiter, Tamara; Kroutil, Wolfgang; ChemCatChem; vol. 10; nb. 4; (2018); p. 763 - 768, View in Reaxys

b'2

Wang, Ding; Bruneau-Voisine, Antoine; Sortais, Jean-Baptiste; Catalysis Communications; vol. 105; (2018); p. 31 36, View in Reaxys

Qin, Chao; Hou, Chuan-Jin; Liu, Hongzhu; Liu, Yan-Jun; Huang, De-Zhi; Hu, Xiang-Ping; Tetrahedron Letters; vol. 59; nb. 8; (2018); p. 719 - 722, View in Reaxys

(S)-10c

Qu, Ge; Lonsdale, Richard; Yao, Peiyuan; Li, Guangyue; Liu, Beibei; Reetz, Manfred T.; Sun, Zhoutong; ChemBioChem; vol. 19; nb. 3; (2018); p. 239 - 246, View in Reaxys

Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys

18a

Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys

Liu, Huan; Liu, Sensheng; Zhou, Haifeng; Liu, Qixing; Wang, Chunqin; RSC Advances; vol. 8; nb. 27; (2018); p. 14829 - 14832, View in Reaxys

Tashenov, Yerbolat; Daniels, Mathias; Robeyns, Koen; Van Meervelt, Luc; Dehaen, Wim; Suleimen, Yerlan M.; Szakonyi, Zsolt; Molecules; vol. 23; nb. 4; (2018); Art.No: Y, View in Reaxys

Szakonyi, Zsolt; Gonda, Tímea; Ötvös, Sándor Balázs; Fülöp, Ferenc; Tetrahedron Asymmetry; vol. 25; nb. 15; (2014); p. 1138 - 1145, View in Reaxys; Gonda, Tímea; Balázs, Attila; Tóth, Gábor; Fülöp, Ferenc; Szakonyi, Zsolt; Tetrahedron; vol. 73; nb. 18; (2017); p. 2638 - 2648, View in Reaxys

Cettolin, Mattia; Puylaert, Pim; Pignataro, Luca; Hinze, Sandra; Gennari, Cesare; de Vries, Johannes G.; ChemCatChem; vol. 9; nb. 16; (2017); p. 3125 - 3130, View in Reaxys

(S)-1P1P

Zhang, Shi-Yuan; Yang, Cheng-Xiong; Shi, Wei; Yan, Xiu-Ping; Cheng, Peng; Wojtas, Lukasz; Zaworotko, Michael J.; Chem; vol. 3; nb. 2; (2017); p. 281 - 289, View in Reaxys

(S)-5-61

Patent; Chinese Academy Of Sciences Shanghai Organic Chemistry Institute; Tang Wenjun; Li Chengxi; Wan Feng; (49 pag.); CN107445999; (2017); (A) Chinese, View in Reaxys

Salvi; Chattopadhyay; Tetrahedron; vol. 57; nb. 14; (2001); p. 2833 - 2839, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Liardo, Elisa; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Angewandte Chemie - International Edition; vol. 55; nb. 30; (2016); p. 8691 - 8695; Angew. Chem.; vol. 128; nb. 30; (2016); p. 8833 - 8837,5, View in Reaxys

Kamal, Ahmed; Sandbhor, Mahendra; Ramana; Tetrahedron Asymmetry; vol. 13; nb. 8; (2002); p. 815 - 820, View in Reaxys; Courmarcel, James; Mostefai, Naouel; Sirol, Sabine; Choppin, Sabine; Riant, Olivier; Israel Journal of Chemistry; vol. 41; nb. 4; (2001); p. 231 - 240, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Contente, Martina Letizia; Molinari, Francesco; Zambelli, Paolo; De Vitis, Valerio; Gandolfi, Raffaella; Pinto, Andrea; Romano, Diego; Tetrahedron Letters; vol. 55; nb. 51; (2014); p. 7051 - 7053, View in Reaxys; Renom-Carrasco, Marc; Gajewski, Piotr; Pignataro, Luca; De Vries, Johannes G.; Piarulli, Umberto; Gennari, Cesare; Lefort, Laurent; Advanced Synthesis and Catalysis; vol. 358; nb. 4; (2016); p. 515 - 519, View in Reaxys; Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys

Dong, Zhen-Rong; Li, Yan-Yun; Chen, Jian-Shan; Li, Bao-Zhu; Xing, Yan; Gao, Jing-Xing; Organic Letters; vol. 7; nb. 6; (2005); p. 1043 - 1045, View in Reaxys; Lee, Dong-Sheng; Chang, Shu-Ming; Ho, Chun-Ying; Lu, TaJung; Chirality; vol. 28; nb. 1; (2016); p. 65 - 71, View in Reaxys

(S)-3

Priego; Garcia Mancheno; Cabrera; Carretero; Chemical Communications; nb. 19; (2001); p. 2026 - 2027, View in Reaxys; Abato; Seto; Journal of the American Chemical Society; vol. 123; nb. 37; (2001); p. 9206 - 9207, View in Reaxys; Ghanem, Ashraf; Schurig, Volker; Tetrahedron Asymmetry; vol. 14; nb. 17; (2003); p. 2547 - 2555, View in Reaxys; Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron Asymmetry; vol. 16; nb. 4; (2005); p. 851 - 855, View in Reaxys; Mastranzo, Virginia M.; Santacruz, Ericka; Huelgas, Gabriela; Paz, Evelyn; Sosa-Rivadeneyra, Martha V.; Bernes, Sylvain; Juaristi, Eusebio; Quintero, Leticia; de Parrodi, Cecilia Anaya; Tetrahedron Asymmetry; vol. 17; nb. 11; (2006); p. 1663 - 1670, View in Reaxys; Manabe, Yoshiki; Shinohara, Kanako; Nakamura, Ha-

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nako; Teramoto, Hiro; Sakaguchi, Satoshi; Journal of Molecular Catalysis A: Chemical; vol. 421; (2016); p. 138 145, View in Reaxys (S)-5a

Ma, Gaoyuan; Deng, Jun; Sibi, Mukund P.; Angewandte Chemie - International Edition; vol. 53; nb. 44; (2014); p. 11818 - 11821; Angew. Chem.; vol. 53-126; nb. 44; (2014); p. 12180, View in Reaxys; Gao, De-Wei; Gu, Qing; You, Shu-Li; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2544 - 2547, View in Reaxys

(S)-9e

Frensch, Gustavo; Labes, Ricardo; Wosch, Celso Luiz; Munaretto, Laieli Dos Santos; Salomé, Kahlil Schwanka; Guerrero, Palimécio G.; Marques, Francisco A.; Tetrahedron Letters; vol. 57; nb. 3; (2016); p. 420 - 422, View in Reaxys

35&S%

Boyd, Derek R.; Sharma, Narain D.; Malone, John F.; Ljubez, Vera; Murphy, Deirdre; Shepherd, Steven D.; Allen, Christopher C. R.; Organic and Biomolecular Chemistry; vol. 14; nb. 9; (2016); p. 2651 - 2664, View in Reaxys

(S)-23a

Szakonyi, Zsolt; Csör, Árpád; Csámpai, Antal; Fülöp, Ferenc; Chemistry - A European Journal; vol. 22; nb. 21; (2016); p. 7163 - 7173, View in Reaxys

(S)-1o

Hernández, José G.; Frings, Marcus; Bolm, Carsten; ChemCatChem; vol. 8; nb. 10; (2016); p. 1769 - 1772, View in Reaxys

(S)-4c

Sun, Zhoutong; Li, Guangyue; Ilie, Adriana; Reetz, Manfred T.; Tetrahedron Letters; vol. 57; nb. 32; (2016); p. 3648 - 3651, View in Reaxys

(S)-15a

Zhang, Pengxiang; Yu, Jipan; Peng, Fei; Wu, Xudong; Jie, Jiyang; Liu, Can; Tian, Hua; Yang, Haijun; Fu, Hua; Chemistry - A European Journal; vol. 22; nb. 48; (2016); p. 17477 - 17484, View in Reaxys

Heldmann, Dieter K.; Seebach, Dieter; Helvetica Chimica Acta; vol. 82; nb. 7; (1999); p. 1096 - 1110, View in Reaxys; Li, Aipeng; Ye, Lidan; Guo, Fei; Yang, Xiaohong; Yu, Hongwei; Journal of Molecular Catalysis B: Enzymatic; vol. 117; (2015); p. 31 - 37, View in Reaxys

(S)-6

Shiina, Isamu; Konishi, Katsuhiko; Kuramoto, Yu-suke; Chemistry Letters; nb. 2; (2002); p. 164 - 165, View in Reaxys; Braese, Stefan; Dahmen, Stefan; Lauterwasser, Frank; Leadbeater, Nicholas E; Sharp, Emma L; Bioorganic and medicinal chemistry letters; vol. 12; nb. 14; (2002); p. 1849 - 1851, View in Reaxys; Reigada, Juliana B.; Tcacenco, Celize. M.; Andrade, Leandro H.; Kato, Massuo J.; Porto, Andre L.M.; Lago, Joao Henrique G.; Tetrahedron Asymmetry; vol. 18; nb. 9; (2007); p. 1054 - 1058, View in Reaxys; Escorihuela, Jorge; Altava, Beln; Burguete, M. Isabel; Luis, Santiago V.; RSC Advances; vol. 5; nb. 19; (2015); p. 14653 - 14662, View in Reaxys

Coldham, Iain; Patel, Jignesh J.; Raimbault, Sophie; Whittaker, David T. E.; Adams, Harry; Fang, Guang Y.; Aggarwal, Varinder K.; Organic Letters; vol. 10; nb. 1; (2008); p. 141 - 143, View in Reaxys; Faigl; Deák; Erdélyi; Holczbauer; Czugler; Nyerges; Mátravölgyi; Chirality; vol. 27; nb. 3; (2015); p. 216 - 222, View in Reaxys

(S)-2a

Cobb, Alexander J. A.; Marson, Charles M.; Tetrahedron Asymmetry; vol. 12; nb. 11; (2001); p. 1547 - 1550, View in Reaxys; Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1561 - 1568, View in Reaxys; El-Shehawy, Ashraf A.; Sugiyama, Kenji; Hirao, Akira; Tetrahedron Asymmetry; vol. 19; nb. 4; (2008); p. 425 - 434, View in Reaxys; Zheng, Gao-Wei; Liu, Xu-Yun; Zhang, Zhi-Jun; Tian, Ping; Lin, Guo-Qiang; Xu, Jian-He; RSC Advances; vol. 3; nb. 43; (2013); p. 20446 - 20449, View in Reaxys; Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys; Patent; RESEARCH & BUSINESS FOUNDATION SUNGKYUNKWAN UNIVERSITY; SONG, CHOON GEUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114445; (2015); (A) Korean, View in Reaxys

Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 2725, View in Reaxys; Wang, Xiaojuan; Zhao, Wenxian; Li, Gaowei; Liu, Guanjun; Wang, Jin; Wang, Mincan; Liu, Lantao; Tetrahedron Asymmetry; vol. 26; nb. 15-16; (2015); p. 815 - 820; Art.No: 59322, View in Reaxys

Pieczonka, Adam M.; Les̈niak, Stanisław; Jarzyński, Szymon; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 26; nb. 2-3; (2015); p. 148 - 151, View in Reaxys

Gajewski, Piotr; Renom-Carrasco, Marc; Facchini, Sofia Vailati; Pignataro, Luca; Lefort, Laurent; De Vries, Johannes G.; Ferraccioli, Raffaella; Forni, Alessandra; Piarulli, Umberto; Gennari, Cesare; European Journal of Organic Chemistry; vol. 2015; nb. 9; (2015); p. 1887 - 1893, View in Reaxys; Gajewski, Piotr; Renom-Carrasco, Marc; Facchini, Sofia Vailati; Pignataro, Luca; Lefort, Laurent; De Vries, Johannes G.; Ferraccioli, Raffaella; Piarulli, Umberto; Gennari, Cesare; European Journal of Organic Chemistry; vol. 2015; nb. 25; (2015); p. 5526 - 5536, View in Reaxys

Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys

(S)-7; (S)-7b; 7

Yoshida, Kazuhiro; Kamimura, Takumi; Kuwabara, Hiroshi; Yanagisawa, Akira; Chemical Communications; vol. 51; nb. 84; (2015); p. 15442 - 15445, View in Reaxys

32-S

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Szewczyk, Marcin; Stanek, Filip; Bezłada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3727 - 3731, View in Reaxys

Jones, Simon; Atherton; Tetrahedron Asymmetry; vol. 11; nb. 22; (2000); p. 4543 - 4548, View in Reaxys; Laufer, Radoslaw; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Canadian Journal of Chemistry; vol. 84; nb. 2; (2006); p. 356 - 369, View in Reaxys; Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 - 350, View in Reaxys

Bussche-Huennefeld, Joanna Linda v.; Seebach, Dieter; Tetrahedron; vol. 48; nb. 27; (1992); p. 5719 - 5730, View in Reaxys; Bauer, Tomasz; Tarasiuk, Joanna; Tetrahedron Letters; vol. 43; nb. 4; (2002); p. 687 - 689, View in Reaxys; Prasad, Kavirayani R.; Revu, Omkar; Tetrahedron; vol. 69; nb. 39; (2013); p. 8422 - 8428, View in Reaxys; Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys

(S)-17

Wipf, Peter; Wang, Xiaodong; Organic Letters; vol. 4; nb. 7; (2002); p. 1197 - 1199, View in Reaxys; Jurcik, Vaclav; Gilani, Mazhar; Wilhelm, Rene; European Journal of Organic Chemistry; nb. 22; (2006); p. 5103 - 5109, View in Reaxys; Marchalin, Stefan; Valigura, Dusan; Varecka, Ludovit; Lakatos, Boris; Vanekova, Monika; Baran, Peter; Lawson, Ata Martin; Daich, Adam; Monatshefte fur Chemie; vol. 145; nb. 5; (2014); p. 835 - 847, View in Reaxys

(S)-4

Keller, Felix; Rippert, Andreas Johannes; Helvetica Chimica Acta; vol. 82; nb. 1; (1999); p. 125 - 137, View in Reaxys; Adair, Gareth R. A.; Williams, Jonathan M. J.; Chemical Communications; nb. 25; (2007); p. 2608 2609, View in Reaxys; Janeczko, Tomasz; Kostrzewa-Suslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys

(S)-7

Rudolph, Jens; Hermanns, Nina; Bolm, Carsten; Journal of Organic Chemistry; vol. 69; nb. 11; (2004); p. 3997 4000, View in Reaxys; Kleijn, Henk; Rijnberg, Evelien; Jastrzebski, Johann T. B. H.; Van Koten, Gerard; Organic Letters; vol. 1; nb. 6; (1999); p. 853 - 855, View in Reaxys; Coronel, Camila; Arce, Gabriel; Iglesias, Cesar; Noguera, Cynthia Magallanes; Bonnecarrere, Paula Rodriguez; Giordano, Sonia Rodriguez; Gonzalez, David; Journal of Molecular Catalysis B: Enzymatic; vol. 102; (2014); p. 94 - 98, View in Reaxys

12a

Szakonyi, Zsolt; Balazs, Arpad; Martinek, Tamas A.; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 17; nb. 2; (2006); p. 199 - 204, View in Reaxys; Rodriguez-Escrich, Sergi; Reddy, Katamreddy Subba; Jimeno, Ciril; Colet, Gisela; Rodriguez-Escrich, Carles; Sola, Lluis; Vidal-Ferran, Anton; Pericas, Miquel A.; Journal of Organic Chemistry; vol. 73; nb. 14; (2008); p. 5340 - 5353, View in Reaxys; Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys

Rachwalski, Michal; Jarzynski, Szymon; Jasinski, Marcin; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 689 - 693, View in Reaxys; Li, Yanyun; Yu, Shenluan; Wu, Xiaofeng; Xiao, Jianliang; Shen, Weiyi; Dong, Zhenrong; Gao, Jingxing; Journal of the American Chemical Society; vol. 136; nb. 10; (2014); p. 4031 4039, View in Reaxys

(S)-37a

Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys

Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 - 2688, View in Reaxys

15g

Boukachabia, Mourad; Vriamont, Nicolas; Lambin, Dominique; Riant, Olivier; Aribi-Zouioueche, Louisa; Comptes Rendus Chimie; vol. 17; nb. 5; (2014); p. 403 - 412, View in Reaxys

ent-SRC 1240

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys

Hesse, Matthew J.; Essafi, Stephanie; Watson, Charlotte G.; Harvey, Jeremy N.; Hirst, David; Willis, Christine L.; Aggarwal, Varinder K.; Angewandte Chemie - International Edition; vol. 53; nb. 24; (2014); p. 6145 - 6149; Angew. Chem.; vol. 126; nb. 24; (2014); p. 6259 - 6263,5, View in Reaxys

1-PPP

Lin, Lang; Yu, Rongmin; Wu, Xiao-Yuan; Yang, Wen-Bin; Zhang, Jian; Guo, Xiang-Guang; Lin, Zu-Jin; Lu, Can-Zhong; Inorganic Chemistry; vol. 53; nb. 10; (2014); p. 4794 - 4796, View in Reaxys

S-6a

Karabuga, Semistan; Karakaya, Idris; Ulukanli, Sabri; Tetrahedron Asymmetry; vol. 25; nb. 10-11; (2014); p. 851 855, View in Reaxys

Zheng, Jun; You, Shu-Li; Chemical Communications; vol. 50; nb. 60; (2014); p. 8204 - 8207, View in Reaxys

Szaleniec, Maciej; Dudzik, Agnieszka; Kozik, Bartłomiej; Borowski, Tomasz; Heider, Johann; Witko, Małgorzata; Journal of Inorganic Biochemistry; vol. 139; (2014); p. 9 - 20, View in Reaxys

Kang, Guowei; Lin, Silong; Shiwakoti, Atul; Ni, Bukuo; Catalysis Communications; vol. 57; (2014); p. 111 - 114, View in Reaxys; Kang, Guowei; Lin, Silong; Shiwakoti, Atul; Ni, Bukuo; Catalysis Communications; vol. 57; (2014); p. 111 - 114, View in Reaxys

7; 9

Faigl, Ferenc; Erdlyi, Zsuzsa; Dek, Szilvia; Nyerges, Mikls; Mtravölgyi, Bla; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6891 - 6894, View in Reaxys

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Yin, Yue-Cai; Yu, Hui-Lei; Luan, Zheng-Jiao; Li, Ren-Jie; Ouyang, Peng-Fei; Liu, Jing; Xu, Jian-He; ChemBioChem; vol. 15; nb. 16; (2014); p. 2443 - 2449, View in Reaxys; Yin, Yue-Cai; Yu, Hui-Lei; Luan, Zheng-Jiao; Li, Ren-Jie; Ouyang, Peng-Fei; Liu, Jing; Xu, Jian-He; ChemBioChem; vol. 15; nb. 16; (2014); p. 2443 - 2449, View in Reaxys

Boyle, Grant A.; Govender, Thavendran; Kruger, Hendrik G.; Maguire, Glenn E.M.; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2661 - 2666, View in Reaxys; Csillag, Kinga; Szakonyi, Zsolt; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 24; nb. 9-10; (2013); p. 553 - 561, View in Reaxys

(S)-2k

Kuwano, Ryoichi; Sawamura, Masaya; Shirai, Junya; Takahashi, Masatoshi; Ito, Yoshihiko; Bulletin of the Chemical Society of Japan; vol. 73; nb. 2; (2000); p. 485 - 496, View in Reaxys; Rudolph, Jens; Schmidt, Frank; Bolm, Carsten; Advanced Synthesis and Catalysis; vol. 346; nb. 7; (2004); p. 867 - 872, View in Reaxys; Krabbe, Scott W.; Hatcher, Mark A.; Bowman, Roy K.; Mitchell, Mark B.; McClure, Michael S.; Johnson, Jeffrey S.; Organic Letters; vol. 15; nb. 17; (2013); p. 4560 - 4563, View in Reaxys

Liu, Shuanglong; Wolf, Christian; Organic Letters; vol. 9; nb. 16; (2007); p. 2965 - 2968, View in Reaxys; Cheng, Ying-Ni; Wu, Hsyueh-Liang; Wu, Ping-Yu; Shen, Ying-Ying; Uang, Biing-Jiun; Chemistry - An Asian Journal; vol. 7; nb. 12; (2012); p. 2921 - 2924, View in Reaxys; Gou, Shaohua; Ye, Zhongbin; Feng, Mingming; Jiang, Wenchao; Synthetic Communications; vol. 43; nb. 7; (2013); p. 941 - 950, View in Reaxys

10a

Na, Risong; Wang, Bo; Liu, Honglei; Bian, Qinghua; Zhong, Jiangchun; Wang, Min; Guo, Hongchao; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 622 - 627, View in Reaxys; Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys

tbl 4 ent 4 pdt

Hosoda, Naoya; Kamito, Hideaki; Takano, Miki; Takebe, Yoshitaka; Yamaguchi, Yoshitaka; Asami, Masatoshi; Tetrahedron; vol. 69; nb. 6; (2013); p. 1739 - 1746, View in Reaxys

Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys

Zhou, Han; Huang, Hanmin; ChemCatChem; vol. 5; nb. 8; (2013); p. 2253 - 2257, View in Reaxys

(S)-PPA

Li, Zi-Jian; Yao, Jia; Tao, Qian; Jiang, Long; Lu, Tong-Bu; Inorganic Chemistry; vol. 52; nb. 20; (2013); p. 11694 11696, View in Reaxys

Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys

Table 4, entry 2

Jiang, Heyan; Journal of Chemical Research; vol. 37; nb. 12; (2013); p. 761 - 763, View in Reaxys

(S)-10

Knollmueller, Max; Ferencic, Mathias; Gaertner, Peter; Tetrahedron Asymmetry; vol. 10; nb. 20; (1999); p. 3969 3975, View in Reaxys; Kostova, Kalina; Genov, Miroslav; Philipova, Irena; Dimitrov, Vladimir; Tetrahedron Asymmetry; vol. 11; nb. 16; (2000); p. 3253 - 3256, View in Reaxys; Jones; Butler; Richards; Tetrahedron Letters; vol. 41; nb. 48; (2000); p. 9351 - 9354, View in Reaxys; Bolm, Carsten; Tanyeli, Cihangir; Grenz, Achim; Dinter, Christian L.; Advanced Synthesis and Catalysis; vol. 344; nb. 6-7; (2002); p. 649 - 656, View in Reaxys; Munoz-Muniz, Omar; Juaristi, Eusebio; Journal of Organic Chemistry; vol. 68; nb. 10; (2003); p. 3781 - 3785, View in Reaxys; Takizawa, Shinobu; Patil, Mahesh L.; Marubayashi, Kazuyoshi; Sasai, Hiroaki; Tetrahedron; vol. 63; nb. 28; (2007); p. 6512 6528, View in Reaxys; Kataoka, Noriyuki; Okudomi, Masayuki; Chihara, Naoka; Matsumoto, Kazutsugu; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 615 - 621, View in Reaxys

(S)-1

Hodge, Philip; Sung, David W. L.; Stratford, Peter W.; Journal of the Chemical Society - Perkin Transactions 1; nb. 16; (1999); p. 2335 - 2342, View in Reaxys; Sung, David W. L.; Hodge, Philip; Stratford, Peter W.; Journal of the Chemical Society - Perkin Transactions 1; nb. 11; (1999); p. 1463 - 1472, View in Reaxys; Harada, Toshiro; Hiraoka, Yuki; Kusukawa, Takahiro; Marutani, Yasuhisa; Matsui, Shinichiro; Nakatsugawa, Masashi; Kanda, Koso; Organic Letters; vol. 5; nb. 26; (2003); p. 5059 - 5062, View in Reaxys; Bachu, Prabhakar; Gibson, Jennifer S.; Sperry, Jonathan; Brimble, Margaret A.; Tetrahedron Asymmetry; vol. 18; nb. 13; (2007); p. 1618 - 1624, View in Reaxys; Shiina, Isamu; Nakata, Kenya; Ono, Keisuke; Mukaiyama, Teruaki; Helvetica Chimica Acta; vol. 95; nb. 10; (2012); p. 1891 - 1911,21, View in Reaxys; Shiina, Isamu; Nakata, Kenya; Ono, Keisuke; Mukaiyama, Teruaki; Helvetica Chimica Acta; vol. 95; nb. 10; (2012); p. 1891 - 1911, View in Reaxys

(S)-26

Naito, Tatsuo; Yoneda, Takuma; Ito, Jun-Ichi; Nishiyama, Hisao; Synlett; vol. 23; nb. 20; (2012); p. 2957 - 2960, View in Reaxys

Tab.2, entry.1: prod. Dong, Zhi-Bing; Liu, Bing; Fang, Cao; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 693; nb. 1; (2008); p. 17 - 22, View in Reaxys (S)-41

Melgar-Fernandez, Roberto; Gonzalez-Olvera, Rodrigo; Olivares-Romero, J. Luis; Gonzalez-Lopez, Vianney; Romero-Ponce, Leticia; Ramirez-Zarate, Maria Del Refugio; Demare, Patricia; Regla, Ignacio; Juaristi, Eusebio; European Journal of Organic Chemistry; nb. 4; (2008); p. 655 - 672, View in Reaxys

(S)-16

Szakonyi, Zsolt; Hetenyi, Anasztazia; Fueloep, Ferenc; Tetrahedron; vol. 64; nb. 6; (2008); p. 1034 - 1039, View in Reaxys

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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(S)-30

Hernandez-Rodriguez, Marcos; Avila-Ortiz, Claudia Gabriela; Del Campo, Jorge M.; Hernandez-Romero, Delia; Rosales-Hoz, Maria J.; Juaristi, Eusebio; Australian Journal of Chemistry; vol. 61; nb. 5; (2008); p. 364 - 375, View in Reaxys

Taniguchi, Tomohiro; Fukuba, Taka-Aki; Nakatsuka, Shuhei; Hayase, Shuichi; Kawatsura, Motoi; Uno, Hidemitsu; Itoh, Toshiyuki; Journal of Organic Chemistry; vol. 73; nb. 10; (2008); p. 3875 - 3884, View in Reaxys

Table 1; entry 10

Sui-Seng, Christine; Freutel, Friederike; Lough, Alan J.; Morris, Robert H.; Angewandte Chemie - International Edition; vol. 47; nb. 5; (2008); p. 940 - 943, View in Reaxys

(S)-9n

Niu, Yan-Ning; Yan, Ze-Yi; Li, Gao-Qiang; Wei, Hai-Long; Gao, Guo-Lin; Wu, Lu-Yong; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 8; (2008); p. 912 - 920, View in Reaxys

(S)-1c

Muramatsu, Yusuke; Harada, Toshiro; Angewandte Chemie - International Edition; vol. 47; nb. 6; (2008); p. 1088 1090, View in Reaxys

(S)-Prod.8

Liu, Juntao; Wu, Yinuo; Li, Xingshu; Chan, Albert S.C.; Journal of Organometallic Chemistry; vol. 693; nb. 12; (2008); p. 2177 - 2180, View in Reaxys

(S)-13a

11b

Vinogradov; Mikhalev; Pavlov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 5; (2001); p. 843 - 845, View in Reaxys; Lavandera, Ivan; Kern, Alexander; Ferreira-Silva, Bianca; Glieder, Anton; De Wildeman, Stefaan; Kroutil, Wolfgang; Journal of Organic Chemistry; vol. 73; nb. 15; (2008); p. 6003 - 6005, View in Reaxys

Hwang, Chyuan-Der; Uang, Biing-Jiun; Tetrahedron Asymmetry; vol. 9; nb. 22; (1998); p. 3979 - 3984, View in Reaxys; Salvi, Neeta A.; Chattopadhyay, Subrata; Tetrahedron Asymmetry; vol. 19; nb. 16; (2008); p. 1992 1997, View in Reaxys

Zolle, Ilse M.; Berger, Michael L.; Hammerschmidt, Friedrich; Hahner, Stefanie; Schirbel, Andreas; Peric-Simov, Biljana; Journal of Medicinal Chemistry; vol. 51; nb. 7; (2008); p. 2244 - 2253, View in Reaxys

(S)-9

Paleo, M. Rita; Cabeza, Isabel; Sardina, F. Javier; Journal of Organic Chemistry; vol. 65; nb. 7; (2000); p. 2108 2113, View in Reaxys; Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron; vol. 59; nb. 50; (2003); p. 10009 - 10012, View in Reaxys; Jones, Geraint; Richards, Christopher J.; Tetrahedron Asymmetry; vol. 15; nb. 4; (2004); p. 653 664, View in Reaxys; Du, Haifeng; Zhang, Xue; Wang, Zheng; Ding, Kuiling; Tetrahedron; vol. 61; nb. 40; (2005); p. 9465 - 9477, View in Reaxys; Birman, Vladimir B.; Jiang, Hui; Li, Ximin; Organic Letters; vol. 9; nb. 17; (2007); p. 3237 - 3240, View in Reaxys; Rachwalski, Michal; Kwiatkowska, Malgorzata; Drabowicz, Jozef; Klos, Marcin; Wieczorek, Wanda M.; Szyrej, Malgorzata; Sieron, Leslaw; Kielbasinski, Piotr; Tetrahedron Asymmetry; vol. 19; nb. 17; (2008); p. 2096 - 2101, View in Reaxys

(S)-2c

Shaikh, Nadim S.; Enthaler, Stephan; Junge, Kathrin; Beller, Matthias; Angewandte Chemie - International Edition; vol. 47; nb. 13; (2008); p. 2497 - 2501, View in Reaxys

(S)-3b

Zhang, Huichang; Chan, Kin Shing; Journal of the Chemical Society - Perkin Transactions 1; nb. 4; (1999); p. 381 382, View in Reaxys; He, Wei; Zhang, Bang-Le; Jiang, Ru; Liu, Peng; Sun, Xiao-Li; Zhang, Sheng-Yong; Tetrahedron Letters; vol. 47; nb. 30; (2006); p. 5367 - 5370, View in Reaxys; Patent; THE HONG KONG POLYTECHNIC UNIVERSITY; US2008/269490; (2008); (A1) English, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys

S-product Table 3 E. 1

Hua, Genghong; Liu, Delong; Xie, Fang; Zhang, Wanbin; Tetrahedron Letters; vol. 48; nb. 3; (2007); p. 385 - 388, View in Reaxys

Product, Tab.1, run 1

Omote, Masaaki; Tanaka, Naoya; Tarui, Atsushi; Sato, Kazuyuki; Kumadaki, Itsumaro; Ando, Akira; Tetrahedron Letters; vol. 48; nb. 17; (2007); p. 2989 - 2991, View in Reaxys

Clive, Derrick L. J.; Stoffman, Elia J. L.; Chemical Communications; nb. 21; (2007); p. 2151 - 2153, View in Reaxys

Tab. 5, entry 5

Kantam, M. Lakshmi; Laha, Soumi; Yadav, Jagjit; Likhar, Pravin R.; Sreedhar; Choudary; Advanced Synthesis and Catalysis; vol. 349; nb. 10; (2007); p. 1797 - 1802, View in Reaxys

Table 3, entry 4

Tanyeli, Cihangir; Odabas, Serhat; Erdem, Mine; Cakir, Esen; Keskin, Eda; Tetrahedron Asymmetry; vol. 18; nb. 19; (2007); p. 2349 - 2357, View in Reaxys

(S)-product, R=Ph

Jiang, Fu-Yong; Liu, Bing; Dong, Zhi-Bing; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 692; nb. 20; (2007); p. 4377 - 4380, View in Reaxys

13, Tab.2; entry 2

Casarotto, Virginie; Li, Zhongtao; Boucau, Julie; Lin, Yun-Ming; Tetrahedron Letters; vol. 48; nb. 31; (2007); p. 5561 - 5564, View in Reaxys

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(-)-(S)-47

Driver, Tom G.; Harris, Jason R.; Woerpel; Journal of the American Chemical Society; vol. 129; nb. 13; (2007); p. 3836 - 3837, View in Reaxys

(S)-10a

Reddy, Katamreddy Subba; Sola, Lluis; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Journal of Organic Chemistry; vol. 64; nb. 11; (1999); p. 3969 - 3974, View in Reaxys; Wilken, Joerg; Erny, Silke; Wassmann, Suzanne; Martens, Juergen; Tetrahedron Asymmetry; vol. 11; nb. 10; (2000); p. 2143 - 2148, View in Reaxys; Enthaler, Stephan; Hagemann, Bernhard; Bhor, Santosh; Anilkumar, Gopinathan; Tse, Man Kin; Bitterlich, Bianca; Junge, Kathrin; Erre, Giulia; Beller, Matthias; Advanced Synthesis and Catalysis; vol. 349; nb. 6; (2007); p. 853 - 860, View in Reaxys

(S)-1, T3, E1-7

Shiina, Isamu; Nakata, Kenya; Tetrahedron Letters; vol. 48; nb. 47; (2007); p. 8314 - 8317, View in Reaxys

(S)-7a

Palmieri, Gianni; European Journal of Organic Chemistry; nb. 4; (1999); p. 805 - 811, View in Reaxys; Nagaoka; Kayahara; Wakabayashi; Bioscience, biotechnology, and biochemistry; vol. 65; nb. 3; (2001); p. 634 - 637, View in Reaxys; Bandini, Marco; Melucci, Manuela; Piccinelli, Fabio; Sinisi, Riccardo; Tommasi, Simona; Umani-Ronchi, Achille; Chemical Communications; nb. 43; (2007); p. 4519 - 4521, View in Reaxys

Tab 3/6 (S)-product Eagon, Scott; Kim, Jinsoo; Yan, Katie; Haddenham, Dustin; Singaram, Bakthan; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 9025 - 9029, View in Reaxys Table 3, entry 1

Nakamura, Yutaka; Takeuchi, Seiji; Okumura, Kazuo; Ohgo, Yoshiaki; Tetrahedron; vol. 57; nb. 26; (2001); p. 5565 - 5571, View in Reaxys; Liu, Bing; Jiang, Fu-Yong; Song, Hai-Bin; Li, Jin-Shan; Tetrahedron Asymmetry; vol. 17; nb. 14; (2006); p. 2149 - 2153, View in Reaxys

(S)-4b

Pavlov; Vinogradov; Starodubtseva; Chel'tsova; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 4; (2001); p. 734 - 735, View in Reaxys; Spivey, Alan C.; Arseniyadis, Stellios; Fekner, Tomasz; Maddaford, Adrian; Leese, David P.; Tetrahedron; vol. 62; nb. 2-3; (2006); p. 295 - 301, View in Reaxys

(S)-8b

Maillard, David; Pozzi, Gianluca; Quici, Silvio; Sinou, Denis; Tetrahedron; vol. 58; nb. 20; (2002); p. 3971 - 3976, View in Reaxys; Matsumura, Yoshihiro; Ogura, Kanako; Kouchi, Yoshimi; Iwasaki, Fumiaki; Onomura, Osamu; Organic Letters; vol. 8; nb. 17; (2006); p. 3789 - 3792, View in Reaxys; Bandini, Marco; Bottoni, Andrea; Cozzi, Pier Giorgio; Miscione, Gian Pietro; Monari, Magda; Pierciaccante, Rossana; Umani-Ronchi, Achille; European Journal of Organic Chemistry; nb. 20; (2006); p. 4596 - 4608, View in Reaxys

Table 2, entry 1

Huang, Hanmin; Zheng, Zhuo; Chen, Huilin; Bai, Changmin; Wang, Junwei; Tetrahedron Asymmetry; vol. 14; nb. 10; (2003); p. 1285 - 1289, View in Reaxys; Wang, Min-Can; Hou, Xue-Hui; Chi, Chao-Xian; Tang, Ming-Sheng; Tetrahedron Asymmetry; vol. 17; nb. 14; (2006); p. 2126 - 2132, View in Reaxys

(S)-5b

Vinogradov; Gorshkova; Chel'tsova; Pavlov; Razmanov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 52; nb. 2; (2003); p. 471 - 479, View in Reaxys; Birman, Vladimir B.; Li, Ximin; Organic Letters; vol. 8; nb. 7; (2006); p. 1351 - 1354, View in Reaxys

Tab.2. run 1, product

Guo, Qun-Sheng; Lu, Yong-Na; Liu, Bing; Xiao, Jian; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 691; nb. 6; (2006); p. 1282 - 1287, View in Reaxys

(S)-23j

Schiffers, Ingo; Rantanen, Toni; Schmidt, Frank; Bergmans, Werner; Zani, Lorenzo; Bolm, Carsten; Journal of Organic Chemistry; vol. 71; nb. 6; (2006); p. 2320 - 2331, View in Reaxys

9-(S)

Roudeau, Remi; Gomez Pardo, Domingo; Cossy, Janine; Tetrahedron; vol. 62; nb. 10; (2006); p. 2388 - 2394, View in Reaxys

Yang, Wei; Xu, Jian-He; Xie, Yan; Xu, Yi; Zhao, Gang; Lin, Guo-Qiang; Tetrahedron Asymmetry; vol. 17; nb. 12; (2006); p. 1769 - 1774, View in Reaxys

5a (S) (minor)

MacLeod, Patricia D.; Li, Zhiping; Feng, Jianqing; Li, Chao-Jun; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6791 - 6794, View in Reaxys

4b, S

Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys

(S)-6i

Reetz, Manfred T.; Li, Xiaoguang; Journal of the American Chemical Society; vol. 128; nb. 4; (2006); p. 1044 - 1045, View in Reaxys

(S) pr. table 1.

Bauer, Michael; Kazmaier, Uli; Journal of Organometallic Chemistry; vol. 691; nb. 10; (2006); p. 2155 - 2158, View in Reaxys

(S)-9a, Tab 3, entry 1

Mino, Takashi; Suzuki, Atsushi; Yamashita, Masakazu; Narita, Shusaku; Shirae, Yoshiaki; Sakamoto, Masami; Fujita, Tsutomu; Journal of Organometallic Chemistry; vol. 691; nb. 20; (2006); p. 4297 - 4303, View in Reaxys

(S)-6f

Anwar, Shaik; Periasamy, Mariappan; Tetrahedron Asymmetry; vol. 17; nb. 23; (2006); p. 3244 - 3247, View in Reaxys

Malkov, Andrei V.; Stewart Liddon, Angus J. P.; Ramirez-Lopez, Pedro; Bendova, Lada; Haigh, David; Kocovsky, Pavel; Angewandte Chemie - International Edition; vol. 45; nb. 9; (2006); p. 1432 - 1435, View in Reaxys

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Tab 1/8-9 Product(S)

Cortez, Norma A.; Rodriguez-Apodaca, Ramon; Aguirre, Gerardo; Parra-Hake, Miguel; Cole, Thomas; Somanathan, Ratnasamy; Tetrahedron Letters; vol. 47; nb. 48; (2006); p. 8515 - 8518, View in Reaxys

15a

Zhang, Yi-Li; Zhang, Feng; Tang, Wei-Jun; Wu, Qing-Lai; Fan, Qing-Hua; Synlett; nb. 8; (2006); p. 1250 - 1254, View in Reaxys

(S)PhCH(OH)CH2CH 3

Bulman Page, Philip C.; Allin, Steven M.; Maddocks, Suzanne J.; Elsegood, Mark R.J.; Journal of the Chemical Society. Perkin Transactions 1; nb. 24; (2002); p. 2827 - 2832, View in Reaxys; Harada, Toshiro; Nakatsugawa, Masashi; Synlett; nb. 2; (2006); p. 321 - 323, View in Reaxys

(S)-11

Bolm, Carsten; Dinter, Christian L.; Seger, Andreas; Hoecker, Hartwig; Brozio, Joerg; Journal of Organic Chemistry; vol. 64; nb. 16; (1999); p. 5730 - 5731, View in Reaxys; Bauer, Tomasz; Tarasiuk, Joanna; Paniczek, Konrad; Tetrahedron Asymmetry; vol. 13; nb. 1; (2002); p. 77 - 82, View in Reaxys; Braun, Manfred; Fleischer, Ralf; Mai, Brigitte; Schneider, Marc-Andre; Lachenicht, Stefan; Advanced Synthesis and Catalysis; vol. 346; nb. 4; (2004); p. 474 - 482, View in Reaxys; Danilova, Tatyana I.; Rozenberg, Valeria I.; Starikova, Zoya A.; Braese, Stefan; Tetrahedron Asymmetry; vol. 15; nb. 2; (2004); p. 223 - 229, View in Reaxys; Emmerson, Daniel P G; Villard, Renaud; Mugnaini, Claudia; Batsanov, Andrei; Howard, Judith A K; Hems, William P; Tooze, Robert P; Davis, Benjamin G; Organic and biomolecular chemistry; vol. 1; nb. 21; (2003); p. 3826 - 3838, View in Reaxys; Takizawa, Shinobu; Patil, Mahesh L.; Yonezawa, Fumiko; Marubayashi, Kazuyoshi; Tanaka, Hiroyuki; Kawai, Tomoji; Sasai, Hiroaki; Tetrahedron Letters; vol. 46; nb. 7; (2005); p. 1193 - 1197, View in Reaxys; Kourist, Robert; Gonzalez-Sabin, Javier; Liz, Ramon; Rebolledo, Francisca; Advanced Synthesis and Catalysis; vol. 347; nb. 5; (2005); p. 695 - 702, View in Reaxys; Birman, Vladimir B.; Li, Ximin; Jiang, Hui; W. Uffman, Eric; Tetrahedron; vol. 62; nb. 2-3; (2006); p. 285 - 294, View in Reaxys

(S)-5, R1 = Ph

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Synlett; nb. 11; (2006); p. 1762 - 1764, View in Reaxys

(S)-6a

Sola, Lluis; Reddy, Katamreddy Subba; Vidal-Ferran, Anton; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Alvarez-Larena, Angel; Piniella, Joan-F.; Journal of Organic Chemistry; vol. 63; nb. 20; (1998); p. 7078 - 7082, View in Reaxys; Hanyu, Naoto; Mino, Takashi; Sakamoto, Masami; Fujita, Tsutomu; Tetrahedron Letters; vol. 41; nb. 23; (2000); p. 4587 - 4590, View in Reaxys; Hanyu, Naoto; Aoki, Tasuku; Mino, Takashi; Sakamoto, Masami; Fujita, Tsutomu; Tetrahedron Asymmetry; vol. 11; nb. 14; (2000); p. 2971 - 2979, View in Reaxys; Satyanarayana, Tummanapalli; Kagan, Henri B.; Chemistry - A European Journal; vol. 12; nb. 22; (2006); p. 5785 - 5789, View in Reaxys

(S)-13

Santi, Claudio; Wirth, Thomas; Tetrahedron Asymmetry; vol. 10; nb. 6; (1999); p. 1019 - 1023, View in Reaxys; Schlatter, Alain; Kundu, Mrinal K.; Woggon, Wolf-D.; Angewandte Chemie - International Edition; vol. 43; nb. 48; (2004); p. 6731 - 6734, View in Reaxys; Birman, Vladimir B.; Jiang, Hui; Organic Letters; vol. 7; nb. 16; (2005); p. 3445 - 3447, View in Reaxys

(S)-14

Wipf, Peter; Pierce, Joshua G.; Wang, Xiaodong; Tetrahedron Asymmetry; vol. 14; nb. 22; (2003); p. 3605 - 3611, View in Reaxys; Thienthong, Neeranat; Perlmutter, Patrick; Journal of Organometallic Chemistry; vol. 690; nb. 8 SPEC. ISS.; (2005); p. 2027 - 2034, View in Reaxys

prod. S

Omote, Masaaki; Nishimura, Yuji; Sato, Kazuyuki; Ando, Akira; Kumadaki, Itsumaro; Tetrahedron Letters; vol. 46; nb. 2; (2005); p. 319 - 322, View in Reaxys

product Tab. run 8

Ngo, Helen L.; Hu, Aiguo; Lin, Wenbin; Tetrahedron Letters; vol. 46; nb. 4; (2005); p. 595 - 597, View in Reaxys

(S)-4g

Lapis, Alexandre A. M.; De Fatima, Angelo; Martins, Jose E. D.; Costa, Valentim E. U.; Pilli, Ronaldo A.; Tetrahedron Letters; vol. 46; nb. 3; (2005); p. 495 - 498, View in Reaxys

Tab.2. Ent.2-3. Sprod.

