1-Phenylpropan-1-one (1-Phenyl-1-propanone; Propiophenone) [C9H10O] by Asch

Query Query

Results

Date

1 substances in Reaxys

2018-07-03 19h:01m:09s (UTC)

1. Query

Search as: As drawn ) AND (IDE.RN='93-55-0') AND (IDE.INCHI='KRIOVPPHQSLHCZ-UHFFFAOYSA-N') AND (IDE.XRN=606215))

1/126

2018-07-03 19:01:53

Reaxys ID 606215 View in Reaxys

1/1 CAS Registry Number: 93-55-0 Chemical Name: 1-phenyl-propan-1-one; 1-phenylpropanone; propiophenone; Propiophenone Linear Structure Formula: C6H5C(O)CH2CH3 Molecular Formula: C9H10O Molecular Weight: 134.178 Type of Substance: isocyclic InChI Key: KRIOVPPHQSLHCZ-UHFFFAOYSA-N Note:

Substance Label (433) Label References a2

Yu, Jianhua; Hu, Yulai; Huang, Qibing; Ma, Ronghua; Yang, Shiyan; Synthetic Communications; vol. 29; nb. 15; (1999); p. 2567 - 2574, View in Reaxys; 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; Wang, Ding; Bruneau-Voisine, Antoine; Sortais, Jean-Baptiste; Catalysis Communications; vol. 105; (2018); p. 31 36, View in Reaxys

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; Gevorgyan, Ashot; Mkrtchyan, Satenik; Grigoryan, Tatevik; Iaroshenko, Viktor O.; ChemPlusChem; vol. 83; nb. 5; (2018); p. 375 - 382, 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; Concellon, Jose M; Cuervo, Humildad; Fernandez-Fano, Ramon; Tetrahedron; vol. 57; nb. 43; (2001); p. 8983 - 8987, 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; 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; Chen, ZhengWang; Ye, Dong-Nai; Ye, Min; Liu, Liang-Xian; Chemistry Letters; vol. 42; nb. 11; (2013); p. 1388 - 1390, View in Reaxys; Ananthan, Bakthavachalam; Yan, Tu-Hsin; Synthetic Communications; vol. 48; nb. 7; (2018); p. 753 - 760, 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; Arakawa, Yukihiro; Haraguchi, Naoki; Itsuno, Shinichi; Tetrahedron Letters; vol. 47; nb. 19; (2006); p. 3239 - 3243, View in Reaxys; Hatano, Manabu; Suzuki, Shinji; Ishihara, Kazuaki; Journal of the American Chemical Society; vol. 128; nb. 31; (2006); p. 9998 - 9999, View in Reaxys; Chatupheeraphat, Adisak; Liao, Hsuan-Hung; Srimontree, Watchara; Guo, Lin; Minenkov, Yury; Poater, Albert; Cavallo, Luigi; Rueping, Magnus; Journal of the American Chemical Society; vol. 140; nb. 10; (2018); p. 3724 - 3735, View in Reaxys

Pavlov; Vinogradov; Starodubtseva; Chel'tsova; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 4; (2001); p. 734 - 735, View in Reaxys; Miyamoto; Yasaka; Takaoka; Tanaka; Toda; Enantiomer; vol. 6; nb. 1; (2001); p. 51 - 55, View in Reaxys; Oguma, Kazuaki; Miura, Masahiro; Satoh, Tetsuya; Nomura, Masakatsu; Journal of Organometalic Chemistry; vol. 648; nb. 1-2; (2002); p. 297 - 301, View in Reaxys; Sano, Shigeki; Takehisa, Tomoka; Ogawa, Shiho; Yokoyama, Kenji; Nagao, Yoshimitsu; Chemical and Pharmaceutical Bulletin; vol. 50; nb. 9; (2002); p. 1300 - 1302, View in Reaxys; Kubota, Jun; Shimizu, Yusuke; Mitsudo, Koichi; Tanaka, Hideo; Tetrahedron Letters; vol. 46; nb. 52; (2005); p. 8975 - 8979, 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; Kamimura, Akio; Nozaki, Yuichiro; Nishiyama, Mai; Nakayama, Masaharu; RSC Advances; vol. 3; nb. 2; (2013); p. 468 - 472, View in Reaxys; Kotani, Shunsuke; Kukita, Kenji; Tanaka, Kana; Ichibakase, Tomonori; Nakajima, Makoto; Journal of Organic Chemistry; vol. 79; nb. 11; (2014); p. 4817 - 4825, View in Reaxys; Han, Sang-Woo; Park, Eul-Soo; Dong, Joo-Young; Shin, Jong-Shik; Advanced Synthesis and Catalysis; vol. 357; nb. 12; (2015); p. 2712 - 2720, View in Reaxys; Sagir, Hozeyfa; Rai, Pragati; Neha, Shamshun; Singh, Prashant Kumar; Tiwari, Shailendra; Siddiqui; RSC Advances; vol. 6; nb. 77; (2016); p. 73924 - 73932, View in Reaxys; Sun, Jin-Shi; Jing, Li-Ping; Tian, Yuyang; Sun, Fuxing; Chen, Peng; Zhu, Guangshan; Chemical Communications; vol. 54; nb. 13; (2018); p. 1603 - 1606, View in Reaxys

Nishiguchi, Ikuzo; Sakai, Masahiro; Maekawa, Hirofumi; Ohno, Toshinobu; Yamamoto, Yoshimasa; Ishino, Yoshio; Tetrahedron Letters; vol. 43; nb. 4; (2002); p. 635 - 637, View in Reaxys; Liu, Yu-Xiu; Xu, Cheng-Fu; Liu, Lun-Zu; Synthesis; nb. 9; (2003); p. 1335 - 1338, View in Reaxys; Huang; Hou; Wang; Chen; Organic Preparations and Procedures International; vol. 38; nb. 5; (2006); p. 473 - 476, View in Reaxys; Kitamura, Tsugio; Muta, Kensuke; Muta, Kazutaka; Journal of Organic Chemistry; vol. 79; nb. 12; (2014); p. 5842 - 5846, View in Reaxys; Zhang, Bijun; Han, Liuquan; Hu, Jiantao; Yan, Jie; Tetrahedron Letters; vol. 55; nb. 42; (2014); p. 5851 - 5854, View in Reaxys; Zhang, Bijun; Han, Liuquan; Hu, Jiantao; Yan, Jie; Synthetic Communications; vol. 44; nb. 22; (2014); p. 3264 - 3270, View in Reaxys; Sandoval, Cosme; Lim, Ngiap-Kie; Zhang, Haiming; Organic Letters; vol. 20; nb. 4; (2018); p. 1252 - 1255, View in Reaxys; Silva, Saúl; Maycock, Christopher D.; Tetrahedron Letters; vol. 59; nb. 13; (2018); p. 1233 - 1238, View in Reaxys

2/126

2018-07-03 19:01:53

Vinogradov; Gorshkova; Chel'tsova; Kurilov; Ferapontov; Shishkin; Heise; Russian Chemical Bulletin; vol. 52; nb. 8; (2003); p. 1841 - 1846, View in Reaxys; Prebil, Rok; Stavber, Stojan; Advanced Synthesis and Catalysis; vol. 356; nb. 6; (2014); p. 1266 - 1274, View in Reaxys; Bolje, Aljosa; Hohloch, Stephan; Urankar, Damijana; Pevec, Andrej; Gazvoda, Martin; Sarkar, Biprajit; Kosmrlj, Janez; Organometallics; vol. 33; nb. 10; (2014); p. 2588 - 2598, View in Reaxys; Pavlidis, Ioannis V.; Weiß, Martin S.; Genz, Maika; Spurr, Paul; Hanlon, Steven P.; Wirz, Beat; Iding, Hans; Bornscheuer, Uwe T.; Nature Chemistry; vol. 8; nb. 11; (2016); p. 1076 - 1082, View in Reaxys; Reddy, G. Trivikram; Kumar; Reddy, N. C. Gangi; Advanced Synthesis and Catalysis; vol. 360; nb. 5; (2018); p. 995 - 1006, View in Reaxys