Tan, Duan-Ming; Chan, Kin Shing; Tetrahedron Letters; vol. 46; nb. 3; (2005); p. 503 - 505, View in Reaxys

(S)-11e

Castellnou, David; Sola, Lluis; Jimeno, Ciril; Fraile, Jose M.; Mayoral, Jose A.; Riera, Antoni; Pericas, Miquel A.; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 433 - 438, View in Reaxys

Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 - 2153, View in Reaxys

Tab. 1, entry 3

Vorontsova, Natalia; Vorontsov, Evgenii; Antonov, Dmitrii; Starikova, Zoya; Butin, Kim; Braese, Stefan; Hoefener, Sebastian; Rozenberg, Valeria; Advanced Synthesis and Catalysis; vol. 347; nb. 1; (2005); p. 129 - 135, View in Reaxys

25a (S)

Cobb, Alexander J.A.; Marson, Charles M.; Tetrahedron; vol. 61; nb. 5; (2005); p. 1269 - 1279, View in Reaxys

21S

Matsuda, Hisashi; Ando, Shin; Morikawa, Toshio; Kataoka, Shinya; Yoshikawa, Masayuki; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 7; (2005); p. 1949 - 1953, View in Reaxys

(S)-product from 11 Liu, Pei-Nian; Gu, Pei-Ming; Deng, Jin-Gen; Tu, Yong-Qiang; Ma, Ya-Ping; European Journal of Organic Chemistry; nb. 15; (2005); p. 3221 - 3227, View in Reaxys (S)-5, tab. 3, ent. 1

Song, Chun; Ma, Changqin; Ma, Yudao; Feng, Wenhua; Ma, Shutao; Chai, Qiang; Andrus, Merritt B.; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3241 - 3244, View in Reaxys

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(S)-6s

Jing, Qing; Zhang, Xue; Sun, Jie; Ding, Kuiling; Advanced Synthesis and Catalysis; vol. 347; nb. 9; (2005); p. 1193 1197, View in Reaxys

12e maj

Dalicsek, Zoltan; Pollreisz, Ferenc; Goemoery, Agnes; Soos, Tibor; Organic Letters; vol. 7; nb. 15; (2005); p. 3243 3246, View in Reaxys

(S)-20

Fennie, Michael W.; DiMauro, Erin F.; O'Brien, Erin M.; Annamalai, Venkatachalam; Kozlowski, Marisa C.; Tetrahedron; vol. 61; nb. 26; (2005); p. 6249 - 6265, View in Reaxys

Scheme 2. product 1

Johansson, Anna; Wingstrand, Erica; Hakansson, Mikael; Journal of Organometallic Chemistry; vol. 690; nb. 16; (2005); p. 3846 - 3853, View in Reaxys

byproduct, T 2/run 4

Cordes, David B.; Nguyen, Thao M.; Kwong, Tracey J.; Suri, Jeff T.; Luibrand, Richard T.; Singaram, Bakthan; European Journal of Organic Chemistry; nb. 24; (2005); p. 5289 - 5295, View in Reaxys

(S)-(-)-5a

Biswas, Kallolmay; Prieto, Oscar; Goldsmith, Paul J.; Woodward, Simon; Angewandte Chemie - International Edition; vol. 44; nb. 15; (2005); p. 2232 - 2234, View in Reaxys

Kawasaki, Ikuo; Tsunoda, Kazuya; Tsuji, Tomoko; Yamaguchi, Tomoko; Shibuta, Hiroki; Uchida, Nozomi; Yamashita, Masayuki; Ohta, Shunsaku; Chemical Communications; nb. 16; (2005); p. 2134 - 2136, View in Reaxys

(S)-19a

Lauterwasser, Frank; Nieger, Martin; Mansikkamaeki, Heidi; Naettinen, Kalle; Braese, Stefan; Chemistry - A European Journal; vol. 11; nb. 15; (2005); p. 4509 - 4525, View in Reaxys

(S)-1b

Adam, Waldemar; Lukacs, Zoltan; Viebach, Kirsten; Humpf, Hans-Ulrich; Saha-Moeller, Chantu R.; Schreier, Peter; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 186 - 190, View in Reaxys; Verzijl, Gerard K.M.; De Vries, Johannes G.; Broxterman, Quirinus B.; Tetrahedron Asymmetry; vol. 16; nb. 9; (2005); p. 1603 - 1610, View in Reaxys

product, isomer 2

Barros, M. Teresa; Maycock, Christopher D.; Phillips, Ana Maria Faisca; European Journal of Organic Chemistry; nb. 8; (2004); p. 1820 - 1829, View in Reaxys

Tab. 2

Hu, Aiguo; Ngo, Helen L.; Lin, Wenbin; Organic Letters; vol. 6; nb. 17; (2004); p. 2937 - 2940, View in Reaxys

4, R = Et

Dahmen, Stefan; Organic Letters; vol. 6; nb. 13; (2004); p. 2113 - 2116, View in Reaxys

Table 1, entry 6

Kuwano, Ryoichi; Uemura, Takashi; Saitoh, Makoto; Ito, Yoshihiko; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2263 - 2271, View in Reaxys

(S)-11, R1=C6H5

Scarpi, Dina; Lo Galbo, Fabrizio; Occhiato, Ernesto G.; Guarna, Antonio; Tetrahedron Asymmetry; vol. 15; nb. 8; (2004); p. 1319 - 1324, View in Reaxys

(S)-PhCH(Et)OH

Cuervo, Dario; Gamasa, M. Pilar; Gimeno, Jose; Chemistry - A European Journal; vol. 10; nb. 2; (2004); p. 425 432, View in Reaxys

Gilmore, Nathan J.; Jones, Simon; Muldowney, Mark P.; Organic Letters; vol. 6; nb. 16; (2004); p. 2805 - 2808, View in Reaxys

Scheme 4 (R = CH2CH3)

Cheng, Xiaohui; Horton, Peter N.; Hursthouse, Michael B.; Hii, King Kuok; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2241 - 2246, View in Reaxys

(S)-7i

Basavaiah, Deevi; Reddy, Gone Jayapal; Rao, Kalapala Venkateswara; Tetrahedron Asymmetry; vol. 15; nb. 12; (2004); p. 1881 - 1888, View in Reaxys

t.5, α-product, (S)

Connolly, David J.; Lacey, Patrick M.; McCarthy, Mary; Saunders, Cormac P.; Carroll, Anne-Marie; Goddard, Richard; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6572 - 6589, View in Reaxys

9, enantiomer

Sibi, Mukund P.; Stanley, Levi M.; Tetrahedron Asymmetry; vol. 15; nb. 21; (2004); p. 3353 - 3356, View in Reaxys

3n, (S)

Xu, Jiaxi; Wei, Tiezheng; Zhang, Qihan; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6860 - 6866, View in Reaxys

Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys

t.2, entry 1, enant.

Sprout, Christopher M.; Richmond, Meaghan L.; Seto, Christopher T.; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6666 - 6673, View in Reaxys

(S)-product of 3

Kriis, Kadri; Kanger, Tonis; Lopp, Margus; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2687 - 2691, View in Reaxys

Bagdanoff, Jeffrey T.; Stoltz, Brian M.; Angewandte Chemie - International Edition; vol. 43; nb. 3; (2004); p. 353 357, View in Reaxys

Tab. 1, Ent. 1, prod. Zhong, Yu-Wu; Jiang, Chang-Sheng; Xu, Ming-Hua; Lin, Guo-Qiang; Tetrahedron; vol. 60; nb. 40; (2004); p. 8861 S - 8868, View in Reaxys S-3

Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron; vol. 60; nb. 41; (2004); p. 9163 - 9170, View in Reaxys

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Prod.(S), Tab.1,run 9

Lee, Dong-Won; Yun, Jaesook; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5415 - 5417, View in Reaxys

prod., Tab. 1, entry 2

Bogevig, Anders; Pastor, Isidro M.; Adolfsson, Hans; Chemistry - A European Journal; vol. 10; nb. 1; (2004); p. 294 302, View in Reaxys

4a (S)

Homann, Michael J.; Vail, Robert B.; Previte, Edward; Tamarez, Maria; Morgan, Brian; Dodds, David R.; Zaks, Aleksey; Tetrahedron; vol. 60; nb. 3; (2004); p. 789 - 797, View in Reaxys

11, (S)-alcohol

Li, Xiaoguang; Chen, Weiping; Hems, William; King, Frank; Xiao, Jianliang; Tetrahedron Letters; vol. 45; nb. 5; (2004); p. 951 - 953, View in Reaxys

S-alcohol T. 1, e. 3

Chen, Jian-Shan; Li, Yan-Yun; Dong, Zhen-Rong; Li, Bao-Zhu; Gao, Jing-Xing; Tetrahedron Letters; vol. 45; nb. 45; (2004); p. 8415 - 8418, View in Reaxys

(S)-9a

Reddy, Katamreddy Subba; Sola, Lluis; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Synthesis; nb. 1; (2000); p. 165 - 176, View in Reaxys; Okuyama, Yuko; Nakano, Hiroto; Igarashi, Mayumi; Kabuto, Chizuko; Hongo, Hiroshi; Heterocycles; vol. 59; nb. 2; (2003); p. 635 - 643, View in Reaxys

(S)-2

Bakker; Spruijt; Van Rantwijk; Sheldon; Tetrahedron Asymmetry; vol. 11; nb. 8; (2000); p. 1801 - 1808, View in Reaxys; Ghanem, Ashraf; Schurig, Volker; Monatshefte fur Chemie; vol. 134; nb. 8; (2003); p. 1151 - 1157, View in Reaxys; Sosa-Rivadeneyra, Martha; Munoz-Muniz, Omar; Anaya de Parrodi, Cecilia; Quintero, Leticia; Juaristi, Eusebio; Journal of Organic Chemistry; vol. 68; nb. 6; (2003); p. 2369 - 2375, View in Reaxys

Vinogradov; Gorshkova; Pavlov; Mikhalev; Chel'tsova; Razmanov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 49; nb. 3; (2000); p. 460 - 465, View in Reaxys; Huertas, Ramon E.; Corella, Joseph A.; Soderquist, John A.; Tetrahedron Letters; vol. 44; nb. 24; (2003); p. 4435 - 4437, View in Reaxys

(S)-7, R1=Ph

Casey, Mike; Smyth, Martin P.; Synlett; nb. 1; (2003); p. 102 - 106, View in Reaxys

(S)C6H5CH(OH)Et

Jiang, Hua; Hu, Aiguo; Lin, Wenbin; Chemical Communications; nb. 1; (2003); p. 96 - 97, View in Reaxys

24j

Evans, David A.; Michael, Forrest E.; Tedrow, Jason S.; Campos, Kevin R.; Journal of the American Chemical Society; vol. 125; nb. 12; (2003); p. 3534 - 3543, View in Reaxys

(S)-alcohol, entry 9

Hegarty, Philip; Lau, Raymond; Motherwell, William B.; Tetrahedron Letters; vol. 44; nb. 9; (2003); p. 1851 - 1853, View in Reaxys

14a-(S), R=Ph

Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Tetrahedron Asymmetry; vol. 14; nb. 9; (2003); p. 1103 - 1114, View in Reaxys

(S)-4a

Joshi, Sudhir N.; Malhotra, Sanjay V.; Tetrahedron Asymmetry; vol. 14; nb. 13; (2003); p. 1763 - 1766, View in Reaxys

Tab.2., run 1, prod. 2

Anyanwu, Uche K.; Venkataraman; Tetrahedron Letters; vol. 44; nb. 34; (2003); p. 6445 - 6448, View in Reaxys

3b(S)

Nishibayashi, Yoshiaki; Yamauchi, Akiyoshi; Onodera, Gen; Uemura, Sakae; Journal of Organic Chemistry; vol. 68; nb. 15; (2003); p. 5875 - 5880, View in Reaxys

S-isomer

Garcia Martinez, Antonio; Teso Vilar, Enrique; Garcia Fraile, Amelia; De La Moya Cerero, Santiago; Lora Maroto, Beatriz; Tetrahedron Asymmetry; vol. 14; nb. 14; (2003); p. 1959 - 1963, View in Reaxys

13, S

Danilova, Tatyana I.; Rozenberg, Valeria I.; Sergeeva, Elena V.; Starikova, Zoya A.; Braese, Stefan; Tetrahedron Asymmetry; vol. 14; nb. 14; (2003); p. 2013 - 2019, View in Reaxys

6, (S)-enantiomer

Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 458, View in Reaxys

13 (S)

Burguete, M. Isabel; Collado, Manuel; Escorihuela, Jorge; Galindo, Francisco; Garcia-Verdugo, Eduardo; Luis, Santiago V.; Vicent, Maria J.; Tetrahedron Letters; vol. 44; nb. 36; (2003); p. 6891 - 6894, View in Reaxys

S-product(table,entry1)

Muniz, Kilian; Tetrahedron Letters; vol. 44; nb. 17; (2003); p. 3547 - 3549, View in Reaxys

16-(S)

Bonini, Bianca F.; Fochi, Mariafrancesca; Comes-Franchini, Mauro; Ricci, Alfredo; Thijs, Lambertus; Zwanenburg, Binne; Tetrahedron Asymmetry; vol. 14; nb. 21; (2003); p. 3321 - 3327, View in Reaxys

(S)-35b

Stampfer, Wolfgang; Kosjek, Birgit; Faber, Kurt; Kroutil, Wolfgang; Journal of Organic Chemistry; vol. 68; nb. 2; (2003); p. 402 - 406, View in Reaxys

Bosman, Anton W.; Vestberg, Robert; Heumann, Andi; Frechet, Jean M. J.; Hawker, Craig J.; Journal of the American Chemical Society; vol. 125; nb. 3; (2003); p. 715 - 728, View in Reaxys

(S)-PhCH(OH)Et

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card; Brunel; Chemical Communications; nb. 18; (2000); p. 1773 - 1774, View in Reaxys; Zhang; Yoshinaga; Imai; Kida; Nakatsuji; Ikeda; Synlett; nb. 10; (2000); p. 1512 - 1514, View in Reaxys; Jimeno; Moyano; Pericas; Riera; Synlett; nb. 7; (2001); p. 1155 - 1157, View in Reaxys; Hermsen; Cremers; Thijs; Zwanenburg; Tetrahedron Letters; vol. 42; nb. 25; (2001); p. 4243 - 4245, View in Reaxys; Nakano, Hiroto; Okuyama, Yuko; Fushimi, Kazuyuki; Yamakawa, Ryo; Kayaoka, Daisuke; Hongo, Hiroshi; Heterocycles; vol. 56; nb. 1-2; (2002); p. 457 - 466, View in Reaxys; Zhang, Hui; Yang, Chuan-Bo; Li, Yan-Yun; Donga, Zhen-Rong; Gao, Jing-Xing; Nakamura, Hideaki; Murata, Kunihiko; Ikariya, Takao; Chemical Communications; nb. 1; (2003); p. 142 - 143, View in Reaxys; Segarra, Anna M.; Guerrero, Ramon; Claver, Carmen; Fernandez, Elena; Chemistry - A European Journal; vol. 9; nb. 1; (2003); p. 191 - 200, View in Reaxys (S)-11a

Pericas, Miquel A.; Castellnou, David; Rodriguez, Israel; Riera, Antoni; Sola, Lluis; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1305 - 1313, View in Reaxys

(S)-9b

Palmieri, Gianni; Tetrahedron Asymmetry; vol. 11; nb. 16; (2000); p. 3361 - 3373, View in Reaxys; Ruzziconi, Renzo; Piermatti, Oriana; Ricci, Giacomo; Vinci, Daniele; Synlett; nb. 5; (2002); p. 747 - 750, View in Reaxys

Prod.(S), Tab.1/2,run 1

Braga, Antonio L; Vargas, Fabricio; Silveira, Claudio C; De Andrade, Leandro H; Tetrahedron Letters; vol. 43; nb. 13; (2002); p. 2335 - 2337, View in Reaxys

Pastor, Isidro M; Adolfsson, Hans; Tetrahedron Letters; vol. 43; nb. 9; (2002); p. 1743 - 1746, View in Reaxys

(S)-a

Kim, Tae-Jeong; Lee, Hee-Yeol; Ryu, Eun-Sook; Park, Dong-Kyu; Cho, Chan Sik; Shim, Sang Chul; Jeong, Jong Hwa; Journal of Organometalic Chemistry; vol. 649; nb. 2; (2002); p. 258 - 267, View in Reaxys

6-(S)

Wolf, Christian; Francis, Christopher J.; Hawes, Pili A.; Shah, Mirage; Tetrahedron Asymmetry; vol. 13; nb. 16; (2002); p. 1733 - 1741, View in Reaxys

t.1, major pr.

Superchi, Stefano; Giorgio, Egidio; Scafato, Patrizia; Rosini, Carlo; Tetrahedron Asymmetry; vol. 13; nb. 13; (2002); p. 1385 - 1391, View in Reaxys

(S)-IIb

Yadav, Ashok K.; Singh, Arpita; Bulletin of the Chemical Society of Japan; vol. 75; nb. 3; (2002); p. 587 - 588, View in Reaxys

Prod.(major),Tab.1,run8

Kim, Geon-Joong; Kim, Sang-Han; Chong, Pong-Hyun; Kwon, Mi-Ae; Tetrahedron Letters; vol. 43; nb. 45; (2002); p. 8059 - 8062, View in Reaxys

(S)-sec-alc. from PhCHO

Shaikh, Nadim S; Deshpande, Vishnu H; Bedekar, Ashutosh V; Tetrahedron Letters; vol. 43; nb. 32; (2002); p. 5587 - 5589, View in Reaxys

Product (S) (major)

Nagasawa, Tomomi; Miyata, Hideto; Kudo, Nozomi; Nakatani, Motoi; Ito, Kazuaki; Ohba, Yoshihiro; Heterocyclic Communications; vol. 8; nb. 5; (2002); p. 423 - 426, View in Reaxys

pure enantiomer 3a

Klein, Guenter; Pandiaraju, Subramaniam; Reiser, Oliver; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7503 7506, View in Reaxys

(S)-product

Lake, Fredrik; Moberg, Christina; European Journal of Organic Chemistry; nb. 18; (2002); p. 3179 - 3188, View in Reaxys

tab. 1,entry 2 (S)alc.

Jeong, Kyu-Sung; Kim, Soong-Hyun; Park, Hyun-Jin; Chang, Kyoung-Jin; Kwan, Soo Kim; Chemistry Letters; nb. 11; (2002); p. 1114 - 1115, View in Reaxys

(S)-12

Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Tetrahedron Asymmetry; vol. 13; nb. 14; (2002); p. 1573 - 1579, View in Reaxys; Burguete, M. Isabel; Garcia-Verdugo, Eduardo; Vicent, Maria J.; Luis, Santiago V.; Pennemann, Helmut; Graf Von Keyserling, Nikolai; Martens, Jurgen; Organic Letters; vol. 4; nb. 22; (2002); p. 3947 - 3950, View in Reaxys

ent-6

Wolf, Christian; Hawes, Pili A.; Journal of Organic Chemistry; vol. 67; nb. 8; (2002); p. 2727 - 2729, View in Reaxys

(S)-5

Priego, Julian; Garcia Mancheno, Olga; Cabrera, Silvia; Carretero, Juan Carlos; Journal of Organic Chemistry; vol. 67; nb. 4; (2002); p. 1346 - 1353, View in Reaxys

ent-4b

Yong, Kelvin H.; Taylor, Nicholas J.; Chong, J. Michael; Organic Letters; vol. 4; nb. 21; (2002); p. 3553 - 3556, View in Reaxys

table 1, entry 1

Long, Jiang; Ding, Kuiling; Angewandte Chemie - International Edition; vol. 40; nb. 3; (2001); p. 544 - 547, View in Reaxys; Yang, Xiao-Wu; Shen, Jian-Heng; Da, Chao-Shan; Wang, Heng-Shan; Su, Wu; Liu, Da-Xue; Wang, Rui; Choi, Michael C.K.; Chan, Albert S.C.; Tetrahedron Letters; vol. 42; nb. 37; (2001); p. 6573 - 6575, View in Reaxys

7a (S)

Nakano, Hiroto; Okuyama, Yuko; Iwasa, Kazuto; Hongo, Hiroshi; Heterocycles; vol. 54; nb. 1; (2001); p. 411 - 418, View in Reaxys

(S)

Xu, Qianyong; Wang, Guoxing; Pan, Xinfu; Chan, Albert S.C.; Tetrahedron Asymmetry; vol. 12; nb. 3; (2001); p. 381 - 385, View in Reaxys; Panev, Stefan; Linden, Anthony; Dimitrov, Vladimir; Tetrahedron Asymmetry; vol. 12; nb. 9; (2001); p. 1313 - 1321, View in Reaxys

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8A-(S)

Okamoto, Kazuya; Kimachi, Tetsutaro; Ibuka, Toshiro; Takemoto, Yoshiji; Tetrahedron Asymmetry; vol. 12; nb. 3; (2001); p. 463 - 467, View in Reaxys

table 1, entry 8

Wu, Xun-Wei; Hou, Xue-Long; Dai, Li-Xin; Tao, Ju; Cao, Bo-Xun; Sun, Jie; Tetrahedron Asymmetry; vol. 12; nb. 4; (2001); p. 529 - 532, View in Reaxys

table 1, entry 6

Braga, Antonio L; Appelt, Helmoz R; Schneider, Paulo H; Rodrigues, Oscar E.D; Silveira, Claudio C; Wessjohann, Ludger A; Tetrahedron; vol. 57; nb. 16; (2001); p. 3291 - 3295, View in Reaxys

(S)-alcohol from 4

Maj, Anna M.; Pietrusiewicz; Suisse, Isabelle; Agbossou, Francine; Mortreux, Andre; Journal of Organometallic Chemistry; vol. 626; nb. 1-2; (2001); p. 157 - 160, View in Reaxys

Product (S), Table 1 Xu, Qianyong; Wang, Hui; Pan, Xinfu; Chan, Albert S.C; Yang, Teng-Kuei; Tetrahedron Letters; vol. 42; nb. 35; (2001); p. 6171 - 6173, View in Reaxys (S)-alcohol from 3c Rhyoo, Hae Yoon; Yoon, Young-Ae; Park, Hee-Jung; Chung, Young Keun; Tetrahedron Letters; vol. 42; nb. 30; (2001); p. 5045 - 5048, View in Reaxys Prod.,Tab.1,run 1,minor

Hu, Qiao-Sheng; Sun, Chaode; Monaghan, Colleen E; Tetrahedron Letters; vol. 42; nb. 44; (2001); p. 7725 - 7728, View in Reaxys

(S)-3 (R=H)

Ooi, Takashi; Saito, Akira; Maruoka, Keiji; Chemistry Letters; nb. 11; (2001); p. 1108 - 1109, View in Reaxys

(-)-4b

Miyamoto; Yasaka; Takaoka; Tanaka; Toda; Enantiomer; vol. 6; nb. 1; (2001); p. 51 - 55, View in Reaxys

7 (en)

Fan, Qing-Hua; Liu, Guo-Hua; Deng, Guo-Jun; Chen, Xiao-Min; Chan, Albert S.C.; Tetrahedron Letters; vol. 42; nb. 51; (2001); p. 9047 - 9050, View in Reaxys

(S)-7b

Lin, Yang-Miin; Fu, I-Pin; Uang, Biing-Jiun; Tetrahedron Asymmetry; vol. 12; nb. 23; (2001); p. 3217 - 3221, View in Reaxys

ent-12

Jayaprakash, Doss; Sasai, Hiroaki; Tetrahedron Asymmetry; vol. 12; nb. 18; (2001); p. 2589 - 2595, View in Reaxys

(S)-9a ((S)-3g)

Jiang, Biao; Feng, Yan; Hang, Jian-Feng; Tetrahedron Asymmetry; vol. 12; nb. 16; (2001); p. 2323 - 2329, View in Reaxys

Tab.2.,entry 2A,alcohol

Sarvary, Ian; Almqvist, Fredrik; Frejd, Torbjoern; Chemistry - A European Journal; vol. 7; nb. 10; (2001); p. 2158 2166, View in Reaxys

Schinnerl, Marina; Seitz, Michael; Kaiser, Anja; Reiser, Oliver; Organic Letters; vol. 3; nb. 26; (2001); p. 4259 4262, View in Reaxys

(S)-PP

Cavazzini; Kaczmarski; Szabelski; Zhou; Liu; Guiochon; Analytical Chemistry; vol. 73; nb. 23; (2001); p. 5704 5715, View in Reaxys

14a, S

DiMauro, Erin F.; Kozlowski, Marisa C.; Organic Letters; vol. 3; nb. 19; (2001); p. 3053 - 3056, View in Reaxys

(S)-2b

Ford, Alan; Woodward, Simon; Angewandte Chemie - International Edition; vol. 38; nb. 3; (1999); p. 335 - 336, View in Reaxys; Adam, Waldemar; Lukacs, Zoltan; Harmsen, Dag; Saha-Moeller, Chantu R.; Schreier, Peter; Journal of Organic Chemistry; vol. 65; nb. 3; (2000); p. 878 - 882, View in Reaxys; Sirol, Sabine; Courmarcel, James; Mostefai, Naouel; Riant, Olivier; Organic Letters; vol. 3; nb. 25; (2001); p. 4111 - 4113, View in Reaxys

(S)-Ph-CH(OH)-Et

Nakamura, Yutaka; Takeuchi, Seiji; Ohgo, Yoshiaki; Curran, Dennis P.; Tetrahedron Letters; vol. 41; nb. 1; (2000); p. 57 - 60, View in Reaxys

29a-ent

Spieler, Jan; Huttenloch, Oliver; Waldmann, Herbert; European Journal of Organic Chemistry; nb. 3; (2000); p. 391 - 399, View in Reaxys

(S)PhCH(OH)C2H5

Imai, Yoshitane; Matsuo, Shigeaki; Zhang, Wanbin; Nakatsuji, Yohji; Ikeda, Isao; Synlett; nb. 2; (2000); p. 239 241, View in Reaxys

Heckel, Alexander; Seebach, Dieter; Angewandte Chemie - International Edition; vol. 39; nb. 1; (2000); p. 163 - 165, View in Reaxys; Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 - 26, View in Reaxys

(S)-8a

Okaniwa, Masanori; Yanada, Reiko; Ibuka, Toshiro; Tetrahedron Letters; vol. 41; nb. 7; (2000); p. 1047 - 1050, View in Reaxys

ent-16

Prieto, Oscar; Ramon, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 11; nb. 7; (2000); p. 1629 - 1644, View in Reaxys

byproduct, T.3 run 4

Asami, Masatoshi; Sato, Shinsuke; Watanabe, Hiroyasu; Chemistry Letters; nb. 9; (2000); p. 990 - 991, View in Reaxys

(S)-19

Dai, Wei-Min; Zhu, Hua-Jie; Hao, Xiao-Jiang; Tetrahedron Asymmetry; vol. 11; nb. 11; (2000); p. 2315 - 2337, View in Reaxys

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(S)-product T5/enty Saluzzo, Christine; Ter Halle, Rob; Touchard, Francois; Fache, Fabienne; Schulz, Emmanuelle; Lemaire, Marc; 4 Journal of Organometallic Chemistry; vol. 603; nb. 1; (2000); p. 30 - 39, View in Reaxys Tab.1, entry 7, Sisom.

McCarthy, Mary; Hooper, Mark W.; Guiry, Patrick J.; Chemical Communications; nb. 14; (2000); p. 1333 - 1334, View in Reaxys

(S)-10d

Kita, Yasuyuki; Takebe, Yasushi; Murata, Kenji; Naka, Tadaatsu; Akai, Shuji; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 83 - 88, View in Reaxys

(S)-3C

Boyd, Derek R.; Sharma, Narain D.; Bowers, Nigel I.; Duffy, John; Harrison, John S.; Dalton, Howard; Journal of the Chemical Society, Perkin Transactions 1; nb. 9; (2000); p. 1345 - 1350, View in Reaxys

(S)-3a

(S)-24b

Petra, Danielle G. I.; Kamer, Paul C. J.; Spek, Anthony L.; Schoemaker, Hans E.; Van Leeuwen, Piet W. N. M.; Journal of Organic Chemistry; vol. 65; nb. 10; (2000); p. 3010 - 3017, View in Reaxys

(S)-16c

Spivey, Alan C.; Fekner, Tomasz; Spey, Sharon E.; Journal of Organic Chemistry; vol. 65; nb. 10; (2000); p. 3154 3159, View in Reaxys

ent-2b

Blake, Alexander J.; Cunningham, Anthony; Ford, Alan; Teat, Simon J.; Woodward, Simon; Chemistry - A European Journal; vol. 6; nb. 19; (2000); p. 3586 - 3594, View in Reaxys

prod.(S) Tab. 1, run 13

Arikawa, Yasuyoshi; Ueoka, Masanao; Matoba, Kazutaka; Nishibayashi, Yoshiaki; Hidai, Masanobu; Uemura, Sakae; Journal of Organometallic Chemistry; vol. 572; nb. 2; (1999); p. 163 - 168, View in Reaxys

Tab. col.5. run 5

Sibi, Mukund P.; Chen, Jian-xie; Cook, Gregory R.; Tetrahedron Letters; vol. 40; nb. 17; (1999); p. 3301 - 3304, View in Reaxys

19a

Cherng, Yie-Jia; Fang, Jim-Min; Lu, Ta-Jung; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 3207 - 3212, View in Reaxys

Cao, Ping; Zhang, Xumu; Journal of Organic Chemistry; vol. 64; nb. 6; (1999); p. 2127 - 2129, View in Reaxys

2, R=phenyl

Ding, Kuiling; Ishii, Akihiro; Mikami, Koichi; Angewandte Chemie - International Edition; vol. 38; nb. 4; (1999); p. 497 - 501, View in Reaxys

(S)-10b

Derdau, Volker; Laschat, Sabine; Hupe, Eike; Koenig, Wilfried A.; Dix, Ina; Jones, Peter G.; European Journal of Inorganic Chemistry; nb. 6; (1999); p. 1001 - 1007, View in Reaxys

(S)-8

Omote, Masaaki; Kominato, Akane; Sugawara, Michi; Sato, Kazuyuki; Ando, Akira; Kumadaki, Itsumaro; Tetrahedron Letters; vol. 40; nb. 30; (1999); p. 5583 - 5585, View in Reaxys

Cho, Byung Tae; Chun, Yu Sung; Synthetic Communications; vol. 29; nb. 3; (1999); p. 521 - 531, View in Reaxys

(S)-2d

Adam, Waldemar; Mock-Knoblauch, Cordula; Saha-Moeller, Chantu R.; Journal of Organic Chemistry; vol. 64; nb. 13; (1999); p. 4834 - 4839, View in Reaxys

(S)-9g

Puigjaner, Cristina; Vidal-Ferran, Anton; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Journal of Organic Chemistry; vol. 64; nb. 21; (1999); p. 7902 - 7911, View in Reaxys

(S), Table (1-7)

Cardellicchio, Cosimo; Ciccarella, Giuseppe; Naso, Francesco; Perna, Filippo; Tortorella, Paolo; Tetrahedron; vol. 55; nb. 51; (1999); p. 14685 - 14692, View in Reaxys

Table 3 entry 54

Mimoun, Hubert; De Saint Laumer, Jean Yves; Giannini, Luca; Scopelliti, Rosario; Floriani, Carlo; Journal of the American Chemical Society; vol. 121; nb. 26; (1999); p. 6158 - 6166, View in Reaxys

byproduct T 2/entry Yanagi, Takashi; Kikuchi, Ken; Takeuchi, Hideki; Ishikawa, Takehiro; Nishimura, Toshihiro; Kamijo, Tetsuhide; 4 Chemistry Letters; nb. 11; (1999); p. 1203 - 1204, View in Reaxys (S)-8d

Gao, Jing-Xing; Yi, Xiao-Dong; Xu, Pian-Pian; Tang, Chun-Liang; Wan, Hui-Lin; Ikariya, Takao; Journal of Organometallic Chemistry; vol. 592; nb. 2; (1999); p. 290 - 295, View in Reaxys

Hodge, Philip; Kell, Roger J.; Ma, Jianbiao; Morris, Hugh; Australian Journal of Chemistry; vol. 52; nb. 11; (1999); p. 1041 - 1046, View in Reaxys

ent-10a

Deng, Wei-Ping; Hou, Xue-Long; Dai, Li-Xin; Tetrahedron Asymmetry; vol. 10; nb. 24; (1999); p. 4689 - 4693, View in Reaxys

(S)C6H5CH(OH)CH3 CH3

Rheiner, P. Beat; Seebach, Dieter; Chemistry - A European Journal; vol. 5; nb. 11; (1999); p. 3221 - 3236, View in Reaxys

product, Table1, en- Legrand, Olivier; Brunel, Jean-Michel; Buono, Gerard; Tetrahedron Letters; vol. 39; nb. 51; (1998); p. 9419 - 9422, try8 View in Reaxys

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21a-(S)

Vyskocil, Stepn; Jaracz, Stanislav; Smrcina, Martin; Sticha, Martin; Hanus, Vladimir; Miroslav Poldsek; Kocovsky, Pavel; Journal of Organic Chemistry; vol. 63; nb. 22; (1998); p. 7727 - 7737, View in Reaxys

(S)-23b

Nakamura; Matsuda; Journal of Organic Chemistry; vol. 63; nb. 24; (1998); p. 8957 - 8964, View in Reaxys

ent-21

Hu, Qiao-Sheng; Huang, Wei-Sheng; Vitharana, Dilrukshi; Zheng, Xiao-Fan; Pu, Lin; Journal of the American Chemical Society; vol. 119; nb. 51; (1997); p. 12454 - 12464, View in Reaxys

(-)-(S)-18

Davis, Franklin A.; Reddy, R. Thimma; Journal of Organic Chemistry; vol. 57; nb. 9; (1992); p. 2599 - 2606, View in Reaxys

Chan, T. H.; Pellon, P.; Journal of the American Chemical Society; vol. 111; nb. 23; (1989); p. 8737 - 8738, View in Reaxys

Tab., run 1, byprod. Soai, Kenso; Nishi, Mitsugu; Ito, Yuhki; Chemistry Letters; (1987); p. 2405 - 2406, View in Reaxys (S)-(-)-28

Tanno; Terashima; Chemical and Pharmaceutical Bulletin; vol. 31; nb. 3; (1983); p. 837 - 851, View in Reaxys

Patent-Specific Data (3) References Patent; Fourth Military Medical University,People's Liberation Army; Chen, Weiping; Zhang, sheng Yong; cheng, sikun; li, xiaoye; Nie, Huifang; (10 pag.); CN103012498; (2016); (B) Chinese, View in Reaxys Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys Patent; KANEKA CORPORATION; WO2007/37242; (2007); (A1) Japanese, View in Reaxys Druglikeness (1) 1 of 1

LogP

2.095

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

20.23

Lipinski Number

Veber Number

Related Structure (3) Related Structure Referenced Compound The author has (R)-1-phenyl-1doubts about the propanol constitution/configuration of the title compound. The following alternatives are discussed/ proposed: /BRN= 2041555/

References Ishizaki, Miyuki; Hoshino, Osamu; Tetrahedron: Asymmetry; vol. 5; nb. 10; (1994); p. 1901 1904, View in Reaxys

Boireau,G. et al.; Tetrahedron; vol. 35; (1979); p. 1457 - 1461, View in Reaxys; Yamamoto,K. et al.; Journal of Organometallic Chemistry; vol. 46; (1972); p. C65 - C67, View in Reaxys Configuration.

Derivative (5) Derivative

(S)-1-phenylpropyl Braun, Manfred; Fleischer, Ralf; Mai, Brigitte; Schneider, Marc-Andre; Lachenicht, Stefan; Advanced Synthesis (S)-α-methoxy-α-triand Catalysis; vol. 346; nb. 4; (2004); p. 474 - 482, View in Reaxys fluoromethylphenylacetate (4S,7S)-2,5-dioxo-4,7-diphen-

Aurich, Hans Guenter; Soeberdt, Michael; Harms, Klaus; Tetrahedron; vol. 55; nb. 5; (1999); p. 1249 - 1270, View in Reaxys

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yl-3,6-dioxa-nonane 3,3,3-Trifluoro-2Hodge, Philip; Sung, David W. L.; Stratford, Peter W.; Journal of the Chemical Society - Perkin Transactions 1; nb. methoxy-2-phenyl- 16; (1999); p. 2335 - 2342, View in Reaxys propionic acid (S)-1-phenyl-propyl ester (S)-1-Phenylpropan-1-yl (R)-(-)-αmethoxy-α-(trifluoromethyl)phenyl acetate

Bolm, Carsten; Schlingloff, Gunther; Harms, Klaus; Chemische Berichte; vol. 125; nb. 5; (1992); p. 1191 - 1204, View in Reaxys

Carbonic acid Corey; Yuen; Hannon; Wierda; Journal of Organic Chemistry; vol. 55; nb. 3; (1990); p. 784 - 786, View in Reaxys (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester (S)-1-phenyl-propyl ester Purification (10) Purification (method) acetylation of epimer by (CH3CO)2O, <(α %5&-C5Ph5)Fe(α %5&C10H11N2)>, NEt3, Et2O at r.t.

References Ruble; Latham; Fu; Journal of the American Chemical Society; vol. 119; nb. 6; (1997); p. 1492 - 1493, View in Reaxys

esterification of the Faraldos, Juan; Arroyo, Elisa; Herradon, Bernardo; Synlett; vol. 1997; nb. 4; (1997); p. 367 - 370, View in Reaxys (R)-enantiomer with vinyl butyrate in toluene catalyzed by enzyme acylase I (AA-I) from Aspergillus species via Novozym Guibe-Jampel, Eryka; Chalecki, Zbigniew; Bassir, Mohamed; Gelo-Pujic, Mirjana; Tetrahedron; vol. 52; nb. 12; SP435 catalyzed re- (1996); p. 4397 - 4402, View in Reaxys action with mixed carboxylic-carbonic anhydride via acylation with isopropenyl acetate in the presence of QL lipase from Alcaligenes sp.