Yamasaki; Iida; Shibasaki; Tetrahedron Letters; vol. 40; nb. 2; (1999); p. 307 - 310, View in Reaxys; Yamasaki, Shingo; Iida, Takehiko; Shibasaki, Masakatsu; Tetrahedron; vol. 55; nb. 29; (1999); p. 8857 - 8867, View in Reaxys; De Luca, Lidia; Giacomelli, Giampaolo; Porcheddu, Andrea; Organic Letters; vol. 3; nb. 10; (2001); p. 1519 - 1521, View in Reaxys; Rodrigues, J. Augusto R.; Siqueira-Filho, Ezequias P.; De Mancilha, Moacir; Moran, Paulo J. S.; Synthetic Communications; vol. 33; nb. 2; (2003); p. 331 - 340, View in Reaxys; Li, Xiaoqing; Zhou, Can; Hu, Zhiyan; Xu, Xiangsheng; Journal of Chemical Research; vol. 37; nb. 9; (2013); p. 579 - 581, View in Reaxys; GhorbaniChoghamarani, Arash; Zamani, Parisa; Journal of Chemical Sciences; vol. 126; nb. 1; (2014); p. 103 - 109, View in Reaxys; Bogolubsky, Andrey V.; Moroz, Yurii S.; Pipko, Sergey E.; Panov, Dmitriy M.; Konovets, Anzhelika I.; Doroschuk, Roman; Tolmachev, Andrey; Synthesis (Germany); vol. 46; nb. 13; (2014); p. 1765 - 1772; Art.No: SS-2014-Z0090-OP, View in Reaxys; Grigalunas, Michael; Ankner, Tobias; Norrby, Per-Ola; Wiest, Olaf; Helquist, Paul; Organic Letters; vol. 16; nb. 15; (2014); p. 3970 - 3973, View in Reaxys; Agudo, Rubén; Roiban, GheorgheDoru; Lonsdale, Richard; Ilie, Adriana; Reetz, Manfred T.; Journal of Organic Chemistry; vol. 80; nb. 2; (2015); p. 950 - 956, View in Reaxys; Xi, Long-Yi; Zhang, Ruo-Yi; Zhang, Lei; Chen, Shan-Yong; Yu, Xiao-Qi; Organic and Biomolecular Chemistry; vol. 13; nb. 13; (2015); p. 3924 - 3930, View in Reaxys; Naveen, Naganaboina; Koppolu, Srinivasa Rao; Balamurugan, Rengarajan; Advanced Synthesis and Catalysis; vol. 357; nb. 7; (2015); p. 1463 - 1473, View in Reaxys; Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys; Bettadapur, Kiran R.; Lanke, Veeranjaneyulu; Prabhu, Kandikere Ramaiah; Organic Letters; vol. 17; nb. 19; (2015); p. 4658 - 4661, View in Reaxys; Lu, Ailing; Huang, Danfeng; Wang, Ke-Hu; Su, Yingpeng; Ma, Junyan; Xu, Yanli; Hu, Yulai; Synthesis (Germany); vol. 48; nb. 2; (2016); p. 293 - 301, View in Reaxys; Ghorbani-Choghamarani, Arash; Zamani, Parisa; Journal of Chemical Sciences; vol. 126; nb. 1; (2014); p. 103 - 109, View in Reaxys; Wang, Tao; Di, Xiao; Wang, Chao; Zhou, Li; Sun, Jian; Organic Letters; vol. 18; nb. 8; (2016); p. 1900 - 1903, View in Reaxys; Xie, Zeqiang; Deng, Jiaojiao; Qiu, Zhiping; Li, Juan; Zhu, Qiang; Chemical Communications; vol. 52; nb. 38; (2016); p. 6467 - 6470, 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; Nayal, Onkar S.; Thakur, Maheshwar S.; Bhatt, Vinod; Kumar, Manoranjan; Kumar, Neeraj; Singh, Bikram; Sharma, Upendra; Chemical Communications; vol. 52; nb. 62; (2016); p. 9648 - 9651, View in Reaxys; Chen, Xu; Lu, Zhan; Organic Letters; vol. 18; nb. 18; (2016); p. 4658 4661, View in Reaxys; Cinar, M. Emin; Schmittel, Michael; Monatshefte fur Chemie; vol. 147; nb. 11; (2016); p. 1925 - 1932, View in Reaxys; Malmedy, Florence; Wirth, Thomas; Chemistry - A European Journal; vol. 22; nb. 45; (2016); p. 16072 - 16077, View in Reaxys; Kim, Jungwon; Hong, Soon Hyeok; Chemical Science; vol. 8; nb. 3; (2017); p. 2401 - 2406, View in Reaxys; Kazi, Imran; Guha, Somraj; Sekar, Govindasamy; Organic Letters; vol. 19; nb. 5; (2017); p. 1244 - 1247, View in Reaxys; Zhang, Zhi-Jie; Yi, Dong; Fu, Qiang; Liang, Wu; Chen, Su-Yuan; Yang, Lu; Du, Feng-Tian; Ji, Jian-Xin; Wei, Wei; Tetrahedron Letters; vol. 58; nb. 25; (2017); p. 2417 - 2420, View in Reaxys; Liu, Yufeng; Zhan, Xi; Ji, Pengyi; Xu, Jingwen; Liu, Qiang; Luo, Weiping; Chen, Tieqiao; Guo, Cancheng; Chemical Communications; vol. 53; nb. 38; (2017); p. 5346 - 5349, View in Reaxys; Xuan, Qingqing; Zhao, Cong; Song, Qiuling; Organic and Biomolecular Chemistry; vol. 15; nb. 24; (2017); p. 5140 - 5144, View in Reaxys; Patent; Jiangsu Aifan Bio-pharmaceutical Co., Ltd.; Feng Bonian; Fan Wenhua; (22 pag.); CN106632142; (2017); (A) Chinese, View in Reaxys; Souza, Gisele C.; Franchi, Gilberto C.; Nowill, Alexandre E.; Santos, Lourivaldo S.; Alves, Cláudio N.; Barata, Lauro E.S.; Andrade, Carlos K. Z.; Journal of the Brazilian Chemical Society; vol. 28; nb. 11; (2017); p. 2229 - 2243, View in Reaxys; Yang, Zan; Li, Jiao; Hua, Jie; Yang, Tao; Yi, Jianmin; Zhou, Congshan; Synlett; vol. 28; nb. 17; (2017); p. 2325 - 2329; Art.No: ST-2017-R0233-L, View in Reaxys; Wang, Peng; Verma, Pritha; Xia, Guoqin; Shi, Jun; Qiao, Jennifer X.; Tao, Shiwei; Cheng, Peter T. W.; Poss, Michael A.; Farmer, Marcus E.; Yeung, Kap-Sun; Yu, Jin-Quan; Nature; vol. 551; nb. 7681; (2017); p. 489 - 493, View in Reaxys; Zhang, Jingyu; Li, Shiguang; Deng, Guo-Jun; Gong, Hang; ChemCatChem; vol. 10; nb. 2; (2018); p. 376 - 380, View in Reaxys; Wu, Jiwei; Zhou, Yuchen; Wu, Ting; Zhou, Yi; Chiang, Chien-Wei; Lei, Aiwen; Organic Letters; vol. 19; nb. 23; (2017); p. 6432 - 6435, View in Reaxys; Jiang, Bing; Liang, Qiu-Ju; Han, Yu; Zhao, Meng; Xu, Yun-He; Loh, Teck-Peng; Organic Letters; vol. 20; nb. 11; (2018); p. 3215 - 3219, View in Reaxys