Naemura; Murata; Tanaka; Yano; Hirose; Tobe; Tetrahedron Asymmetry; vol. 7; nb. 6; (1996); p. 1581 - 1584, View in Reaxys

via the esterificaNakamura, Kaoru; Kawasaki, Masashi; Ohno, Atsuyoshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 4; tion with vinyl ace- (1996); p. 1079 - 1085, View in Reaxys tate in the presence of lipase from Pseudomonas cepacia at 35 deg C, 11 h via the acylation with isopropenyl acetate in the presence of lipase QL in diisopropyl ether at 30 deg C during 40 h

Naemura, Koichiro; Murata, Masaki; Tanaka, Rie; Yano, Masashi; Hirose, Keiji; Tobe, Yoshito; Tetrahedron Asymmetry; vol. 7; nb. 11; (1996); p. 3285 - 3294, View in Reaxys

via esterification with isopropenyl acetate in the presence of lipase YS

Naemura; Fukuda; Murata; Konishi; Hirose; Tobe; Tetrahedron Asymmetry; vol. 6; nb. 9; (1995); p. 2385 - 2394, View in Reaxys

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from Pseudomonas fluorescens heptakis(2,3,6-triO-methyl)-α-cyclodextrin

Weber, Beat; Seebach, Dieter; Tetrahedron; vol. 50; nb. 25; (1994); p. 7473 - 7484, View in Reaxys

via selective esterification of the opposite enantiomer in the presence of lipase Amano PS

Gutman, Arie L.; Brenner, Dov; Boltanski, Aviv; Tetrahedron: Asymmetry; vol. 4; nb. 5; (1993); p. 839 - 844, View in Reaxys

via lipase catalysed acylation with propionic anhydride

Bianchi, Daniele; Cesti, Pietro; Battistel, Ezio; Journal of Organic Chemistry; vol. 53; nb. 23; (1988); p. 5531 - 5534, View in Reaxys

Boiling Point (9) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

References

94 - 95

9.976

Yadav, Ashok K.; Kumar, Manoj; Yadav, Tripti; Jain, Renuka; Synlett; nb. 5; (2010); p. 712 714, View in Reaxys

123

1.20012

Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys

103

Bussche-Huennefeld, Joanna Linda v.; Seebach, Dieter; Tetrahedron; vol. 48; nb. 27; (1992); p. 5719 - 5730, View in Reaxys

110

Davis, Franklin A.; Reddy, R. Thimma; Journal of Organic Chemistry; vol. 57; nb. 9; (1992); p. 2599 - 2606, View in Reaxys

Zadel, Guido; Rieger, Rainer; Breitmaier, Eberhard; Liebigs Annalen der Chemie; nb. 12; (1991); p. 1343 - 1346, View in Reaxys

175

Tanno; Terashima; Chemical and Pharmaceutical Bulletin; vol. 31; nb. 3; (1983); p. 837 - 851, View in Reaxys

94 - 95

Levene; Rothen; Kuna; Journal of Biological Chemistry; vol. 120; (1937); p. 789, View in Reaxys

119 - 120

Levene; Mikeska; Journal of Biological Chemistry; vol. 70; (1926); p. 377, View in Reaxys

115 - 116

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys

Refractive Index (1) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C] 1.518

589

References Levene; Rothen; Journal of Biological Chemistry; vol. 127; (1937); p. 237,240, 245, View in Reaxys

Density (3) 1 of 3

Density [g·cm-3]

0.9025

Reference Temperature [°C]

Measurement Temperature 129 [°C] Pickard; Kenyon; Journal of the Chemical Society; vol. 105; (1914); p. 1124, View in Reaxys 2 of 3

Density [g·cm-3]

1.0129

Reference Temperature [°C]

Smith; Journal of the Chemical Society; vol. 105; (1914); p. 1709, View in Reaxys 3 of 3

Density [g·cm-3]

0.9538 - 0.9982

Reference Temperature [°C]

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Measurement Temperature 13.8 - 69.5 [°C] Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys Adsorption (MCS) (1) 1 of 1

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

22.5 - 24.5

Partner (Adsorption (MCS))

cellulose tribenzoate

Cavazzini; Kaczmarski; Szabelski; Zhou; Liu; Guiochon; Analytical Chemistry; vol. 73; nb. 23; (2001); p. 5704 - 5715, View in Reaxys Association (MCS) (1) 1 of 1

Description (Association (MCS))

Enthalpy of association

Walden,W. et al.; Tetrahedron; vol. 33; (1977); p. 419 - 421, View in Reaxys Chromatographic Data (12) Chromatographic Original string data HPLC (High performance liquid chromatography)

Location

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GC (Gas chromatography)

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(2013); p. 10343 - 10352, View in Reaxys; Soni, Rina; Jolley, Katherine E.; Clarkson, Guy J.; Wills, Martin; Organic Letters; vol. 15; nb. 19; (2013); p. 5110 - 5113, View in Reaxys; Li, Yanyun; Yu, Shenluan; Wu, Xiaofeng; Xiao, Jianliang; Shen, Weiyi; Dong, Zhenrong; Gao, Jingxing; Journal of the American Chemical Society; vol. 136; nb. 10; (2014); p. 4031 - 4039, View in Reaxys; Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 - 2688, View in Reaxys; Lin, Lang; Yu, Rongmin; Wu, Xiao-Yuan; Yang, Wen-Bin; Zhang, Jian; Guo, Xiang-Guang; Lin, Zu-Jin; Lu, CanZhong; Inorganic Chemistry; vol. 53; nb. 10; (2014); p. 4794 - 4796, View in Reaxys; Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys; Faigl, Ferenc; Erdlyi, Zsuzsa; Dek, Szilvia; Nyerges, Mikls; Mtravölgyi, Bla; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6891 - 6894, View in Reaxys; Faigl; Deák; Erdélyi; Holczbauer; Czugler; Nyerges; Mátravölgyi; Chirality; vol. 27; nb. 3; (2015); p. 216 - 222, View in Reaxys; Gajewski, Piotr; Renom-Carrasco, Marc; Facchini, Sofia Vailati; Pignataro, Luca; Lefort, Laurent; De Vries, Johannes G.; Ferraccioli, Raffaella; Forni, Alessandra; Piarulli, Umberto; Gennari, Cesare; European Journal of Organic Chemistry; vol. 2015; nb. 9; (2015); p. 1887 - 1893, View in Reaxys; Coverdale, James P. C.; SanchezCano, Carlos; Clarkson, Guy J.; Soni, Rina; Wills, Martin; Sadler, Peter J.; Chemistry - A European Journal; vol. 21; nb. 22; (2015); p. 8043 8046, View in Reaxys; Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 - 2546, View in Reaxys; Gajewski, Piotr; Renom-Carrasco, Marc; Facchini, Sofia Vailati; Pignataro, Luca; Lefort, Laurent; De Vries, Johannes G.; Ferraccioli, Raffaella; Piarulli, Umberto; Gennari, Cesare; European Journal of Organic Chemistry; vol. 2015; nb. 25; (2015); p. 5526 - 5536, View in Reaxys; Gonda, Tímea; Szakonyi, Zsolt; Csámpai, Antal; Haukka, Matti; Fülöp, Ferenc; Tetrahedron Asymmetry; vol. 27; nb. 11-12; (2016); p. 480 - 486, View in Reaxys; Agac, Ahmet; Karakaya, Idris; Sahin, Irfan; Emir, Sedat; Karabuga, Semistan; Ulukanli, Sabri; Journal of Organometallic Chemistry; vol. 819; (2016); p. 189 - 193, View in Reaxys; Jadhav, Dipesh D.; Patil, Harshal S.; Chaya, Patil S.; Thulasiram, Hirekodathakallu V.; Tetrahedron Letters; vol. 57; nb. 41; (2016); p. 4563 4567, View in Reaxys; Liu, Juan; Wang, Fei; Ding, Qing-Rong; Zhang, Jian; Inorganic Chemistry; vol. 55; nb. 24; (2016); p. 12520 - 12522, View in Reaxys; Margalef, Jèssica; Slagbrand, Tove; Tinnis, Fredrik; Adolfsson, Hans; Diéguez, Montserrat; Pàmies, Oscar; Advanced Synthesis and Catalysis; vol. 358; nb. 24; (2016); p. 4006 - 4018, View in Reaxys; Tao, Meng; Wu, Fang; Li, Teng; Li, Yan-Yun; Gao, Jing-Xing; Chinese Chemical Letters; vol. 28; nb. 1; (2017); p. 97 - 100, View in Reaxys; Smith, Samantha A. M.; Lagaditis, Paraskevi O.; Lüpke, Anne; Lough, Alan J.; Morris, Robert H.; Chemistry - A European Journal; vol. 23; nb. 30; (2017); p. 7212 - 7216, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys; Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys; de Jesús Cázares-Marinero, José; Przybylski, Cédric; Salmain, Michèle; European Journal of Inorganic Chemistry; vol. 2018; nb. 12; (2018); p. 1383 - 1393, View in Reaxys TLC (Thin layer chromatography)

supporting informa- Hesse, Matthew J.; Essafi, Stephanie; Watson, Charlotte G.; Harvey, tion Jeremy N.; Hirst, David; Willis, Christine L.; Aggarwal, Varinder K.; Angewandte Chemie - International Edition; vol. 53; nb. 24; (2014); p. 6145 - 6149; Angew. Chem.; vol. 126; nb. 24; (2014); p. 6259 - 6263,5, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys

GC (Gas chromatography)

Silva, Camila R.; Souza, Juliana C.; Araujo, Lidiane S.; Kagohara, Edna; Garcia, Thais P.; Pelizzari, Vivian H.; Andrade, Leandro H.; Journal of Molecular Catalysis B: Enzymatic; vol. 83; (2012); p. 23 - 28, View in Reaxys; Bian, Guangling; Huang, Huayin; Zong, Hua; Song, Ling; Chirality; vol. 24; nb. 10; (2012); p. 825 - 832, View in Reaxys;

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Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 - 10434, View in Reaxys; Kataoka, Noriyuki; Okudomi, Masayuki; Chihara, Naoka; Matsumoto, Kazutsugu; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 615 621, View in Reaxys; Csillag, Kinga; Szakonyi, Zsolt; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 24; nb. 9-10; (2013); p. 553 - 561, View in Reaxys; Zhang, Zhanbin; Li, Min; Zi, Guofu; Chirality; vol. 19; nb. 10; (2007); p. 802 - 808, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys; Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys; Nieto, Ismael; Wooten, Alfred J.; Robinson, Jerome R.; Carroll, Patrick J.; Schelter, Eric J.; Walsh, Patrick J.; Organometallics; vol. 32; nb. 24; (2013); p. 7431 - 7439, View in Reaxys; Boukachabia, Mourad; Vriamont, Nicolas; Lambin, Dominique; Riant, Olivier; Aribi-Zouioueche, Louisa; Comptes Rendus Chimie; vol. 17; nb. 5; (2014); p. 403 - 412, View in Reaxys; Jiang, Heyan; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 410 - 413, View in Reaxys; Janeczko, Tomasz; KostrzewaSuslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys; Li, Aipeng; Ye, Lidan; Guo, Fei; Yang, Xiaohong; Yu, Hongwei; Journal of Molecular Catalysis B: Enzymatic; vol. 117; (2015); p. 31 - 37, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys; Wang, Dan; Yang, Zhirong; Zhang, Jinhua; Han, Yunlei; Hao, Junli; He, Lang; Catalysis Letters; vol. 146; nb. 6; (2016); p. 1079 - 1086, View in Reaxys; Sun, Zhoutong; Li, Guangyue; Ilie, Adriana; Reetz, Manfred T.; Tetrahedron Letters; vol. 57; nb. 32; (2016); p. 3648 - 3651, View in Reaxys; KamenovaNacheva, Mariana; Dobrikov, Georgi M.; Dimitrov, Vladimir; Tetrahedron Asymmetry; vol. 27; nb. 17-18; (2016); p. 852 - 864, View in Reaxys HPLC (High performance liquid chromatography)

tR(mm) 19.19

Paragraph 0182

Patent; The Governing Council of the University of Toronto; MORRIS, Robert H.; LAGADITIS, Paraskevi Olympia; SONNENBERG, Jessica; (73 pag.); US2016/326202; (2016); (A1) English, View in Reaxys

TLC (Thin layer chromatography)

Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 - 26, View in Reaxys; Nottingham, Chris; Benson, Robert; Müller-Bunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 80; nb. 20; (2015); p. 10163 10176, View in Reaxys

HPLC (High performance liquid chromatography); GPC (Gel permeation chromatography)

Zhang, An-Lin; Yu, Zeng-Da; Yang, Li-Wen; Yang, Nian-Fa; Tetrahedron Asymmetry; vol. 26; nb. 4; (2015); p. 173 - 179, View in Reaxys

GC (Gas chromatography)

retention time [min] Page/Page column 13 24

HPLC (High performance liquid chromatography) GC (Gas chromatography)

S isomer 21.00 min

Paragraph 0136

Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys

SFC (Supercritical fluid chromatography) Crystal Property Description (7) Colour & Other Location Properties

Patent; B.R.A.I.N. AG; Liebeton, Klaus; Eck, Jürgen; Bornscheuer, Uwe; Böttcher, Dominique; Langer, Peter; Bellur, Esen; US9193961; (2015); (B2) English, View in Reaxys

Kitamura, Masato; Oka, Hiromasa; Suga, Seiji; Noyori, Ryoji; Kaelin, David E.; Martin, Stephen F.; Beutner, Gregory L.; Denmark, Scott E.; Organic Syntheses; vol. 79; (2002); p. 139 - 139, View in Reaxys References

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colourless

Bian, Guangling; Huang, Huayin; Zong, Hua; Song, Ling; Chirality; vol. 24; nb. 10; (2012); p. 825 - 832, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys; Chen, Qian; Ou, Jun; Chen, Guo-Shu; Liu, Tian-Hui; Xie, Bin; Liang, Hai-Bo; Xie, Li-Qiong; Chen, Yi-Xin; Chirality; vol. 26; nb. 5; (2014); p. 268 - 271, View in Reaxys; Janeczko, Tomasz; Kostrzewa-Suslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys; Kitamura, Masato; Oka, Hiromasa; Suga, Seiji; Noyori, Ryoji; Kaelin, David E.; Martin, Stephen F.; Beutner, Gregory L.; Denmark, Scott E.; Organic Syntheses; vol. 79; (2002); p. 139 - 139, View in Reaxys; Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys

colourless

supporting informa- Li, Yanyun; Yu, Shenluan; Wu, Xiaofeng; Xiao, Jianliang; Shen, Weiyi; Dong, Zhenrong; tion Gao, Jingxing; Journal of the American Chemical Society; vol. 136; nb. 10; (2014); p. 4031 4039, View in Reaxys; Hesse, Matthew J.; Essafi, Stephanie; Watson, Charlotte G.; Harvey, Jeremy N.; Hirst, David; Willis, Christine L.; Aggarwal, Varinder K.; Angewandte Chemie International Edition; vol. 53; nb. 24; (2014); p. 6145 - 6149; Angew. Chem.; vol. 126; nb. 24; (2014); p. 6259 - 6263,5, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 - 2546, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys; Qin, Chao; Hou, Chuan-Jin; Liu, Hongzhu; Liu, Yan-Jun; Huang, De-Zhi; Hu, Xiang-Ping; Tetrahedron Letters; vol. 59; nb. 8; (2018); p. 719 - 722, View in Reaxys; Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys

yellow

Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 - 1816, View in Reaxys

colourless

Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 - 597, View in Reaxys; Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 - 4470, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; Tetrahedron Asymmetry; vol. 23; nb. 10; (2012); p. 789 - 794, View in Reaxys

yellow

supporting informa- Stegink, Bart; Van Boxtel, Lonneke; Lefort, Laurent; Minnaard, Adriaan J.; Feringa, Ben tion L.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 352; nb. 14-15; (2010); p. 2621 - 2628, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; European Journal of Organic Chemistry; nb. 20; (2012); p. 3732 - 3736, View in Reaxys

light-yellow

Bandini, Marco; Melucci, Manuela; Piccinelli, Fabio; Sinisi, Riccardo; Tommasi, Simona; Umani-Ronchi, Achille; Chemical Communications; nb. 43; (2007); p. 4519 - 4521, View in Reaxys

yellow

Lipshutz, Bruce H.; Noson, Kevin; Chrisman, Will; Lower, Asher; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8779 - 8789, View in Reaxys

Dynamic Viscosity (1) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

References

0.1306

Thole; Journal of the Chemical Society; vol. 103; (1913); p. 24, View in Reaxys

Optical Rotatory Power (141) 1 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.5 g/100ml

Enantiomeric excess [%ee] 83 Length of Path [cm]

Solvent (Optical Rotatory Power)

chloroform

73/229

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Optical Rotatory Power [deg]

-28

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 2 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.38 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-54.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Qin, Chao; Hou, Chuan-Jin; Liu, Hongzhu; Liu, Yan-Jun; Huang, De-Zhi; Hu, Xiang-Ping; Tetrahedron Letters; vol. 59; nb. 8; (2018); p. 719 - 722, View in Reaxys 3 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-48.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys 4 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.3 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.2

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Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform-d1

Optical Rotatory Power [deg]

-14.8

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Utecht, Greta; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1774 - 1779, View in Reaxys 6 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 83 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-10.9

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 7 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 87 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-11.1

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 8 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 94

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Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-12.7

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 9 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-13.4

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 10 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-13.9

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 11 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-14.1

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 12 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 98

76/229

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Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-14.5

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 13 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-14.7

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 14 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-14.8

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 15 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-15

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 16 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.3 g/100ml

Enantiomeric excess [%ee] 98

77/229

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Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-15.2

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 17 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-50.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Gao, De-Wei; Gu, Qing; You, Shu-Li; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2544 - 2547, View in Reaxys 18 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 80 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-35.9

Wavelength (Optical Rota- 589 tory Power) [nm] Chrzanowski, Jacek; Rachwalski, Michal; Pieczonka, Adam M.; Leniak, Stanislaw; Drabowicz, Jzef; Kielbasiski, Piotr; Tetrahedron; vol. 72; nb. 21; (2016); p. 2649 - 2655, View in Reaxys 19 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-38.6

Type (Optical Rotatory Power)

[alpha]

78/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 87 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-39.3

Wavelength (Optical Rota- 589 tory Power) [nm] Jarzyski, Szymon; Lesniak, Stanislaw; Pieczonka, Adam M.; Rachwalski, Michal; Tetrahedron Asymmetry; vol. 26; nb. 1; (2015); p. 35 - 40, View in Reaxys 21 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 88 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-39.5

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 89 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-40

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-41.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

79/229

2018-07-03 16:52:46

Pieczonka, Adam M.; Les̈niak, Stanisław; Jarzyński, Szymon; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 26; nb. 2-3; (2015); p. 148 - 151, View in Reaxys; Jarzyski, Szymon; Lesniak, Stanislaw; Pieczonka, Adam M.; Rachwalski, Michal; Tetrahedron Asymmetry; vol. 26; nb. 1; (2015); p. 35 - 40, View in Reaxys 24 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-43.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Pieczonka, Adam M.; Les̈niak, Stanisław; Jarzyński, Szymon; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 26; nb. 2-3; (2015); p. 148 - 151, View in Reaxys 25 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.0 g/100ml

Enantiomeric excess [%ee] 93.6 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-96.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 2546, View in Reaxys 26 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-45.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Yoshida, Kazuhiro; Kamimura, Takumi; Kuwabara, Hiroshi; Yanagisawa, Akira; Chemical Communications; vol. 51; nb. 84; (2015); p. 15442 - 15445, View in Reaxys 27 of 141

Type (Optical Rotatory Power)

[alpha]

80/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

0.65 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform-d1

Optical Rotatory Power [deg]

-58.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

19.9

Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys 28 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.72 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, Yanyun; Yu, Shenluan; Wu, Xiaofeng; Xiao, Jianliang; Shen, Weiyi; Dong, Zhenrong; Gao, Jingxing; Journal of the American Chemical Society; vol. 136; nb. 10; (2014); p. 4031 - 4039, View in Reaxys 29 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.4 g/100ml

Solvent (Optical Rotatory Power)

diethyl ether

Optical Rotatory Power [deg]

-59.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.13 mol/l

Enantiomeric excess [%ee] 20 Solvent (Optical Rotatory Power)

chloroform

81/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

3.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Zheng, Jun; You, Shu-Li; Chemical Communications; vol. 50; nb. 60; (2014); p. 8204 - 8207, View in Reaxys 31 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.03 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-46.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Kang, Guowei; Lin, Silong; Shiwakoti, Atul; Ni, Bukuo; Catalysis Communications; vol. 57; (2014); p. 111 - 114, View in Reaxys 32 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.5 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-4.78

Wavelength (Optical Rota- 589 tory Power) [nm] Location

supporting information

Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 16106, View in Reaxys 33 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.95 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

82/229

2018-07-03 16:52:46

Janeczko, Tomasz; Kostrzewa-Suslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys 34 of 141

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 91.4 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-38

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zeng, Xiaofeng; Malik, Debasis; Chen, Ryan; Lee-Ruff, Edward; Synthetic Communications; vol. 43; nb. 8; (2013); p. 1168 - 1172, View in Reaxys 35 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 80 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-36

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys 36 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-40.2

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys 37 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.7

Wavelength (Optical Rota- 589 tory Power) [nm]

83/229

2018-07-03 16:52:46

Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys; Rachwalski, Michal; Jarzynski, Szymon; Jasinski, Marcin; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 689 - 693, View in Reaxys 38 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-44.1

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys 39 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Enantiomeric excess [%ee] 84 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-34.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Michigami, Kyosuke; Hayashi, Masahiko; Tetrahedron; vol. 69; nb. 21; (2013); p. 4221 - 4225, View in Reaxys 40 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 42 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-18.9

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Jarzynski, Szymon; Jasinski, Marcin; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 689 - 693, View in Reaxys 41 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

84/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-41.4

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 52 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-27.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Roszkowski, Piotr; Maurin, Jan K.; Czarnocki, Zbigniew; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 643 - 650, View in Reaxys 43 of 141

Type (Optical Rotatory Power)

alpha

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 89.2 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-39.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Prasad, Kavirayani R.; Revu, Omkar; Tetrahedron; vol. 69; nb. 39; (2013); p. 8422 - 8428, View in Reaxys 44 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 40 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-18

Wavelength (Optical Rota- 589 tory Power) [nm] Lesniak, Stanislaw; Rachwalski, Michal; Jarzynski, Szymon; Obijalska, Emilia; Tetrahedron Asymmetry; vol. 24; nb. 20; (2013); p. 1336 - 1340, View in Reaxys 45 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

85/229

2018-07-03 16:52:46

Enantiomeric excess [%ee] 80 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-36

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.2

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 75 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-33.8

Wavelength (Optical Rota- 589 tory Power) [nm] Lesniak, Stanislaw; Pieczonka, Adam M.; Jarzynski, Szymon; Justyna, Katarzyna; Rachwalski, Michal; Tetrahedron Asymmetry; vol. 24; nb. 20; (2013); p. 1341 - 1344, View in Reaxys 48 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-41

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

86/229

2018-07-03 16:52:46

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-41.9

Concentration (Optical Rotatory Power)

5.0 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

ethanol

Optical Rotatory Power [deg]

-30.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Jiang, Heyan; Journal of Chemical Research; vol. 37; nb. 12; (2013); p. 761 - 763, View in Reaxys 51 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.25 g/100ml

Enantiomeric excess [%ee] 79 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-44.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

20.6

Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys 52 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.25 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-40.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Faigl, Ferenc; Matravolgyi, Bela; Szoellosy, Aron; Czugler, Matyas; Tarkanyi, Gabor; Vekey, Karoly; Kubinyi, Miklos; Chirality; vol. 24; nb. 7; (2012); p. 532 - 542, View in Reaxys

87/229

2018-07-03 16:52:46

53 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Faigl, Ferenc; Matravolgyi, Bela; Szoellosy, Aron; Czugler, Matyas; Tarkanyi, Gabor; Vekey, Karoly; Kubinyi, Miklos; Chirality; vol. 24; nb. 7; (2012); p. 532 - 542, View in Reaxys 54 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 90 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-38

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; Tetrahedron Asymmetry; vol. 23; nb. 10; (2012); p. 789 - 794, View in Reaxys 55 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.973 g/100ml

Enantiomeric excess [%ee] 56.6 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-27.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Ema, Tadashi; Nakano, Yasuko; Yoshida, Daiki; Kamata, Shusuke; Sakai, Takashi; Organic and Biomolecular Chemistry; vol. 10; nb. 31; (2012); p. 6299 - 6308, View in Reaxys 56 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

88/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-39.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; European Journal of Organic Chemistry; nb. 20; (2012); p. 3732 3736, View in Reaxys 57 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 11 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-5.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Roszkowski, Piotr; Maurin, Jan K.; Czarnocki, Zbigniew; Tetrahedron Asymmetry; vol. 23; nb. 14; (2012); p. 1106 - 1110, View in Reaxys 58 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, Yuehui; Zhou, Yougui; Shi, Qixun; Ding, Kuiling; Noyori, Ryoji; Sandoval, Christian A.; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 495 - 500, View in Reaxys 59 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.46 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-49.6

Wavelength (Optical Rota- 589 tory Power) [nm]

89/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Zhu, Qiming; Shi, Dengjian; Xia, Chungu; Huang, Hanmin; Chemistry - A European Journal; vol. 17; nb. 28; (2011); p. 7760 - 7763, View in Reaxys 60 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-44.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Xie, Jian-Hua; Liu, Xiao-Yan; Xie, Jian-Bo; Wang, Li-Xin; Zhou, Qi-Lin; Angewandte Chemie - International Edition; vol. 50; nb. 32; (2011); p. 7329 - 7332, View in Reaxys 61 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.3 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-33.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys 62 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.02 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-38.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

90/229

2018-07-03 16:52:46

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.3 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yadav, Ashok K.; Kumar, Manoj; Yadav, Tripti; Jain, Renuka; Synlett; nb. 5; (2010); p. 712 - 714, View in Reaxys 64 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.5 g/100ml

Enantiomeric excess [%ee] 89 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-32.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, Wei Jie; Qiu, Sheng Xiang; Advanced Synthesis and Catalysis; vol. 352; nb. 7; (2010); p. 1119 - 1122, View in Reaxys 65 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-46.7

Wavelength (Optical Rota- 589 tory Power) [nm] Location

supporting information

Patil; Gonnade; Joshi; Tetrahedron; vol. 66; nb. 27-28; (2010); p. 5036 - 5041, View in Reaxys 66 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.5 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

91/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-37

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, Wei Jie; Qiu, Sheng Xiang; Xu, Zun Le; Beilstein Journal of Organic Chemistry; vol. 6; (2010); Art.No: 29, View in Reaxys 67 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.48 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, De Run; He, Anyu; Falck; Organic Letters; vol. 12; nb. 8; (2010); p. 1756 - 1759, View in Reaxys 68 of 141

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 90 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 69 of 141

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 33 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-15.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys

92/229

2018-07-03 16:52:46

70 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.93 g/100ml

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.4

Wavelength (Optical Rota- 589 tory Power) [nm] Location

supporting information

Stegink, Bart; Van Boxtel, Lonneke; Lefort, Laurent; Minnaard, Adriaan J.; Feringa, Ben L.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 352; nb. 14-15; (2010); p. 2621 - 2628, View in Reaxys 71 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.00 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-46.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Li, Yuehui; Ding, Kuiling; Sandoval, Christian A.; Organic Letters; vol. 11; nb. 4; (2009); p. 907 - 910, View in Reaxys 72 of 141

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 93 Optical Rotatory Power [deg]

-21.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Comment (Optical Rotato- neat (no solvent) ry Power) Binder, Caitlin M.; Bautista, April; Zaidlewicz, Marek; Krzeminski, Marek P.; Oliver, Allen; Singaram, Bakthan; Journal of Organic Chemistry; vol. 74; nb. 6; (2009); p. 2337 - 2343, View in Reaxys 73 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.01 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

hexane

93/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-49

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 4470, View in Reaxys 74 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.48 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-47.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Patent; Board of Regents; US2009/253919; (2009); (A1) English, View in Reaxys 75 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.00 g/100ml

Enantiomeric excess [%ee] 81 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-39.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Kantam, M. Lakshmi; Yadav, Jagjit; Laha, Soumi; Srinivas, Pottabathula; Sreedhar, Bojja; Figueras; Journal of Organic Chemistry; vol. 74; nb. 12; (2009); p. 4608 - 4611, View in Reaxys 76 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.76 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

-32.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

94/229

2018-07-03 16:52:46

Noh, Dongwan; Chea, Heesung; Ju, Junghwan; Yun, Jaesook; Angewandte Chemie, International Edition; vol. 48; nb. 33; (2009); p. 6062 - 6064; Angewandte Chemie; vol. 121; nb. 33; (2009); p. 6178 - 6180, View in Reaxys 77 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 50 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-22

Wavelength (Optical Rota- 589 tory Power) [nm] Lesniak, Stanislaw; Rachwalski, Michal; Sznajder, Ewelina; Kielbasinski, Piotr; Tetrahedron Asymmetry; vol. 20; nb. 20; (2009); p. 2311 - 2314, View in Reaxys 78 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-45.7

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-44.2

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.85 g/100ml

Enantiomeric excess [%ee] 66 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-40

Wavelength (Optical Rota- 589 tory Power) [nm]

95/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Martins, Jose E.D.; Morris, David J.; Wills, Martin; Tetrahedron Letters; vol. 50; nb. 6; (2009); p. 688 - 692, View in Reaxys 81 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.30 g/100ml

Enantiomeric excess [%ee] 85 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-36.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Dean, Melissa A.; Hitchcock, Shawn R.; Tetrahedron Asymmetry; vol. 19; nb. 22; (2008); p. 2563 - 2567, View in Reaxys 82 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.85 g/100ml

Length of Path [cm]

Solvent (Optical Rotatory Power)

acetone

Optical Rotatory Power [deg]

-30.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 597, View in Reaxys 83 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.02 g/100ml

Enantiomeric excess [%ee] 67 Solvent (Optical Rotatory Power)

dichloromethane

Optical Rotatory Power [deg]

-18.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

24.1

Chang, Tien-Chu; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 55; nb. 3; (2008); p. 606 - 615, View in Reaxys 84 of 141

Type (Optical Rotatory Power)

[alpha]

96/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

1.23 g/100ml

Enantiomeric excess [%ee] 76 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-29.26

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Clive, Derrick L. J.; Stoffman, Elia J. L.; Organic and Biomolecular Chemistry; vol. 6; nb. 10; (2008); p. 1831 - 1842, View in Reaxys 85 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.00 g/100ml

Enantiomeric excess [%ee] 84 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-42.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.73 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-50.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Reigada, Juliana B.; Tcacenco, Celize. M.; Andrade, Leandro H.; Kato, Massuo J.; Porto, Andre L.M.; Lago, Joao Henrique G.; Tetrahedron Asymmetry; vol. 18; nb. 9; (2007); p. 1054 - 1058, View in Reaxys 87 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.8 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

97/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-46

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Bachu, Prabhakar; Gibson, Jennifer S.; Sperry, Jonathan; Brimble, Margaret A.; Tetrahedron Asymmetry; vol. 18; nb. 13; (2007); p. 1618 - 1624, View in Reaxys 88 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.03 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-50.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yang, Wei; Xu, Jian-He; Xie, Yan; Xu, Yi; Zhao, Gang; Lin, Guo-Qiang; Tetrahedron Asymmetry; vol. 17; nb. 12; (2006); p. 1769 - 1774, View in Reaxys 89 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-46

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Jing, Qing; Sandoval, Christian A.; Wang, Zheng; Ding, Kuiling; European Journal of Organic Chemistry; nb. 16; (2006); p. 3606 - 3616, View in Reaxys 90 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.2 g/100ml

Solvent (Optical Rotatory Power)

hexane

Optical Rotatory Power [deg]

-47

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Hajji, Chakib; Testa, M. Luisa; Zaballos-Garcia, Elena; Sepulveda-Arques, Jose; Journal of Chemical Research; nb. 7; (2005); p. 420 - 421, View in Reaxys

98/229

2018-07-03 16:52:46

91 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.20 g/100ml

Solvent (Optical Rotatory Power)

hexane

Optical Rotatory Power [deg]

-47.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Sakoh, Hiroki; Sakuraba, Shunji; Sugimoto, Yuichi; Imamura, Hideaki; Jona, Hideki; Yamada, Koji; Bamba-Nagano, Rie; Hashizume, Terutaka; Morishima, Hajime; Chemical and Pharmaceutical Bulletin; vol. 52; nb. 1; (2004); p. 163 - 165, View in Reaxys 92 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

ethanol

Optical Rotatory Power [deg]

-34.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

24.7

Homann, Michael J.; Vail, Robert B.; Previte, Edward; Tamarez, Maria; Morgan, Brian; Dodds, David R.; Zaks, Aleksey; Tetrahedron; vol. 60; nb. 3; (2004); p. 789 - 797, View in Reaxys 93 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.6 g/100ml

Enantiomeric excess [%ee] 98.8 Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

-48.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.3 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-45.6

Wavelength (Optical Rota- 589 tory Power) [nm]

99/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Kamal, Ahmed; Sandbhor, Mahendra; Ramana; Tetrahedron Asymmetry; vol. 13; nb. 8; (2002); p. 815 - 820, View in Reaxys 95 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat liquid

Optical Rotatory Power [deg]

-20.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

De Luca, Lidia; Giacomelli, Giampaolo; Porcheddu, Andrea; Organic Letters; vol. 4; nb. 4; (2002); p. 553 - 555, View in Reaxys 96 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.55 g/100ml

Enantiomeric excess [%ee] 95.4 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-45.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.23 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-50

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Hayashi; Hirate; Kitayama; Tsuji; Torii; Uozumi; Journal of Organic Chemistry; vol. 66; nb. 4; (2001); p. 1441 - 1449, View in Reaxys 98 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

-28

100/229

2018-07-03 16:52:46

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Bakker; Spruijt; Van Rantwijk; Sheldon; Tetrahedron Asymmetry; vol. 11; nb. 8; (2000); p. 1801 - 1808, View in Reaxys 99 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.19 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Lutz, Christian; Jones, Philip; Knochel, Paul; Synthesis; nb. 2; (1999); p. 312 - 316, View in Reaxys 100 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.18 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-49.2

Wavelength (Optical Rota- 589 tory Power) [nm] Yun, Jaesook; Buchwald, Stephen L.; Journal of the American Chemical Society; vol. 121; nb. 24; (1999); p. 5640 - 5644, View in Reaxys 101 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.643 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-47.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Nakamura; Matsuda; Journal of Organic Chemistry; vol. 63; nb. 24; (1998); p. 8957 - 8964, View in Reaxys 102 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat liquid

Optical Rotatory Power [deg]

-24.7

Wavelength (Optical Rota- 589 tory Power) [nm]

101/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 26, View in Reaxys 103 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.2 g/100ml

Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

-27.9

Wavelength (Optical Rota- 589 tory Power) [nm] Faraldos, Juan; Arroyo, Elisa; Herradon, Bernardo; Synlett; vol. 1997; nb. 4; (1997); p. 367 - 370, View in Reaxys 104 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-46.7

Wavelength (Optical Rota- 589 tory Power) [nm] Prasad; Joshi; Journal of Organic Chemistry; vol. 62; nb. 11; (1997); p. 3770 - 3771, View in Reaxys 105 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.31 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Lutz, Christian; Knochel, Paul; Journal of Organic Chemistry; vol. 62; nb. 22; (1997); p. 7895 - 7898, View in Reaxys 106 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

9.8 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-37.8

Wavelength (Optical Rota- 589 tory Power) [nm] Takeshita, Mitsuhiro; Miura, Masatomo; Unuma, Yukiko; Iwai, Sakiko; Sato, Izumi; Hongo, Takahiko; Arai, Toshie; Kosaka, Kazuhiro; Heterocycles; vol. 42; nb. 2; (1996); p. 831 - 836, View in Reaxys

102/229

2018-07-03 16:52:46

107 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.130 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-59

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Nakamura, Kaoru; Kawasaki, Masashi; Ohno, Atsuyoshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 4; (1996); p. 1079 - 1085, View in Reaxys 108 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.12 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-46.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Wirth, Thomas; Kulicke, Klaus J.; Fragale, Gianfranco; Helvetica Chimica Acta; vol. 79; nb. 7; (1996); p. 1957 - 1966, View in Reaxys 109 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.425 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-49.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Nakamura, Kaoru; Matsuda, Tomoko; Ohno, Atsuyoshi; Tetrahedron Asymmetry; vol. 7; nb. 10; (1996); p. 3021 - 3024, View in Reaxys 110 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.2 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-46.3

Wavelength (Optical Rota- 589 tory Power) [nm]

103/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Shono, Tatsuya; Kise, Naoki; Fujimoto, Taku; Yamanami, Ayuko; Nomura, Ryoji; Journal of Organic Chemistry; vol. 59; nb. 7; (1994); p. 1730 - 1740, View in Reaxys 111 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4.91 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.94

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Watanabe, Masami; Soai, Kenso; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 7; (1994); p. 837 - 842, View in Reaxys 112 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soai, Kenso; Hirose, Yuji; Ohno, Yoshiaki; Tetrahedron: Asymmetry; vol. 4; nb. 7; (1993); p. 1473 - 1474, View in Reaxys 113 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.13 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yoshioka, Masato; Kawakita, Takashi; Ohno, Masaji; Tetrahedron Letters; vol. 30; nb. 13; (1989); p. 1657 - 1660, View in Reaxys; Takahashi, Hideyo; Kawakita, Takashi; Ohno, Masaji; Yoshioka, Masato; Kobayashi, Susumu; Tetrahedron; vol. 48; nb. 27; (1992); p. 5691 - 5700, View in Reaxys 114 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4 g/100ml

Length of Path [cm]

Solvent (Optical Rotatory Power)

CHCl3

104/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-44.24

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Conti; Falorni; Giacomelli; Soccolini; Tetrahedron; vol. 48; nb. 41; (1992); p. 8993 - 9000, View in Reaxys 115 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4.3 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-45.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Shono, Tatsuya; Kise, Naoki; Fujimoto, Taku; Tominaga, Naoto; Morita, Hiroshi; Journal of Organic Chemistry; vol. 57; nb. 28; (1992); p. 7175 - 7187, View in Reaxys 116 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2 g/100ml

Length of Path [cm]

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-45.82

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Falorni, Massimo; Giacomelli, Giampaolo; Gazzetta Chimica Italiana; vol. 122; nb. 8; (1992); p. 339 - 340, View in Reaxys 117 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.68 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.01

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Li; Jiang; Mi; Tetrahedron Asymmetry; vol. 3; nb. 11; (1992); p. 1467 - 1474, View in Reaxys 118 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat (no solvent)

105/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-21.16

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Davis, Franklin A.; Reddy, R. Thimma; Journal of Organic Chemistry; vol. 57; nb. 9; (1992); p. 2599 - 2606, View in Reaxys 119 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.38 g/100ml

Length of Path [cm]

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.3

Wavelength (Optical Rota- 589 tory Power) [nm] Bussche-Huennefeld, Joanna Linda v.; Seebach, Dieter; Tetrahedron; vol. 48; nb. 27; (1992); p. 5719 - 5730, View in Reaxys 120 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4.9 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.49

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soai, Kenso; Watanabe, Masami; Tetrahedron: Asymmetry; vol. 2; nb. 2; (1991); p. 97 - 100, View in Reaxys 121 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.5 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-46.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Shono, Tatsuya; Kise, Naoki; Shirakawa, Eiji; Matsumoto, Hideshi; Okazaki, Eiichi; Journal of Organic Chemistry; vol. 56; (1991); p. 3063 - 3067, View in Reaxys 122 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.21 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

106/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-47.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Watanabe, Makoto; Araki, Shuki; Butsugan, Yasuo; Journal of Organic Chemistry; vol. 56; nb. 6; (1991); p. 2218 - 2224, View in Reaxys 123 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.28 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Watanabe, Makoto; Araki, Shuki; Butsugan, Yasuo; Journal of Organic Chemistry; vol. 56; nb. 6; (1991); p. 2218 - 2224, View in Reaxys 124 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.94 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-48.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Watanabe, Makoto; Araki, Shuki; Butsugan, Yasuo; Journal of Organic Chemistry; vol. 56; nb. 6; (1991); p. 2218 - 2224, View in Reaxys 125 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.24

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Chelucci, Giorgio; Conti, Sandra; Falorni, Massimo; Giacomelli, Giampaolo; Tetrahedron; vol. 47; nb. 38; (1991); p. 8251 8258, View in Reaxys 126 of 141

Type (Optical Rotatory Power)

[alpha]

107/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

6.11 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-47.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Noyori, R.; Suga, S.; Kawai, K.; Okada, S.; Kitamura, M.; et al.; Journal of Organometallic Chemistry; vol. 382; nb. 1-2; (1990); p. 19 - 37, View in Reaxys; Kitamura, M.; Suga, S.; Kawai, K.; Noyori, R.; Journal of the American Chemical Society; vol. 108; nb. 19; (1986); p. 6071 - 6072, View in Reaxys 127 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

CDCl3

Optical Rotatory Power [deg]

-44

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Chan, T. H.; Pellon, P.; Journal of the American Chemical Society; vol. 111; nb. 23; (1989); p. 8737 - 8738, View in Reaxys 128 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.95

Wavelength (Optical Rota- 589 tory Power) [nm] Soai, Kenso; Ookawa, Atsuhiro; Kaba, Tatsuya; Ogawa, Kazuo; Journal of the American Chemical Society; vol. 109; nb. 23; (1987); p. 7111 - 7115, View in Reaxys 129 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.15 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-40.74

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soai, Kenso; Yokoyama, Shuji; Ebihara, Katsumi; Hayasaka, Tomoiki; Journal of the Chemical Society, Chemical Communications; nb. 22; (1987); p. 1690 - 1691, View in Reaxys

108/229

2018-07-03 16:52:46

130 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4.6 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

32.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soai, Kenso; Ookawa, Atsuhiro; Ogawa, Kazuo; Kaba, Tatsuya; Journal of the Chemical Society, Chemical Communications; nb. 6; (1987); p. 467 - 468, View in Reaxys 131 of 141

Patent; Noe; Christian; US4497960; (1985); (A) English, View in Reaxys

132 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat (no solvent)

Optical Rotatory Power [deg]

-0.284

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Noyori; Tomino; Tanimoto; Nishizawa; Journal of the American Chemical Society; vol. 106; nb. 22; (1984); p. 6709 - 6716, View in Reaxys 133 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.54 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yamamoto, Koji; Fukushima, Hitoshi; Nakazaki, Masao; Journal of the Chemical Society, Chemical Communications; nb. 22; (1984); p. 1490 - 1491, View in Reaxys 134 of 141

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-5.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Boireau,G. et al.; Tetrahedron; vol. 35; (1979); p. 1457 - 1461, View in Reaxys 135 of 141

Type (Optical Rotatory Power)

[alpha]

109/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-26.77

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Gallina, Carlo; Lucente, Gino; Pinnen, Francesco; Tetrahedron; vol. 34; nb. 15; (1978); p. 2361 - 2363, View in Reaxys 136 of 141

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

-2.21

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yamamoto,K. et al.; Journal of Organometallic Chemistry; vol. 46; (1972); p. C65 - C67, View in Reaxys 137 of 141

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat (no solvent)

Optical Rotatory Power [deg]

-22.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Levene; Rothen; Kuna; Journal of Biological Chemistry; vol. 120; (1937); p. 789, View in Reaxys 138 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

c=10

Solvent (Optical Rotatory Power)

diethyl ether

Optical Rotatory Power [deg]

-55.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Levene; Mikeska; Journal of Biological Chemistry; vol. 70; (1926); p. 377, View in Reaxys 139 of 141

Type (Optical Rotatory Power)

alpha

Length of Path [cm]

Optical Rotatory Power [deg]

18.5 - 163

Wavelength (Optical Rota- 589 tory Power) [nm] Pickard; Kenyon; Journal of the Chemical Society; vol. 105; (1914); p. 1124, View in Reaxys 140 of 141

Type (Optical Rotatory Power)

[alpha]

110/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

-35.58 - -24.76

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

5.3 - 94

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys 141 of 141

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

c=5

Solvent (Optical Rotatory Power)

ethanol

Optical Rotatory Power [deg]

-32.48

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys NMR Spectroscopy (120) 1 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; European Journal of Organic Chemistry; nb. 20; (2012); p. 3732 3736, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 - 10434, View in Reaxys; Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys; Wang, Xiuren; Zhang, Jie; Liu, Yan; Cui, Yong; Bulletin of the Chemical Society of Japan; vol. 87; nb. 3; (2014); p. 435 - 440, View in Reaxys; Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 - 2688, View in Reaxys; Hesse, Matthew J.; Essafi, Stephanie; Watson, Charlotte G.; Harvey, Jeremy N.; Hirst, David; Willis, Christine L.; Aggarwal, Varinder K.; Angewandte Chemie - International Edition; vol. 53; nb. 24; (2014); p. 6145 - 6149; Angew. Chem.; vol. 126; nb. 24; (2014); p. 6259 - 6263,5, View in Reaxys; Zheng, Jun; You, Shu-Li; Chemical Communications; vol. 50; nb. 60; (2014); p. 8204 - 8207, View in Reaxys; An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, View in Reaxys; Kang, Guowei; Lin, Silong; Shiwakoti, Atul; Ni, Bukuo; Catalysis Communications; vol. 57; (2014); p. 111 - 114, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Gao, DeWei; Gu, Qing; You, Shu-Li; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2544 - 2547, View in Reaxys; Wang, Xiuren; Han, Xing; Zhang, Jie; Wu, Xiaowei; Liu, Yan; Cui, Yong; Journal of the American Chemical Society; vol. 138; nb. 38; (2016); p. 12332 - 12335, View in Reaxys; Zhang, Pengxiang; Yu, Jipan; Peng, Fei; Wu, Xudong; Jie, Jiyang; Liu, Can; Tian, Hua; Yang, Haijun; Fu, Hua; Chemistry - A European Journal; vol. 22; nb. 48; (2016); p. 17477 - 17484, View in Reaxys; Qin, Chao; Hou, Chuan-Jin; Liu, Hongzhu; Liu, Yan-Jun; Huang, De-Zhi; Hu, XiangPing; Tetrahedron Letters; vol. 59; nb. 8; (2018); p. 719 - 722, View in Reaxys; Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys 2 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

111/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Jolley, Katherine E.; Prokes, Ivan; Morris, David J.; Wills, Martin; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damian M.; Medlock, Jonathan A.; Nedden, Hans G.; Le Paih, Jacques J. M.; Roseblade, Stephen J.; Seger, Andreas; Sivakumar, Vilvanathan; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2545 - 2555,11, View in Reaxys; Jolley, Katherine E.; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damian M.; Medlock, Jonathan A.; Nedden, Hans G.; Le Paih, Jacques J. M.; Roseblade, Stephen J.; Seger, Andreas; Sivakumar, Vilvanathan; Prokes, Ivan; Morris, David J.; Wills, Martin; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2545 2555, View in Reaxys; Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 350, View in Reaxys; Botta, María C.; Biava, Hernán D.; Spanevello, Rolando A.; Mata, Ernesto G.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 57; nb. 20; (2016); p. 2186 - 2189, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Liardo, Elisa; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Angewandte Chemie - International Edition; vol. 55; nb. 30; (2016); p. 8691 - 8695; Angew. Chem.; vol. 128; nb. 30; (2016); p. 8833 - 8837,5, View in Reaxys; Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys 3 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 10434, View in Reaxys; Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys; Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys; Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys; Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 - 2688, View in Reaxys; An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, View in Reaxys; Kang, Guowei; Lin, Silong; Shiwakoti, Atul; Ni, Bukuo; Catalysis Communications; vol. 57; (2014); p. 111 - 114, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Hodgkinson, Roy; Jurk, Vclav; Zanotti-Gerosa, Antonio; Nedden, Hans Günter; Blackaby, Andrew; Clarkson, Guy J.; Wills, Martin; Organometallics; vol. 33; nb. 19; (2014); p. 5517 - 5524, View in Reaxys; Zhang, Pengxiang; Yu, Jipan; Peng, Fei; Wu, Xudong; Jie, Jiyang; Liu, Can; Tian, Hua; Yang, Haijun; Fu, Hua; Chemistry - A European Journal; vol. 22; nb. 48; (2016); p. 17477 - 17484, View in Reaxys; Liu, Sensheng; Liu, Huan; Zhou, Haifeng; Liu, Qixing; Lv, Jinliang; Organic Letters; vol. 20; nb. 4; (2018); p. 1110 - 1113, View in Reaxys 4 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Zanardi, María M.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 56; nb. 24; (2015); p. 3762 - 3765, View in Reaxys; Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys 5 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