Talukdar; Fang; Journal of Organic Chemistry; vol. 66; nb. 1; (2001); p. 330 - 333, View in Reaxys; Poisson, Thomas; Belhomme, Marie-Charlotte; Pannecoucke, Xavier; Journal of Organic Chemistry; vol. 77; nb. 20; (2012); p. 9277 9285,9, View in Reaxys; Poisson, Thomas; Belhomme, Marie-Charlotte; Pannecoucke, Xavier; Journal of Organic Chemistry; vol. 77; nb. 20; (2012); p. 9277 - 9285, View in Reaxys; Wu, Kun; Huang, Zhiliang; Liu, Chao; Zhang, Heng; Lei, Aiwen; Chemical Communications; vol. 51; nb. 12; (2015); p. 2286 - 2289, View in Reaxys; Mandal, Rajib; Emayavaramban, Balakumar; Sundararaju, Basker; Organic Letters; vol. 20; nb. 10; (2018); p. 2835 - 2838, View in Reaxys

Pasto, Mireia; Riera, Antoni; Pericas, Miquel A.; European Journal of Organic Chemistry; nb. 14; (2002); p. 2337 2341, View in Reaxys; Shen, Yongcun; Feng, Xiaoming; Li, Yan; Zhang, Guolin; Jiang, Yaozhong; Tetrahedron; vol. 59; nb. 30; (2003); p. 5667 - 5675, View in Reaxys; Kawasaki, Ikuo; Tsunoda, Kazuya; Tsuji, Tomoko; Yamaguchi, Tomoko; Shibuta, Hiroki; Uchida, Nozomi; Yamashita, Masayuki; Ohta, Shunsaku; Chemical Communica-

3/126

2018-07-03 19:01:53

tions; nb. 16; (2005); p. 2134 - 2136, View in Reaxys; Lopez-Iglesias, Maria; Busto, Eduardo; Gotor, Vicente; Gotor-Fernandez, Vicente; Journal of Organic Chemistry; vol. 77; nb. 18; (2012); p. 8049 - 8055,7, View in Reaxys; Lopez-Iglesias, Maria; Busto, Eduardo; Gotor, Vicente; Gotor-Fernandez, Vicente; Journal of Organic Chemistry; vol. 77; nb. 18; (2012); p. 8049 - 8055, View in Reaxys; Hokamp, Tobias; Storm, Alena Therese; Yusubov, Mekhman; Wirth, Thomas; Synlett; vol. 29; nb. 4; (2018); p. 415 - 418; Art.No: ST-2017-R0670-C, View in Reaxys 2