112/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Zanardi, María M.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 56; nb. 24; (2015); p. 3762 - 3765, View in Reaxys; Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys 6 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.04

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Hara, Nanami; Fujisawa, Shu; Fujita, Mizuki; Miyazawa, Mikako; Ochiai, Kazuma; Katsuda, Satoshi; Fujimoto, Tetsuya; Tetrahedron; vol. 74; nb. 2; (2018); p. 296 - 302, View in Reaxys 7 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 8 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 9 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

113/229

2018-07-03 16:52:46

Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys 10 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Vidal, Marc; Schmitzer, Andreea R.; Organometallics; vol. 33; nb. 13; (2014); p. 3328 - 3340, View in Reaxys; Liu, Lijia; Long, Qing; Aoki, Toshiki; Zhang, Geng; Kaneko, Takashi; Teraguchi, Masahiro; Zhang, Chunhong; Wang, Yudan; Chirality; vol. 27; nb. 8; (2015); p. 454 - 458, View in Reaxys; Ferrari Bach, Mariana; Herzer Griebeler, Cassiana; Gross Jacoby, Caroline; Schneider, Paulo Henrique; European Journal of Organic Chemistry; vol. 2017; nb. 46; (2017); p. 6997 7004, View in Reaxys 11 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Original Text (NMR Spec- 1H NMR (600αMHz, CDCl3) α: 0.96 (t, 3H, Jα=α7.4αHz), 1.72-1.91 (m, 2H), 1.94 (s, 1H), 4.63 (t, 1H, troscopy) Jα=α6.6αHz), 7.29-7.40 (m, 5H) ppm Location

supporting information

Signals [ppm]

0.96; 1.72 - 1.91; 1.94; 4.63; 7.29 - 7.4

Kind of signal

t, 3H, Jα=α7.4αHz; m, 2H; s, 1H; t, 1H, Jα=α6.6αHz; m, 5H

Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 12 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Ferrari Bach, Mariana; Herzer Griebeler, Cassiana; Gross Jacoby, Caroline; Schneider, Paulo Henrique; European Journal of Organic Chemistry; vol. 2017; nb. 46; (2017); p. 6997 - 7004, View in Reaxys 13 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

114/229

2018-07-03 16:52:46

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys 14 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys; Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys; Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys 15 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; Tetrahedron Asymmetry; vol. 23; nb. 10; (2012); p. 789 - 794, View in Reaxys; Bian, Guangling; Huang, Huayin; Zong, Hua; Song, Ling; Chirality; vol. 24; nb. 10; (2012); p. 825 - 832, View in Reaxys; Jiang, Heyan; Journal of Chemical Research; vol. 37; nb. 12; (2013); p. 761 - 763, View in Reaxys; Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys; Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys; Jiang, Heyan; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 410 - 413, View in Reaxys; Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys; Lee, Dong-Sheng; Chang, Shu-Ming; Ho, Chun-Ying; Lu, Ta-Jung; Chirality; vol. 28; nb. 1; (2016); p. 65 - 71, View in Reaxys; Pandia Kumar, Arun Kumar; Samuelson, Ashoka G; Journal of Chemical Sciences; vol. 128; nb. 9; (2016); p. 1405 - 1415, View in Reaxys; Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys; Kitamura, Masato; Oka, Hiromasa; Suga, Seiji; Noyori, Ryoji; Kaelin, David E.; Martin, Stephen F.; Beutner, Gregory L.; Denmark, Scott E.; Organic Syntheses; vol. 79; (2002); p. 139 - 139, View in Reaxys 16 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys; Botta, María C.; Biava, Hernán D.; Spanevello, Rolando A.; Mata, Ernesto G.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 57; nb. 20; (2016); p. 2186 - 2189, View in Reaxys 17 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

115/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Faigl; Deák; Erdélyi; Holczbauer; Czugler; Nyerges; Mátravölgyi; Chirality; vol. 27; nb. 3; (2015); p. 216 - 222, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys 18 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.4

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 19 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.4

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 20 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Margalef, Jèssica; Slagbrand, Tove; Tinnis, Fredrik; Adolfsson, Hans; Diéguez, Montserrat; Pàmies, Oscar; Advanced Synthesis and Catalysis; vol. 358; nb. 24; (2016); p. 4006 - 4018, View in Reaxys 21 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

116/229

2018-07-03 16:52:46

Location

supporting information

Cheng, Ying-Ni; Wu, Hsyueh-Liang; Wu, Ping-Yu; Shen, Ying-Ying; Uang, Biing-Jiun; Chemistry - An Asian Journal; vol. 7; nb. 12; (2012); p. 2921 - 2924, View in Reaxys; Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys 22 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H NMR (400 MHz, CDCl3) α: 7.38-7.34 (m, 4H, Ar-H), 4.63-4.57 (m, 1H, CH), 1.85-1.72 (m, 3H, troscopy) CH2), 0.94-0.90 (t, J = 7.4 Hz, 3H, CH3) Signals [ppm]

7.34 - 7.38; 4.57 - 4.63; 1.72 - 1.85; 0.9 - 0.94

Kind of signal

m, 4H, Ar-H; m, 1H, CH; m, 3H, CH&2%; t, J = 7.4 Hz, 3H, CH&3%

Zhang, An-Lin; Yu, Zeng-Da; Yang, Li-Wen; Yang, Nian-Fa; Tetrahedron Asymmetry; vol. 26; nb. 4; (2015); p. 173 - 179, View in Reaxys 23 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Original Text (NMR Spectroscopy)

13C

Signals [ppm]

144.7; 128.3; 127.4; 126.1; 75.9; 31.9; 10.2

NMR (100 MHz, CDCl3) α: 144.7, 128.3, 127.4, 126.1, 75.9, 31.9, 10.2

Zhang, An-Lin; Yu, Zeng-Da; Yang, Li-Wen; Yang, Nian-Fa; Tetrahedron Asymmetry; vol. 26; nb. 4; (2015); p. 173 - 179, View in Reaxys 24 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys 25 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 299.9 scopy) [MHz]

117/229

2018-07-03 16:52:46

Location

supporting information

Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 2546, View in Reaxys 26 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Nottingham, Chris; Benson, Robert; Müller-Bunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 80; nb. 20; (2015); p. 10163 - 10176, View in Reaxys 27 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Temperature (NMR Spectroscopy) [°C]

Location

supporting information

Yoshida, Kazuhiro; Kamimura, Takumi; Kuwabara, Hiroshi; Yanagisawa, Akira; Chemical Communications; vol. 51; nb. 84; (2015); p. 15442 - 15445, View in Reaxys 28 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

Paragraph 0137

Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys; Patent; RESEARCH & BUSINESS FOUNDATION SUNGKYUNKWAN UNIVERSITY; SONG, CHOON GEUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114445; (2015); (A) Korean, View in Reaxys 29 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

Paragraph 0138

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

118/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Zhang, Anlin; Yang, Nianfa; Yang, Liwen; Peng, Dan; Chemistry Letters; vol. 43; nb. 4; (2014); p. 462 - 464, View in Reaxys 32 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Martins, Jose E.D.; Morris, David J.; Wills, Martin; Tetrahedron Letters; vol. 50; nb. 6; (2009); p. 688 - 692, View in Reaxys; Cambeiro, Xacobe C.; Pericas, Miquel A.; Advanced Synthesis and Catalysis; vol. 353; nb. 1; (2011); p. 113 - 124, View in Reaxys; Zhou, Xiao-Yu; Wang, Duo-Sheng; Bao, Ming; Zhou, Yong-Gui; Tetrahedron Letters; vol. 52; nb. 22; (2011); p. 2826 - 2829, View in Reaxys; Zhang, Anlin; Yang, Nianfa; Yang, Liwen; Peng, Dan; Chemistry Letters; vol. 43; nb. 4; (2014); p. 462 - 464, View in Reaxys 33 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys; Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys; Hodgkinson, Roy; Jurk, Vclav; Zanotti-Gerosa, Antonio; Nedden, Hans Günter; Blackaby, Andrew; Clarkson, Guy J.; Wills, Martin; Organometallics; vol. 33; nb. 19; (2014); p. 5517 - 5524, View in Reaxys 34 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

119/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Krabbe, Scott W.; Hatcher, Mark A.; Bowman, Roy K.; Mitchell, Mark B.; McClure, Michael S.; Johnson, Jeffrey S.; Organic Letters; vol. 15; nb. 17; (2013); p. 4560 - 4563, View in Reaxys; Li, Yanyun; Yu, Shenluan; Wu, Xiaofeng; Xiao, Jianliang; Shen, Weiyi; Dong, Zhenrong; Gao, Jingxing; Journal of the American Chemical Society; vol. 136; nb. 10; (2014); p. 4031 - 4039, View in Reaxys 35 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.46 scopy) [MHz] Location

supporting information

Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 - 350, View in Reaxys 36 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys 37 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Lowicki, Daniel; Bezlada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 591 595, View in Reaxys 39 of 120

Description (NMR Spectroscopy)

Chemical shifts

120/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- α(400 MHz, CDC13) 7.36-7.25 (5H, m, Ph), 4.58 (1H, t, / 6.4, -CH), 2.03 (1α, br s, -OH), 1.87- 1.68 α troscopy) (2α, m, -CH2), 1.48 (3α, d, / 7.4, -CH3) Location

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys 40 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Original Text (NMR Spec- αC (100 MHz, CDC13): 144.55, 128.36(2C), 127.46, 125.94(2C), 75.99, 31.84, 10.11; troscopy) Location

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys 41 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300.1 scopy) [MHz] Location

supporting information

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys 43 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

121/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H NMR (400 MHz, CDCl3): α 0.92 (t, J=7.2 Hz, 3H, CH2CH3), 1.7-1.8 (m, 2H, CH2CH3), 4.61 (t, troscopy) J=7.2 Hz, 1H, PhCH), 7.3-7.4 (m, 5H, PhH) Location

supporting information

Signals [ppm]

0.92; 1.7 - 1.8; 4.61; 7.3 - 7.4

Kind of signal

t, J=7.2 Hz, 3H, CH&2%CH&3%; m, 2H, CH&2%CH&3%; t, J=7.2 Hz, 1H, PhCH; m, 5H, PhH

Michigami, Kyosuke; Hayashi, Masahiko; Tetrahedron; vol. 69; nb. 21; (2013); p. 4221 - 4225, View in Reaxys 44 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Pericas, Miquel A.; Herrerias, Clara I.; Sola, Lluis; Advanced Synthesis and Catalysis; vol. 350; nb. 6; (2008); p. 927 - 932, View in Reaxys; Kawabata, Shun; Tokura, Hiromu; Chiyojima, Hiroyuki; Okamoto, Masaki; Sakaguchi, Satoshi; Advanced Synthesis and Catalysis; vol. 354; nb. 5; (2012); p. 807 - 812, View in Reaxys 45 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Martins, Jose E.D.; Wills, Martin; Tetrahedron; vol. 65; nb. 29-30; (2009); p. 5782 - 5786, View in Reaxys; Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys 46 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Yadav, Ashok K.; Kumar, Manoj; Yadav, Tripti; Jain, Renuka; Synlett; nb. 5; (2010); p. 712 - 714, View in Reaxys; Gong, Zhiyong; Liu, Qingwen; Xue, Pengchong; Li, Kechang; Song, Zhiguang; Liu, Zaiqun; Jin, Yinghua; Applied Organometallic Chemistry; vol. 26; nb. 3; (2012); p. 121 - 129, View in Reaxys 47 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

122/229

2018-07-03 16:52:46

Kantam, M. Lakshmi; Laha, Soumi; Yadav, Jagjit; Likhar, Pravin R.; Sreedhar, Bojja; Jha, Shailendra; Bhargava, Suresh; Udayakiran; Jagadeesh; Organic Letters; vol. 10; nb. 14; (2008); p. 2979 - 2982, View in Reaxys; Kantam, M. Lakshmi; Laha, Soumi; Yadav, Jagjit; Likhar, Pravin R.; Sreedhar; Jha, Shailendra; Bhargava, Suresh; Udayakiran; Jagadeesh; Organic Letters; vol. 10; nb. 19; (2008); p. 4391 - 4391, View in Reaxys; Li, Yuehui; Ding, Kuiling; Sandoval, Christian A.; Organic Letters; vol. 11; nb. 4; (2009); p. 907 - 910, View in Reaxys; Kantam, M. Lakshmi; Yadav, Jagjit; Laha, Soumi; Srinivas, Pottabathula; Sreedhar, Bojja; Figueras; Journal of Organic Chemistry; vol. 74; nb. 12; (2009); p. 4608 - 4611, View in Reaxys; Da, Chao-Shan; Wang, Jun-Rul; Yin, Xiao-Gang; Fan, Xin-Yuan; Liu, Yi; Yu, Sheng-Li; Organic Letters; vol. 11; nb. 24; (2009); p. 5578 - 5581, View in Reaxys; Li, De Run; He, Anyu; Falck; Organic Letters; vol. 12; nb. 8; (2010); p. 1756 - 1759, View in Reaxys; Naik, Anu; Maji, Tapan; Reiser, Oliver; Chemical Communications; vol. 46; nb. 25; (2010); p. 4475 - 4477, View in Reaxys; Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys 48 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Kantam, M. Lakshmi; Yadav, Jagjit; Laha, Soumi; Srinivas, Pottabathula; Sreedhar, Bojja; Figueras; Journal of Organic Chemistry; vol. 74; nb. 12; (2009); p. 4608 - 4611, View in Reaxys; Li, De Run; He, Anyu; Falck; Organic Letters; vol. 12; nb. 8; (2010); p. 1756 - 1759, View in Reaxys; Naik, Anu; Maji, Tapan; Reiser, Oliver; Chemical Communications; vol. 46; nb. 25; (2010); p. 4475 - 4477, View in Reaxys; Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys 49 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Yadav, Ashok K.; Kumar, Manoj; Yadav, Tripti; Jain, Renuka; Synlett; nb. 5; (2010); p. 712 - 714, View in Reaxys; Xu, Geng; Liu, Zhan Zhu; Chinese Chemical Letters; vol. 21; nb. 3; (2010); p. 309 - 311, View in Reaxys; Gong, Zhiyong; Liu, Qingwen; Xue, Pengchong; Li, Kechang; Song, Zhiguang; Liu, Zaiqun; Jin, Yinghua; Applied Organometallic Chemistry; vol. 26; nb. 3; (2012); p. 121 - 129, View in Reaxys 50 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Dean, Melissa A.; Hitchcock, Shawn R.; Tetrahedron Asymmetry; vol. 19; nb. 22; (2008); p. 2563 - 2567, View in Reaxys; Martins, Jose E.D.; Wills, Martin; Tetrahedron; vol. 65; nb. 29-30; (2009); p. 5782 - 5786, View in Reaxys; Tasgin, Dilek Isik; Unaleroglu, Canan; Applied Organometallic Chemistry; vol. 24; nb. 1; (2010); p. 33 - 37, View in Reaxys; Cakici, Murat; Catir, Mustafa; Karabuga, Semistan; Ulukanli, Sabri; Kilic, Hamdullah; Tetrahedron Asymmetry; vol. 22; nb. 3; (2011); p. 300 - 308, View in Reaxys; Hirose, Takuji; Sugawara, Kazuyuki; Kodama, Koichi; Journal of Organic Chemistry; vol. 76; nb. 13; (2011); p. 5413 - 5428, View in Reaxys; Hatano, Manabu; Mizuno, Tomokazu; Ishihara, Kazuaki; Tetrahedron; vol. 67; nb. 24; (2011); p. 4417 - 4424, View in Reaxys; Wang, Bo; Jiang, Ling; Wang, Jue; Ma, Jingbo; Liu, Min; Yu, Hongwei; Tetrahedron Asymmetry; vol. 22; nb. 9; (2011); p. 980 - 985, View in Reaxys; Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys 51 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

123/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; European Journal of Organic Chemistry; nb. 20; (2012); p. 3732 - 3736, View in Reaxys 52 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Pericas, Miquel A.; Herrerias, Clara I.; Sola, Lluis; Advanced Synthesis and Catalysis; vol. 350; nb. 6; (2008); p. 927 - 932, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys; Yu, Feng; Zhou, Ji-Ning; Zhang, Xi-Chang; Sui, Yao-Zong; Wu, Fei-Fei; Xie, Lin-Jie; S. C. Chan, Albert; Wu, Jing; Chemistry - A European Journal; vol. 17; nb. 50; (2011); p. 14234 14240, View in Reaxys; Kawabata, Shun; Tokura, Hiromu; Chiyojima, Hiroyuki; Okamoto, Masaki; Sakaguchi, Satoshi; Advanced Synthesis and Catalysis; vol. 354; nb. 5; (2012); p. 807 - 812, View in Reaxys 53 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Osorio-Planes, Laura; Rodriguez-Escrich, Carles; Pericas, Miquel A.; Organic Letters; vol. 14; nb. 7; (2012); p. 1816 1819, View in Reaxys 54 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Osorio-Planes, Laura; Rodriguez-Escrich, Carles; Pericas, Miquel A.; Organic Letters; vol. 14; nb. 7; (2012); p. 1816 1819, View in Reaxys 55 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz]

124/229

2018-07-03 16:52:46

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; Tetrahedron Asymmetry; vol. 23; nb. 10; (2012); p. 789 - 794, View in Reaxys 56 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Shiina, Isamu; Nakata, Kenya; Ono, Keisuke; Mukaiyama, Teruaki; Helvetica Chimica Acta; vol. 95; nb. 10; (2012); p. 1891 - 1911,21, View in Reaxys; Shiina, Isamu; Nakata, Kenya; Ono, Keisuke; Mukaiyama, Teruaki; Helvetica Chimica Acta; vol. 95; nb. 10; (2012); p. 1891 - 1911, View in Reaxys; Wu, Nan; Bo, Rongcheng; Zhang, Rongli; Jiang, Xi; Wan, Yu; Xu, Zhou; Wu, Hui; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 644 - 649, View in Reaxys 57 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene-d6

Temperature (NMR Spectroscopy) [°C]

22.84

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie - International Edition; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys 59 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Temperature (NMR Spectroscopy) [°C]

22.84

Frequency (NMR Spectro- 75.4 scopy) [MHz] Location

supporting information

Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie - International Edition; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys 60 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

125/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 250 scopy) [MHz] Location

supporting information

Aupoix, Audrey; Bournaud, Chloee; Vo-Thanh, Giang; European Journal of Organic Chemistry; nb. 15; (2011); p. 2772 2776, View in Reaxys 61 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 90 scopy) [MHz] Location

supporting information

Aupoix, Audrey; Bournaud, Chloee; Vo-Thanh, Giang; European Journal of Organic Chemistry; nb. 15; (2011); p. 2772 2776, View in Reaxys 62 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Zhang, Xi-Chang; Wu, Fei-Fei; Li, Shijun; Zhou, Ji-Ning; Wu, Jing; Li, Ning; Fang, Wenjun; Lam, Kim Hung; Chan, Albert S. C.; Advanced Synthesis and Catalysis; vol. 353; nb. 9; (2011); p. 1457 - 1462, View in Reaxys 63 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.5

Frequency (NMR Spectro- 300.4 scopy) [MHz] Location

supporting information

Nakata, Kenya; Shiina, Isamu; Organic and Biomolecular Chemistry; vol. 9; nb. 20; (2011); p. 7092 - 7096, View in Reaxys 64 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

126/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.5

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Nakata, Kenya; Shiina, Isamu; Organic and Biomolecular Chemistry; vol. 9; nb. 20; (2011); p. 7092 - 7096, View in Reaxys 65 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Eidamshaus, Christian; Reissig, Hans-Ulrich; Tetrahedron Asymmetry; vol. 22; nb. 16-17; (2011); p. 1644 - 1652, View in Reaxys 66 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Xu, Zhou; Bo, Rongcheng; Wu, Nan; Wan, Yu; Wu, Hui; Letters in Organic Chemistry; vol. 8; nb. 8; (2011); p. 582 - 586, View in Reaxys 67 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Chen, Xi; Liu, Qiang; Sun, Hong-Bao; Yu, Xiao-Qi; Pu, Lin; Tetrahedron Letters; vol. 51; nb. 17; (2010); p. 2345 - 2347, View in Reaxys 68 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Chen, Xi; Liu, Qiang; Sun, Hong-Bao; Yu, Xiao-Qi; Pu, Lin; Tetrahedron Letters; vol. 51; nb. 17; (2010); p. 2345 - 2347, View in Reaxys

127/229

2018-07-03 16:52:46

69 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Li, Wei Jie; Qiu, Sheng Xiang; Advanced Synthesis and Catalysis; vol. 352; nb. 7; (2010); p. 1119 - 1122, View in Reaxys 70 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys 71 of 120

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys 72 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Location

supporting information

Gastl, Christoph; Laschat, Sabine; Synthesis; nb. 15; (2010); p. 2643 - 2651; Art.No: Z07810SS, View in Reaxys 73 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 63 scopy) [MHz] Location

supporting information

Gastl, Christoph; Laschat, Sabine; Synthesis; nb. 15; (2010); p. 2643 - 2651; Art.No: Z07810SS, View in Reaxys 74 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

128/229

2018-07-03 16:52:46

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 4470, View in Reaxys 77 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 4470, View in Reaxys 78 of 120

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spec- 1H NMR (CDCl3, 300 MHz) α=7.38-7.26 (m, 5H), 4.57 (t, J=6.3 Hz, 1 H), 2.25 (br s, 1 H), troscopy) 1.87-1.69 (m, 2H), 0.91 (t, J=7.8 Hz, 3H) Comment (NMR Spectroscopy)

Signals given

Signals [ppm]

7.26 - 7.38; 4.57; 2.25; 1.69 - 1.87; 0.91

Kind of signal

m, 5H; t, J=6.3 Hz, 1 H; br s, 1 H; m, 2H; t, J=7.8 Hz, 3H

Patent; Board of Regents; US2009/253919; (2009); (A1) English, View in Reaxys 79 of 120

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz]

129/229

2018-07-03 16:52:46

Original Text (NMR Spectroscopy)

13C

Comment (NMR Spectroscopy)

Signals given

Signals [ppm]

145; 128.5; 127.6; 126.1; 74.5; 41.3; 19.1; 14.1

Kind of signal

2C; 2C

NMR (CDCl3, 75 MHz) α=145.0, 128.5 (2C), 127.6, 126.1 (2C), 74.5, 41.3, 19.1, 14.1

Patent; Board of Regents; US2009/253919; (2009); (A1) English, View in Reaxys 80 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Martins, Jose E.D.; Morris, David J.; Wills, Martin; Tetrahedron Letters; vol. 50; nb. 6; (2009); p. 688 - 692, View in Reaxys 81 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Kamal, Ahmed; Sandbhor, Mahendra; Ramana; Tetrahedron Asymmetry; vol. 13; nb. 8; (2002); p. 815 - 820, View in Reaxys; Lipshutz, Bruce H.; Noson, Kevin; Chrisman, Will; Lower, Asher; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8779 - 8789, View in Reaxys; Matsunaga, Hirofumi; Ishizuka, Tadao; Kunieda, Takehisa; Tetrahedron Letters; vol. 46; nb. 21; (2005); p. 3645 - 3648, View in Reaxys; Buckley, Benjamin R.; Boxhall, Jonathan Y.; Bulman Page, Philip C.; Chan, Yohan; Elsegood, Mark R. J.; Heaney, Harry; Holmes, Kathryn E.; McIldowie, Matthew J.; McKee, Vickie; McGrath, Matthew J.; Mocerino, Mauro; Poulton, Andrew M.; Sampler, Edward P.; Skelton, Brian W.; White, Allan H.; European Journal of Organic Chemistry; nb. 22; (2006); p. 5117 - 5134, View in Reaxys; Bachu, Prabhakar; Gibson, Jennifer S.; Sperry, Jonathan; Brimble, Margaret A.; Tetrahedron Asymmetry; vol. 18; nb. 13; (2007); p. 1618 - 1624, View in Reaxys; Taniguchi, Tomohiro; Fukuba, Taka-Aki; Nakatsuka, Shuhei; Hayase, Shuichi; Kawatsura, Motoi; Uno, Hidemitsu; Itoh, Toshiyuki; Journal of Organic Chemistry; vol. 73; nb. 10; (2008); p. 3875 - 3884, View in Reaxys 82 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 597, View in Reaxys; Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 - 26, View in Reaxys 83 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz]

130/229

2018-07-03 16:52:46

Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 597, View in Reaxys 84 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Lombardo, Marco; Chiarucci, Michel; Trombini, Claudio; Chemistry - A European Journal; vol. 14; nb. 36; (2008); p. 11288 - 11291, View in Reaxys 85 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Lombardo, Marco; Chiarucci, Michel; Trombini, Claudio; Chemistry - A European Journal; vol. 14; nb. 36; (2008); p. 11288 - 11291, View in Reaxys 86 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

27.5

Frequency (NMR Spectro- 300 scopy) [MHz] Clive, Derrick L. J.; Stoffman, Elia J. L.; Chemical Communications; nb. 21; (2007); p. 2151 - 2153, View in Reaxys 87 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Du, Haifeng; Ding, Kuiling; Organic Letters; vol. 5; nb. 7; (2003); p. 1091 - 1093, View in Reaxys; Rudolph, Jens; Schmidt, Frank; Bolm, Carsten; Advanced Synthesis and Catalysis; vol. 346; nb. 7; (2004); p. 867 - 872, View in Reaxys; Bastin, Stephanie; Eaves, Richard J.; Edwards, Christopher W.; Ichihara, Osamu; Whittaker, Mark; Wills, Martin; Journal of Organic Chemistry; vol. 69; nb. 16; (2004); p. 5405 - 5412, View in Reaxys; Du, Haifeng; Zhang, Xue; Wang, Zheng; Ding, Kuiling; Tetrahedron; vol. 61; nb. 40; (2005); p. 9465 - 9477, View in Reaxys; Liu, Shuanglong; Wolf, Christian; Organic Letters; vol. 9; nb. 16; (2007); p. 2965 - 2968, View in Reaxys 88 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Liu, Shuanglong; Wolf, Christian; Organic Letters; vol. 9; nb. 16; (2007); p. 2965 - 2968, View in Reaxys 89 of 120

Description (NMR Spectroscopy)

Chemical shifts

131/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Rudolph, Jens; Schmidt, Frank; Bolm, Carsten; Advanced Synthesis and Catalysis; vol. 346; nb. 7; (2004); p. 867 - 872, View in Reaxys; Liu, Shuanglong; Wolf, Christian; Organic Letters; vol. 9; nb. 16; (2007); p. 2965 - 2968, View in Reaxys 90 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Liu, Shuanglong; Wolf, Christian; Organic Letters; vol. 9; nb. 16; (2007); p. 2965 - 2968, View in Reaxys 91 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Lipshutz, Bruce H.; Noson, Kevin; Chrisman, Will; Lower, Asher; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8779 - 8789, View in Reaxys; Buckley, Benjamin R.; Boxhall, Jonathan Y.; Bulman Page, Philip C.; Chan, Yohan; Elsegood, Mark R. J.; Heaney, Harry; Holmes, Kathryn E.; McIldowie, Matthew J.; McKee, Vickie; McGrath, Matthew J.; Mocerino, Mauro; Poulton, Andrew M.; Sampler, Edward P.; Skelton, Brian W.; White, Allan H.; European Journal of Organic Chemistry; nb. 22; (2006); p. 5117 - 5134, View in Reaxys; Bachu, Prabhakar; Gibson, Jennifer S.; Sperry, Jonathan; Brimble, Margaret A.; Tetrahedron Asymmetry; vol. 18; nb. 13; (2007); p. 1618 - 1624, View in Reaxys 92 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Doucet, Henri; Fernandez, Elena; Layzell, Timothy P.; Brown, John M.; Chemistry - A European Journal; vol. 5; nb. 4; (1999); p. 1320 - 1330, View in Reaxys; Kita, Yasuyuki; Takebe, Yasushi; Murata, Kenji; Naka, Tadaatsu; Akai, Shuji; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 83 - 88, View in Reaxys; Kuwano, Ryoichi; Sawamura, Masaya; Shirai, Junya; Takahashi, Masatoshi; Ito, Yoshihiko; Bulletin of the Chemical Society of Japan; vol. 73; nb. 2; (2000); p. 485 - 496, View in Reaxys; Salvi; Chattopadhyay; Tetrahedron; vol. 57; nb. 14; (2001); p. 2833 - 2839, View in Reaxys; Jones, Simon; Atherton; Tetrahedron Asymmetry; vol. 11; nb. 22; (2000); p. 4543 - 4548, View in Reaxys; Courmarcel, James; Mostefai, Naouel; Sirol, Sabine; Choppin, Sabine; Riant, Olivier; Israel Journal of Chemistry; vol. 41; nb. 4; (2001); p. 231 240, View in Reaxys; Emmerson, Daniel P G; Villard, Renaud; Mugnaini, Claudia; Batsanov, Andrei; Howard, Judith A K; Hems, William P; Tooze, Robert P; Davis, Benjamin G; Organic and biomolecular chemistry; vol. 1; nb. 21; (2003); p. 3826 - 3838, View in Reaxys; Dalicsek, Zoltan; Pollreisz, Ferenc; Goemoery, Agnes; Soos, Tibor; Organic Letters; vol. 7; nb. 15; (2005); p. 3243 - 3246, View in Reaxys; Bandini, Marco; Melucci, Manuela; Piccinelli, Fabio; Sinisi, Riccardo; Tommasi, Simona; Umani-Ronchi, Achille; Chemical Communications; nb. 43; (2007); p. 4519 - 4521, View in Reaxys 93 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

132/229

2018-07-03 16:52:46

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Evans, David A.; Michael, Forrest E.; Tedrow, Jason S.; Campos, Kevin R.; Journal of the American Chemical Society; vol. 125; nb. 12; (2003); p. 3534 - 3543, View in Reaxys; Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 - 2153, View in Reaxys; Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys; Yang, Wei; Xu, Jian-He; Xie, Yan; Xu, Yi; Zhao, Gang; Lin, Guo-Qiang; Tetrahedron Asymmetry; vol. 17; nb. 12; (2006); p. 1769 - 1774, View in Reaxys 95 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Unaleroglu, Canan; Aydin, A. Ebru; Demir, Ayhan S.; Tetrahedron Asymmetry; vol. 17; nb. 5; (2006); p. 742 - 749, View in Reaxys 97 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz]

133/229

2018-07-03 16:52:46

Comment (NMR Spectroscopy)

ambient temperature

Unaleroglu, Canan; Aydin, A. Ebru; Demir, Ayhan S.; Tetrahedron Asymmetry; vol. 17; nb. 5; (2006); p. 742 - 749, View in Reaxys 98 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Alberts, Albert H.; Wynberg, Hans; Journal of the American Chemical Society; vol. 111; nb. 18; (1989); p. 7265 - 7266, View in Reaxys; Tanno; Terashima; Chemical and Pharmaceutical Bulletin; vol. 31; nb. 3; (1983); p. 837 - 851, View in Reaxys; Seebach, Dieter; Plattner, Dietmar A.; Beck, Albert K.; Wang, Yan Ming; Hunziker, Daniel; Petter, Walter; Helvetica Chimica Acta; vol. 75; nb. 7; (1992); p. 2171 - 2209, View in Reaxys; Carter, Mary Beth; Schiott, Birgit; Gutierrez, Alberto; Buchwald, Stephen L.; Journal of the American Chemical Society; vol. 116; nb. 26; (1994); p. 11667 11670, View in Reaxys; Ramoen, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 8; nb. 14; (1997); p. 2479 - 2496, View in Reaxys; Lutz, Christian; Knochel, Paul; Journal of Organic Chemistry; vol. 62; nb. 22; (1997); p. 7895 - 7898, View in Reaxys; Palmer; Walsgrove; Wills; Journal of Organic Chemistry; vol. 62; nb. 15; (1997); p. 5226 - 5228, View in Reaxys; Hailes, Helen C.; Madden, James; Synlett; nb. 1; (1999); p. 105 - 107, View in Reaxys; Laufer, Radoslaw S.; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Organic Letters; vol. 2; nb. 5; (2000); p. 629 - 631, View in Reaxys; Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 - 458, View in Reaxys; Hu, Aiguo; Ngo, Helen L.; Lin, Wenbin; Journal of the American Chemical Society; vol. 125; nb. 38; (2003); p. 11490 - 11491, View in Reaxys; Wipf, Peter; Pierce, Joshua G.; Wang, Xiaodong; Tetrahedron Asymmetry; vol. 14; nb. 22; (2003); p. 3605 - 3611, View in Reaxys; Song, Chun; Ma, Changqin; Ma, Yudao; Feng, Wenhua; Ma, Shutao; Chai, Qiang; Andrus, Merritt B.; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3241 - 3244, View in Reaxys; Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys 99 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Laufer, Radoslaw S.; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Organic Letters; vol. 2; nb. 5; (2000); p. 629 - 631, View in Reaxys; Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 - 458, View in Reaxys; Hu, Aiguo; Ngo, Helen L.; Lin, Wenbin; Journal of the American Chemical Society; vol. 125; nb. 38; (2003); p. 11490 - 11491, View in Reaxys; Wipf, Peter; Pierce, Joshua G.; Wang, Xiaodong; Tetrahedron Asymmetry; vol. 14; nb. 22; (2003); p. 3605 - 3611, View in Reaxys; Song, Chun; Ma, Changqin; Ma, Yudao; Feng, Wenhua; Ma, Shutao; Chai, Qiang; Andrus, Merritt B.; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3241 - 3244, View in Reaxys; Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys 100 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 - 2153, View in Reaxys; Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys 101 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

134/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 125 scopy) [MHz] Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 - 2153, View in Reaxys; Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys 102 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Song, Chun; Ma, Changqin; Ma, Yudao; Feng, Wenhua; Ma, Shutao; Chai, Qiang; Andrus, Merritt B.; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3241 - 3244, View in Reaxys 104 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 50 scopy) [MHz] Dalicsek, Zoltan; Pollreisz, Ferenc; Goemoery, Agnes; Soos, Tibor; Organic Letters; vol. 7; nb. 15; (2005); p. 3243 - 3246, View in Reaxys 105 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

135/229

2018-07-03 16:52:46

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Kuwano, Ryoichi; Uemura, Takashi; Saitoh, Makoto; Ito, Yoshihiko; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2263 - 2271, View in Reaxys 108 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Kuwano, Ryoichi; Uemura, Takashi; Saitoh, Makoto; Ito, Yoshihiko; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2263 - 2271, View in Reaxys 109 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Dangel, Brian D.; Polt, Robin; Organic Letters; vol. 2; nb. 19; (2000); p. 3003 - 3006, View in Reaxys; Palmer, Matthew J.; Kenny, Jennifer A.; Walsgrove, Tim; Kawamoto, Aparecida M.; Wills, Martin; Journal of the Chemical Society. Perkin Transactions 1; nb. 3; (2002); p. 416 - 427, View in Reaxys; Steiner, Derek; Sethofer, Steven G.; Goralski, Christian T.; Singaram, Bakthan; Tetrahedron Asymmetry; vol. 13; nb. 14; (2002); p. 1477 - 1483, View in Reaxys; Gilmore, Nathan J.; Jones, Simon; Muldowney, Mark P.; Organic Letters; vol. 6; nb. 16; (2004); p. 2805 - 2808, View in Reaxys 110 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Dangel, Brian D.; Polt, Robin; Organic Letters; vol. 2; nb. 19; (2000); p. 3003 - 3006, View in Reaxys; Gilmore, Nathan J.; Jones, Simon; Muldowney, Mark P.; Organic Letters; vol. 6; nb. 16; (2004); p. 2805 - 2808, View in Reaxys

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111 of 120

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Dangel, Brian D.; Polt, Robin; Organic Letters; vol. 2; nb. 19; (2000); p. 3003 - 3006, View in Reaxys; Palmer, Matthew J.; Kenny, Jennifer A.; Walsgrove, Tim; Kawamoto, Aparecida M.; Wills, Martin; Journal of the Chemical Society. Perkin Transactions 1; nb. 3; (2002); p. 416 - 427, View in Reaxys; Gilmore, Nathan J.; Jones, Simon; Muldowney, Mark P.; Organic Letters; vol. 6; nb. 16; (2004); p. 2805 - 2808, View in Reaxys 112 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Kitamura, Masato; Oka, Hiromasa; Suga, Seiji; Noyori, Ryoji; Kaelin, David E.; Martin, Stephen F.; Beutner, Gregory L.; Denmark, Scott E.; Organic Syntheses; vol. 79; (2002); p. 139 - 139, View in Reaxys 113 of 120

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Ulrich, Claudia; Bargon, Joachim; Magnetic Resonance in Chemistry; vol. 38; nb. 1; (2000); p. 33 - 37, View in Reaxys 114 of 120

Description (NMR Spectroscopy)

NMR with shift reagents

Nucleus (NMR Spectroscopy)

Ulrich, Claudia; Bargon, Joachim; Magnetic Resonance in Chemistry; vol. 38; nb. 1; (2000); p. 33 - 37, View in Reaxys 115 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Ramoen, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 8; nb. 14; (1997); p. 2479 - 2496, View in Reaxys; Lutz, Christian; Knochel, Paul; Journal of Organic Chemistry; vol. 62; nb. 22; (1997); p. 7895 - 7898, View in Reaxys; Hailes, Helen C.; Madden, James; Synlett; nb. 1; (1999); p. 105 - 107, View in Reaxys; Aurich, Hans Guenter; Soeberdt, Michael; Harms, Klaus; Tetrahedron; vol. 55; nb. 5; (1999); p. 1249 - 1270, View in Reaxys; Laufer, Radoslaw S.; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Organic Letters; vol. 2; nb. 5; (2000); p. 629 - 631, View in Reaxys 116 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

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Aurich, Hans Guenter; Soeberdt, Michael; Harms, Klaus; Tetrahedron; vol. 55; nb. 5; (1999); p. 1249 - 1270, View in Reaxys; Yun, Jaesook; Buchwald, Stephen L.; Journal of the American Chemical Society; vol. 121; nb. 24; (1999); p. 5640 - 5644, View in Reaxys 117 of 120

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Tanno; Terashima; Chemical and Pharmaceutical Bulletin; vol. 31; nb. 3; (1983); p. 837 - 851, View in Reaxys; Seebach, Dieter; Plattner, Dietmar A.; Beck, Albert K.; Wang, Yan Ming; Hunziker, Daniel; Petter, Walter; Helvetica Chimica Acta; vol. 75; nb. 7; (1992); p. 2171 - 2209, View in Reaxys; Carter, Mary Beth; Schiott, Birgit; Gutierrez, Alberto; Buchwald, Stephen L.; Journal of the American Chemical Society; vol. 116; nb. 26; (1994); p. 11667 - 11670, View in Reaxys; Ramoen, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 8; nb. 14; (1997); p. 2479 - 2496, View in Reaxys; Lutz, Christian; Knochel, Paul; Journal of Organic Chemistry; vol. 62; nb. 22; (1997); p. 7895 - 7898, View in Reaxys; Palmer; Walsgrove; Wills; Journal of Organic Chemistry; vol. 62; nb. 15; (1997); p. 5226 - 5228, View in Reaxys; Hailes, Helen C.; Madden, James; Synlett; nb. 1; (1999); p. 105 - 107, View in Reaxys 118 of 120

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Bussche-Huennefeld, Joanna Linda v.; Seebach, Dieter; Tetrahedron; vol. 48; nb. 27; (1992); p. 5719 - 5730, View in Reaxys; Prasad; Joshi; Journal of Organic Chemistry; vol. 62; nb. 11; (1997); p. 3770 - 3771, View in Reaxys 119 of 120

Description (NMR Spectroscopy)

Spin-spin coupling constants

Comment (NMR Spectroscopy)

1H-1H

Description (NMR Spectroscopy)

NMR

Gallina, Carlo; Lucente, Gino; Pinnen, Francesco; Tetrahedron; vol. 34; nb. 15; (1978); p. 2361 - 2363, View in Reaxys IR Spectroscopy (18) 1 of 18

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 2 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys; Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 4 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

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Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys 5 of 18

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 2688, View in Reaxys; Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys 6 of 18

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands; Spectrum

Location

supporting information

Lowicki, Daniel; Bezlada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 591 595, View in Reaxys 7 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 597, View in Reaxys; Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 781, View in Reaxys 8 of 18

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat (no solvent)

Yadav, Ashok K.; Kumar, Manoj; Yadav, Tripti; Jain, Renuka; Synlett; nb. 5; (2010); p. 712 - 714, View in Reaxys; Hatano, Manabu; Mizuno, Tomokazu; Ishihara, Kazuaki; Tetrahedron; vol. 67; nb. 24; (2011); p. 4417 - 4424, View in Reaxys 9 of 18

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Solvent (IR Spectroscopy)

chloroform

Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 4470, View in Reaxys 10 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

Lipshutz, Bruce H.; Noson, Kevin; Chrisman, Will; Lower, Asher; Journal of the American Chemical Society; vol. 125; nb. 29; (2003); p. 8779 - 8789, View in Reaxys; Adair, Gareth R. A.; Williams, Jonathan M. J.; Chemical Communications; nb. 25; (2007); p. 2608 - 2609, View in Reaxys; Bachu, Prabhakar; Gibson, Jennifer S.; Sperry, Jonathan; Brimble, Margaret A.; Tetrahedron Asymmetry; vol. 18; nb. 13; (2007); p. 1618 - 1624, View in Reaxys 11 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Salvi; Chattopadhyay; Tetrahedron; vol. 57; nb. 14; (2001); p. 2833 - 2839, View in Reaxys; Buckley, Benjamin R.; Boxhall, Jonathan Y.; Bulman Page, Philip C.; Chan, Yohan; Elsegood, Mark R. J.; Heaney, Harry; Holmes, Kathryn E.; McIldowie, Matthew J.; McKee, Vickie; McGrath, Matthew J.; Mocerino, Mauro; Poulton, Andrew M.; Sampler, Edward P.; Skelton, Brian W.; White, Allan H.; European Journal of Organic Chemistry; nb. 22; (2006); p. 5117 - 5134, View in Reaxys 12 of 18

Description (IR Spectroscopy)

Bands

Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys 13 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

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Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 - 2153, View in Reaxys; Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys 14 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Kita, Yasuyuki; Takebe, Yasushi; Murata, Kenji; Naka, Tadaatsu; Akai, Shuji; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 83 - 88, View in Reaxys; Kamal, Ahmed; Sandbhor, Mahendra; Ramana; Tetrahedron Asymmetry; vol. 13; nb. 8; (2002); p. 815 - 820, View in Reaxys 15 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Laufer, Radoslaw S.; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Organic Letters; vol. 2; nb. 5; (2000); p. 629 - 631, View in Reaxys 16 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3360 - 1031 cm**(-1)

Lutz, Christian; Knochel, Paul; Journal of Organic Chemistry; vol. 62; nb. 22; (1997); p. 7895 - 7898, View in Reaxys 17 of 18

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3380 cm**(-1)

Tanno; Terashima; Chemical and Pharmaceutical Bulletin; vol. 31; nb. 3; (1983); p. 837 - 851, View in Reaxys 18 of 18

Description (IR Spectroscopy)

Walden,W. et al.; Tetrahedron; vol. 33; (1977); p. 419 - 421, View in Reaxys Mass Spectrometry (18) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); electron impact (EI); spectrum

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys

gas chromatography mass spectrometry (GCMS); spectrum

Sarkar, Md. Raihan; Lee, Joel H. Z.; Bell, Stephen G.; ChemBioChem; vol. 18; nb. 21; (2017); p. 2119 - 2128, View in Reaxys

electrospray ionisa- supporting information (ESI); spection trum

An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation

Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys

supporting information

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(ESI); time-offlight mass spectra (TOFMS); spectrum high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

supporting information

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys

EI (Electron impact); Spectrum EI (Electron impact); GCMS (Gas chromatography mass spectrometry); Spectrum

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; Tetrahedron Asymmetry; vol. 23; nb. 10; (2012); p. 789 - 794, View in Reaxys supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Yus, Miguel; European Journal of Organic Chemistry; nb. 20; (2012); p. 3732 - 3736, View in Reaxys

HRMS (High resolution mass spectrometry); ESI (Electrospray ionisation); TOFMS (Time of flight mass spectrum); Spectrum

Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys

FAB (Fast atom bombardment); HRMS (High resolution mass spectrometry); Spectrum

Hatano, Manabu; Mizuno, Tomokazu; Ishihara, Kazuaki; Tetrahedron; vol. 67; nb. 24; (2011); p. 4417 - 4424, View in Reaxys

EI (Electron impact); Spectrum

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys

ESI (Electrospray ionisation); Spectrum

supporting information

Li, Wei Jie; Qiu, Sheng Xiang; Advanced Synthesis and Catalysis; vol. 352; nb. 7; (2010); p. 1119 - 1122, View in Reaxys; Li, Wei Jie; Qiu, Sheng Xiang; Xu, Zun Le; Beilstein Journal of Organic Chemistry; vol. 6; (2010); Art.No: 29, View in Reaxys

EI (Electron impact); Spectrum

mol peak

Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 - 4470, View in Reaxys

HRMS (High resolution mass spectrometry); EI (Electron impact)

mol peak

Miyabe, Hideto; Matsumura, Akira; Yoshida, Kazumasa; Takemoto, Yoshiji; Tetrahedron; vol. 65; nb. 23; (2009); p. 4464 - 4470, View in Reaxys

ESI (Electrospray ionisation)

mol peak

Eppacher, Simon; Giester, Gerald; Bats, Jan W.; Noe, Christian R.; Helvetica Chimica Acta; vol. 91; nb. 4; (2008); p. 581 - 597, View in Reaxys

spectrum; electron impact (EI)

Laufer, Radoslaw S.; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Organic Letters; vol. 2; nb. 5; (2000); p. 629 - 631, View in Reaxys; Miyabe, Hideto; Yoshida, Kazumasa; Yamauchi, Masashige; Takemoto, Yoshiji; Journal of Organic Chemistry; vol. 70; nb. 6; (2005); p. 2148 2153, View in Reaxys; Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys; Bandini, Marco; Melucci, Manuela; Piccinelli, Fabio; Sinisi, Riccardo; Tommasi, Simona; Umani-Ronchi, Achille; Chemical Communications; nb. 43; (2007); p. 4519 - 4521, View in Reaxys

electron impact (EI); spectrum

Miyabe, Hideto; Matsumura, Akira; Moriyama, Katsuhiko; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 24; (2004); p. 4631 - 4634, View in Reaxys

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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spectrum

Salvi; Chattopadhyay; Tetrahedron; vol. 57; nb. 14; (2001); p. 2833 - 2839, View in Reaxys

UV/VIS Spectroscopy (1) 1 of 1

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

Comment (UV/VIS Spectroscopy)

220 - 280 nm

Levene; Rothen; Journal of Biological Chemistry; vol. 127; (1937); p. 237,240, 245, View in Reaxys Medchem (6) 1 of 6

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Inhibitory concentration of compound on nitric oxide (NO) production in lipopolysaccharide activated mouse peritoneal macrophages

Biological Species/NCBI ID

mouse

Cells/Cell Lines

peritoneal macrophage

Substance RN

2041556View in Reaxys

Measurement Parameter

IC50

Unit

ÂľM

Measurement Object

nitric oxide production

Qualitative value

Quantitative value

100

Measurement pX

Matsuda, Hisashi; Ando, Shin; Morikawa, Toshio; Kataoka, Shinya; Yoshikawa, Masayuki; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 7; (2005); p. 1949 - 1953, View in Reaxys 2 of 6

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent inhibition of nitric oxide (NO) production in lipopolysaccharide activated mouse peritoneal macrophages at 100uM of compound

Biological Species/NCBI ID

mouse

Cells/Cell Lines

peritoneal macrophage

Substance RN

2041556View in Reaxys

Measurement Parameter

inhibition rate

Unit

Measurement Object

nitric oxide (NO) production in lipopolysaccharide activated mouse peritoneal macrophages

Qualitative value

Quantitative value

-4

Matsuda, Hisashi; Ando, Shin; Morikawa, Toshio; Kataoka, Shinya; Yoshikawa, Masayuki; Bioorganic and Medicinal Chemistry Letters; vol. 15; nb. 7; (2005); p. 1949 - 1953, View in Reaxys 3 of 6

Target Name

Sulfotransferase 1A1 [rat]

Target Synonyms

aryl sulfotransferase; aryl sulfotransferase iv; astiv; minoxidil sulfotransferase; mx-st; phenol sulfotransferase; pst-1; st1a1; sulfokinase; sulfotransferase 1a1; sult1a1; tyrosine-ester sulfotransferase

Target Uniprot ID

p17988

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4 of 6

5 of 6

Target, Subunit, Species

Sulfotransferase 1A1 [rat]

Target Mutant/Chimera Details

Sulfotransferase 1A1 [rat]:Wild

Target Species (Bioactivity)

rat

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Apparent Michaelis constant of the compound towards rat hepatic Aryl sulfotransferase (AST IV) incubated with 0.25 M potassium phosphate buffer at pH 7.0 for 10 min at 37 degree C

Biological Species/NCBI ID

rat

Substance RN

2041556View in Reaxys

Measurement Parameter

Km (Michaelis constant)

Unit

Qualitative value

Quantitative value

0.24

Measurement pX

3.62

Target Name

Sulfotransferase 1A1 [rat]

Target Synonyms

Target Uniprot ID

p17988

Target, Subunit, Species

Sulfotransferase 1A1 [rat]

Target Mutant/Chimera Details

Sulfotransferase 1A1 [rat]:Wild

Target Species (Bioactivity)

rat

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Ratio of kcat/Km of the compound towards rat hepatic Aryl sulfotransferase (AST IV) incubated with 0.25 M potassium phosphate buffer at pH 7.0 for 10 min at 37 degree C

Biological Species/NCBI ID

rat

Substance RN

2041556View in Reaxys

Measurement Parameter

ratio

Quantitative value

1.4

Target Name

Sulfotransferase 1A1 [rat]

Target Synonyms

Target Uniprot ID

p17988

Target, Subunit, Species

Sulfotransferase 1A1 [rat]

Target Mutant/Chimera Details

Sulfotransferase 1A1 [rat]:Wild

Target Species (Bioactivity)

rat

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Maximal velocity of the compound towards rat hepatic Aryl sulfotransferase (AST IV) incubated with 0.25 M potassium phosphate buffer at pH 7.0 for 2 min at 37 degree C

Biological Species/NCBI ID

rat

Substance RN

2041556View in Reaxys

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6 of 6

Measurement Parameter

Vmax

Unit

nM/min

Qualitative value

Quantitative value

9.9

Target Name

carbonyl reductase (NADPH) [Bacillus]

Target Synonyms

carbonyl reductase (nadph)

Target, Subunit, Species

carbonyl reductase (NADPH) [Bacillus]

Target Mutant/Chimera Details

carbonyl reductase (NADPH) [Bacillus]:Wild

Target Species (Bioactivity)

Bacillus

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Specific activity of compound towards Bacillus sp. ECU0013 carbonyl reductase expressed in Escherichia coli BL21(DE3) upon incubation in 50 mM phosphate buffer, pH 7 in presence of 0.05 mM NADP+

Biological Species/NCBI ID

Bacillus ECU0013

Substance RN

2041556View in Reaxys

Unit

U/mg protein

Qualitative value

Quantitative value

0.014

Concomitants: Compound name

NADP+

Concomitants: Compound role

COM

Reaxys ID 2041555 View in Reaxys

3/3 CAS Registry Number: 1565-74-8 Chemical Name: (R)-1-phenyl-1-propanol; 1-phenyl-propan-1-ol Linear Structure Formula: C6H5C(OH)HCH2CH3 Molecular Formula: C9H12O Molecular Weight: 136.194 Type of Substance: isocyclic InChI Key: DYUQAZSOFZSPHD-SECBINFHSA-N Note:

H OH

Substance Label (275) Label References 21

Hu, Qiao-Sheng; Huang, Wei-Sheng; Vitharana, Dilrukshi; Zheng, Xiao-Fan; Pu, Lin; Journal of the American Chemical Society; vol. 119; nb. 51; (1997); p. 12454 - 12464, View in Reaxys; Tashenov, Yerbolat; Daniels, Mathias; Robeyns, Koen; Van Meervelt, Luc; Dehaen, Wim; Suleimen, Yerlan M.; Szakonyi, Zsolt; Molecules; vol. 23; nb. 4; (2018); Art.No: Y, View in Reaxys

14a

Jarzyski, Szymon; Lesniak, Stanislaw; Pieczonka, Adam M.; Rachwalski, Michal; Tetrahedron Asymmetry; vol. 26; nb. 1; (2015); p. 35 - 40, View in Reaxys; Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys

b'2

Wang, Ding; Bruneau-Voisine, Antoine; Sortais, Jean-Baptiste; Catalysis Communications; vol. 105; (2018); p. 31 36, View in Reaxys

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Hara, Nanami; Fujisawa, Shu; Fujita, Mizuki; Miyazawa, Mikako; Ochiai, Kazuma; Katsuda, Satoshi; Fujimoto, Tetsuya; Tetrahedron; vol. 74; nb. 2; (2018); p. 296 - 302, View in Reaxys

Gonda, Tímea; Bérdi, Péter; Zupkó, István; Fülöp, Ferenc; Szakonyi, Zsolt; International Journal of Molecular Sciences; vol. 19; nb. 1; (2018); Art.No: 81, View in Reaxys

(R)-10c

Qu, Ge; Lonsdale, Richard; Yao, Peiyuan; Li, Guangyue; Liu, Beibei; Reetz, Manfred T.; Sun, Zhoutong; ChemBioChem; vol. 19; nb. 3; (2018); p. 239 - 246, View in Reaxys

(R)-1e

Dorau, Robin; Görbe, Tamás; Svedendahl Humble, Maria; ChemBioChem; vol. 19; nb. 4; (2018); p. 338 - 346, View in Reaxys

18a

Liu, Huan; Liu, Sensheng; Zhou, Haifeng; Liu, Qixing; Wang, Chunqin; RSC Advances; vol. 8; nb. 27; (2018); p. 14829 - 14832, View in Reaxys

Sarkar, Shaheen M.; Yusoff, Mashitah Mohd; Rahman, Md. Lutfor; Journal of the Chinese Chemical Society; vol. 62; nb. 2; (2015); p. 177 - 181, View in Reaxys; Yu, Jianfei; Duan, Meng; Wu, Weilong; Qi, Xiaotian; Xue, Peng; Lan, Yu; Dong, Xiu-Qin; Zhang, Xumu; Chemistry - A European Journal; vol. 23; nb. 4; (2017); p. 970 - 975, View in Reaxys; Yu, Jianfei; Long, Jiao; Yang, Yuhong; Wu, Weilong; Xue, Peng; Chung, Lung Wa; Dong, XiuQin; Zhang, Xumu; Organic Letters; vol. 19; nb. 3; (2017); p. 690 - 693, View in Reaxys; Patent; Wuhan Kaitelisi Technology Co., Ltd.; Zhang Xumu; Yu Jianfei; (13 pag.); CN106632511; (2017); (A) Chinese, View in Reaxys

Sánchez-Carnerero, Esther M.; Sandoval-Torrientes, Rafael; Urieta-Mora, Javier; Moreno, Florencio; Maroto, Beatriz L.; de la Moya, Santiago; Reactive and Functional Polymers; vol. 113; (2017); p. 23 - 30, View in Reaxys

Gonda, Tímea; Balázs, Attila; Tóth, Gábor; Fülöp, Ferenc; Szakonyi, Zsolt; Tetrahedron; vol. 73; nb. 18; (2017); p. 2638 - 2648, View in Reaxys

Guo, Jun; Cheng, Biao; Shen, Xuzhong; Lu, Zhan; Journal of the American Chemical Society; vol. 139; nb. 43; (2017); p. 15316 - 15319, View in Reaxys

(R)-2e

Benítez-Mateos, Ana I.; San Sebastian, Eneko; Ríos-Lombardía, Nicolás; Morís, Francisco; González-Sabín, Javier; López-Gallego, Fernando; Chemistry - A European Journal; vol. 23; nb. 66; (2017); p. 16843 - 16852, View in Reaxys

(R)-3

Priego; Garcia Mancheno; Cabrera; Carretero; Chemical Communications; nb. 19; (2001); p. 2026 - 2027, View in Reaxys; Abato; Seto; Journal of the American Chemical Society; vol. 123; nb. 37; (2001); p. 9206 - 9207, View in Reaxys; Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron Asymmetry; vol. 16; nb. 4; (2005); p. 851 - 855, View in Reaxys; Mastranzo, Virginia M.; Santacruz, Ericka; Huelgas, Gabriela; Paz, Evelyn; Sosa-Rivadeneyra, Martha V.; Bernes, Sylvain; Juaristi, Eusebio; Quintero, Leticia; de Parrodi, Cecilia Anaya; Tetrahedron Asymmetry; vol. 17; nb. 11; (2006); p. 1663 - 1670, View in Reaxys; Manabe, Yoshiki; Shinohara, Kanako; Nakamura, Hanako; Teramoto, Hiro; Sakaguchi, Satoshi; Journal of Molecular Catalysis A: Chemical; vol. 421; (2016); p. 138 145, View in Reaxys

Blake, Alexander J.; Cunningham, Anthony; Ford, Alan; Teat, Simon J.; Woodward, Simon; Chemistry - A European Journal; vol. 6; nb. 19; (2000); p. 3586 - 3594, View in Reaxys; Rodriguez, Cristina; Borzecka, Wioleta; Sattler, Johann H.; Kroutil, Wolfgang; Lavandera, Ivan; Gotor, Vicente; Organic and Biomolecular Chemistry; vol. 12; nb. 4; (2014); p. 673 - 681, View in Reaxys; Renom-Carrasco, Marc; Gajewski, Piotr; Pignataro, Luca; De Vries, Johannes G.; Piarulli, Umberto; Gennari, Cesare; Lefort, Laurent; Advanced Synthesis and Catalysis; vol. 358; nb. 4; (2016); p. 515 - 519, View in Reaxys; Kaldun, Johannes; Krimalowski, Alexander; Breuning, Matthias; Tetrahedron Letters; vol. 57; nb. 23; (2016); p. 2492 - 2495, View in Reaxys; Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys

Fang, Guang Y.; Wallner, Olov A.; Di Blasio, Nadia; Ginesta, Xavier; Harvey, Jeremy N.; Aggarwal, Varinder K.; Journal of the American Chemical Society; vol. 129; nb. 47; (2007); p. 14632 - 14639, View in Reaxys; Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys; Wang, Xiaojuan; Zhao, Wenxian; Li, Gaowei; Liu, Guanjun; Wang, Jin; Wang, Mincan; Liu, Lantao; Tetrahedron Asymmetry; vol. 26; nb. 15-16; (2015); p. 815 - 820; Art.No: 59322, View in Reaxys; Wu, Hsyueh-Liang; Wu, Ping-Yu; Cheng, Ying-Ni; Uang, Biing-Jiun; Tetrahedron; vol. 72; nb. 21; (2016); p. 2656 2665, View in Reaxys

Yong, Kelvin H.; Taylor, Nicholas J.; Chong, J. Michael; Organic Letters; vol. 4; nb. 21; (2002); p. 3553 - 3556, View in Reaxys; Patent; UANG, Biing-Jiun; Wu, Ping-Yu; Wu, Hsyueh-Liang; US2011/295042; (2011); (A1) English, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Liardo, Elisa; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Angewandte Chemie - International Edition; vol. 55; nb. 30; (2016); p. 8691 - 8695; Angew. Chem.; vol. 128; nb. 30; (2016); p. 8833 - 8837,5, View in Reaxys

Escorihuela, Jorge; Altava, Belen; Burguete, M. Isabel; Luis, Santiago V.; Tetrahedron; vol. 69; nb. 2; (2013); p. 551 - 558, View in Reaxys; Faigl; Deák; Erdélyi; Holczbauer; Czugler; Nyerges; Mátravölgyi; Chirality; vol. 27; nb. 3;

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(2015); p. 216 - 222, View in Reaxys; Jadhav, Dipesh D.; Patil, Harshal S.; Chaya, Patil S.; Thulasiram, Hirekodathakallu V.; Tetrahedron Letters; vol. 57; nb. 41; (2016); p. 4563 - 4567, View in Reaxys 2o

Perna; Ricci; Scilimati; Mena; Pisano; Palmieri; Agrimi; Vitale; Journal of Molecular Catalysis B: Enzymatic; vol. 124; (2016); p. 29 - 37, View in Reaxys; Tian, Cheng; Gong, Lei; Meggers, Eric; Chemical Communications; vol. 52; nb. 22; (2016); p. 4207 - 4210, View in Reaxys

(R)-9e

Contente, Martina Letizia; Serra, Immacolata; Brambilla, Marta; Eberini, Ivano; Gianazza, Elisabetta; De Vitis, Valerio; Molinari, Francesco; Zambelli, Paolo; Romano, Diego; Applied Microbiology and Biotechnology; vol. 100; nb. 1; (2016); p. 193 - 201, View in Reaxys

Lee, Dong-Sheng; Chang, Shu-Ming; Ho, Chun-Ying; Lu, Ta-Jung; Chirality; vol. 28; nb. 1; (2016); p. 65 - 71, View in Reaxys

(R)-5a

Gao, De-Wei; Gu, Qing; You, Shu-Li; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2544 2547, View in Reaxys

35&R%

(R)-23a

Szakonyi, Zsolt; Csör, Árpád; Csámpai, Antal; Fülöp, Ferenc; Chemistry - A European Journal; vol. 22; nb. 21; (2016); p. 7163 - 7173, View in Reaxys

2-2

Wu, Weilong; Liu, Shaodong; Duan, Meng; Tan, Xuefeng; Chen, Caiyou; Xie, Yun; Lan, Yu; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 18; nb. 12; (2016); p. 2938 - 2941, View in Reaxys

(R)-4c

Sun, Zhoutong; Li, Guangyue; Ilie, Adriana; Reetz, Manfred T.; Tetrahedron Letters; vol. 57; nb. 32; (2016); p. 3648 - 3651, View in Reaxys

Hernández, José G.; Frings, Marcus; Bolm, Carsten; ChemCatChem; vol. 8; nb. 10; (2016); p. 1769 - 1772, View in Reaxys

11t

Bigler, Raphael; Huber, Raffael; Stöckli, Marco; Mezzetti, Antonio; ACS Catalysis; vol. 6; nb. 10; (2016); p. 6455 6464, View in Reaxys

Patent; Hangzhou Normal University; Li, Li; Xu, Liwen; Lu, Xing; Yang, Kefang; Zheng, Zhanjiang; Deng, Wenhui; (14 pag.); CN103396429; (2016); (B) Chinese, View in Reaxys

Chen, Xu; Lu, Zhan; Organic Letters; vol. 18; nb. 18; (2016); p. 4658 - 4661, View in Reaxys

(R)-3b

Zhang, Huichang; Chan, Kin Shing; Journal of the Chemical Society - Perkin Transactions 1; nb. 4; (1999); p. 381 382, View in Reaxys; He, Wei; Zhang, Bang-Le; Jiang, Ru; Liu, Peng; Sun, Xiao-Li; Zhang, Sheng-Yong; Tetrahedron Letters; vol. 47; nb. 30; (2006); p. 5367 - 5370, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys; Liu, Wei-Peng; Yuan, Ming-Lei; Yang, Xiao-Hui; Li, Ke; Xie, Jian-Hua; Zhou, Qi-Lin; Chemical Communications; vol. 51; nb. 28; (2015); p. 6123 - 6125, View in Reaxys

Harada, Toshiro; Kanda, Kousou; Hiraoka, Yuuki; Marutani, Yasuhisa; Nakatsugawa, Masashi; Tetrahedron Asymmetry; vol. 15; nb. 24; (2004); p. 3879 - 3883, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12614 - 12619, View in Reaxys

(R)-6

Wolf, Christian; Hawes, Pili A.; Journal of Organic Chemistry; vol. 67; nb. 8; (2002); p. 2727 - 2729, View in Reaxys; Shiina, Isamu; Konishi, Katsuhiko; Kuramoto, Yu-suke; Chemistry Letters; nb. 2; (2002); p. 164 - 165, View in Reaxys; Braese, Stefan; Dahmen, Stefan; Lauterwasser, Frank; Leadbeater, Nicholas E; Sharp, Emma L; Bioorganic and medicinal chemistry letters; vol. 12; nb. 14; (2002); p. 1849 - 1851, View in Reaxys; Escorihuela, Jorge; Altava, Beln; Burguete, M. Isabel; Luis, Santiago V.; RSC Advances; vol. 5; nb. 19; (2015); p. 14653 - 14662, View in Reaxys

(R)-2a

Cobb, Alexander J. A.; Marson, Charles M.; Tetrahedron Asymmetry; vol. 12; nb. 11; (2001); p. 1547 - 1550, View in Reaxys; El-Shehawy, Ashraf A.; Sugiyama, Kenji; Hirao, Akira; Tetrahedron Asymmetry; vol. 19; nb. 4; (2008); p. 425 - 434, View in Reaxys; Zheng, Gao-Wei; Liu, Xu-Yun; Zhang, Zhi-Jun; Tian, Ping; Lin, Guo-Qiang; Xu, Jian-He; RSC Advances; vol. 3; nb. 43; (2013); p. 20446 - 20449, View in Reaxys; Wang, Zheng; Ye, Jinjin; Wu, Rui; Liu, Yang-Zi; Fossey, John S.; Cheng, Jiagao; Deng, Wei-Ping; Catalysis Science and Technology; vol. 4; nb. 7; (2014); p. 1909 - 1913, View in Reaxys; Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys; Patent; RESEARCH & BUSINESS FOUNDATION SUNGKYUNKWAN UNIVERSITY; SONG, CHOON GEUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114445; (2015); (A) Korean, View in Reaxys

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Rachwalski, Michal; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 219 - 223, View in Reaxys; Pieczonka, Adam M.; Les̈niak, Stanisław; Jarzyński, Szymon; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 26; nb. 2-3; (2015); p. 148 - 151, View in Reaxys

Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys

3aa

Guo, Jun; Chen, Jianhui; Lu, Zhan; Chemical Communications; vol. 51; nb. 26; (2015); p. 5725 - 5727, View in Reaxys

15b

Romero, R. Martín; Fra, Laura; Lishchynskyi, Anton; Martínez, Claudio; Streuff, Jan; Muñiz, Kilian; Tetrahedron; vol. 71; nb. 26-27; (2015); p. 4465 - 4472, View in Reaxys

32-R

Vinogradov; Gorshkova; Pavlov; Mikhalev; Chel'tsova; Razmanov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 49; nb. 3; (2000); p. 460 - 465, View in Reaxys; Tang, Tuo-Xian; Liu, Yan; Wu, Zhong-Liu; Journal of Molecular Catalysis B: Enzymatic; vol. 105; (2014); p. 82 - 88, View in Reaxys

(R)-17

McNulty, James; Capretta, Alfredo; Laritchev, Vladimir; Dyck, Jeff; Robertson, Al J.; Journal of Organic Chemistry; vol. 68; nb. 4; (2003); p. 1597 - 1600, View in Reaxys; Sibi, Mukund P.; Stanley, Levi M.; Tetrahedron Asymmetry; vol. 15; nb. 21; (2004); p. 3353 - 3356, View in Reaxys; Laufer, Radoslaw; Veith, Ulrich; Taylor, Nicholas J.; Snieckus, Victor; Canadian Journal of Chemistry; vol. 84; nb. 2; (2006); p. 356 - 369, View in Reaxys; Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 - 350, View in Reaxys

(R)-4

(R)-37a

Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys

15g

Boukachabia, Mourad; Vriamont, Nicolas; Lambin, Dominique; Riant, Olivier; Aribi-Zouioueche, Louisa; Comptes Rendus Chimie; vol. 17; nb. 5; (2014); p. 403 - 412, View in Reaxys

SRC 1240

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys

1-PPP

Lin, Lang; Yu, Rongmin; Wu, Xiao-Yuan; Yang, Wen-Bin; Zhang, Jian; Guo, Xiang-Guang; Lin, Zu-Jin; Lu, Can-Zhong; Inorganic Chemistry; vol. 53; nb. 10; (2014); p. 4794 - 4796, View in Reaxys

R-6a

Karabuga, Semistan; Karakaya, Idris; Ulukanli, Sabri; Tetrahedron Asymmetry; vol. 25; nb. 10-11; (2014); p. 851 855, View in Reaxys

Zheng, Jun; You, Shu-Li; Chemical Communications; vol. 50; nb. 60; (2014); p. 8204 - 8207, View in Reaxys

Szakonyi, Zsolt; Gonda, Tímea; Ötvös, Sándor Balázs; Fülöp, Ferenc; Tetrahedron Asymmetry; vol. 25; nb. 15; (2014); p. 1138 - 1145, View in Reaxys

7; 9

Faigl, Ferenc; Erdlyi, Zsuzsa; Dek, Szilvia; Nyerges, Mikls; Mtravölgyi, Bla; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6891 - 6894, View in Reaxys

Bigler, Raphael; Huber, Raffael; Mezzetti, Antonio; Angewandte Chemie - International Edition; vol. 54; nb. 17; (2014); p. 5171 - 5174; Angew. Chem.; vol. 127; nb. 17; (2014); p. 5260 - 5263,4, View in Reaxys

ent-4

Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys

Matsumura, Yoshihiro; Ogura, Kanako; Kouchi, Yoshimi; Iwasaki, Fumiaki; Onomura, Osamu; Organic Letters; vol. 8; nb. 17; (2006); p. 3789 - 3792, View in Reaxys; Nie, Huifang; Zhou, Gang; Wang, Quanjun; Chen, Weiping; Zhang, Shengyong; Tetrahedron Asymmetry; vol. 24; nb. 24; (2013); p. 1567 - 1571, View in Reaxys

(R)-2k

147/229

2018-07-03 16:52:46

10a

Sato, Itaru; Shibata, Takanori; Ohtake, Koji; Kodaka, Ryo; Hirokawa, Yutaka; Shirai, Nobuaki; Soai, Kenso; Tetrahedron Letters; vol. 41; nb. 17; (2000); p. 3123 - 3126, View in Reaxys; Deng, Wei-Ping; Hou, Xue-Long; Dai, Li-Xin; Tetrahedron Asymmetry; vol. 10; nb. 24; (1999); p. 4689 - 4693, View in Reaxys; Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul; Synthesis; nb. 24; (2007); p. 3877 - 3885, View in Reaxys; Na, Risong; Wang, Bo; Liu, Honglei; Bian, Qinghua; Zhong, Jiangchun; Wang, Min; Guo, Hongchao; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 622 - 627, View in Reaxys; Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys

Patent; NORTH CAROLINA STATE UNIVERSITY; COMINS, Daniel, L.; CAPRACOTTA, Sonja, S.; WO2010/40059; (2010); (A1) English, View in Reaxys; Zammit, Charlotte M.; Wills, Martin; Tetrahedron Asymmetry; vol. 24; nb. 13-14; (2013); p. 844 - 852, View in Reaxys

tbl 4 ent 4 pdt

Hosoda, Naoya; Kamito, Hideaki; Takano, Miki; Takebe, Yoshitaka; Yamaguchi, Yoshitaka; Asami, Masatoshi; Tetrahedron; vol. 69; nb. 6; (2013); p. 1739 - 1746, View in Reaxys

Li, Jiahong; Li, Xuefeng; Ma, Yaping; Wu, Jiashou; Wang, Fei; Xiang, Jing; Zhu, Jin; Wang, Qiwei; Deng, Jingen; RSC Advances; vol. 3; nb. 6; (2013); p. 1825 - 1834, View in Reaxys

Csillag, Kinga; Szakonyi, Zsolt; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 24; nb. 9-10; (2013); p. 553 - 561, View in Reaxys

6a_R

Rachwalski, Michal; Jarzynski, Szymon; Jasinski, Marcin; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 689 - 693, View in Reaxys

Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys

Zhou, Han; Huang, Hanmin; ChemCatChem; vol. 5; nb. 8; (2013); p. 2253 - 2257, View in Reaxys

(R)-PPA

Li, Zi-Jian; Yao, Jia; Tao, Qian; Jiang, Long; Lu, Tong-Bu; Inorganic Chemistry; vol. 52; nb. 20; (2013); p. 11694 11696, View in Reaxys

Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys

(R)-10

Compound 41

Patent; UANG, Biing-Jiun; Yang, Bo-Yao; US2012/77976; (2012); (A1) English, View in Reaxys

(R)-26

(R)-1,(R)-3

Cheng, Ying-Ni; Wu, Hsyueh-Liang; Wu, Ping-Yu; Shen, Ying-Ying; Uang, Biing-Jiun; Chemistry - An Asian Journal; vol. 7; nb. 12; (2012); p. 2921 - 2924, View in Reaxys

Tab.2, entry.1: byprod.

Dong, Zhi-Bing; Liu, Bing; Fang, Cao; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 693; nb. 1; (2008); p. 17 - 22, View in Reaxys

(R)-41

(R)-15

Szakonyi, Zsolt; Hetenyi, Anasztazia; Fueloep, Ferenc; Tetrahedron; vol. 64; nb. 6; (2008); p. 1034 - 1039, View in Reaxys

Table 2, entry 16

Li, Gao-Qiang; Yan, Ze-Yi; Niu, Yan-Ning; Wu, Lu-Yong; Wei, Hai-Long; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 7; (2008); p. 816 - 821, View in Reaxys

(R)-30

Wang, Fei; Liu, Hui; Cun, Linfeng; Zhu, Jin; Deng, Jingen; Jiang, Yaozhong; Journal of Organic Chemistry; vol. 70; nb. 23; (2005); p. 9424 - 9429, View in Reaxys; Taniguchi, Tomohiro; Fukuba, Taka-Aki; Nakatsuka, Shuhei;

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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Hayase, Shuichi; Kawatsura, Motoi; Uno, Hidemitsu; Itoh, Toshiyuki; Journal of Organic Chemistry; vol. 73; nb. 10; (2008); p. 3875 - 3884, View in Reaxys (R)-9n

Niu, Yan-Ning; Yan, Ze-Yi; Li, Gao-Qiang; Wei, Hai-Long; Gao, Guo-Lin; Wu, Lu-Yong; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 8; (2008); p. 912 - 920, View in Reaxys

(R)-1c

Muramatsu, Yusuke; Harada, Toshiro; Angewandte Chemie - International Edition; vol. 47; nb. 6; (2008); p. 1088 1090, View in Reaxys

(R)-Prod.8

Liu, Juntao; Wu, Yinuo; Li, Xingshu; Chan, Albert S.C.; Journal of Organometallic Chemistry; vol. 693; nb. 12; (2008); p. 2177 - 2180, View in Reaxys

(R)-13a

(R)-13

(R)-19b

Lavandera, Ivan; Hoeller, Brigitte; Kern, Alexander; Ellmer, Ursula; Glieder, Anton; de Wildeman, Stefaan; Kroutil, Wolfgang; Tetrahedron Asymmetry; vol. 19; nb. 16; (2008); p. 1954 - 1958, View in Reaxys

(R)-9

Paleo, M. Rita; Cabeza, Isabel; Sardina, F. Javier; Journal of Organic Chemistry; vol. 65; nb. 7; (2000); p. 2108 2113, View in Reaxys; Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron; vol. 59; nb. 50; (2003); p. 10009 - 10012, View in Reaxys; Jones, Geraint; Richards, Christopher J.; Tetrahedron Asymmetry; vol. 15; nb. 4; (2004); p. 653 664, View in Reaxys; Birman, Vladimir B.; Jiang, Hui; Li, Ximin; Organic Letters; vol. 9; nb. 17; (2007); p. 3237 3240, View in Reaxys; Rachwalski, Michal; Kwiatkowska, Malgorzata; Drabowicz, Jozef; Klos, Marcin; Wieczorek, Wanda M.; Szyrej, Malgorzata; Sieron, Leslaw; Kielbasinski, Piotr; Tetrahedron Asymmetry; vol. 19; nb. 17; (2008); p. 2096 - 2101, View in Reaxys

(R)-2c

Shaikh, Nadim S.; Enthaler, Stephan; Junge, Kathrin; Beller, Matthias; Angewandte Chemie - International Edition; vol. 47; nb. 13; (2008); p. 2497 - 2501, View in Reaxys

R-product Table 3 E. 1

Hua, Genghong; Liu, Delong; Xie, Fang; Zhang, Wanbin; Tetrahedron Letters; vol. 48; nb. 3; (2007); p. 385 - 388, View in Reaxys

(R)-1

(R)-product, R=Ph

Jiang, Fu-Yong; Liu, Bing; Dong, Zhi-Bing; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 692; nb. 20; (2007); p. 4377 - 4380, View in Reaxys

byprod., Tab.2; entry 2

Casarotto, Virginie; Li, Zhongtao; Boucau, Julie; Lin, Yun-Ming; Tetrahedron Letters; vol. 48; nb. 31; (2007); p. 5561 - 5564, View in Reaxys

(+)-(R)-47

Driver, Tom G.; Harris, Jason R.; Woerpel; Journal of the American Chemical Society; vol. 129; nb. 13; (2007); p. 3836 - 3837, View in Reaxys

table 2, entry 2

Harada, Toshiro; Ukon, Takahiro; Tetrahedron Asymmetry; vol. 18; nb. 21; (2007); p. 2499 - 2502, View in Reaxys

(R)-10a

Reddy, Katamreddy Subba; Sola, Lluis; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Journal of Organic Chemistry; vol. 64; nb. 11; (1999); p. 3969 - 3974, View in Reaxys; Wilken, Joerg; Erny, Silke; Wassmann, Suzanne; Martens, Juergen; Tetrahedron Asymmetry; vol. 11; nb. 10; (2000); p. 2143 - 2148, View in Reaxys; Bringmann, Gerhard; Pfeifer, Robert-Michael; Rummey, Christian; Hartner, Kristina; Breuning, Matthias; Journal of Organic Chemistry; vol. 68; nb. 18; (2003); p. 6859 - 6863, View in Reaxys; Enthaler, Stephan; Hagemann, Bernhard; Bhor, Santosh; Anilkumar, Gopinathan; Tse, Man Kin; Bitterlich, Bianca; Junge, Kathrin; Erre, Giulia; Beller, Matthias; Advanced Synthesis and Catalysis; vol. 349; nb. 6; (2007); p. 853 - 860, View in Reaxys

(R)-1, T3, E1-7

Shiina, Isamu; Nakata, Kenya; Tetrahedron Letters; vol. 48; nb. 47; (2007); p. 8314 - 8317, View in Reaxys

(R)-7a

Tab 3/6 (R)-product Eagon, Scott; Kim, Jinsoo; Yan, Katie; Haddenham, Dustin; Singaram, Bakthan; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 9025 - 9029, View in Reaxys

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Table 2, entry 1

Huang, Hanmin; Zheng, Zhuo; Chen, Huilin; Bai, Changmin; Wang, Junwei; Tetrahedron Asymmetry; vol. 14; nb. 10; (2003); p. 1285 - 1289, View in Reaxys; Tanaka, Takanori; Yasuda, Yorinobu; Hayashi, Masahiko; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7091 - 7093, View in Reaxys

(R)-5b

Tab.2. run 1, byprod.

Guo, Qun-Sheng; Lu, Yong-Na; Liu, Bing; Xiao, Jian; Li, Jin-Shan; Journal of Organometallic Chemistry; vol. 691; nb. 6; (2006); p. 1282 - 1287, View in Reaxys

(R)-23j

Schiffers, Ingo; Rantanen, Toni; Schmidt, Frank; Bergmans, Werner; Zani, Lorenzo; Bolm, Carsten; Journal of Organic Chemistry; vol. 71; nb. 6; (2006); p. 2320 - 2331, View in Reaxys

9-(R)

Roudeau, Remi; Gomez Pardo, Domingo; Cossy, Janine; Tetrahedron; vol. 62; nb. 10; (2006); p. 2388 - 2394, View in Reaxys

11a

Szakonyi, Zsolt; Balazs, Arpad; Martinek, Tamas A.; Fueloep, Ferenc; Tetrahedron Asymmetry; vol. 17; nb. 2; (2006); p. 199 - 204, View in Reaxys

tbl.2, ent.2, product

Arakawa, Yukihiro; Haraguchi, Naoki; Itsuno, Shinichi; Tetrahedron Letters; vol. 47; nb. 19; (2006); p. 3239 - 3243, View in Reaxys

5a (R) (major)

MacLeod, Patricia D.; Li, Zhiping; Feng, Jianqing; Li, Chao-Jun; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6791 - 6794, View in Reaxys

4b, R

Utsukihara, Takamitsu; Misumi, Osami; Kato, Nakahide; Kuroiwa, Tsuneyoshi; Horiuchi, C. Akira; Tetrahedron Asymmetry; vol. 17; nb. 8; (2006); p. 1179 - 1185, View in Reaxys

(R)-6i

Reetz, Manfred T.; Li, Xiaoguang; Journal of the American Chemical Society; vol. 128; nb. 4; (2006); p. 1044 - 1045, View in Reaxys

(R) pr. table 1.

Bauer, Michael; Kazmaier, Uli; Journal of Organometallic Chemistry; vol. 691; nb. 10; (2006); p. 2155 - 2158, View in Reaxys

(R)-8b

Bandini, Marco; Bottoni, Andrea; Cozzi, Pier Giorgio; Miscione, Gian Pietro; Monari, Magda; Pierciaccante, Rossana; Umani-Ronchi, Achille; European Journal of Organic Chemistry; nb. 20; (2006); p. 4596 - 4608, View in Reaxys

(R)-3f

Huang, Hanmin; Okuno, Tomoko; Tsuda, Kazuomi; Yoshimura, Masahiro; Kitamura, Masato; Journal of the American Chemical Society; vol. 128; nb. 27; (2006); p. 8716 - 8717, View in Reaxys

(R)-9a, Tab3, run 1

(R)-6f

Anwar, Shaik; Periasamy, Mariappan; Tetrahedron Asymmetry; vol. 17; nb. 23; (2006); p. 3244 - 3247, View in Reaxys

(R)-(+)-3e

Tab 1/8-9 Product(R)

Cortez, Norma A.; Rodriguez-Apodaca, Ramon; Aguirre, Gerardo; Parra-Hake, Miguel; Cole, Thomas; Somanathan, Ratnasamy; Tetrahedron Letters; vol. 47; nb. 48; (2006); p. 8515 - 8518, View in Reaxys

Tab. 2, entry 9

Issenhuth, Jean Thomas; Dagorne, Samuel; Bellemin-Laponnaz, Stephane; Advanced Synthesis and Catalysis; vol. 348; nb. 14; (2006); p. 1991 - 1994, View in Reaxys

Table 1, entry 13

Morris, David J.; Hayes, Aidan M.; Wills, Martin; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7035 7044, View in Reaxys

(R)-6d

Boren, Linnea; Martin-Matute, Belen; Xu, Yongmei; Cordova, Armando; Baeckvall, Jan-E.; Chemistry - A European Journal; vol. 12; nb. 1; (2006); p. 225 - 232, View in Reaxys

ent-15a

Zhang, Yi-Li; Zhang, Feng; Tang, Wei-Jun; Wu, Qing-Lai; Fan, Qing-Hua; Synlett; nb. 8; (2006); p. 1250 - 1254, View in Reaxys

alc., Tab. 3, entry 8

Li, Xiaohong; Blacker, John; Houson, Ian; Wu, Xiaofeng; Xiao, Jianliang; Synlett; nb. 8; (2006); p. 1155 - 1160, View in Reaxys

(R)PhCH(OH)CH2CH 3

(R)-5, R1 = Ph

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Synlett; nb. 11; (2006); p. 1762 - 1764, View in Reaxys

(R)-6a

Soai, Kenso; Niwa, Seiji; Watanabe, Masami; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1989); p. 109 - 113, View in Reaxys; Hanyu, Naoto; Mino, Takashi; Sakamoto, Masami; Fujita, Tsutomu; Tetrahedron Letters; vol. 41; nb. 23; (2000); p. 4587 - 4590, View in Reaxys; Hanyu, Nao-

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to; Aoki, Tasuku; Mino, Takashi; Sakamoto, Masami; Fujita, Tsutomu; Tetrahedron Asymmetry; vol. 11; nb. 14; (2000); p. 2971 - 2979, View in Reaxys; Satyanarayana, Tummanapalli; Kagan, Henri B.; Chemistry - A European Journal; vol. 12; nb. 22; (2006); p. 5785 - 5789, View in Reaxys (+)-(R)-PA2a

Patent; UNIVERSITY OF NOTTINGHAM; WO2006/79819; (2006); (A2) English, View in Reaxys

Matharu, Daljit S.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Chemical Communications; nb. 30; (2006); p. 3232 - 3234, View in Reaxys

(R)-19a

Cherng, Yie-Jia; Fang, Jim-Min; Lu, Ta-Jung; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 3207 - 3212, View in Reaxys; Lauterwasser, Frank; Nieger, Martin; Mansikkamaeki, Heidi; Naettinen, Kalle; Braese, Stefan; Chemistry - A European Journal; vol. 11; nb. 15; (2005); p. 4509 - 4525, View in Reaxys

(R)-14

prod. R

Omote, Masaaki; Nishimura, Yuji; Sato, Kazuyuki; Ando, Akira; Kumadaki, Itsumaro; Tetrahedron Letters; vol. 46; nb. 2; (2005); p. 319 - 322, View in Reaxys

enan. Tab. run 8

Ngo, Helen L.; Hu, Aiguo; Lin, Wenbin; Tetrahedron Letters; vol. 46; nb. 4; (2005); p. 595 - 597, View in Reaxys

(R)-4g

Lapis, Alexandre A. M.; De Fatima, Angelo; Martins, Jose E. D.; Costa, Valentim E. U.; Pilli, Ronaldo A.; Tetrahedron Letters; vol. 46; nb. 3; (2005); p. 495 - 498, View in Reaxys

Tab.2. Ent.2-3. Rprod.