Ross, Nathan A.; Bartsch, Richard A.; Journal of Organic Chemistry; vol. 68; nb. 2; (2003); p. 360 - 366, View in Reaxys; Spaggiari, Alberto; Vaccari, Daniele; Davoli, Paolo; Torre, Giovanni; Prati, Fabio; Journal of Organic Chemistry; vol. 72; nb. 6; (2007); p. 2216 - 2219, View in Reaxys; Osako, Takao; Uozumi, Yasuhiro; Chemistry Letters; vol. 38; nb. 9; (2009); p. 902 - 903, View in Reaxys; Shang, Yaping; Jie, Xiaoming; Zhou, Jun; Hu, Peng; Huang, Shijun; Su, Weiping; Angewandte Chemie - International Edition; vol. 52; nb. 4; (2013); p. 1299 - 1303; Angew. Chem.; vol. 125; nb. 4; (2013); p. 1337 - 1341,5, View in Reaxys; Bagdi, Avik Kumar; Rahman, Matiur; Santra, Sougata; Majee, Adinath; Hajra, Alakananda; Advanced Synthesis and Catalysis; vol. 355; nb. 9; (2013); p. 1741 - 1747, View in Reaxys; John, Lukas C.; Gunay, Ahmet; Wood, Andrew J.; Emmert, Marion H.; Tetrahedron; vol. 69; nb. 27-28; (2013); p. 5758 - 5764, View in Reaxys; Cabrero-Antonino, Jose R.; Leyva-Perez, Antonio; Corma, Avelino; Chemistry - A European Journal; vol. 19; nb. 26; (2013); p. 8627 - 8633, View in Reaxys; Zhou, Yuhan; Gao, Guchao; Song, Yuming; Qu, Jingping; Synthetic Communications; vol. 44; nb. 10; (2014); p. 1515 - 1520, View in Reaxys; Meng, Xu; Wang, Yanmin; Yu, Chaoying; Zhao, Peiqing; RSC Advances; vol. 4; nb. 52; (2014); p. 27301 - 27307, View in Reaxys; Undeela, Sridhar; Ramchandra, Joshi P.; Menon, Rajeev S.; Tetrahedron Letters; vol. 55; nb. 41; (2014); p. 5667 - 5670, View in Reaxys; Janeczko, Tomasz; Kostrzewa-Suslow, Edyta; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1264 - 1269, View in Reaxys; Gunay, Ahmet; Mantell, Mark A.; Field, Kathleen D.; Wu, Wenbo; Chin, Michael; Emmert, Marion H.; Catalysis Science and Technology; vol. 5; nb. 2; (2015); p. 1198 - 1205, View in Reaxys; Quan, Xu; Kerdphon, Sutthichat; Andersson, Pher G.; Chemistry - A European Journal; vol. 21; nb. 9; (2015); p. 3576 - 3579, View in Reaxys; Liu, Wei-Peng; Yuan, Ming-Lei; Yang, XiaoHui; Li, Ke; Xie, Jian-Hua; Zhou, Qi-Lin; Chemical Communications; vol. 51; nb. 28; (2015); p. 6123 - 6125, View in Reaxys; Xu, Guo-Chao; Shang, Yue-Peng; Yu, Hui-Lei; Xu, Jian-He; Chemical Communications; vol. 51; nb. 86; (2015); p. 15728 - 15731, View in Reaxys; Ouyang, Lu; Qi, Chaorong; He, Haitao; Peng, Youbin; Xiong, Wenfang; Ren, Yanwei; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 81; nb. 3; (2016); p. 912 - 919, View in Reaxys; Qiu, Fadong; Yang, Junjuan; Shi, Daxin; Zhang, Qi; Li, Jiarong; Tetrahedron Letters; vol. 57; nb. 11; (2016); p. 1210 - 1214, 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; Siddaraju, Yogesh; Prabhu, Kandikere Ramaiah; Organic Letters; vol. 18; nb. 23; (2016); p. 6090 - 6093, View in Reaxys; Casnati, Alessandra; Maggi, Raimondo; Maestri, Giovanni; Della Ca, Nicola; Motti, Elena; Journal of Organic Chemistry; vol. 82; nb. 15; (2017); p. 8296 - 8303, View in Reaxys; Das, Sudarshan; Santra, Sougata; Jana, Sourav; Zyryanov, Grigory V.; Majee, Adinath; Hajra, Alakananda; European Journal of Organic Chemistry; vol. 2017; nb. 33; (2017); p. 4955 - 4962, View in Reaxys; Patent; Chinese Academy Of Sciences Chemical Institute; Shi Yian; Tan Xiangyu; Pan Hongjie; Tian Hua; (23 pag.); CN107162997; (2017); (A) Chinese, View in Reaxys; Wei, Wei; Dai, Xi-Jie; Wang, Haining; Li, Chenchen; Yang, Xiaobo; Li, Chao-Jun; Chemical Science; vol. 8; nb. 12; (2017); p. 8193 - 8197, View in Reaxys; Ling, Fei; Xiao, Lian; Fang, Lu; Lv, Yaping; Zhong, Weihui; Advanced Synthesis and Catalysis; vol. 360; nb. 3; (2018); p. 444 - 448, View in Reaxys; Löwe, Jana; Ingram, Aaron A.; Gröger, Harald; Bioorganic and Medicinal Chemistry; vol. 26; nb. 7; (2018); p. 1387 - 1392, View in Reaxys

Mino, Takashi; Matsuda, Terumi; Hiramatsu, Dai; Yamashita, Masakazu; Tetrahedron Letters; vol. 41; nb. 9; (2000); p. 1461 - 1463, View in Reaxys; Jiang, Biao; Feng, Yan; Hang, Jian-Feng; Tetrahedron Asymmetry; vol. 12; nb. 16; (2001); p. 2323 - 2329, View in Reaxys; Yasuda, Makoto; Hirata, Kay; Nishino, Mitsuyoshi; Yamamoto, Akihiro; Baba, Akio; Journal of the American Chemical Society; vol. 124; nb. 45; (2002); p. 13442 - 13447, View in Reaxys; Fesko, Kateryna; Steiner, Kerstin; Breinbauer, Rolf; Schwab, Helmut; Schuermann, Martin; Strohmeier, Gernot A.; Journal of Molecular Catalysis B: Enzymatic; vol. 96; (2013); p. 103 - 110, View in Reaxys; Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 - 6104, View in Reaxys; Zhang, Yan; He, Yu; Li, Lisha; Ji, Mingming; Li, Xiao-Zong; Zhu, Gangguo; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2898 - 2903, View in Reaxys

Miura, Katsukiyo; Yamada, Yusuke; Tomita, Mitsuru; Hosomi, Akira; Synlett; nb. 11; (2004); p. 1985 - 1989, View in Reaxys; Kim, Seong Jin; Lee, Hyun Seung; Kim, Jae Nyoung; Tetrahedron Letters; vol. 48; nb. 6; (2007); p. 1069 - 1072, View in Reaxys; Sheng, Wen-Bing; Jiang, Qing; Luo, Wei-Ping; Guo, Can-Cheng; Journal of Organic Chemistry; vol. 78; nb. 11; (2013); p. 5691 - 5693, 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; Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; vol. 16; nb. 1; (2014); p. 66 - 69, View in Reaxys; Slagbrand, Tove; Lundberg, Helena; Adolfsson, Hans; Chemistry - A European Journal; vol. 20; nb. 49; (2014); p. 16102 - 16106, View in Reaxys; Wu, Fengtian; Bai, Rongxian; Gu, Yanlong; Advanced Synthesis and Catalysis; vol. 358; nb. 14; (2016); p. 2307 - 2316, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24; (2017); p. 6760 - 6762, View in Reaxys; Popłoński, Jarosław; Reiter, Tamara; Kroutil, Wolfgang; ChemCatChem; vol. 10; nb. 4; (2018); p. 763 - 768, View in Reaxys

Togo, Hideo; Abe, Seiichiro; Nogami, Genki; Yokohama, Masataka; Bulletin of the Chemical Society of Japan; vol. 72; nb. 10; (1999); p. 2351 - 2356, View in Reaxys; Fu, I.-Pin; Uang, Biing-Jiun; Tetrahedron Asymmetry; vol. 12; nb. 1; (2001); p. 45 - 48, View in Reaxys; Kriis, Kadri; Kanger, Tonis; Lopp, Margus; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2687 - 2691, 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; Yang, Xiao-Hui; Zhou, Yong-Hong; Zhang, Ping-Hu; Zhang, Li-Yun; Journal of Heterocyclic Chemistry; vol. 50; nb. 6; (2013); p. 1346 - 1350, View in Reaxys;