Tan, Duan-Ming; Chan, Kin Shing; Tetrahedron Letters; vol. 46; nb. 3; (2005); p. 503 - 505, View in Reaxys

(R)-11e

Castellnou, David; Sola, Lluis; Jimeno, Ciril; Fraile, Jose M.; Mayoral, Jose A.; Riera, Antoni; Pericas, Miquel A.; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 433 - 438, View in Reaxys

12an

Aggarwal, Varinder K.; Guang, Yu Fang; Schmidt, Andreas T.; Journal of the American Chemical Society; vol. 127; nb. 6; (2005); p. 1642 - 1643, View in Reaxys

Tab.1.,Ent.1.,(R)prod.

Jin, Myung-Jong; Kim, Young-Mok; Lee, Kyoung-Soo; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2695 - 2696, View in Reaxys

Tab. 1, entry 3

25a (R)

Cobb, Alexander J.A.; Marson, Charles M.; Tetrahedron; vol. 61; nb. 5; (2005); p. 1269 - 1279, View in Reaxys

(R)-product from 11

Liu, Pei-Nian; Gu, Pei-Ming; Deng, Jin-Gen; Tu, Yong-Qiang; Ma, Ya-Ping; European Journal of Organic Chemistry; nb. 15; (2005); p. 3221 - 3227, View in Reaxys

(R)-5, tab. 3, ent. 1

Song, Chun; Ma, Changqin; Ma, Yudao; Feng, Wenhua; Ma, Shutao; Chai, Qiang; Andrus, Merritt B.; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3241 - 3244, View in Reaxys

12e min

Dalicsek, Zoltan; Pollreisz, Ferenc; Goemoery, Agnes; Soos, Tibor; Organic Letters; vol. 7; nb. 15; (2005); p. 3243 3246, View in Reaxys

(R)-20

Fennie, Michael W.; DiMauro, Erin F.; O'Brien, Erin M.; Annamalai, Venkatachalam; Kozlowski, Marisa C.; Tetrahedron; vol. 61; nb. 26; (2005); p. 6249 - 6265, View in Reaxys

ent-7a

Dong, Zhen-Rong; Li, Yan-Yun; Chen, Jian-Shan; Li, Bao-Zhu; Xing, Yan; Gao, Jing-Xing; Organic Letters; vol. 7; nb. 6; (2005); p. 1043 - 1045, View in Reaxys

Inoue, Kousuke; Makino, Yoshihide; Itoh, Nobuya; Tetrahedron Asymmetry; vol. 16; nb. 15; (2005); p. 2539 - 2549, View in Reaxys

Scheme 2. product 2

Johansson, Anna; Wingstrand, Erica; Hakansson, Mikael; Journal of Organometallic Chemistry; vol. 690; nb. 16; (2005); p. 3846 - 3853, View in Reaxys

(R)-2a, Tab. 1, entry 1

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1561 - 1568, View in Reaxys

product, table 2/run Cordes, David B.; Nguyen, Thao M.; Kwong, Tracey J.; Suri, Jeff T.; Luibrand, Richard T.; Singaram, Bakthan; 4 European Journal of Organic Chemistry; nb. 24; (2005); p. 5289 - 5295, View in Reaxys (R)-(+)-5a

Biswas, Kallolmay; Prieto, Oscar; Goldsmith, Paul J.; Woodward, Simon; Angewandte Chemie - International Edition; vol. 44; nb. 15; (2005); p. 2232 - 2234, View in Reaxys

ent-7e

(R)-1b

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Organic Chemistry; vol. 66; nb. 19; (2001); p. 6495 - 6497, View in Reaxys; Verzijl, Gerard K.M.; De Vries, Johannes G.; Broxterman, Quirinus B.; Tetrahedron Asymmetry; vol. 16; nb. 9; (2005); p. 1603 - 1610, View in Reaxys (R)-11

product, isomer 1

Barros, M. Teresa; Maycock, Christopher D.; Phillips, Ana Maria Faisca; European Journal of Organic Chemistry; nb. 8; (2004); p. 1820 - 1829, View in Reaxys

Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys

Guo, Xun-Xiang; Xie, Jian-Hua; Hou, Guo-Hua; Shi, Wen-Jian; Wang, Li-Xin; Zhou, Qi-Lin; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2231 - 2234, View in Reaxys

(R)-PhCH(Et)OH

Cuervo, Dario; Gamasa, M. Pilar; Gimeno, Jose; Chemistry - A European Journal; vol. 10; nb. 2; (2004); p. 425 432, View in Reaxys

Scheme 4 (R = CH2CH3)

Cheng, Xiaohui; Horton, Peter N.; Hursthouse, Michael B.; Hii, King Kuok; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2241 - 2246, View in Reaxys

Basavaiah, Deevi; Reddy, Gone Jayapal; Rao, Kalapala Venkateswara; Tetrahedron Asymmetry; vol. 15; nb. 12; (2004); p. 1881 - 1888, View in Reaxys

t.5, α-product, (R)

Tab. 2,entry 13,alcohol

Wu, Xiaofeng; Li, Xiaoguang; Hems, William; King, Frank; Xiao, Jianliang; Organic and Biomolecular Chemistry; vol. 2; nb. 13; (2004); p. 1818 - 1821, View in Reaxys

13, t.2, entry 1

Tseng, Shi-Liang; Yang, Teng-Kuei; Tetrahedron Asymmetry; vol. 15; nb. 21; (2004); p. 3375 - 3380, View in Reaxys

Xu, Jiaxi; Wei, Tiezheng; Zhang, Qihan; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6860 - 6866, View in Reaxys

t.2, entry 1

Sprout, Christopher M.; Richmond, Meaghan L.; Seto, Christopher T.; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6666 - 6673, View in Reaxys

32, enantiomer

Boyle, Grant A.; Govender, Thavendran; Kruger, Hendrik G.; Maguire, Glenn E.M.; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2661 - 2666, View in Reaxys

(R)-product of 3

Kriis, Kadri; Kanger, Tonis; Lopp, Margus; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2687 - 2691, View in Reaxys

Tab. 1, Ent. 1, prod. Zhong, Yu-Wu; Jiang, Chang-Sheng; Xu, Ming-Hua; Lin, Guo-Qiang; Tetrahedron; vol. 60; nb. 40; (2004); p. 8861 R - 8868, View in Reaxys R-3

Bauer, Tomasz; Gajewiak, Joanna; Tetrahedron; vol. 60; nb. 41; (2004); p. 9163 - 9170, View in Reaxys

Prod.(R), Tab.1,run 9

Lee, Dong-Won; Yun, Jaesook; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5415 - 5417, View in Reaxys

4a (R)

Homann, Michael J.; Vail, Robert B.; Previte, Edward; Tamarez, Maria; Morgan, Brian; Dodds, David R.; Zaks, Aleksey; Tetrahedron; vol. 60; nb. 3; (2004); p. 789 - 797, View in Reaxys

11, (R)-alcohol

Li, Xiaoguang; Chen, Weiping; Hems, William; King, Frank; Xiao, Jianliang; Tetrahedron Letters; vol. 45; nb. 5; (2004); p. 951 - 953, View in Reaxys

R-alcohol T. 1, e. 3

Chen, Jian-Shan; Li, Yan-Yun; Dong, Zhen-Rong; Li, Bao-Zhu; Gao, Jing-Xing; Tetrahedron Letters; vol. 45; nb. 45; (2004); p. 8415 - 8418, View in Reaxys

(R)-7

(R)-8

Omote, Masaaki; Kominato, Akane; Sugawara, Michi; Sato, Kazuyuki; Ando, Akira; Kumadaki, Itsumaro; Tetrahedron Letters; vol. 40; nb. 30; (1999); p. 5583 - 5585, View in Reaxys; Marubayashi, Kazuyoshi; Takizawa, Shino-

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bu; Kawakusu, Tetsuo; Arai, Takayoshi; Sasai, Hiroaki; Organic Letters; vol. 5; nb. 23; (2003); p. 4409 - 4412, View in Reaxys (R)-7, R1=Ph

Casey, Mike; Smyth, Martin P.; Synlett; nb. 1; (2003); p. 102 - 106, View in Reaxys

(R)C6H5CH(OH)Et

Jiang, Hua; Hu, Aiguo; Lin, Wenbin; Chemical Communications; nb. 1; (2003); p. 96 - 97, View in Reaxys

(R)-alcohol, entry 9 Hegarty, Philip; Lau, Raymond; Motherwell, William B.; Tetrahedron Letters; vol. 44; nb. 9; (2003); p. 1851 - 1853, View in Reaxys 14a-(R), R=Ph

Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Tetrahedron Asymmetry; vol. 14; nb. 9; (2003); p. 1103 - 1114, View in Reaxys

(R)-2

Sosa-Rivadeneyra, Martha; Munoz-Muniz, Omar; Anaya de Parrodi, Cecilia; Quintero, Leticia; Juaristi, Eusebio; Journal of Organic Chemistry; vol. 68; nb. 6; (2003); p. 2369 - 2375, View in Reaxys

(R)-4a

Joshi, Sudhir N.; Malhotra, Sanjay V.; Tetrahedron Asymmetry; vol. 14; nb. 13; (2003); p. 1763 - 1766, View in Reaxys

Tab.2., run 1, prod. 1

Anyanwu, Uche K.; Venkataraman; Tetrahedron Letters; vol. 44; nb. 34; (2003); p. 6445 - 6448, View in Reaxys

byproduct 3b

Huertas, Ramon E.; Corella, Joseph A.; Soderquist, John A.; Tetrahedron Letters; vol. 44; nb. 24; (2003); p. 4435 4437, View in Reaxys

(R)-9a

Okuyama, Yuko; Nakano, Hiroto; Igarashi, Mayumi; Kabuto, Chizuko; Hongo, Hiroshi; Heterocycles; vol. 59; nb. 2; (2003); p. 635 - 643, View in Reaxys

3b(R)

Nishibayashi, Yoshiaki; Yamauchi, Akiyoshi; Onodera, Gen; Uemura, Sakae; Journal of Organic Chemistry; vol. 68; nb. 15; (2003); p. 5875 - 5880, View in Reaxys

R-isomer

Garcia Martinez, Antonio; Teso Vilar, Enrique; Garcia Fraile, Amelia; De La Moya Cerero, Santiago; Lora Maroto, Beatriz; Tetrahedron Asymmetry; vol. 14; nb. 14; (2003); p. 1959 - 1963, View in Reaxys

13, R

Danilova, Tatyana I.; Rozenberg, Valeria I.; Sergeeva, Elena V.; Starikova, Zoya A.; Braese, Stefan; Tetrahedron Asymmetry; vol. 14; nb. 14; (2003); p. 2013 - 2019, View in Reaxys

6, (R)-enantiomer

Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 458, View in Reaxys

13 (R)

R-product(table,en- Muniz, Kilian; Tetrahedron Letters; vol. 44; nb. 17; (2003); p. 3547 - 3549, View in Reaxys try1) 16-(R)

Bonini, Bianca F.; Fochi, Mariafrancesca; Comes-Franchini, Mauro; Ricci, Alfredo; Thijs, Lambertus; Zwanenburg, Binne; Tetrahedron Asymmetry; vol. 14; nb. 21; (2003); p. 3321 - 3327, View in Reaxys

(R)-6b

Vinogradov; Gorshkova; Chel'tsova; Kurilov; Ferapontov; Shishkin; Heise; Russian Chemical Bulletin; vol. 52; nb. 8; (2003); p. 1841 - 1846, View in Reaxys

P&R%

Scuderi; Paladini; Satta; Catone; Rondino; Tacconi; Filippi; Piccirillo; Giardini Guidoni; Speranza; Physical Chemistry Chemical Physics; vol. 5; nb. 20; (2003); p. 4570 - 4575, View in Reaxys

(R)-35b

Stampfer, Wolfgang; Kosjek, Birgit; Faber, Kurt; Kroutil, Wolfgang; Journal of Organic Chemistry; vol. 68; nb. 2; (2003); p. 402 - 406, View in Reaxys

Bosman, Anton W.; Vestberg, Robert; Heumann, Andi; Frechet, Jean M. J.; Hawker, Craig J.; Journal of the American Chemical Society; vol. 125; nb. 3; (2003); p. 715 - 728, View in Reaxys

(R)-PhCH(OH)Et

Lawrence, Corrine F.; Nayak, Sandip K.; Thijs, Lambertus; Zwanenburg, Binne; Synlett; nb. 10; (1999); p. 1571 1572, View in Reaxys; Nakamura, Kaoru; Fujii, Mikio; Ida, Yoshiteru; Journal of the Chemical Society, Perkin Transactions 1; nb. 19; (2000); p. 3205 - 3211, View in Reaxys; Abramson; Lasperas; Galarneau; Desplantier-Giscard; Brunel; Chemical Communications; nb. 18; (2000); p. 1773 - 1774, View in Reaxys; Zhang; Yoshinaga; Imai; Kida; Nakatsuji; Ikeda; Synlett; nb. 10; (2000); p. 1512 - 1514, View in Reaxys; Jimeno; Moyano; Pericas; Riera; Synlett; nb. 7; (2001); p. 1155 - 1157, View in Reaxys; Hermsen; Cremers; Thijs; Zwanenburg; Tetrahedron Letters; vol. 42; nb. 25; (2001); p. 4243 - 4245, View in Reaxys; Nakano, Hiroto; Okuyama, Yuko; Fushimi, Kazuyuki; Yamakawa, Ryo; Kayaoka, Daisuke; Hongo, Hiroshi; Heterocycles; vol. 56; nb. 1-2; (2002); p. 457 - 466, View in Reaxys; Zhang, Hui; Yang, Chuan-Bo; Li, Yan-Yun; Donga, Zhen-Rong; Gao, Jing-Xing; Nakamura, Hideaki; Murata, Kunihiko; Ikariya, Takao; Chemical Communications; nb. 1; (2003); p. 142 - 143, View in Reaxys; Segarra, Anna M.; Guerrero, Ramon; Claver, Carmen; Fernandez, Elena; Chemistry - A European Journal; vol. 9; nb. 1; (2003); p. 191 - 200, View in Reaxys

(R)-11a

Pericas, Miquel A.; Castellnou, David; Rodriguez, Israel; Riera, Antoni; Sola, Lluis; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1305 - 1313, View in Reaxys

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Patent; CYTEC CANADA INC.; WO2004/778; (2003); (A1) English, View in Reaxys

Cho, Byung Tae; Chun, Yu Sung; Synthetic Communications; vol. 29; nb. 3; (1999); p. 521 - 531, View in Reaxys; Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys; Scuderi; Paladini; Piccirillo; Satta; Catone; Giardini; Filippi; Speranza, Maurizio; Chemical Communications; nb. 20; (2002); p. 2438 - 2439, View in Reaxys

(R)-9b

Prod.(R), Tab.1/2,run 1

Braga, Antonio L; Vargas, Fabricio; Silveira, Claudio C; De Andrade, Leandro H; Tetrahedron Letters; vol. 43; nb. 13; (2002); p. 2335 - 2337, View in Reaxys

Pastor, Isidro M; Adolfsson, Hans; Tetrahedron Letters; vol. 43; nb. 9; (2002); p. 1743 - 1746, View in Reaxys

(R)-a

12a

Sato, Itaru; Kodaka, Ryo; Hosoi, Kenji; Soai, Kenso; Tetrahedron Asymmetry; vol. 13; nb. 8; (2002); p. 805 - 808, View in Reaxys

6-(R)

Wolf, Christian; Francis, Christopher J.; Hawes, Pili A.; Shah, Mirage; Tetrahedron Asymmetry; vol. 13; nb. 16; (2002); p. 1733 - 1741, View in Reaxys

t.1, minor enantiomer

Superchi, Stefano; Giorgio, Egidio; Scafato, Patrizia; Rosini, Carlo; Tetrahedron Asymmetry; vol. 13; nb. 13; (2002); p. 1385 - 1391, View in Reaxys

(R)-IIb

Yadav, Ashok K.; Singh, Arpita; Bulletin of the Chemical Society of Japan; vol. 75; nb. 3; (2002); p. 587 - 588, View in Reaxys

Prod.(minor),Tab.1,run8

Kim, Geon-Joong; Kim, Sang-Han; Chong, Pong-Hyun; Kwon, Mi-Ae; Tetrahedron Letters; vol. 43; nb. 45; (2002); p. 8059 - 8062, View in Reaxys

(R)-sec-alc. from PhCHO

Shaikh, Nadim S; Deshpande, Vishnu H; Bedekar, Ashutosh V; Tetrahedron Letters; vol. 43; nb. 32; (2002); p. 5587 - 5589, View in Reaxys

Product (R) (minor) Nagasawa, Tomomi; Miyata, Hideto; Kudo, Nozomi; Nakatani, Motoi; Ito, Kazuaki; Ohba, Yoshihiro; Heterocyclic Communications; vol. 8; nb. 5; (2002); p. 423 - 426, View in Reaxys (R)-adduct from PhCHO

Lu, Jun; Xu, Xuenong; Wang, Cunde; He, Jiangang; Hu, Yuefei; Hu, Hongwen; Tetrahedron Letters; vol. 43; nb. 46; (2002); p. 8367 - 8369, View in Reaxys

(R)-product

Lake, Fredrik; Moberg, Christina; European Journal of Organic Chemistry; nb. 18; (2002); p. 3179 - 3188, View in Reaxys

table 1, entry 3

Shi, Min; Wang, Chun-Jiang; Tetrahedron Asymmetry; vol. 13; nb. 19; (2002); p. 2161 - 2166, View in Reaxys

tab. 1,entry 2 (R)alc.

Jeong, Kyu-Sung; Kim, Soong-Hyun; Park, Hyun-Jin; Chang, Kyoung-Jin; Kwan, Soo Kim; Chemistry Letters; nb. 11; (2002); p. 1114 - 1115, View in Reaxys

(R)-12

Jensen, Jakob F.; Svendsen, Bo Y.; La Cour, Thomas V.; Pedersen, Henriette L.; Johannsen, Mogens; Journal of the American Chemical Society; vol. 124; nb. 17; (2002); p. 4558 - 4559, View in Reaxys

(R)-5

Priego, Julian; Garcia Mancheno, Olga; Cabrera, Silvia; Carretero, Juan Carlos; Journal of Organic Chemistry; vol. 67; nb. 4; (2002); p. 1346 - 1353, View in Reaxys

Gamble, Mark P.; Smith, Athene R. C.; Wills, Martin; Journal of Organic Chemistry; vol. 63; nb. 17; (1998); p. 6068 - 6071, View in Reaxys; Fan, Qing-Hua; Liu, Guo-Hua; Deng, Guo-Jun; Chen, Xiao-Min; Chan, Albert S.C.; Tetrahedron Letters; vol. 42; nb. 51; (2001); p. 9047 - 9050, View in Reaxys

11b

Petra, Danielle G. I.; Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M.; Goubitz, Kees; Van Loon, Arjen M.; De Vries, Johannes G.; Schoemaker, Hans E.; European Journal of Inorganic Chemistry; nb. 12; (1999); p. 2335 - 2341, View in Reaxys; Vinogradov; Mikhalev; Pavlov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 5; (2001); p. 843 - 845, View in Reaxys

Uozumi, Yasuhiro; Mizutani, Kanako; Nagai, Shin-ichi; Tetrahedron Letters; vol. 42; nb. 3; (2001); p. 407 - 410, View in Reaxys

7a (R)

Nakano, Hiroto; Okuyama, Yuko; Iwasa, Kazuto; Hongo, Hiroshi; Heterocycles; vol. 54; nb. 1; (2001); p. 411 - 418, View in Reaxys

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(R)

8A-(R)

Okamoto, Kazuya; Kimachi, Tetsutaro; Ibuka, Toshiro; Takemoto, Yoshiji; Tetrahedron Asymmetry; vol. 12; nb. 3; (2001); p. 463 - 467, View in Reaxys

table 1, entry 1

Wu, Xun-Wei; Hou, Xue-Long; Dai, Li-Xin; Tao, Ju; Cao, Bo-Xun; Sun, Jie; Tetrahedron Asymmetry; vol. 12; nb. 4; (2001); p. 529 - 532, View in Reaxys

(R)-alcohol from 4

Maj, Anna M.; Pietrusiewicz; Suisse, Isabelle; Agbossou, Francine; Mortreux, Andre; Journal of Organometallic Chemistry; vol. 626; nb. 1-2; (2001); p. 157 - 160, View in Reaxys

Table 3, entry 1

Nakamura, Yutaka; Takeuchi, Seiji; Okumura, Kazuo; Ohgo, Yoshiaki; Tetrahedron; vol. 57; nb. 26; (2001); p. 5565 - 5571, View in Reaxys

Product (R), Table 1

Xu, Qianyong; Wang, Hui; Pan, Xinfu; Chan, Albert S.C; Yang, Teng-Kuei; Tetrahedron Letters; vol. 42; nb. 35; (2001); p. 6171 - 6173, View in Reaxys

table 1, entry 1, ent

Yang, Xiao-Wu; Shen, Jian-Heng; Da, Chao-Shan; Wang, Heng-Shan; Su, Wu; Liu, Da-Xue; Wang, Rui; Choi, Michael C.K.; Chan, Albert S.C.; Tetrahedron Letters; vol. 42; nb. 37; (2001); p. 6573 - 6575, View in Reaxys

(R)-alcohol from 3c Rhyoo, Hae Yoon; Yoon, Young-Ae; Park, Hee-Jung; Chung, Young Keun; Tetrahedron Letters; vol. 42; nb. 30; (2001); p. 5045 - 5048, View in Reaxys 4

Chrisman, Will; Camara, Jason N.; Marcellini, Kim; Singaram, Bakthan; Goralski, Christian T.; Hasha, Dennis L.; Rudolf, Philip R.; Nicholson, Lawrence W.; Borodychuk, Karen K.; Tetrahedron Letters; vol. 42; nb. 34; (2001); p. 5805 - 5807, View in Reaxys

(R)-4b

Pavlov; Vinogradov; Starodubtseva; Chel'tsova; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 4; (2001); p. 734 - 735, View in Reaxys

Prod.,Tab.1,run 1,major

Hu, Qiao-Sheng; Sun, Chaode; Monaghan, Colleen E; Tetrahedron Letters; vol. 42; nb. 44; (2001); p. 7725 - 7728, View in Reaxys

(R)-3 (R=H)

Ooi, Takashi; Saito, Akira; Maruoka, Keiji; Chemistry Letters; nb. 11; (2001); p. 1108 - 1109, View in Reaxys

(+)-4b

Miyamoto; Yasaka; Takaoka; Tanaka; Toda; Enantiomer; vol. 6; nb. 1; (2001); p. 51 - 55, View in Reaxys

(R)-7b

Lin, Yang-Miin; Fu, I-Pin; Uang, Biing-Jiun; Tetrahedron Asymmetry; vol. 12; nb. 23; (2001); p. 3217 - 3221, View in Reaxys

Jayaprakash, Doss; Sasai, Hiroaki; Tetrahedron Asymmetry; vol. 12; nb. 18; (2001); p. 2589 - 2595, View in Reaxys

(R)-9a ((R)-3g)

Jiang, Biao; Feng, Yan; Hang, Jian-Feng; Tetrahedron Asymmetry; vol. 12; nb. 16; (2001); p. 2323 - 2329, View in Reaxys

2, R=Et, Ar=Ph

Lipshutz; Noson; Chrisman; Journal of the American Chemical Society; vol. 123; nb. 51; (2001); p. 12917 - 12918, View in Reaxys

Tab.2.,entry 2A,alcohol

Sarvary, Ian; Almqvist, Fredrik; Frejd, Torbjoern; Chemistry - A European Journal; vol. 7; nb. 10; (2001); p. 2158 2166, View in Reaxys

ent-6

Schinnerl, Marina; Seitz, Michael; Kaiser, Anja; Reiser, Oliver; Organic Letters; vol. 3; nb. 26; (2001); p. 4259 4262, View in Reaxys

(R)-PP

Cavazzini; Kaczmarski; Szabelski; Zhou; Liu; Guiochon; Analytical Chemistry; vol. 73; nb. 23; (2001); p. 5704 5715, View in Reaxys

14a, R

DiMauro, Erin F.; Kozlowski, Marisa C.; Organic Letters; vol. 3; nb. 19; (2001); p. 3053 - 3056, View in Reaxys

(R)-2b

(R)-3a

Soai, Kenso; Konishi, Takashi; Shibata, Takanori; Heterocycles; vol. 51; nb. 6; (1999); p. 1421 - 1426, View in Reaxys; Sato; Saito; Soai; Chemical Communications; nb. 24; (2000); p. 2471 - 2472, View in Reaxys; Nakamura, Kaoru; Fujii, Mikio; Ida, Yoshiteru; Tetrahedron Asymmetry; vol. 12; nb. 22; (2001); p. 3147 - 3153, View in Reaxys

Hodge, Philip; Kell, Roger J.; Ma, Jianbiao; Morris, Hugh; Australian Journal of Chemistry; vol. 52; nb. 11; (1999); p. 1041 - 1046, View in Reaxys; Mikami, Koichi; Angelaud, Remy; Ding, Kuiling; Ishii, Akihiro; Tanaka, Akito; Sawada, Naotaka; Kudo, Kenichi; Senda, Masaaki; Chemistry - A European Journal; vol. 7; nb. 3; (2001); p. 730 737, View in Reaxys

(R)-Ph-CH(OH)-Et

Nakamura, Yutaka; Takeuchi, Seiji; Ohgo, Yoshiaki; Curran, Dennis P.; Tetrahedron Letters; vol. 41; nb. 1; (2000); p. 57 - 60, View in Reaxys

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29a

Spieler, Jan; Huttenloch, Oliver; Waldmann, Herbert; European Journal of Organic Chemistry; nb. 3; (2000); p. 391 - 399, View in Reaxys

(R)PhCH(OH)C2H5

Imai, Yoshitane; Matsuo, Shigeaki; Zhang, Wanbin; Nakatsuji, Yohji; Ikeda, Isao; Synlett; nb. 2; (2000); p. 239 241, View in Reaxys

ent-3

Heckel, Alexander; Seebach, Dieter; Angewandte Chemie - International Edition; vol. 39; nb. 1; (2000); p. 163 - 165, View in Reaxys

(R)-8a

Okaniwa, Masanori; Yanada, Reiko; Ibuka, Toshiro; Tetrahedron Letters; vol. 41; nb. 7; (2000); p. 1047 - 1050, View in Reaxys

Prieto, Oscar; Ramon, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 11; nb. 7; (2000); p. 1629 - 1644, View in Reaxys

product, T.3 run 4

Asami, Masatoshi; Sato, Shinsuke; Watanabe, Hiroyasu; Chemistry Letters; nb. 9; (2000); p. 990 - 991, View in Reaxys

Table 2 Entry 1 product

Lipshutz; Shin; Tetrahedron Letters; vol. 41; nb. 49; (2000); p. 9515 - 9521, View in Reaxys

table 2, entry 3

Yun, Hongying; Wu, Yangjie; Wu, Yusheng; Ding, Kuiling; Zhou, Ying; Tetrahedron Letters; vol. 41; nb. 52; (2000); p. 10263 - 10266, View in Reaxys

entry 2

Jiang, Biao; Feng, Yan; Zheng, Jian; Tetrahedron Letters; vol. 41; nb. 52; (2000); p. 10281 - 10283, View in Reaxys

(R)-19

Dai, Wei-Min; Zhu, Hua-Jie; Hao, Xiao-Jiang; Tetrahedron Asymmetry; vol. 11; nb. 11; (2000); p. 2315 - 2337, View in Reaxys

(R)-product T7/ enty 2

Saluzzo, Christine; Ter Halle, Rob; Touchard, Francois; Fache, Fabienne; Schulz, Emmanuelle; Lemaire, Marc; Journal of Organometallic Chemistry; vol. 603; nb. 1; (2000); p. 30 - 39, View in Reaxys

Tab.1, entry 7, Risom.

McCarthy, Mary; Hooper, Mark W.; Guiry, Patrick J.; Chemical Communications; nb. 14; (2000); p. 1333 - 1334, View in Reaxys

(R)-10d

Kita, Yasuyuki; Takebe, Yasushi; Murata, Kenji; Naka, Tadaatsu; Akai, Shuji; Journal of Organic Chemistry; vol. 65; nb. 1; (2000); p. 83 - 88, View in Reaxys

(R)-3C

(R)-24b

Petra, Danielle G. I.; Kamer, Paul C. J.; Spek, Anthony L.; Schoemaker, Hans E.; Van Leeuwen, Piet W. N. M.; Journal of Organic Chemistry; vol. 65; nb. 10; (2000); p. 3010 - 3017, View in Reaxys

(R)-16c

Spivey, Alan C.; Fekner, Tomasz; Spey, Sharon E.; Journal of Organic Chemistry; vol. 65; nb. 10; (2000); p. 3154 3159, View in Reaxys

prod.(R) Tab. 1, run Arikawa, Yasuyoshi; Ueoka, Masanao; Matoba, Kazutaka; Nishibayashi, Yoshiaki; Hidai, Masanobu; Uemura, 13 Sakae; Journal of Organometallic Chemistry; vol. 572; nb. 2; (1999); p. 163 - 168, View in Reaxys Tab. col.5. run 10

Sibi, Mukund P.; Chen, Jian-xie; Cook, Gregory R.; Tetrahedron Letters; vol. 40; nb. 17; (1999); p. 3301 - 3304, View in Reaxys

table 1, entry 5

Cao, Ping; Zhang, Xumu; Journal of Organic Chemistry; vol. 64; nb. 6; (1999); p. 2127 - 2129, View in Reaxys

ent-13

Heldmann, Dieter K.; Seebach, Dieter; Helvetica Chimica Acta; vol. 82; nb. 7; (1999); p. 1096 - 1110, View in Reaxys

(R)-10b

Derdau, Volker; Laschat, Sabine; Hupe, Eike; Koenig, Wilfried A.; Dix, Ina; Jones, Peter G.; European Journal of Inorganic Chemistry; nb. 6; (1999); p. 1001 - 1007, View in Reaxys

(R)-(+)-2d

Adam, Waldemar; Mock-Knoblauch, Cordula; Saha-Moeller, Chantu R.; Journal of Organic Chemistry; vol. 64; nb. 13; (1999); p. 4834 - 4839, View in Reaxys

(R)-9g

Puigjaner, Cristina; Vidal-Ferran, Anton; Moyano, Albert; Pericas, Miquel A.; Riera, Antoni; Journal of Organic Chemistry; vol. 64; nb. 21; (1999); p. 7902 - 7911, View in Reaxys

8, R=Ph

Paquette, Leo A.; Zhou, Renjie; Journal of Organic Chemistry; vol. 64; nb. 21; (1999); p. 7929 - 7934, View in Reaxys

(R), Table (8)

Cardellicchio, Cosimo; Ciccarella, Giuseppe; Naso, Francesco; Perna, Filippo; Tortorella, Paolo; Tetrahedron; vol. 55; nb. 51; (1999); p. 14685 - 14692, View in Reaxys

product T 2/entry 4

Yanagi, Takashi; Kikuchi, Ken; Takeuchi, Hideki; Ishikawa, Takehiro; Nishimura, Toshihiro; Kamijo, Tetsuhide; Chemistry Letters; nb. 11; (1999); p. 1203 - 1204, View in Reaxys

(R)-8d

Gao, Jing-Xing; Yi, Xiao-Dong; Xu, Pian-Pian; Tang, Chun-Liang; Wan, Hui-Lin; Ikariya, Takao; Journal of Organometallic Chemistry; vol. 592; nb. 2; (1999); p. 290 - 295, View in Reaxys

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(R)C6H5CH(OH)CH3 CH3

Rheiner, P. Beat; Seebach, Dieter; Chemistry - A European Journal; vol. 5; nb. 11; (1999); p. 3221 - 3236, View in Reaxys

product, Table1, en- Legrand, Olivier; Brunel, Jean-Michel; Buono, Gerard; Tetrahedron Letters; vol. 39; nb. 51; (1998); p. 9419 - 9422, try5 View in Reaxys 21a-(R)

Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 - 26, View in Reaxys

(+)-3, R = Et

Srivastava; Mital; Kumar; Journal of the Chemical Society - Series Chemical Communications; nb. 6; (1992); p. 493 494, View in Reaxys

Tab., run 1, product

Soai, Kenso; Nishi, Mitsugu; Ito, Yuhki; Chemistry Letters; (1987); p. 2405 - 2406, View in Reaxys

(+)(R)-12

Davis, Franklin A.; Stringer, Orum D.; McCauley, John P., Jr.; Tetrahedron; vol. 41; nb. 21; (1985); p. 4747 - 4758, View in Reaxys

Table 1. line 2

Soai, Kenso; Yamanoi, Takashi; Oyamada, Hidekazu; Chemistry Letters; (1984); p. 251 - 254, View in Reaxys

Patent-Specific Data (3) References Patent; Fourth Military Medical University,People's Liberation Army; Chen, Weiping; Zhang, sheng Yong; cheng, sikun; li, xiaoye; Nie, Huifang; (10 pag.); CN103012498; (2016); (B) Chinese, View in Reaxys Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys Patent; CIBA SPECIALTY CHEMICALS HOLDING INC.; WO2004/31109; (2004); (A2) English, View in Reaxys Druglikeness (1) 1 of 1

LogP

2.095

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

20.23

Lipinski Number

Veber Number

Related Structure (3) Related Structure Referenced Compound The author has (S)-1-phenyl-1doubts about the propanol constitution/configuration of the title compound. The following alternatives are discussed/ proposed: /BRN= 2041556/

References Ishizaki, Miyuki; Hoshino, Osamu; Tetrahedron: Asymmetry; vol. 5; nb. 10; (1994); p. 1901 1904, View in Reaxys

Yamamoto,K. et al.; Journal of Organometallic Chemistry; vol. 46; (1972); p. C65 - C67, View in Reaxys Configuration.

Derivative (4) Derivative (R)-1-phenyl-propyl (S)-2-methoxy-2-trifluoro-

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methyl-2-phenylacetate (4S,7R)-2,5-dioxo-4,7-diphenyl-3,6-dioxa-nonane

Aurich, Hans Guenter; Soeberdt, Michael; Harms, Klaus; Tetrahedron; vol. 55; nb. 5; (1999); p. 1249 - 1270, View in Reaxys

3,3,3-Trifluoro-2methoxy-2-phenylpropionic acid (R)-1-phenyl-propyl ester

Hodge, Philip; Sung, David W. L.; Stratford, Peter W.; Journal of the Chemical Society - Perkin Transactions 1; nb. 16; (1999); p. 2335 - 2342, View in Reaxys

(R)-1-Phenylpropan-1-yl (R)-(-)-αmethoxy-α-(trifluoromethyl)phenyl acetate

Bolm, Carsten; Schlingloff, Gunther; Harms, Klaus; Chemische Berichte; vol. 125; nb. 5; (1992); p. 1191 - 1204, View in Reaxys

Purification (3) Purification (method)

References

via selective acylation with succinic anhydride in the presence of lipase Amano Sam 2 and subsequent hydrolysis

Gutman, Arie L.; Brenner, Dov; Boltanski, Aviv; Tetrahedron: Asymmetry; vol. 4; nb. 5; (1993); p. 839 - 844, View in Reaxys

by using goat liver acetone powder (GLAP) in two phase medium (ether:aqueous phosphate buffer)

Basavaiah; Raju; Synthetic Communications; vol. 21; nb. 18-19; (1991); p. 1859 - 1863, View in Reaxys

clathrate formation Kanoh, Shigeyoshi; Hongoh, Yukihiko; Katoh, Shingo; Motoi, Masatoshi; Suda, Hiroshi; Journal of the Chemical with (S)-1,1'-biSociety, Chemical Communications; nb. 6; (1988); p. 405 - 406, View in Reaxys naphthyl-2,2'-dicarboxylic acid and decomposition with aq. NaOH Boiling Point (6) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

Location

0.00120012

supporting informa- Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie tion - International Edition; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys

62 - 68

0.675068 0.975098

47 - 50

Patent; The Dow Chemical Company; Singaram, Bakthan; Chrisman, William; US6362373; (2002); (B1) English, View in Reaxys

103

Zadel, Guido; Rieger, Rainer; Breitmaier, Eberhard; Liebigs Annalen der Chemie; nb. 12; (1991); p. 1343 - 1346, View in Reaxys

105

Duveen; Kenyon; Journal of the Chemical Society; (1939); p. 1697,1700, View in Reaxys

115 - 116

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys

Refractive Index (2) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

References

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2018-07-03 16:52:46

1.5196

589

Duveen; Kenyon; Journal of the Chemical Society; (1939); p. 1697,1700, View in Reaxys

1.52

589

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys

Density (3) 1 of 3

Density [g·cm-3]

1.61

Type (Density)

crystallographic

Balsells, Jaume; Davis, Timothy J.; Carroll, Patrick; Walsh, Patrick J.; Journal of the American Chemical Society; vol. 124; nb. 35; (2002); p. 10336 - 10348, View in Reaxys 2 of 3

Density [g·cm-3]

0.994

Reference Temperature [°C]

Measurement Temperature 20 [°C] Lowry; Journal of the Chemical Society; vol. 105; (1914); p. 91, View in Reaxys; Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys 3 of 3

Density [g·cm-3]

0.9962

Reference Temperature [°C]

Measurement Temperature 17 [°C] Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys Adsorption (MCS) (1) 1 of 1

Description (Adsorption (MCS))

Adsorption isotherm

Temperature (Adsorption (MCS)) [°C]

22.5 - 24.5

Partner (Adsorption (MCS))

cellulose tribenzoate

Cavazzini; Kaczmarski; Szabelski; Zhou; Liu; Guiochon; Analytical Chemistry; vol. 73; nb. 23; (2001); p. 5704 - 5715, View in Reaxys Association (MCS) (20) 1 of 20

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(2R)-propane-1,2-diol

Scuderi; Paladini; Satta; Catone; Rondino; Tacconi; Filippi; Piccirillo; Giardini Guidoni; Speranza; Physical Chemistry Chemical Physics; vol. 5; nb. 20; (2003); p. 4570 - 4575, View in Reaxys 2 of 20

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(S)-1,2-Propanediol

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(R,R)-2,3-butandiol

Scuderi; Paladini; Satta; Catone; Rondino; Tacconi; Filippi; Piccirillo; Giardini Guidoni; Speranza; Physical Chemistry Chemical Physics; vol. 5; nb. 20; (2003); p. 4570 - 4575, View in Reaxys

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4 of 20

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(2S,3S)-butane-2,3-diol

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(2R,3S)-2,3-butanediol

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(2R,4R)-pentanediol

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

(2S,4S)-pentane-2,4-diol

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

methanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 9 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

ethanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 10 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

propan-1-ol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 11 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

isopropyl alcohol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 12 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

butan-1-ol

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Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 13 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

(2R)-butan-2-ol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 14 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

(S)-2-butanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 15 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

pentan-1-ol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 16 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

(R)-2-pentanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 17 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

(S)-2-pentanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 18 of 20

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

2-pentanol

Latini, Andrea; Satta, Mauro; Giardini Guidoni, Anna; Piccirillo, Susanna; Speranza, Maurizio; Chemistry - A European Journal; vol. 6; nb. 6; (2000); p. 1042 - 1049, View in Reaxys 19 of 20

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gas

Partner (Association (MCS))

(2R)-butan-2-ol

Piccirillo; Bosman; Toja; Giardini-Guidoni; Pierini; Troiani; Speranza; Angewandte Chemie - International Edition in English; vol. 36; nb. 16; (1997); p. 1729 - 1731, View in Reaxys 20 of 20

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

gas

Partner (Association (MCS))

(S)-2-butanol

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Piccirillo; Bosman; Toja; Giardini-Guidoni; Pierini; Troiani; Speranza; Angewandte Chemie - International Edition in English; vol. 36; nb. 16; (1997); p. 1729 - 1731, View in Reaxys Chromatographic Data (10) Chromatographic Original string data GC (Gas chromatography)

Location

References

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GC (Gas chromatography)

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TLC (Thin layer chromatography) GC (Gas chromatography)

Nottingham, Chris; Benson, Robert; Müller-Bunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 80; nb. 20; (2015); p. 10163 10176, View in Reaxys retention time [min] Page/Page column 12.1 24

HPLC (High performance liquid chromatography) GC (Gas chromatography)

Paragraph 0130

R isomer 19.39 min Page/Page column 49

Patent; B.R.A.I.N. AG; Liebeton, Klaus; Eck, Jürgen; Bornscheuer, Uwe; Böttcher, Dominique; Langer, Peter; Bellur, Esen; US9193961; (2015); (B2) English, View in Reaxys Patent; SUNGKYUNKWAN UNIVERSITY RESEARCH & BUSINESS FOUNDATION; SONG, CHUNG EUI; PARK, SANG YEON; LEE, JI WOONG; (43 pag.); KR2015/114167; (2015); (A) Korean, View in Reaxys Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys

Circular Dichroism (1) Location Comment (Circular Dichroism)

References

supporting informa- Circular dichroism tion given

Lin, Chung-Yon; Lim, Stephanie; Anslyn, Eric V.; Journal of the American Chemical Society; vol. 138; nb. 26; (2016); p. 8045 - 8047, View in Reaxys

Crystal Phase (1) Description (Crystal Phase)

Temperature (Crystal Phase) [°C]

References

-156.16

Balsells, Jaume; Davis, Timothy J.; Carroll, Patrick; Walsh, Patrick J.; Journal of the American Chemical Society; vol. 124; nb. 35; (2002); p. 10336 - 10348, View in Reaxys

Crystal structure determination

Crystal Property Description (7) Colour & Other Location Properties colourless

References Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 - 10434, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys; Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys; Marques, Francisco A.; Wosch, Celso L.; Frensch, Gustavo; Labes, Ricardo; Maia, Beatriz H. L. N. S.; Salom, Kahlil S.; Barisona, Andersson; Guerrero, Palimcio G.; Journal of the Brazilian Chemical Society; vol. 26; nb. 1; (2015); p. 165 - 170, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12614 - 12619, View in Reaxys; Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 1092, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys; Soni, Rina; Jolley, Katherine E.; Gosiewska, Silvia; Clarkson, Guy J.; Fang, Zhijia; Hall, Thomas H.; Treloar, Ben N.; Knighton, Richard C.; Wills, Martin; Organometallics; vol. 37; nb. 1; (2018); p. 48 - 64, View in Reaxys; Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys

166/229

2018-07-03 16:52:46

colourless

supporting informa- Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; tion (2013); p. 2722 - 2725, View in Reaxys; Guo, Jun; Chen, Jianhui; Lu, Zhan; Chemical Communications; vol. 51; nb. 26; (2015); p. 5725 - 5727, View in Reaxys; Al-Hunaiti, Afnan; Räisänen, Minna; Pihko, Petri; Leskelä, Markku; Repo, Timo; European Journal of Organic Chemistry; vol. 2014; nb. 28; (2014); p. 6141 - 6144, View in Reaxys; Wu, Weilong; Liu, Shaodong; Duan, Meng; Tan, Xuefeng; Chen, Caiyou; Xie, Yun; Lan, Yu; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 18; nb. 12; (2016); p. 2938 - 2941, View in Reaxys; Chen, Xu; Lu, Zhan; Organic Letters; vol. 18; nb. 18; (2016); p. 4658 - 4661, View in Reaxys; Yu, Jianfei; Long, Jiao; Yang, Yuhong; Wu, Weilong; Xue, Peng; Chung, Lung Wa; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 19; nb. 3; (2017); p. 690 - 693, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys

yellow

Zheng, Long-Sheng; Llopis, Quentin; Echeverria, Pierre-Georges; Férard, Charlène; Guillamot, Gérard; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie; Journal of Organic Chemistry; vol. 82; nb. 11; (2017); p. 5607 - 5615, View in Reaxys

yellow

supporting informa- Tian, Cheng; Gong, Lei; Meggers, Eric; Chemical Communications; vol. 52; nb. 22; (2016); p. tion 4207 - 4210, View in Reaxys

colourless

Paragraph 0133; 0134; 0135

colourless

supporting informa- Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie - International Edition tion; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys; Manville, Charles V.; Docherty, Gordon; Padda, Ranbir; Wills, Martin; European Journal of Organic Chemistry; nb. 34; (2011); p. 6893 - 6901, View in Reaxys

colourless

Patent; SCINOPHARM TAIWAN, LTD.; HENSCHKE, Julian Paul; WU, Ping-Yu; WO2013/80049; (2013); (A2) English, View in Reaxys

Wang, Jin; Liu, Han; Du, Da-Ming; Tetrahedron Asymmetry; vol. 20; nb. 5; (2009); p. 605 609, View in Reaxys; Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys

Crystal System (1) Crystal System References triclinic

Balsells, Jaume; Davis, Timothy J.; Carroll, Patrick; Walsh, Patrick J.; Journal of the American Chemical Society; vol. 124; nb. 35; (2002); p. 10336 - 10348, View in Reaxys

Dynamic Viscosity (1) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

References

0.1393

Thole; Journal of the Chemical Society; vol. 103; (1913); p. 24, View in Reaxys

Interatomic Distances and Angles (1) Description Comment (Interatomic Distances and Angles) Interatomic distances and angles

References

Method of determi- Balsells, Jaume; Davis, Timothy J.; Carroll, Patrick; Walsh, Patrick J.; Journal of the Amerination: single crys- can Chemical Society; vol. 124; nb. 35; (2002); p. 10336 - 10348, View in Reaxys tal X-ray diffraction

Optical Rotatory Power (119) 1 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.39 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

69.7

Wavelength (Optical Rota- 589 tory Power) [nm] Soni, Rina; Jolley, Katherine E.; Gosiewska, Silvia; Clarkson, Guy J.; Fang, Zhijia; Hall, Thomas H.; Treloar, Ben N.; Knighton, Richard C.; Wills, Martin; Organometallics; vol. 37; nb. 1; (2018); p. 48 - 64, View in Reaxys

167/229

2018-07-03 16:52:46

2 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

46.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Yu, Jianfei; Long, Jiao; Yang, Yuhong; Wu, Weilong; Xue, Peng; Chung, Lung Wa; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 19; nb. 3; (2017); p. 690 - 693, View in Reaxys 4 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Yu, Jianfei; Duan, Meng; Wu, Weilong; Qi, Xiaotian; Xue, Peng; Lan, Yu; Dong, Xiu-Qin; Zhang, Xumu; Chemistry - A European Journal; vol. 23; nb. 4; (2017); p. 970 - 975, View in Reaxys 5 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98

168/229

2018-07-03 16:52:46

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

alpha

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

-22.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Perna; Ricci; Scilimati; Mena; Pisano; Palmieri; Agrimi; Vitale; Journal of Molecular Catalysis B: Enzymatic; vol. 124; (2016); p. 29 - 37, View in Reaxys 7 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.2 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

20.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

45.7

Wavelength (Optical Rota- 589 tory Power) [nm]

169/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Tian, Cheng; Gong, Lei; Meggers, Eric; Chemical Communications; vol. 52; nb. 22; (2016); p. 4207 - 4210, View in Reaxys 9 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 75 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

33.7

Wavelength (Optical Rota- 589 tory Power) [nm] Location

supporting information

Chrzanowski, Jacek; Rachwalski, Michal; Pieczonka, Adam M.; Leniak, Stanislaw; Drabowicz, Jzef; Kielbasiski, Piotr; Tetrahedron; vol. 72; nb. 21; (2016); p. 2649 - 2655, View in Reaxys 10 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.27 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

46.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Wu, Weilong; Liu, Shaodong; Duan, Meng; Tan, Xuefeng; Chen, Caiyou; Xie, Yun; Lan, Yu; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 18; nb. 12; (2016); p. 2938 - 2941, View in Reaxys 11 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.5 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

4.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Ríos-Lombardía, Nicolás; Vidal, Cristian; Liardo, Elisa; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Angewandte Chemie - International Edition; vol. 55; nb. 30; (2016); p. 8691 - 8695; Angew. Chem.; vol. 128; nb. 30; (2016); p. 8833 - 8837,5, View in Reaxys

170/229

2018-07-03 16:52:46

12 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.03 g/100ml

Enantiomeric excess [%ee] 45.455 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

4.54

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 13 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.2 g/100ml

Enantiomeric excess [%ee] 88 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

27.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys 14 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.07 g/100ml

Enantiomeric excess [%ee] 96.8 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

47.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Chen, Xu; Lu, Zhan; Organic Letters; vol. 18; nb. 18; (2016); p. 4658 - 4661, View in Reaxys 15 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

chloroform

171/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

32.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Marques, Francisco A.; Wosch, Celso L.; Frensch, Gustavo; Labes, Ricardo; Maia, Beatriz H. L. N. S.; Salom, Kahlil S.; Barisona, Andersson; Guerrero, Palimcio G.; Journal of the Brazilian Chemical Society; vol. 26; nb. 1; (2015); p. 165 - 170, View in Reaxys 16 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

40.9

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

40.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Pieczonka, Adam M.; Les̈niak, Stanisław; Jarzyński, Szymon; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 26; nb. 2-3; (2015); p. 148 - 151, View in Reaxys 18 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.56 g/100ml

Enantiomeric excess [%ee] 86 Solvent (Optical Rotatory Power)

dichloromethane

Optical Rotatory Power [deg]

26.28

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

172/229

2018-07-03 16:52:46

Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys 19 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.99 g/100ml

Enantiomeric excess [%ee] 97.5 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

45.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Guo, Jun; Chen, Jianhui; Lu, Zhan; Chemical Communications; vol. 51; nb. 26; (2015); p. 5725 - 5727, View in Reaxys 20 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 97 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

44.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Liu, Wei-Peng; Yuan, Ming-Lei; Yang, Xiao-Hui; Li, Ke; Xie, Jian-Hua; Zhou, Qi-Lin; Chemical Communications; vol. 51; nb. 28; (2015); p. 6123 - 6125, View in Reaxys 21 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.47 g/100ml

Enantiomeric excess [%ee] 71 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

33.68

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Ueda, Yuki; Yagishita, Fumitoshi; Ishikawa, Hiroki; Kaji, Yuki; Baba, Nozomi; Kasashima, Yoshio; Mino, Takashi; Sakamoto, Masami; Tetrahedron; vol. 71; nb. 36; (2015); p. 6254 - 6258; Art.No: 26920, View in Reaxys 22 of 119

Type (Optical Rotatory Power)

[alpha]

173/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

0.75 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

53.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soni, Rina; Hall, Thomas H.; Mitchell, Benjamin P.; Owen, Matthew R.; Wills, Martin; Journal of Organic Chemistry; vol. 80; nb. 13; (2015); p. 6784 - 6793, View in Reaxys 23 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

21.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

20.9

Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12614 12619, View in Reaxys 24 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.20 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

36.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys 25 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 89 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

174/229

2018-07-03 16:52:46

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 219 - 223, View in Reaxys 26 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 90 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

40.5

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 219 - 223, View in Reaxys 27 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

42.3

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 219 - 223, View in Reaxys 28 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 96 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

43.1

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 219 - 223, View in Reaxys 29 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.27 g/100ml

Enantiomeric excess [%ee] 81 Length of Path [cm]

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

23.2

Wavelength (Optical Rota- 589 tory Power) [nm]

175/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Boukachabia, Mourad; Vriamont, Nicolas; Lambin, Dominique; Riant, Olivier; Aribi-Zouioueche, Louisa; Comptes Rendus Chimie; vol. 17; nb. 5; (2014); p. 403 - 412, View in Reaxys 30 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.75 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

53.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys 31 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 81 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Jiang, Heyan; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 410 - 413, View in Reaxys 32 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.62 g/100ml

Enantiomeric excess [%ee] 92 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

45.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Hodgkinson, Roy; Jurk, Vclav; Zanotti-Gerosa, Antonio; Nedden, Hans Günter; Blackaby, Andrew; Clarkson, Guy J.; Wills, Martin; Organometallics; vol. 33; nb. 19; (2014); p. 5517 - 5524, View in Reaxys 33 of 119

Type (Optical Rotatory Power)

[alpha]

176/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

35.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Al-Hunaiti, Afnan; Räisänen, Minna; Pihko, Petri; Leskelä, Markku; Repo, Timo; European Journal of Organic Chemistry; vol. 2014; nb. 28; (2014); p. 6141 - 6144, View in Reaxys 34 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.1 g/100ml

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

38.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Li, Jiahong; Li, Xuefeng; Ma, Yaping; Wu, Jiashou; Wang, Fei; Xiang, Jing; Zhu, Jin; Wang, Qiwei; Deng, Jingen; RSC Advances; vol. 3; nb. 6; (2013); p. 1825 - 1834, View in Reaxys 35 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

20.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

20.9

Location

supporting information

Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys 36 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 86

177/229

2018-07-03 16:52:46

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

38.8

Wavelength (Optical Rota- 589 tory Power) [nm] Rachwalski, Michal; Jarzynski, Szymon; Lesniak, Stanislaw; Tetrahedron Asymmetry; vol. 24; nb. 7; (2013); p. 421 - 425, View in Reaxys 37 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.8

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 36 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

19.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Roszkowski, Piotr; Maurin, Jan K.; Czarnocki, Zbigniew; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 643 - 650, View in Reaxys 39 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 90 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Roszkowski, Piotr; Maurin, Jan K.; Czarnocki, Zbigniew; Tetrahedron Asymmetry; vol. 24; nb. 11; (2013); p. 643 - 650, View in Reaxys

178/229

2018-07-03 16:52:46

40 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.885 g/100ml

Enantiomeric excess [%ee] 96.8 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

52.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Soni, Rina; Jolley, Katherine E.; Clarkson, Guy J.; Wills, Martin; Organic Letters; vol. 15; nb. 19; (2013); p. 5110 - 5113, View in Reaxys 41 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

20.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

20.9

Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys 42 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 88 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

39.6

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4.8 g/100ml

Enantiomeric excess [%ee] 68 Solvent (Optical Rotatory Power)

chloroform

179/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Gong, Zhiyong; Liu, Qingwen; Xue, Pengchong; Li, Kechang; Song, Zhiguang; Liu, Zaiqun; Jin, Yinghua; Applied Organometallic Chemistry; vol. 26; nb. 3; (2012); p. 121 - 129, View in Reaxys 44 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zacharia, Jamest.; Tanaka, Takanori; Uesaka, Yumiko; Hayashi, Masahiko; Synthesis (Germany); vol. 44; nb. 11; (2012); p. 1625 - 1627; Art.No: SS-2012-F0262-OP, View in Reaxys 45 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 88 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

46.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Roszkowski, Piotr; Maurin, Jan K.; Czarnocki, Zbigniew; Tetrahedron Asymmetry; vol. 23; nb. 14; (2012); p. 1106 - 1110, View in Reaxys 46 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 89.7 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

47.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

180/229

2018-07-03 16:52:46

View in Reaxys; Jolley, Katherine E.; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damian M.; Medlock, Jonathan A.; Nedden, Hans G.; Le Paih, Jacques J. M.; Roseblade, Stephen J.; Seger, Andreas; Sivakumar, Vilvanathan; Prokes, Ivan; Morris, David J.; Wills, Martin; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2545 2555, View in Reaxys 47 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

20.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

20.9

Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 10434, View in Reaxys 48 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.93 g/100ml

Enantiomeric excess [%ee] 99 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

42.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kataoka, Noriyuki; Okudomi, Masayuki; Chihara, Naoka; Matsumoto, Kazutsugu; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 615 - 621, View in Reaxys 49 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 72 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

23.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Zhou, Xiao-Yu; Wang, Duo-Sheng; Bao, Ming; Zhou, Yong-Gui; Tetrahedron Letters; vol. 52; nb. 22; (2011); p. 2826 - 2829, View in Reaxys 50 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.87 g/100ml

181/229

2018-07-03 16:52:46

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

43.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yamamoto, Yasunori; Shirai, Tomohiko; Watanabe, Momoko; Kurihara, Kazunori; Miyaura, Norio; Molecules; vol. 16; nb. 6; (2011); p. 5020 - 5034, View in Reaxys 51 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 73 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

35.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Kunisu, Takashi; Oguma, Takuya; Katsuki, Tsutomu; Journal of the American Chemical Society; vol. 133; nb. 33; (2011); p. 12937 - 12939, View in Reaxys 52 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.11 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

45.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Xie, Jian-Bo; Xie, Jian-Hua; Liu, Xiao-Yan; Zhang, Qian-Qian; Zhou, Qi-Lin; Chemistry - An Asian Journal; vol. 6; nb. 3; (2011); p. 899 - 908, View in Reaxys 53 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

182/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

45.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Touge, Taichiro; Hakamata, Tomohiko; Nara, Hideki; Kobayashi, Tohru; Sayo, Noboru; Saito, Takao; Kayaki, Yoshihito; Ikariya, Takao; Journal of the American Chemical Society; vol. 133; nb. 38; (2011); p. 14960 - 14963, View in Reaxys 54 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.9 g/100ml

Enantiomeric excess [%ee] 68 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

37.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Wu, Xiang-Fei; Min, Chang; Nyamzundui, Enkhtsetseg; Zhou, Hai-Bing; Dong, Chune; Tetrahedron Asymmetry; vol. 22; nb. 16-17; (2011); p. 1640 - 1643, View in Reaxys 55 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 84 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

46.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Manville, Charles V.; Docherty, Gordon; Padda, Ranbir; Wills, Martin; European Journal of Organic Chemistry; nb. 34; (2011); p. 6893 - 6901, View in Reaxys 56 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 70 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

37.8

Wavelength (Optical Rota- 589 tory Power) [nm]

183/229

2018-07-03 16:52:46

Temperature (Optical Rotatory Power) [°C]

Eidamshaus, Christian; Reissig, Hans-Ulrich; Tetrahedron Asymmetry; vol. 22; nb. 16-17; (2011); p. 1644 - 1652, View in Reaxys 57 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.3 g/100ml

Enantiomeric excess [%ee] 85 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

43.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Qi, Gao; Judeh, Zaher M.A.; Tetrahedron Asymmetry; vol. 21; nb. 4; (2010); p. 429 - 436, View in Reaxys 58 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.3 g/100ml

Enantiomeric excess [%ee] 85 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

43.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Qi, Gao; Ji, Yao Qiong; Judeh, Zaher M.A.; Tetrahedron; vol. 66; nb. 23; (2010); p. 4195 - 4205, View in Reaxys 59 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

46.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 60 of 119

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 95

184/229

2018-07-03 16:52:46

Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

45.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 61 of 119

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

44.1

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 62 of 119

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 91 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

43.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 63 of 119

Type (Optical Rotatory Power)

[alpha]

Enantiomeric excess [%ee] 89 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 64 of 119

Type (Optical Rotatory Power)

[alpha]

185/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

1.2 g/100ml

Enantiomeric excess [%ee] 94 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

41.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Okudomi, Masayuki; Shimojo, Megumi; Nogawa, Masaki; Hamanaka, Ayae; Taketa, Natsue; Nakagawa, Takuya; Matsumoto, Kazutsugu; Bulletin of the Chemical Society of Japan; vol. 83; nb. 2; (2010); p. 182 - 189, View in Reaxys; Okudomi, Masayuki; Ageishi, Kanpei; Yamada, Tomomi; Chihara, Naoka; Nakagawa, Takuya; Mizuochi, Katsumi; Matsumoto, Kazutsugu; Tetrahedron; vol. 66; nb. 40; (2010); p. 8060 - 8067, View in Reaxys 65 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

51.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Martins, Jose E.D.; Contreras Redondo, Miguel A.; Wills, Martin; Tetrahedron Asymmetry; vol. 21; nb. 18; (2010); p. 2258 - 2264, View in Reaxys 66 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.70 g/100ml

Solvent (Optical Rotatory Power)

dichloromethane

Optical Rotatory Power [deg]

37.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

Page/Page column 35

Patent; NORTH CAROLINA STATE UNIVERSITY; COMINS, Daniel, L.; CAPRACOTTA, Sonja, S.; WO2010/40059; (2010); (A1) English, View in Reaxys 67 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.77 g/100ml

Enantiomeric excess [%ee] 87 Solvent (Optical Rotatory Power)

chloroform

186/229

2018-07-03 16:52:46

Optical Rotatory Power [deg]

39.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Xu, Geng; Liu, Zhan Zhu; Chinese Chemical Letters; vol. 21; nb. 3; (2010); p. 309 - 311, View in Reaxys 68 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

4 g/100ml

Enantiomeric excess [%ee] 95 Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

40.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

Binder, Caitlin M.; Bautista, April; Zaidlewicz, Marek; Krzeminski, Marek P.; Oliver, Allen; Singaram, Bakthan; Journal of Organic Chemistry; vol. 74; nb. 6; (2009); p. 2337 - 2343, View in Reaxys 69 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Enantiomeric excess [%ee] 90 Solvent (Optical Rotatory Power)

dichloromethane

Optical Rotatory Power [deg]

20.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Wang, Jin; Liu, Han; Du, Da-Ming; Tetrahedron Asymmetry; vol. 20; nb. 5; (2009); p. 605 - 609, View in Reaxys 70 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 84 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Location

supporting information

187/229

2018-07-03 16:52:46

Yoshida, Kazuhiro; Toyoshima, Takeharu; Akashi, Naohisa; Imamoto, Tsuneo; Yanagisawa, Akira; Chemical Communications; nb. 20; (2009); p. 2923 - 2925, View in Reaxys 71 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 58 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

19.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Coeffard, Vincent; Mueller-Bunz, Helge; Guiry, Patrick J.; Organic and Biomolecular Chemistry; vol. 7; nb. 8; (2009); p. 1723 - 1734, View in Reaxys 72 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 62 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Martins, Jose E.D.; Wills, Martin; Tetrahedron; vol. 65; nb. 29-30; (2009); p. 5782 - 5786, View in Reaxys 73 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 93 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.49 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

42.5

188/229

2018-07-03 16:52:46

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yang, Xiao-Feng; Hirose, Takuji; Zhang, Guang-You; Tetrahedron Asymmetry; vol. 19; nb. 14; (2008); p. 1670 - 1675, View in Reaxys 75 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.31 g/100ml

Enantiomeric excess [%ee] 62 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

29.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Dean, Melissa A.; Hitchcock, Shawn R.; Tetrahedron Asymmetry; vol. 19; nb. 22; (2008); p. 2563 - 2567, View in Reaxys 76 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.14 g/100ml

Enantiomeric excess [%ee] 78 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

22.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zeror, Saoussen; Collin, Jacqueline; Fiaud, Jean-Claude; Zouioueche, Louisa Aribi; Advanced Synthesis and Catalysis; vol. 350; nb. 1; (2008); p. 197 - 204, View in Reaxys 77 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.95 g/100ml

Enantiomeric excess [%ee] 84 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Luis Olivares-Romero; Juaristi, Eusebio; Tetrahedron; vol. 64; nb. 42; (2008); p. 9992 - 9998, View in Reaxys 78 of 119

Type (Optical Rotatory Power)

[alpha]

189/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 77 Solvent (Optical Rotatory Power)

chloroform

Optical Rotatory Power [deg]

36.7

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Sun, Lili; Peng, Guisheng; Niu, Hongmei; Wang, Qiang; Li, Chunbao; Synthesis; nb. 24; (2008); p. 3919 - 3924; Art.No: F17308SS, View in Reaxys 79 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.14 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

45.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Bisai, Alakesh; Singh, Pradeep K.; Singh, Vinod K.; Tetrahedron; vol. 63; nb. 3; (2007); p. 598 - 601, View in Reaxys 80 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.21 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

40.3

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Zhong, Jiangchun; Guo, Hongchao; Wang, Mingan; Yin, Mingming; Wang, Min; Tetrahedron Asymmetry; vol. 18; nb. 6; (2007); p. 734 - 741, View in Reaxys 81 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.20 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

30.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

190/229

2018-07-03 16:52:46

Bulut, Adnan; Aslan, Ayhan; Izgue, Enver Cagri; Dogan, Oezdemir; Tetrahedron Asymmetry; vol. 18; nb. 8; (2007); p. 1013 - 1016, View in Reaxys 82 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

32.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul; Synthesis; nb. 24; (2007); p. 3877 3885, View in Reaxys 83 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.39 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

46.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Huang, Hanmin; Okuno, Tomoko; Tsuda, Kazuomi; Yoshimura, Masahiro; Kitamura, Masato; Journal of the American Chemical Society; vol. 128; nb. 27; (2006); p. 8716 - 8717, View in Reaxys 84 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.00 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

41.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Tanaka, Takanori; Yasuda, Yorinobu; Hayashi, Masahiko; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7091 7093, View in Reaxys 85 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.4 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

46.9

191/229

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Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Matharu, Daljit S.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Chemical Communications; nb. 30; (2006); p. 3232 3234, View in Reaxys 86 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.50 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

42.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kang, Seung-Wan; Ko, Dong-Hyun; Kim, Kyoung Hoon; Ha, Deok-Chan; Organic Letters; vol. 5; nb. 23; (2003); p. 4517 4519, View in Reaxys 87 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1 g/100ml

Enantiomeric excess [%ee] 98.1 Solvent (Optical Rotatory Power)

methanol

Optical Rotatory Power [deg]

47.6

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.4 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

44.4

Wavelength (Optical Rota- 589 tory Power) [nm] Comment (Optical Rotato- ambient temperature ry Power) Jensen, Jakob F.; Svendsen, Bo Y.; La Cour, Thomas V.; Pedersen, Henriette L.; Johannsen, Mogens; Journal of the American Chemical Society; vol. 124; nb. 17; (2002); p. 4558 - 4559, View in Reaxys 89 of 119

Type (Optical Rotatory Power)

[alpha]

192/229

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Concentration (Optical Rotatory Power)

1.00 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-47

Wavelength (Optical Rota- 589 tory Power) [nm] Nakamura, Kaoru; Fujii, Mikio; Ida, Yoshiteru; Tetrahedron Asymmetry; vol. 12; nb. 22; (2001); p. 3147 - 3153, View in Reaxys 90 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Spieler, Jan; Huttenloch, Oliver; Waldmann, Herbert; European Journal of Organic Chemistry; nb. 3; (2000); p. 391 - 399, View in Reaxys 91 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.2 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

43.5

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Lipshutz; Shin; Tetrahedron Letters; vol. 41; nb. 49; (2000); p. 9515 - 9521, View in Reaxys 92 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

45.4

Wavelength (Optical Rota- 589 tory Power) [nm] Yang, Xiaowu; Shen, Jianheng; Da, Chaoshan; Wang, Rui; Choi, Michael C. K.; Yang, Liwei; Wong, Kwok-Yin; Tetrahedron Asymmetry; vol. 10; nb. 1; (1999); p. 133 - 138, View in Reaxys 93 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.62 g/100ml

193/229

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Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

43.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Comment (Optical Rotato- ,single stereoisomer ry Power) Paquette, Leo A.; Zhou, Renjie; Journal of Organic Chemistry; vol. 64; nb. 21; (1999); p. 7929 - 7934, View in Reaxys 94 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Cardellicchio, Cosimo; Ciccarella, Giuseppe; Naso, Francesco; Perna, Filippo; Tortorella, Paolo; Tetrahedron; vol. 55; nb. 51; (1999); p. 14685 - 14692, View in Reaxys 95 of 119

Type (Optical Rotatory Power)

[alpha]

Length of Path [cm]

Solvent (Optical Rotatory Power)

hexane

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Malezieux, Bernard; Andres, Roman; Gruselle, Michel; Rager, Marie-Noelle; Thorimbert, Serge; Tetrahedron Asymmetry; vol. 10; nb. 17; (1999); p. 3253 - 3257, View in Reaxys 96 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

43.6

Wavelength (Optical Rota- 589 tory Power) [nm] Nakano, Hiroto; Kumagai, Noriyuki; Matsuzaki, Hisao; Kabuto, Chizuko; Hongo, Hiroshi; Tetrahedron Asymmetry; vol. 8; nb. 9; (1997); p. 1391 - 1401, View in Reaxys 97 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

3.35 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

194/229

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Optical Rotatory Power [deg]

48.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kitajima, Hiroshi; Ito, Katsuji; Aoki, Yuko; Katsuki, Tsutomu; Bulletin of the Chemical Society of Japan; vol. 70; nb. 1; (1997); p. 207 - 217, View in Reaxys 98 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.41 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

44.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Wilken, Joerg; Kossenjans, Michael; Groeger, Harald; Martens, Juergen; Tetrahedron Asymmetry; vol. 8; nb. 12; (1997); p. 2007 - 2015, View in Reaxys 99 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

43.03

Wavelength (Optical Rota- 589 tory Power) [nm] Prasad; Joshi; Tetrahedron Asymmetry; vol. 7; nb. 11; (1996); p. 3147 - 3152, View in Reaxys 100 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.2 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kang, Jahyo; Lee, Jun Won; Kim, Joo In; Journal of the Chemical Society, Chemical Communications; nb. 17; (1994); p. 2009 - 2010, View in Reaxys 101 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

0.95 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

195/229

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Optical Rotatory Power [deg]

44.15

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Li; Jiang; Mi; Tetrahedron Asymmetry; vol. 3; nb. 11; (1992); p. 1467 - 1474, View in Reaxys 102 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

44.1

Wavelength (Optical Rota- 589 tory Power) [nm] Bolm, Carsten; Zehnder, Margareta; Bur, Daniel; Angewandte Chemie; vol. 102; nb. 2; (1990); p. 206 - 208, View in Reaxys 103 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

2.0 g/100ml

Solvent (Optical Rotatory Power)

ethanol

Optical Rotatory Power [deg]

45.4

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Noyori, R.; Suga, S.; Kawai, K.; Okada, S.; Kitamura, M.; et al.; Journal of Organometallic Chemistry; vol. 382; nb. 1-2; (1990); p. 19 - 37, View in Reaxys 104 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.08 g/100ml

Optical Rotatory Power [deg]

46.9

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Tanaka, Kazuhiko; Ushio, Hideki; Suzuki, Hitomi; Journal of the Chemical Society, Chemical Communications; nb. 22; (1989); p. 1700 - 1701, View in Reaxys 105 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.1 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

47.17

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

196/229

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Soai, Kenso; Ookawa, Atsuhiro; Kaba, Tatsuya; Ogawa, Kazuo; Journal of the American Chemical Society; vol. 109; nb. 23; (1987); p. 7111 - 7115, View in Reaxys 106 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

5.0 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

-44.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Soai, Kenso; Ookawa, Atsuhiro; Ogawa, Kazuo; Kaba, Tatsuya; Journal of the Chemical Society, Chemical Communications; nb. 6; (1987); p. 467 - 468, View in Reaxys 107 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.0 g/100ml

Solvent (Optical Rotatory Power)

neat (no solvent)

Optical Rotatory Power [deg]

25.912

Wavelength (Optical Rota- 589 tory Power) [nm] Davis, Franklin A.; Stringer, Orum D.; McCauley, John P., Jr.; Tetrahedron; vol. 41; nb. 21; (1985); p. 4747 - 4758, View in Reaxys 108 of 119

Patent; Noe; Christian; US4497960; (1985); (A) English, View in Reaxys

109 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

1.52 g/100ml

Solvent (Optical Rotatory Power)

CHCl3

Optical Rotatory Power [deg]

16.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kasai, Masaji; Froussios, Cleanthis; Ziffer, Herman; Journal of Organic Chemistry; vol. 48; nb. 4; (1983); p. 459 - 464, View in Reaxys 110 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

1.94

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Yamamoto,K. et al.; Journal of Organometallic Chemistry; vol. 46; (1972); p. C65 - C67, View in Reaxys

197/229

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111 of 119

Bruer,H.-J.; Haller,R.; Tetrahedron Letters; (1972); p. 5227 - 5230, View in Reaxys

112 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

30.2

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 113 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 546.1 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 114 of 119

Type (Optical Rotatory Power)

[alpha]

Solvent (Optical Rotatory Power)

neat (no solvent)

Optical Rotatory Power [deg]

60.5

Wavelength (Optical Rota- 435.8 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 115 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

Wavelength (Optical Rota- 589 tory Power) [nm] Comment (Optical Rotato- at:17-20 degreeC. ry Power) Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 116 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

47.8

Wavelength (Optical Rota- 546.1 tory Power) [nm] Comment (Optical Rotato- at:17-20 degreeC. ry Power) Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 117 of 119

Type (Optical Rotatory Power)

[alpha]

198/229

2018-07-03 16:52:46

Concentration (Optical Rotatory Power)

c=5

Solvent (Optical Rotatory Power)

benzene

Optical Rotatory Power [deg]

79.2

Wavelength (Optical Rota- 435.8 tory Power) [nm] Comment (Optical Rotato- at:17-20 degreeC. ry Power) Kenyon; Partridge; Phillips; Journal of the Chemical Society; (1937); p. 207,213, View in Reaxys 118 of 119

Type (Optical Rotatory Power)

[alpha]

Concentration (Optical Rotatory Power)

c=8

Solvent (Optical Rotatory Power)

diethyl ether

Optical Rotatory Power [deg]

34.8

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Levene; Mikeska; Journal of Biological Chemistry; vol. 70; (1926); p. 377, View in Reaxys 119 of 119

Type (Optical Rotatory Power)

[alpha]

Optical Rotatory Power [deg]

27.35

Wavelength (Optical Rota- 589 tory Power) [nm] Temperature (Optical Rotatory Power) [°C]

Pickard; Kenyon; Journal of the Chemical Society; vol. 99; (1911); p. 55,71; Journal of the Chemical Society; vol. 105; (1914); p. 1121,1123, 1128, View in Reaxys Space Group (1) Space Group 2

References Balsells, Jaume; Davis, Timothy J.; Carroll, Patrick; Walsh, Patrick J.; Journal of the American Chemical Society; vol. 124; nb. 35; (2002); p. 10336 - 10348, View in Reaxys

NMR Spectroscopy (119) 1 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Bian, Guangling; Huang, Huayin; Zong, Hua; Song, Ling; Chirality; vol. 24; nb. 10; (2012); p. 825 - 832, View in Reaxys; Chaplin, David; Harrison, Paul; Henschke, Julian P.; Lennon, Ian C.; Meek, Graham; Moran, Paul; Pilkington, Christopher J.; Ramsden, James A.; Watkins, Simon; Zanotti-Gerosa, Antonio; Organic Process Research and Development; vol. 7; nb. 1; (2003); p. 89 - 94, View in Reaxys; Jiang, Heyan; Journal of Chemical Research; vol. 37; nb. 12; (2013); p. 761 - 763, View in Reaxys; Yue, Huifeng; Huang, Huayin; Bian, Guangling; Zong, Hua; Li, Fangling; Song, Ling; Tetrahedron Asymmetry; vol. 25; nb. 2; (2014); p. 170 - 180, View in Reaxys; Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys; Jiang, Heyan; Journal of Chemical

199/229

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Research; vol. 38; nb. 7; (2014); p. 410 - 413, View in Reaxys; Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys; Lee, Dong-Sheng; Chang, Shu-Ming; Ho, Chun-Ying; Lu, Ta-Jung; Chirality; vol. 28; nb. 1; (2016); p. 65 - 71, View in Reaxys; Pandia Kumar, Arun Kumar; Samuelson, Ashoka G; Journal of Chemical Sciences; vol. 128; nb. 9; (2016); p. 1405 - 1415, View in Reaxys; Soni, Rina; Jolley, Katherine E.; Gosiewska, Silvia; Clarkson, Guy J.; Fang, Zhijia; Hall, Thomas H.; Treloar, Ben N.; Knighton, Richard C.; Wills, Martin; Organometallics; vol. 37; nb. 1; (2018); p. 48 - 64, View in Reaxys 2 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Jolley, Katherine E.; Prokes, Ivan; Morris, David J.; Wills, Martin; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damian M.; Medlock, Jonathan A.; Nedden, Hans G.; Le Paih, Jacques J. M.; Roseblade, Stephen J.; Seger, Andreas; Sivakumar, Vilvanathan; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2545 - 2555,11, View in Reaxys; Jolley, Katherine E.; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damian M.; Medlock, Jonathan A.; Nedden, Hans G.; Le Paih, Jacques J. M.; Roseblade, Stephen J.; Seger, Andreas; Sivakumar, Vilvanathan; Prokes, Ivan; Morris, David J.; Wills, Martin; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2545 2555, View in Reaxys; Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 350, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Liardo, Elisa; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Angewandte Chemie - International Edition; vol. 55; nb. 30; (2016); p. 8691 - 8695; Angew. Chem.; vol. 128; nb. 30; (2016); p. 8833 - 8837,5, View in Reaxys; Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017N0571-OP, View in Reaxys 3 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Tian, Cheng; Gong, Lei; Meggers, Eric; Chemical Communications; vol. 52; nb. 22; (2016); p. 4207 - 4210, View in Reaxys; Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 4 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.04

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Hara, Nanami; Fujisawa, Shu; Fujita, Mizuki; Miyazawa, Mikako; Ochiai, Kazuma; Katsuda, Satoshi; Fujimoto, Tetsuya; Tetrahedron; vol. 74; nb. 2; (2018); p. 296 - 302, View in Reaxys 5 of 119

Description (NMR Spectroscopy)

Chemical shifts

200/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 6 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Soni, Rina; Jolley, Katherine E.; Gosiewska, Silvia; Clarkson, Guy J.; Fang, Zhijia; Hall, Thomas H.; Treloar, Ben N.; Knighton, Richard C.; Wills, Martin; Organometallics; vol. 37; nb. 1; (2018); p. 48 - 64, View in Reaxys 7 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys 8 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Sappino, Carla; Mari, Alessandra; Mantineo, Agnese; Moliterno, Mauro; Palagri, Matteo; Tatangelo, Chiara; Suber, Lorenza; Bovicelli, Paolo; Ricelli, Alessandra; Righi, Giuliana; Organic and Biomolecular Chemistry; vol. 16; nb. 11; (2018); p. 1860 - 1870, View in Reaxys 9 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys

201/229

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10 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Zheng, Long-Sheng; Llopis, Quentin; Echeverria, Pierre-Georges; Férard, Charlène; Guillamot, Gérard; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie; Journal of Organic Chemistry; vol. 82; nb. 11; (2017); p. 5607 - 5615, View in Reaxys 12 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 10434, View in Reaxys; Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys; Wang, Xiuren; Zhang, Jie; Liu, Yan; Cui, Yong; Bulletin of the Chemical Society of Japan; vol. 87; nb. 3; (2014); p. 435 - 440, View in Reaxys; Zheng, Jun; You, Shu-Li; Chemical Communications; vol. 50; nb. 60; (2014); p. 8204 - 8207, View in Reaxys; An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Soni, Rina; Hall, Thomas H.; Mitchell, Benjamin P.; Owen, Matthew R.; Wills, Martin; Journal of Organic Chemistry; vol. 80; nb. 13; (2015); p. 6784 - 6793, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12614 - 12619, View in Reaxys; Gao, De-Wei; Gu, Qing; You, Shu-Li; Journal of the American Chemical Society; vol. 138; nb. 8; (2016); p. 2544 - 2547, View in Reaxys; Chen, Xu; Lu, Zhan; Organic Letters; vol. 18; nb. 18; (2016); p. 4658 - 4661, View in Reaxys; Wang, Xiuren; Han, Xing; Zhang, Jie; Wu, Xiaowei; Liu, Yan; Cui, Yong; Journal of the American Chemical Society; vol. 138; nb. 38; (2016); p. 12332 - 12335, View in Reaxys; Yu, Jianfei; Long, Jiao; Yang, Yuhong; Wu, Weilong; Xue, Peng; Chung, Lung Wa; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 19; nb. 3; (2017); p. 690 - 693, View in Reaxys 13 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Zhang, Anlin; Yang, Nianfa; Yang, Liwen; Peng, Dan; Chemistry Letters; vol. 43; nb. 4; (2014); p. 462 - 464, View in Reaxys; Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 - 2688, View in Reaxys; Vidal, Marc; Schmitzer, Andreea R.; Organometallics; vol. 33; nb. 13; (2014); p. 3328 - 3340, View in Reaxys; Liu, Lijia; Long, Qing; Aoki, Toshiki; Zhang, Geng; Kaneko, Takashi; Teraguchi, Masahiro; Zhang, Chunhong; Wang, Yudan; Chirality; vol. 27; nb. 8; (2015); p. 454 - 458, View in Reaxys; Ferrari Bach, Mariana;

202/229

2018-07-03 16:52:46

Herzer Griebeler, Cassiana; Gross Jacoby, Caroline; Schneider, Paulo Henrique; European Journal of Organic Chemistry; vol. 2017; nb. 46; (2017); p. 6997 - 7004, View in Reaxys 14 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Li, Min; Li, Bin; Xia, Hong-Feng; Ye, Danru; Wu, Jing; Shi, Yifeng; Green Chemistry; vol. 16; nb. 5; (2014); p. 2680 2688, View in Reaxys; Ferrari Bach, Mariana; Herzer Griebeler, Cassiana; Gross Jacoby, Caroline; Schneider, Paulo Henrique; European Journal of Organic Chemistry; vol. 2017; nb. 46; (2017); p. 6997 - 7004, View in Reaxys 15 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Yu, Jianfei; Long, Jiao; Yang, Yuhong; Wu, Weilong; Xue, Peng; Chung, Lung Wa; Dong, Xiu-Qin; Zhang, Xumu; Organic Letters; vol. 19; nb. 3; (2017); p. 690 - 693, View in Reaxys 16 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

supporting information

Signals [ppm]

0.96; 1.72 - 1.91; 1.94; 4.63; 7.29 - 7.4

Kind of signal

t, 3H, Jα=α7.4αHz; m, 2H; s, 1H; t, 1H, Jα=α6.6αHz; m, 5H

Jarzyński, Szymon; Leśniak, Stanisław; Rachwalski, Michał; Tetrahedron Asymmetry; vol. 28; nb. 12; (2017); p. 1808 1816, View in Reaxys 17 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Gong, Zhiyong; Liu, Qingwen; Xue, Pengchong; Li, Kechang; Song, Zhiguang; Liu, Zaiqun; Jin, Yinghua; Applied Organometallic Chemistry; vol. 26; nb. 3; (2012); p. 121 - 129, View in Reaxys; Contente, Martina Letizia; Serra, Immacolata; Brambilla, Marta; Eberini, Ivano; Gianazza, Elisabetta; De Vitis, Valerio; Molinari, Francesco; Zambelli, Paolo; Romano, Diego; Applied Microbiology and Biotechnology; vol. 100; nb. 1; (2016); p. 193 - 201, View in Reaxys

203/229

2018-07-03 16:52:46

18 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Li, Jiahong; Li, Xuefeng; Ma, Yaping; Wu, Jiashou; Wang, Fei; Xiang, Jing; Zhu, Jin; Wang, Qiwei; Deng, Jingen; RSC Advances; vol. 3; nb. 6; (2013); p. 1825 - 1834, View in Reaxys; Nottingham, Chris; Benson, Robert; Müller-Bunz, Helge; Guiry, Patrick J.; Journal of Organic Chemistry; vol. 80; nb. 20; (2015); p. 10163 - 10176, View in Reaxys; Contente, Martina Letizia; Serra, Immacolata; Brambilla, Marta; Eberini, Ivano; Gianazza, Elisabetta; De Vitis, Valerio; Molinari, Francesco; Zambelli, Paolo; Romano, Diego; Applied Microbiology and Biotechnology; vol. 100; nb. 1; (2016); p. 193 - 201, View in Reaxys 19 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Faigl; Deák; Erdélyi; Holczbauer; Czugler; Nyerges; Mátravölgyi; Chirality; vol. 27; nb. 3; (2015); p. 216 - 222, View in Reaxys; Zanardi, María M.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 56; nb. 24; (2015); p. 3762 - 3765, View in Reaxys; Botta, María C.; Biava, Hernán D.; Spanevello, Rolando A.; Mata, Ernesto G.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 57; nb. 20; (2016); p. 2186 - 2189, View in Reaxys; Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 11136, View in Reaxys 20 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Perna; Ricci; Scilimati; Mena; Pisano; Palmieri; Agrimi; Vitale; Journal of Molecular Catalysis B: Enzymatic; vol. 124; (2016); p. 29 - 37, View in Reaxys 21 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 100 scopy) [MHz] Perna; Ricci; Scilimati; Mena; Pisano; Palmieri; Agrimi; Vitale; Journal of Molecular Catalysis B: Enzymatic; vol. 124; (2016); p. 29 - 37, View in Reaxys 22 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

204/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Botta, María C.; Biava, Hernán D.; Spanevello, Rolando A.; Mata, Ernesto G.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 57; nb. 20; (2016); p. 2186 - 2189, View in Reaxys 23 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Chrzanowski, Jacek; Rachwalski, Michal; Pieczonka, Adam M.; Leniak, Stanislaw; Drabowicz, Jzef; Kielbasiski, Piotr; Tetrahedron; vol. 72; nb. 21; (2016); p. 2649 - 2655, View in Reaxys; Margalef, Jèssica; Slagbrand, Tove; Tinnis, Fredrik; Adolfsson, Hans; Diéguez, Montserrat; Pàmies, Oscar; Advanced Synthesis and Catalysis; vol. 358; nb. 24; (2016); p. 4006 4018, View in Reaxys 24 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.4

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 25 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.4

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 26 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

205/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H NMR (400 MHz, CDCl3) α 0.90 (t, 3H), 1.71-1.92 (m, 2H), 1.96 (br, 1H), 4.51-4.72 (m, 1H), troscopy) 7.25-7.40 (m, 5H) Signals [ppm]

0.9; 1.71 - 1.92; 1.96; 4.51 - 4.72; 7.25 - 7.4

Kind of signal

t, 3H; m, 2H; br, 1H; m, 1H; m, 5H

Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys 27 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Original Text (NMR Spectroscopy)

13C

Signals [ppm]