4/126

2018-07-03 19:01:53

Movassagh, Barahman; Yousefi, Ali; Monatshefte fur Chemie; vol. 145; nb. 7; (2014); p. 1173 - 1177, View in Reaxys; Byre Gowda; Charanraj; Pradeepa Kumara; Ramesh; Thomas; Sadashiva; Junjappa; Tetrahedron Letters; vol. 55; nb. 32; (2014); p. 4475 - 4479, 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; Sun, Kai; Lv, Yunhe; Zhu, Zhonghong; Zhang, Liping; Wu, Hankui; Liu, Lin; Jiang, Yongqing; Xiao, Beibei; Wang, Xin; RSC Advances; vol. 5; nb. 4; (2015); p. 3094 - 3097, View in Reaxys; Szewczyk, Marcin; Stanek, Filip; Bezłada, Agata; Mlynarski, Jacek; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3727 - 3731, View in Reaxys; Chen, Zhiwei; Hu, Lele; Peng, Fei; Synlett; vol. 27; nb. 12; (2016); p. 1888 - 1892; Art.No: ST-2015-W1005-L, View in Reaxys; Liu, Yu-Feng; Ji, Peng-Yi; Xu, Jing-Wen; Hu, Yu-Qun; Liu, Qiang; Luo, Wei-Ping; Guo, Can-Cheng; Journal of Organic Chemistry; vol. 82; nb. 14; (2017); p. 7159 - 7164, View in Reaxys; Cui, Bin; Sun, Hui; Xu, Yibo; Duan, Lili; Li, Yue-Ming; Tetrahedron; vol. 73; nb. 48; (2017); p. 6754 - 6762, View in Reaxys; Zhu; Liang; Gong; Pu; Wang; Zhou; Sun; Synlett; vol. 29; nb. 4; (2018); p. 452 - 456; Art.No: ST-2017-W0695-L, View in Reaxys 2a