144.8; 128.4; 127.4; 126.2; 75.9; 31.9; 10.2

NMR (100 MHz, CDCl3) α 144.8, 128.4, 127.4, 126.2, 75.9, 31.9, 10.2

Zhao, Wen-Xian; Liu, Guan-Jun; Wang, Jingjing; Li, Feng; Liu, Lantao; Tetrahedron Asymmetry; vol. 27; nb. 22-23; (2016); p. 1133 - 1144, View in Reaxys 28 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys 29 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Touge, Taichiro; Hakamata, Tomohiko; Nara, Hideki; Kobayashi, Tohru; Sayo, Noboru; Saito, Takao; Kayaki, Yoshihito; Ikariya, Takao; Journal of the American Chemical Society; vol. 133; nb. 38; (2011); p. 14960 - 14963, View in Reaxys; Zanardi, María M.; Suárez, Alejandra G.; Tetrahedron Letters; vol. 56; nb. 24; (2015); p. 3762 - 3765, View in Reaxys 30 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

206/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Kawabata, Shun; Tokura, Hiromu; Chiyojima, Hiroyuki; Okamoto, Masaki; Sakaguchi, Satoshi; Advanced Synthesis and Catalysis; vol. 354; nb. 5; (2012); p. 807 - 812, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 77; nb. 22; (2012); p. 10427 - 10434, View in Reaxys; Zong, Hua; Huang, Huayin; Bian, Guangling; Song, Ling; Tetrahedron Letters; vol. 54; nb. 21; (2013); p. 2722 - 2725, View in Reaxys; Jiang, Fan; Yuan, Kedong; Achard, Mathieu; Bruneau, Christian; Chemistry - A European Journal; vol. 19; nb. 31; (2013); p. 10343 - 10352, View in Reaxys; Shen, Bin; Huang, Huayin; Bian, Guangling; Zong, Hua; Song, Ling; Chirality; vol. 25; nb. 9; (2013); p. 561 - 566, View in Reaxys; An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Hodgkinson, Roy; Jurk, Vclav; Zanotti-Gerosa, Antonio; Nedden, Hans Günter; Blackaby, Andrew; Clarkson, Guy J.; Wills, Martin; Organometallics; vol. 33; nb. 19; (2014); p. 5517 - 5524, View in Reaxys; Huang, Huayin; Zong, Hua; Bian, Guangling; Song, Ling; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12614 - 12619, View in Reaxys 31 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Cheng, Ying-Ni; Wu, Hsyueh-Liang; Wu, Ping-Yu; Shen, Ying-Ying; Uang, Biing-Jiun; Chemistry - An Asian Journal; vol. 7; nb. 12; (2012); p. 2921 - 2924, View in Reaxys; Soni, Rina; Jolley, Katherine E.; Clarkson, Guy J.; Wills, Martin; Organic Letters; vol. 15; nb. 19; (2013); p. 5110 - 5113, View in Reaxys; Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys 32 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

207/229

2018-07-03 16:52:46

Zuo, Ziqing; Zhang, Lei; Leng, Xuebing; Huang, Zheng; Chemical Communications; vol. 51; nb. 24; (2015); p. 5073 - 5076, View in Reaxys 34 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

Vasiloiu, Maria; Gaertner, Peter; Zirbs, Ronald; Bica, Katharina; European Journal of Organic Chemistry; vol. 2015; nb. 11; (2015); p. 2374 - 2381, View in Reaxys 35 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Soni, Rina; Hall, Thomas H.; Mitchell, Benjamin P.; Owen, Matthew R.; Wills, Martin; Journal of Organic Chemistry; vol. 80; nb. 13; (2015); p. 6784 - 6793, View in Reaxys 36 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Shinohara, Kanako; Kawabata, Shun; Nakamura, Hanako; Manabe, Yoshiki; Sakaguchi, Satoshi; European Journal of Organic Chemistry; vol. 2014; nb. 25; (2014); p. 5532 - 5539, View in Reaxys; Bérubé, Christopher; Cardinal, Sébastien; Boudreault, Pierre-Luc; Barbeau, Xavier; Delcey, Nicolas; Giguère, Martin; Gleeton, Dave; Voyer, Normand; Tetrahedron; vol. 71; nb. 42; (2015); p. 8077 - 8084, View in Reaxys 37 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

Paragraph 0131

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

208/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

Paragraph 0132

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Soni, Rina; Jolley, Katherine E.; Clarkson, Guy J.; Wills, Martin; Organic Letters; vol. 15; nb. 19; (2013); p. 5110 - 5113, View in Reaxys; Zhang, Anlin; Yang, Nianfa; Yang, Liwen; Peng, Dan; Chemistry Letters; vol. 43; nb. 4; (2014); p. 462 464, View in Reaxys 40 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.46 scopy) [MHz] Location

supporting information

Faraji, Laleh; Jadidi, Khosrow; Notash, Behrouz; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 346 - 350, View in Reaxys 41 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys 42 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Lowicki, Daniel; Bezlada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 591 595, View in Reaxys

209/229

2018-07-03 16:52:46

43 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spec- α(400 α MHz, CDC13) 7.36-7.25 (5H, m, Ph), 4.58 (1H, t, / 6.4, -CH), 2.03 (1α, br s, -OH), 1.87- 1.68 troscopy) (2α, m, -CH2), 1.48 (3α, d, / 7.4, -CH3) Location

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys 44 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Original Text (NMR Spec- αC (100 MHz, CDC13): 144.55, 128.36(2C), 127.46, 125.94(2C), 75.99, 31.84, 10.11; troscopy) Location

Page/Page column 49

Patent; THE UNIVERSITY OF WARWICK; WILLS, Martin; JOLLEY, Katherine Emma; SONI, Rina; WO2014/68331; (2014); (A1) English, View in Reaxys 45 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300.1 scopy) [MHz] Location

supporting information

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys 46 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, View in Reaxys 47 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

210/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. 2474 - 2476, View in Reaxys; Martins, Jose E.D.; Morris, David J.; Wills, Martin; Tetrahedron Letters; vol. 50; nb. 6; (2009); p. 688 - 692, View in Reaxys; Cambeiro, Xacobe C.; Pericas, Miquel A.; Advanced Synthesis and Catalysis; vol. 353; nb. 1; (2011); p. 113 - 124, View in Reaxys; Zhou, Xiao-Yu; Wang, Duo-Sheng; Bao, Ming; Zhou, Yong-Gui; Tetrahedron Letters; vol. 52; nb. 22; (2011); p. 2826 - 2829, View in Reaxys; Michigami, Kyosuke; Hayashi, Masahiko; Tetrahedron; vol. 69; nb. 21; (2013); p. 4221 - 4225, View in Reaxys 48 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spec- αH (300 MHz; CDCl3) 7.38-7.24 (5H, m, ArH), 4.59 (1H, td, J 6.6 and 3.3, PhCH(OH)), 1.90-1.68 troscopy) (overlapping 1H, d, J 3.3, OH and 2H, m, CH2), 0.92 (3H, t, J 7.5, CH3) Zammit, Charlotte M.; Wills, Martin; Tetrahedron Asymmetry; vol. 24; nb. 13-14; (2013); p. 844 - 852, View in Reaxys 49 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Original Text (NMR Spec- Cα (75 MHz; CDCl3) 144.56 (C), 128.38 (2 * CH), 127.48 (CH), 125.94 (2 * CH), 76.01 (CH), 31.86 troscopy) (CH2), 10.13 (CH3) Zammit, Charlotte M.; Wills, Martin; Tetrahedron Asymmetry; vol. 24; nb. 13-14; (2013); p. 844 - 852, View in Reaxys 50 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Krabbe, Scott W.; Hatcher, Mark A.; Bowman, Roy K.; Mitchell, Mark B.; McClure, Michael S.; Johnson, Jeffrey S.; Organic Letters; vol. 15; nb. 17; (2013); p. 4560 - 4563, View in Reaxys 51 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz]

211/229

2018-07-03 16:52:46

Location

supporting information

Kantam, M. Lakshmi; Laha, Soumi; Yadav, Jagjit; Likhar, Pravin R.; Sreedhar, Bojja; Jha, Shailendra; Bhargava, Suresh; Udayakiran; Jagadeesh; Organic Letters; vol. 10; nb. 14; (2008); p. 2979 - 2982, View in Reaxys; Li, Yuehui; Ding, Kuiling; Sandoval, Christian A.; Organic Letters; vol. 11; nb. 4; (2009); p. 907 - 910, View in Reaxys; Kantam, M. Lakshmi; Yadav, Jagjit; Laha, Soumi; Srinivas, Pottabathula; Sreedhar, Bojja; Figueras; Journal of Organic Chemistry; vol. 74; nb. 12; (2009); p. 4608 - 4611, View in Reaxys; Da, Chao-Shan; Wang, Jun-Rul; Yin, Xiao-Gang; Fan, Xin-Yuan; Liu, Yi; Yu, Sheng-Li; Organic Letters; vol. 11; nb. 24; (2009); p. 5578 - 5581, View in Reaxys; Naik, Anu; Maji, Tapan; Reiser, Oliver; Chemical Communications; vol. 46; nb. 25; (2010); p. 4475 - 4477, View in Reaxys; Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys 52 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Kantam, M. Lakshmi; Yadav, Jagjit; Laha, Soumi; Srinivas, Pottabathula; Sreedhar, Bojja; Figueras; Journal of Organic Chemistry; vol. 74; nb. 12; (2009); p. 4608 - 4611, View in Reaxys; Naik, Anu; Maji, Tapan; Reiser, Oliver; Chemical Communications; vol. 46; nb. 25; (2010); p. 4475 - 4477, View in Reaxys; Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys 53 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Martins, Jose E.D.; Wills, Martin; Tetrahedron; vol. 65; nb. 29-30; (2009); p. 5782 - 5786, View in Reaxys; Martins, Jose E.D.; Contreras Redondo, Miguel A.; Wills, Martin; Tetrahedron Asymmetry; vol. 21; nb. 18; (2010); p. 2258 - 2264, View in Reaxys; Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys 54 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] MacLeod, Patricia D.; Reckling, Amy M.; Li, Chao-Jun; Heterocycles; vol. 80; nb. 2; (2010); p. 1319 - 1337, View in Reaxys; Xu, Geng; Liu, Zhan Zhu; Chinese Chemical Letters; vol. 21; nb. 3; (2010); p. 309 - 311, View in Reaxys; Zhang, Bo; Wang, Hui; Lin, Guo-Qiang; Xu, Ming-Hua; European Journal of Organic Chemistry; nb. 22; (2011); p. 4205 4211, View in Reaxys; Gong, Zhiyong; Liu, Qingwen; Xue, Pengchong; Li, Kechang; Song, Zhiguang; Liu, Zaiqun; Jin, Yinghua; Applied Organometallic Chemistry; vol. 26; nb. 3; (2012); p. 121 - 129, View in Reaxys 55 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

212/229

2018-07-03 16:52:46

Dean, Melissa A.; Hitchcock, Shawn R.; Tetrahedron Asymmetry; vol. 19; nb. 22; (2008); p. 2563 - 2567, View in Reaxys; Martins, Jose E.D.; Wills, Martin; Tetrahedron; vol. 65; nb. 29-30; (2009); p. 5782 - 5786, View in Reaxys; Tasgin, Dilek Isik; Unaleroglu, Canan; Applied Organometallic Chemistry; vol. 24; nb. 1; (2010); p. 33 - 37, View in Reaxys; Martins, Jose E.D.; Contreras Redondo, Miguel A.; Wills, Martin; Tetrahedron Asymmetry; vol. 21; nb. 18; (2010); p. 2258 - 2264, View in Reaxys; Cakici, Murat; Catir, Mustafa; Karabuga, Semistan; Ulukanli, Sabri; Kilic, Hamdullah; Tetrahedron Asymmetry; vol. 22; nb. 3; (2011); p. 300 - 308, View in Reaxys; Hirose, Takuji; Sugawara, Kazuyuki; Kodama, Koichi; Journal of Organic Chemistry; vol. 76; nb. 13; (2011); p. 5413 - 5428, View in Reaxys; Yamamoto, Yasunori; Shirai, Tomohiko; Watanabe, Momoko; Kurihara, Kazunori; Miyaura, Norio; Molecules; vol. 16; nb. 6; (2011); p. 5020 - 5034, View in Reaxys; Wang, Bo; Jiang, Ling; Wang, Jue; Ma, Jingbo; Liu, Min; Yu, Hongwei; Tetrahedron Asymmetry; vol. 22; nb. 9; (2011); p. 980 - 985, View in Reaxys; Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys 56 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys; Kawabata, Shun; Tokura, Hiromu; Chiyojima, Hiroyuki; Okamoto, Masaki; Sakaguchi, Satoshi; Advanced Synthesis and Catalysis; vol. 354; nb. 5; (2012); p. 807 - 812, View in Reaxys 57 of 119

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H-NMR (400 MHz, CDCl3): α 7.35-7.26 (m, 5H), 4.53 (t, J=6.8 Hz, 1H), 2.46 (br, 1H), 1.81-1.69 troscopy) (m, 2H), 0.89 (t, J=7.6 Hz, 3H). Location

Page/Page column 13

Comment (NMR Spectroscopy)

Signals given

Patent; UANG, Biing-Jiun; Yang, Bo-Yao; US2012/77976; (2012); (A1) English, View in Reaxys 58 of 119

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Original Text (NMR Spec- 13C-NMR (100 MHz, CDCl3): α 144.5 (C), 128.3 (CH), 127.3 (CH), 125.9 (CH), 75.8 (CH), 31.7 troscopy) (CH2), 10.1 (CH3) Location

Page/Page column 13

Comment (NMR Spectroscopy)

Signals given

Patent; UANG, Biing-Jiun; Yang, Bo-Yao; US2012/77976; (2012); (A1) English, View in Reaxys 59 of 119

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

213/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Osorio-Planes, Laura; Rodriguez-Escrich, Carles; Pericas, Miquel A.; Organic Letters; vol. 14; nb. 7; (2012); p. 1816 1819, View in Reaxys 60 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Osorio-Planes, Laura; Rodriguez-Escrich, Carles; Pericas, Miquel A.; Organic Letters; vol. 14; nb. 7; (2012); p. 1816 1819, View in Reaxys 61 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene-d6

Temperature (NMR Spectroscopy) [°C]

22.84

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie - International Edition; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys 64 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

214/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

benzene-d6

Temperature (NMR Spectroscopy) [°C]

22.84

Frequency (NMR Spectro- 75.4 scopy) [MHz] Location

supporting information

Irrgang, Torsten; Friedrich, Denise; Kempe, Rhett; Angewandte Chemie - International Edition; vol. 50; nb. 9; (2011); p. 2183 - 2186, View in Reaxys 65 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 250 scopy) [MHz] Location

supporting information

Aupoix, Audrey; Bournaud, Chloee; Vo-Thanh, Giang; European Journal of Organic Chemistry; nb. 15; (2011); p. 2772 2776, View in Reaxys 66 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 90 scopy) [MHz] Location

supporting information

Aupoix, Audrey; Bournaud, Chloee; Vo-Thanh, Giang; European Journal of Organic Chemistry; nb. 15; (2011); p. 2772 2776, View in Reaxys 67 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.5

Frequency (NMR Spectro- 300.4 scopy) [MHz] Location

supporting information

Nakata, Kenya; Shiina, Isamu; Organic and Biomolecular Chemistry; vol. 9; nb. 20; (2011); p. 7092 - 7096, View in Reaxys 68 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

215/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.5

Frequency (NMR Spectro- 75.5 scopy) [MHz] Location

supporting information

Nakata, Kenya; Shiina, Isamu; Organic and Biomolecular Chemistry; vol. 9; nb. 20; (2011); p. 7092 - 7096, View in Reaxys 69 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Location

supporting information

Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys 70 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Eidamshaus, Christian; Reissig, Hans-Ulrich; Tetrahedron Asymmetry; vol. 22; nb. 16-17; (2011); p. 1644 - 1652, View in Reaxys 71 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Xu, Zhou; Bo, Rongcheng; Wu, Nan; Wan, Yu; Wu, Hui; Letters in Organic Chemistry; vol. 8; nb. 8; (2011); p. 582 - 586, View in Reaxys 72 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Muramatsu, Yusuke; Kanehira, Shinichi; Tanigawa, Masato; Miyawaki, Yuta; Harada, Toshiro; Bulletin of the Chemical Society of Japan; vol. 83; nb. 1; (2010); p. 19 - 32, View in Reaxys 73 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

216/229

2018-07-03 16:52:46

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Chen, Xi; Liu, Qiang; Sun, Hong-Bao; Yu, Xiao-Qi; Pu, Lin; Tetrahedron Letters; vol. 51; nb. 17; (2010); p. 2345 - 2347, View in Reaxys 74 of 119

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Chen, Xi; Liu, Qiang; Sun, Hong-Bao; Yu, Xiao-Qi; Pu, Lin; Tetrahedron Letters; vol. 51; nb. 17; (2010); p. 2345 - 2347, View in Reaxys 75 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Li, Wei Jie; Qiu, Sheng Xiang; Advanced Synthesis and Catalysis; vol. 352; nb. 7; (2010); p. 1119 - 1122, View in Reaxys 76 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Location

supporting information

Gastl, Christoph; Laschat, Sabine; Synthesis; nb. 15; (2010); p. 2643 - 2651; Art.No: Z07810SS, View in Reaxys 77 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 63 scopy) [MHz] Location

supporting information

217/229

2018-07-03 16:52:46

Gastl, Christoph; Laschat, Sabine; Synthesis; nb. 15; (2010); p. 2643 - 2651; Art.No: Z07810SS, View in Reaxys 78 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Zhang, Cong-Hai; Yan, Sheng-Jiao; Pan, Sheng-Qiang; Huang, Rong; Lin, Jun; Bulletin of the Korean Chemical Society; vol. 31; nb. 4; (2010); p. 869 - 873, View in Reaxys 79 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100.6 scopy) [MHz] Location

supporting information

Martins, Jose E.D.; Morris, David J.; Wills, Martin; Tetrahedron Letters; vol. 50; nb. 6; (2009); p. 688 - 692, View in Reaxys 80 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 300 scopy) [MHz] El-Shehawy, Ashraf A.; Sugiyama, Kenji; Hirao, Akira; Tetrahedron Asymmetry; vol. 19; nb. 4; (2008); p. 425 - 434, View in Reaxys 81 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75 scopy) [MHz] El-Shehawy, Ashraf A.; Sugiyama, Kenji; Hirao, Akira; Tetrahedron Asymmetry; vol. 19; nb. 4; (2008); p. 425 - 434, View in Reaxys 82 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

218/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 100.6 scopy) [MHz] Hayes, Aidan M.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Journal of the American Chemical Society; vol. 127; nb. 20; (2005); p. 7318 - 7319, View in Reaxys; Malkov, Andrei V.; Stewart Liddon, Angus J. P.; Ramirez-Lopez, Pedro; Bendova, Lada; Haigh, David; Kocovsky, Pavel; Angewandte Chemie - International Edition; vol. 45; nb. 9; (2006); p. 1432 1435, View in Reaxys; Morris, David J.; Hayes, Aidan M.; Wills, Martin; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7035 - 7044, View in Reaxys; Matharu, Daljit S.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Chemical Communications; nb. 30; (2006); p. 3232 - 3234, View in Reaxys; Martins, Jose E.D.; Wills, Martin; Tetrahedron Asymmetry; vol. 19; nb. 10; (2008); p. 1250 - 1255, View in Reaxys 83 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Rahman, Mohammed S.; Oliana, Marco; Hii, King Kuok; Tetrahedron Asymmetry; vol. 15; nb. 12; (2004); p. 1835 - 1840, View in Reaxys; Inoue, Kousuke; Makino, Yoshihide; Itoh, Nobuya; Tetrahedron Asymmetry; vol. 16; nb. 15; (2005); p. 2539 - 2549, View in Reaxys; Hayes, Aidan M.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Journal of the American Chemical Society; vol. 127; nb. 20; (2005); p. 7318 - 7319, View in Reaxys; Malkov, Andrei V.; Stewart Liddon, Angus J. P.; Ramirez-Lopez, Pedro; Bendova, Lada; Haigh, David; Kocovsky, Pavel; Angewandte Chemie - International Edition; vol. 45; nb. 9; (2006); p. 1432 - 1435, View in Reaxys; Morris, David J.; Hayes, Aidan M.; Wills, Martin; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7035 - 7044, View in Reaxys; Matharu, Daljit S.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Chemical Communications; nb. 30; (2006); p. 3232 - 3234, View in Reaxys; Hernandez-Rodriguez, Marcos; Avila-Ortiz, Claudia Gabriela; Del Campo, Jorge M.; Hernandez-Romero, Delia; Rosales-Hoz, Maria J.; Juaristi, Eusebio; Australian Journal of Chemistry; vol. 61; nb. 5; (2008); p. 364 - 375, View in Reaxys; Martins, Jose E.D.; Wills, Martin; Tetrahedron Asymmetry; vol. 19; nb. 10; (2008); p. 1250 - 1255, View in Reaxys; Yang, Xiao-Feng; Hirose, Takuji; Zhang, Guang-You; Tetrahedron Asymmetry; vol. 19; nb. 14; (2008); p. 1670 - 1675, View in Reaxys 84 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Hernandez-Rodriguez, Marcos; Avila-Ortiz, Claudia Gabriela; Del Campo, Jorge M.; Hernandez-Romero, Delia; Rosales-Hoz, Maria J.; Juaristi, Eusebio; Australian Journal of Chemistry; vol. 61; nb. 5; (2008); p. 364 - 375, View in Reaxys; Yang, Xiao-Feng; Hirose, Takuji; Zhang, Guang-You; Tetrahedron Asymmetry; vol. 19; nb. 14; (2008); p. 1670 - 1675, View in Reaxys 85 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Spieler, Jan; Huttenloch, Oliver; Waldmann, Herbert; European Journal of Organic Chemistry; nb. 3; (2000); p. 391 - 399, View in Reaxys; Steiner, Derek; Sethofer, Steven G.; Goralski, Christian T.; Singaram, Bakthan; Tetrahedron Asymmetry; vol. 13; nb. 14; (2002); p. 1477 - 1483, View in Reaxys; Edwards, Christopher W.; Haddleton, David M.; Morsley, David; Shipton, Mark R.; Wills, Martin; Tetrahedron; vol. 59; nb. 31; (2003); p. 5823 - 5830, View in Reaxys; Grach, Guillaume; Reboul, Vincent; Metzner, Patrick; Tetrahedron Asymmetry; vol. 19; nb. 14; (2008); p. 1744 - 1750, View in Reaxys 86 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

219/229

2018-07-03 16:52:46

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Cobb, Alexander J. A.; Marson, Charles M.; Tetrahedron Asymmetry; vol. 12; nb. 11; (2001); p. 1547 - 1550, View in Reaxys; Yong, Kelvin H.; Taylor, Nicholas J.; Chong, J. Michael; Organic Letters; vol. 4; nb. 21; (2002); p. 3553 3556, View in Reaxys; Cobb, Alexander J.A.; Marson, Charles M.; Tetrahedron; vol. 61; nb. 5; (2005); p. 1269 - 1279, View in Reaxys; Liu, Pei-Nian; Gu, Pei-Ming; Deng, Jin-Gen; Tu, Yong-Qiang; Ma, Ya-Ping; European Journal of Organic Chemistry; nb. 15; (2005); p. 3221 - 3227, View in Reaxys; Xu, Yingjian; Clarkson, Guy C.; Docherty, Gordon; North, Carl L.; Woodward, Gary; Wills, Martin; Journal of Organic Chemistry; vol. 70; nb. 20; (2005); p. 8079 - 8087, View in Reaxys; Wang, Fei; Liu, Hui; Cun, Linfeng; Zhu, Jin; Deng, Jingen; Jiang, Yaozhong; Journal of Organic Chemistry; vol. 70; nb. 23; (2005); p. 9424 - 9429, View in Reaxys; Milburn, Robert R.; Hussain, S. M. Shakil; Prien, Olaf; Ahmed, Zaheer; Snieckus, Victor; Organic Letters; vol. 9; nb. 22; (2007); p. 4403 - 4406, View in Reaxys; Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul; Synthesis; nb. 24; (2007); p. 3877 - 3885, View in Reaxys; Li, GaoQiang; Yan, Ze-Yi; Niu, Yan-Ning; Wu, Lu-Yong; Wei, Hai-Long; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 7; (2008); p. 816 - 821, View in Reaxys; Niu, Yan-Ning; Yan, Ze-Yi; Li, Gao-Qiang; Wei, Hai-Long; Gao, Guo-Lin; Wu, Lu-Yong; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 8; (2008); p. 912 - 920, View in Reaxys; Shaikh, Nadim S.; Enthaler, Stephan; Junge, Kathrin; Beller, Matthias; Angewandte Chemie - International Edition; vol. 47; nb. 13; (2008); p. 2497 - 2501, View in Reaxys 87 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Yong, Kelvin H.; Taylor, Nicholas J.; Chong, J. Michael; Organic Letters; vol. 4; nb. 21; (2002); p. 3553 - 3556, View in Reaxys; Liu, Pei-Nian; Gu, Pei-Ming; Deng, Jin-Gen; Tu, Yong-Qiang; Ma, Ya-Ping; European Journal of Organic Chemistry; nb. 15; (2005); p. 3221 - 3227, View in Reaxys; Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1561 - 1568, View in Reaxys; Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul; Synthesis; nb. 24; (2007); p. 3877 - 3885, View in Reaxys; Li, GaoQiang; Yan, Ze-Yi; Niu, Yan-Ning; Wu, Lu-Yong; Wei, Hai-Long; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 7; (2008); p. 816 - 821, View in Reaxys; Niu, Yan-Ning; Yan, Ze-Yi; Li, Gao-Qiang; Wei, Hai-Long; Gao, Guo-Lin; Wu, Lu-Yong; Liang, Yong-Min; Tetrahedron Asymmetry; vol. 19; nb. 8; (2008); p. 912 - 920, View in Reaxys; Shaikh, Nadim S.; Enthaler, Stephan; Junge, Kathrin; Beller, Matthias; Angewandte Chemie - International Edition; vol. 47; nb. 13; (2008); p. 2497 - 2501, View in Reaxys 88 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Doucet, Henri; Fernandez, Elena; Layzell, Timothy P.; Brown, John M.; Chemistry - A European Journal; vol. 5; nb. 4; (1999); p. 1320 - 1330, View in Reaxys; Prasad; Joshi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 42; nb. 1; (2003); p. 150 - 153, View in Reaxys; Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys; Kelsen, Vinciane; Pierrat, Philippe; Gros, Philippe C.; Tetrahedron; vol. 63; nb. 43; (2007); p. 10693 - 10697, View in Reaxys 89 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75.5 scopy) [MHz]

220/229

2018-07-03 16:52:46

Milburn, Robert R.; Hussain, S. M. Shakil; Prien, Olaf; Ahmed, Zaheer; Snieckus, Victor; Organic Letters; vol. 9; nb. 22; (2007); p. 4403 - 4406, View in Reaxys 90 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Cortez, Norma A.; Aguirre, Gerardo; Parra-Hake, Miguel; Somanathan, Ratnasamy; Tetrahedron Letters; vol. 48; nb. 25; (2007); p. 4335 - 4338, View in Reaxys; Eagon, Scott; Kim, Jinsoo; Yan, Katie; Haddenham, Dustin; Singaram, Bakthan; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 9025 - 9029, View in Reaxys 91 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 125.7 scopy) [MHz] Eagon, Scott; Kim, Jinsoo; Yan, Katie; Haddenham, Dustin; Singaram, Bakthan; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 9025 - 9029, View in Reaxys 92 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Hu, Qiao-Sheng; Huang, Wei-Sheng; Vitharana, Dilrukshi; Zheng, Xiao-Fan; Pu, Lin; Journal of the American Chemical Society; vol. 119; nb. 51; (1997); p. 12454 - 12464, View in Reaxys; Fang, Guang Y.; Wallner, Olov A.; Di Blasio, Nadia; Ginesta, Xavier; Harvey, Jeremy N.; Aggarwal, Varinder K.; Journal of the American Chemical Society; vol. 129; nb. 47; (2007); p. 14632 - 14639, View in Reaxys 93 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

221/229

2018-07-03 16:52:46

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Advanced Synthesis and Catalysis; vol. 347; nb. 11-13; (2005); p. 1561 - 1568, View in Reaxys; Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6474 - 6484, View in Reaxys 95 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6474 6484, View in Reaxys 97 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6474 6484, View in Reaxys 98 of 119

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz]

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Comment (NMR Spectroscopy)

ambient temperature

Hatano, Manabu; Miyamoto, Takashi; Ishihara, Kazuaki; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6474 6484, View in Reaxys 99 of 119

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 500.1 scopy) [MHz] Original Text (NMR Spec- 1H NMR (500.1 MHz, CDCI3) α = 0.99 (t, J = 7.4 Hz, 3 H; CH2CH3), 1.77-1.93 (m, 2 H; CH2CH3), troscopy) 2.67 (d J = 3.4 Hz, 1 H; OH), 4.62 (dt, J = 3.4, 6.6 Hz,1 H; CHOH), 7.21-7.44 (m, 5H; Ph). Comment (NMR Spectroscopy)

Signals given

Patent; UNIVERSITY OF NOTTINGHAM; WO2006/79819; (2006); (A2) English, View in Reaxys 100 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Davis, Franklin A.; Stringer, Orum D.; McCauley, John P., Jr.; Tetrahedron; vol. 41; nb. 21; (1985); p. 4747 - 4758, View in Reaxys; Alberts, Albert H.; Wynberg, Hans; Journal of the American Chemical Society; vol. 111; nb. 18; (1989); p. 7265 - 7266, View in Reaxys; Bolm, Carsten; Schlingloff, Gunther; Harms, Klaus; Chemische Berichte; vol. 125; nb. 5; (1992); p. 1191 - 1204, View in Reaxys; Sakaki, Jun-ichi; Schweizer, W. Bernd; Seebach, Dieter; Helvetica Chimica Acta; vol. 76; (1993); p. 2654 - 2665, View in Reaxys; Ishizaki; Fujita; Shimamoto; Hoshino; Tetrahedron Asymmetry; vol. 5; nb. 3; (1994); p. 411 - 424, View in Reaxys; Prasad; Joshi; Tetrahedron Asymmetry; vol. 7; nb. 7; (1996); p. 1957 - 1960, View in Reaxys; Prasad; Joshi; Tetrahedron Asymmetry; vol. 7; nb. 11; (1996); p. 3147 - 3152, View in Reaxys; Chan; Zheng; Canadian Journal of Chemistry; vol. 75; nb. 6; (1997); p. 629 - 633, View in Reaxys; Anderson, James C.; Cubbon, Rachel; Harding, Michael; James, Daniel S.; Tetrahedron Asymmetry; vol. 9; nb. 19; (1998); p. 3461 - 3490, View in Reaxys; Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 - 458, View in Reaxys; Wipf, Peter; Pierce, Joshua G.; Wang, Xiaodong; Tetrahedron Asymmetry; vol. 14; nb. 22; (2003); p. 3605 3611, View in Reaxys; Eriksen, Heidi S.; Oyaga, Sandra Cotes; Sherrington, David C.; Gibson, Colin L.; Synlett; nb. 8; (2005); p. 1235 - 1238; Art.No: D04005ST, View in Reaxys 101 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Fonseca, Maria Hechavarria; Hjelmgaard, Thomas; Koenig, Burkhard; Molecules; vol. 8; nb. 5; (2003); p. 453 - 458, View in Reaxys; Wipf, Peter; Pierce, Joshua G.; Wang, Xiaodong; Tetrahedron Asymmetry; vol. 14; nb. 22; (2003); p. 3605 3611, View in Reaxys; Eriksen, Heidi S.; Oyaga, Sandra Cotes; Sherrington, David C.; Gibson, Colin L.; Synlett; nb. 8; (2005); p. 1235 - 1238; Art.No: D04005ST, View in Reaxys 102 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500.1 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

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Biswas, Kallolmay; Prieto, Oscar; Goldsmith, Paul J.; Woodward, Simon; Angewandte Chemie - International Edition; vol. 44; nb. 15; (2005); p. 2232 - 2234, View in Reaxys 103 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500.1 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Biswas, Kallolmay; Prieto, Oscar; Goldsmith, Paul J.; Woodward, Simon; Angewandte Chemie - International Edition; vol. 44; nb. 15; (2005); p. 2232 - 2234, View in Reaxys 104 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 200 scopy) [MHz] Doucet, Henri; Fernandez, Elena; Layzell, Timothy P.; Brown, John M.; Chemistry - A European Journal; vol. 5; nb. 4; (1999); p. 1320 - 1330, View in Reaxys; Prasad; Joshi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 42; nb. 1; (2003); p. 150 - 153, View in Reaxys; Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys 106 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 50 scopy) [MHz] Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys 107 of 119

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

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Rudolph, Jens; Hermanns, Nina; Bolm, Carsten; Journal of Organic Chemistry; vol. 69; nb. 11; (2004); p. 3997 - 4000, View in Reaxys 108 of 119

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Rudolph, Jens; Hermanns, Nina; Bolm, Carsten; Journal of Organic Chemistry; vol. 69; nb. 11; (2004); p. 3997 - 4000, View in Reaxys 109 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Chan; Zheng; Canadian Journal of Chemistry; vol. 75; nb. 6; (1997); p. 629 - 633, View in Reaxys; Anderson, James C.; Cubbon, Rachel; Harding, Michael; James, Daniel S.; Tetrahedron Asymmetry; vol. 9; nb. 19; (1998); p. 3461 - 3490, View in Reaxys; Edwards, Christopher W.; Haddleton, David M.; Morsley, David; Shipton, Mark R.; Wills, Martin; Tetrahedron; vol. 59; nb. 31; (2003); p. 5823 - 5830, View in Reaxys 110 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 250 scopy) [MHz] Spieler, Jan; Huttenloch, Oliver; Waldmann, Herbert; European Journal of Organic Chemistry; nb. 3; (2000); p. 391 - 399, View in Reaxys; Edwards, Christopher W.; Haddleton, David M.; Morsley, David; Shipton, Mark R.; Wills, Martin; Tetrahedron; vol. 59; nb. 31; (2003); p. 5823 - 5830, View in Reaxys 111 of 119

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Ulrich, Claudia; Bargon, Joachim; Magnetic Resonance in Chemistry; vol. 38; nb. 1; (2000); p. 33 - 37, View in Reaxys 112 of 119

Description (NMR Spectroscopy)

NMR with shift reagents

Nucleus (NMR Spectroscopy)

Ulrich, Claudia; Bargon, Joachim; Magnetic Resonance in Chemistry; vol. 38; nb. 1; (2000); p. 33 - 37, View in Reaxys 113 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Blake, Alexander J.; Cunningham, Anthony; Ford, Alan; Teat, Simon J.; Woodward, Simon; Chemistry - A European Journal; vol. 6; nb. 19; (2000); p. 3586 - 3594, View in Reaxys 114 of 119

Description (NMR Spectroscopy)

Chemical shifts

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Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Blake, Alexander J.; Cunningham, Anthony; Ford, Alan; Teat, Simon J.; Woodward, Simon; Chemistry - A European Journal; vol. 6; nb. 19; (2000); p. 3586 - 3594, View in Reaxys 115 of 119

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Davis, Franklin A.; Stringer, Orum D.; McCauley, John P., Jr.; Tetrahedron; vol. 41; nb. 21; (1985); p. 4747 - 4758, View in Reaxys; Bolm, Carsten; Schlingloff, Gunther; Harms, Klaus; Chemische Berichte; vol. 125; nb. 5; (1992); p. 1191 1204, View in Reaxys; Sakaki, Jun-ichi; Schweizer, W. Bernd; Seebach, Dieter; Helvetica Chimica Acta; vol. 76; (1993); p. 2654 - 2665, View in Reaxys; Ishizaki; Fujita; Shimamoto; Hoshino; Tetrahedron Asymmetry; vol. 5; nb. 3; (1994); p. 411 424, View in Reaxys; Prasad; Joshi; Tetrahedron Asymmetry; vol. 7; nb. 7; (1996); p. 1957 - 1960, View in Reaxys; Prasad; Joshi; Tetrahedron Asymmetry; vol. 7; nb. 11; (1996); p. 3147 - 3152, View in Reaxys; Chan; Zheng; Canadian Journal of Chemistry; vol. 75; nb. 6; (1997); p. 629 - 633, View in Reaxys; Anderson, James C.; Cubbon, Rachel; Harding, Michael; James, Daniel S.; Tetrahedron Asymmetry; vol. 9; nb. 19; (1998); p. 3461 - 3490, View in Reaxys 116 of 119

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Comina, Paul J.; Beck, Albert K.; Seebach, Dieter; Organic Process Research and Development; vol. 2; nb. 1; (1998); p. 18 26, View in Reaxys 117 of 119

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Smaardijk, Ab. A.; Wynberg, Hans; Journal of Organic Chemistry; vol. 52; nb. 1; (1987); p. 135 - 137, View in Reaxys; Nakagawa; Kawate; Kakikawa; Yamada; Matsui; Hino; Tetrahedron; vol. 49; nb. 9; (1993); p. 1739 - 1748, View in Reaxys 119 of 119

Description (NMR Spectroscopy)

Spin-spin coupling constants

Comment (NMR Spectroscopy)

1H-1H

Nakagawa; Kawate; Kakikawa; Yamada; Matsui; Hino; Tetrahedron; vol. 49; nb. 9; (1993); p. 1739 - 1748, View in Reaxys

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IR Spectroscopy (11) 1 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys; Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571-OP, View in Reaxys 2 of 11

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Location

supporting information

Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; (2018); p. 268 - 286, View in Reaxys 3 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Wu, Pei-Shan; Chen, Chinpiao; Journal of the Chinese Chemical Society; vol. 59; nb. 6; (2012); p. 768 - 781, View in Reaxys; Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys; Fujii, Kazuki; Mitsudo, Koichi; Mandai, Hiroki; Suga, Seiji; Bulletin of the Chemical Society of Japan; vol. 89; nb. 9; (2016); p. 1081 - 1092, View in Reaxys 4 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Escorihuela, Jorge; Burguete, M. Isabel; Ujaque, Gregori; Lledós, Agustí; Luis, Santiago V.; Organic and Biomolecular Chemistry; vol. 14; nb. 47; (2016); p. 11125 - 11136, View in Reaxys 5 of 11

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands; Spectrum

Location

supporting information

Lowicki, Daniel; Bezlada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 591 595, View in Reaxys 7 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Cortez, Norma A.; Aguirre, Gerardo; Parra-Hake, Miguel; Somanathan, Ratnasamy; Tetrahedron Letters; vol. 48; nb. 25; (2007); p. 4335 - 4338, View in Reaxys 8 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3370 cm**(-1)

Anderson, James C.; Cubbon, Rachel; Harding, Michael; James, Daniel S.; Tetrahedron Asymmetry; vol. 9; nb. 19; (1998); p. 3461 - 3490, View in Reaxys 9 of 11

Description (IR Spectroscopy)

Bands

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Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3400 - 800 cm**(-1)

Chan; Zheng; Canadian Journal of Chemistry; vol. 75; nb. 6; (1997); p. 629 - 633, View in Reaxys 10 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

3450 cm**(-1)

Ishizaki; Fujita; Shimamoto; Hoshino; Tetrahedron Asymmetry; vol. 5; nb. 3; (1994); p. 411 - 424, View in Reaxys 11 of 11

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

3350 - 3025 cm**(-1)

Nakagawa; Kawate; Kakikawa; Yamada; Matsui; Hino; Tetrahedron; vol. 49; nb. 9; (1993); p. 1739 - 1748, View in Reaxys Mass Spectrometry (14) Description (Mass Location Spectrometry)

References

gas chromatograsupporting informa- Dilek, Ömer; Tezeren, Mustafa A.; Tilki, Tahir; Ertürk, Erkan; Tetrahedron; vol. 74; nb. 2; phy mass spectrom- tion (2018); p. 268 - 286, View in Reaxys etry (GCMS); electron impact (EI); spectrum high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

Mohebbi, Maryam; Bararjanian, Morteza; Ebrahimi, Samad N.; Smieško, Martin; Salehi, Peyman; Synthesis (Germany); vol. 50; nb. 9; (2018); p. 1841 - 1848; Art.No: SS-2017-N0571OP, View in Reaxys

desorption chemical ionization (DCI); spectrum

gas chromatography mass spectrometry (GCMS); spectrum

Sarkar, Md. Raihan; Lee, Joel H. Z.; Bell, Stephen G.; ChemBioChem; vol. 18; nb. 21; (2017); p. 2119 - 2128, View in Reaxys

electrospray ionisa- supporting informa- An, Wan-Kai; Han, Man-Yi; Wang, Chang-An; Yu, Si-Min; Zhang, Yuan; Bai, Shi; Wang, tion (ESI); spection Wei; Chemistry--A European Journal; vol. 20; nb. 35; (2014); p. 11019 - 11028,10, trum View in Reaxys high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

supporting informa- Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. tion 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys

high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

supporting informa- Bigler, Raphael; Mezzetti, Antonio; Organic Letters; vol. 16; nb. 24; (2014); p. 6460 - 6463, tion View in Reaxys

GCMS (Gas chromatography mass

supporting informa- Yadav, Saroj; Yadav; Canadian Journal of Chemistry; vol. 90; nb. 7; (2012); p. 597 - 599, tion View in Reaxys

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spectrometry); Spectrum HRMS (High resolution mass spectrometry); ESI (Electrospray ionisation); TOFMS (Time of flight mass spectrum); Spectrum

Beckendorf, Stephan; Mancheno, Olga Garcia; Synthesis (Germany); vol. 44; nb. 14; (2012); p. 2162 - 2172; Art.No: SS-2012-C0311-ST, View in Reaxys

HRMS (High resolution mass spectrometry); Spectrum

Yamamoto, Yasunori; Shirai, Tomohiko; Watanabe, Momoko; Kurihara, Kazunori; Miyaura, Norio; Molecules; vol. 16; nb. 6; (2011); p. 5020 - 5034, View in Reaxys

EI (Electron impact); Spectrum

supporting informa- Lindsay, David M.; McArthur, David; Chemical Communications; vol. 46; nb. 14; (2010); p. tion 2474 - 2476, View in Reaxys; Fernandez-Mateos, Emilio; MacIa, Beatriz; Ramon, Diego J.; Yus, Miguel; European Journal of Organic Chemistry; nb. 34; (2011); p. 6851 - 6855, View in Reaxys

ESI (Electrospray ionisation); Spectrum

supporting informa- Li, Wei Jie; Qiu, Sheng Xiang; Advanced Synthesis and Catalysis; vol. 352; nb. 7; (2010); p. tion 1119 - 1122, View in Reaxys

spectrum

Chan; Zheng; Canadian Journal of Chemistry; vol. 75; nb. 6; (1997); p. 629 - 633, View in Reaxys; El-Shehawy, Ashraf A.; Sugiyama, Kenji; Hirao, Akira; Tetrahedron Asymmetry; vol. 19; nb. 4; (2008); p. 425 - 434, View in Reaxys

time-of-flight mass spectra (TOFMS)

Scuderi; Paladini; Piccirillo; Satta; Catone; Giardini; Filippi; Speranza, Maurizio; Chemical Communications; nb. 20; (2002); p. 2438 - 2439, View in Reaxys

Medchem (1) 1 of 1

Bioassay Category

In Vivo (Animal models)

Bioassay Details Substance RN

2041555View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Tang, Tuo-Xian; Liu, Yan; Wu, Zhong-Liu; Journal of Molecular Catalysis B: Enzymatic; vol. 105; (2014); p. 82 - 88, View in Reaxys

Copyright ÂŠ 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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