Rodriguez, Alain Louis; Bunlaksananusorn, Tanasri; Knochel, Paul; Organic Letters; vol. 2; nb. 21; (2000); p. 3285 - 3287, View in Reaxys; Demir, Ayhan S.; Hamamci, Haluk; Sesenoglu, Ozge; Aydogan, Feray; Capanoglu, Doga; Neslihanoglu, Rahsan; Tetrahedron Asymmetry; vol. 12; nb. 13; (2001); p. 1953 - 1956, View in Reaxys; Benati, Luisa; Leardini, Rino; Minozzi, Matteo; Nanni, Daniele; Spagnolo, Piero; Strazzari, Samantha; Zanardi, Giuseppe; Calestani, Gianluca; Tetrahedron; vol. 58; nb. 18; (2002); p. 3485 - 3492, View in Reaxys; Tanabe, Yoo; Mitarai, Kumi; Higashi, Takahiro; Misaki, Tomonori; Nishii, Yoshinori; Chemical Communications; nb. 21; (2002); p. 2542 2543, View in Reaxys; Watanabe, Shin-Ichi; Ikeda, Takahiro; Kataoka, Tadashi; Tanabe, Genzoh; Muraoka, Osamu; Organic Letters; vol. 5; nb. 4; (2003); p. 565 - 567, View in Reaxys; Sano, Shigeki; Takemoto, Yuka; Nagao, Yoshimitsu; Tetrahedron Letters; vol. 44; nb. 49; (2003); p. 8853 - 8855, View in Reaxys; Cui, Sun-Liang; Lin, XuFeng; Wang, Yan-Guang; Journal of Organic Chemistry; vol. 70; nb. 7; (2005); p. 2866 - 2869, View in Reaxys; Concellon, Jose M.; Concellon, Carmen; Diaz, Pamela; European Journal of Organic Chemistry; nb. 9; (2006); p. 2197 2200, View in Reaxys; Singh, Fateh V.; Vatsyayan, Rit; Roy, Uma; Goel, Atul; Bioorganic and Medicinal Chemistry Letters; vol. 16; nb. 10; (2006); p. 2734 - 2737, View in Reaxys; Cho, Chan Sik; Ren, Wen Xiu; Shim, Sang Chul; Tetrahedron Letters; vol. 48; nb. 27; (2007); p. 4665 - 4667, 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; Guo, Songjin; Yu, Jin-Tao; Dai, Qiang; Yang, Haitao; Cheng, Jiang; Chemical Communications; vol. 50; nb. 47; (2014); p. 6240 - 6242, View in Reaxys; Liu, Yangyang; Xie, Aming; Li, Junjian; Xu, Xiao; Dong, Wei; Wang, Boliang; Tetrahedron; vol. 70; nb. 52; (2014); p. 9791 - 9796, View in Reaxys; Mondal, Buddhadeb; Sahoo, Subas Chandra; Pan, Subhas Chandra; European Journal of Organic Chemistry; vol. 2015; nb. 14; (2015); p. 3135 - 3140, View in Reaxys; Ghosh, Monoranjan; Mishra, Subhajit; Hajra, Alakananda; Journal of Organic Chemistry; vol. 80; nb. 10; (2015); p. 5364 - 5368, View in Reaxys; Zhao, Jinwu; Liu, Li; Xiang, Shijian; Liu, Qiang; Chen, Huoji; Organic and Biomolecular Chemistry; vol. 13; nb. 20; (2015); p. 5613 - 5616, View in Reaxys; Fernndez-Salas, Jos A.; Marelli, Enrico; Cordes, David B.; Slawin, Alexandra M.Z.; Nolan, Steven P.; Chemistry - A European Journal; vol. 21; nb. 10; (2014); p. 3906 - 3909, View in Reaxys; Pilgrim, Ben S.; Gatland, Alice E.; Esteves, Carlos H. A.; McTernan, Charlie T.; Jones, Geraint R.; Tatton, Matthew R.; Procopiou, Panayiotis A.; Donohoe, Timothy J.; Organic and Biomolecular Chemistry; vol. 14; nb. 3; (2016); p. 1065 1090, View in Reaxys; Li, Chengliang; Jin, Tao; Zhang, Xinglu; Li, Chunju; Jia, Xueshun; Li, Jian; Organic Letters; vol. 18; nb. 8; (2016); p. 1916 - 1919, View in Reaxys; Li, Jing; Wang, Zhong-Xia; Organic and Biomolecular Chemistry; vol. 14; nb. 31; (2016); p. 7579 - 7584, View in Reaxys; Zhu, Meijuan; Wang, Chao; Tang, Weijun; Xiao, Jianliang; Tetrahedron Letters; vol. 56; nb. 48; (2015); p. 6758 - 6761, View in Reaxys; Chang, Li-Ming; Yuan, GaoQing; Tetrahedron; vol. 72; nb. 44; (2016); p. 7003 - 7007, View in Reaxys; Zhan, Jun-Long; Wu, Meng-Wei; Chen, Fei; Han, Bing; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11994 - 12000, View in Reaxys; Xu, JingWen; Ji, Peng-Yi; Liu, Yu-Feng; Luo, Wei-Ping; Liu, Qiang; Guo, Can-Cheng; European Journal of Organic Chemistry; vol. 2017; nb. 3; (2017); p. 734 - 740, View in Reaxys; Qian, Ping; Deng, Yu; Mei, Haibo; Han, Jianlin; Pan, Yi; Chemical Communications; vol. 53; nb. 20; (2017); p. 2958 - 2961, View in Reaxys; Patent; Henan Normal University; Zhang Xinying; Fan Xuesen; Wang Ze; Chen Guang; (12 pag.); CN106749020; (2017); (A) Chinese, View in Reaxys; Patent; Henan Normal University; Fan Xuesen; Wang Ze; Zhang Xinying; Chen Guang; (18 pag.); CN106749238; (2017); (A) Chinese, View in Reaxys; Cicco, Luciana; Rodríguez-Álvarez, María J.; Perna, Filippo M.; García-Álvarez, Joaquín; Capriati, Vito; Green Chemistry; vol. 19; nb. 13; (2017); p. 3069 - 3077, View in Reaxys; Liu, Qi; Tang, Xinjun; Cai, Yujuan; Ma, Shengming; Organic Letters; vol. 19; nb. 19; (2017); p. 5174 - 5177, View in Reaxys; Levitre, Guillaume; Dumoulin, Audrey; Retailleau, Pascal; Panossian, Armen; Leroux, Frédéric R.; Masson, Géraldine; Journal of Organic Chemistry; vol. 82; nb. 22; (2017); p. 11877 - 11883, View in Reaxys; Xia, Tian; Wei, Zhihong; Spiegelberg, Brian; Jiao, Haijun; Hinze, Sandra; de Vries, Johannes G.; Chemistry - A European Journal; vol. 24; nb. 16; (2018); p. 4043 - 4049, View in Reaxys

Patonay; Hajdu; Jeko; Levai; Micskei; Zucchi; Tetrahedron Letters; vol. 40; nb. 7; (1999); p. 1373 - 1374, View in Reaxys; Nooshabadi, Masoud; Aghapoor, Kioumars; Darabi, Hossein Reza; Mojtahedi, Mohammad Majid; Tetrahedron Letters; vol. 40; nb. 42; (1999); p. 7549 - 7552, View in Reaxys; Xi, Qi; Lin, Xingji; Chang, Jianhua; Ding, Yixiang; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 178; nb. 1; (2003); p. 47 - 54, View in Reaxys; Fujiwara, Shin-Ichi; Nishiyama, Akira; Shin-ike, Tsutomu; Kambe, Nobuaki; Sonoda, Noboru; Organic Letters; vol. 6; nb. 3; (2004); p. 453 - 455, View in Reaxys; Yan, Xiao-Xia; Liang, Chun-Gen; Zhang, Yan; Hong, Wei; Cao, Bo-Xun; Dai, Li-Xin; Hou, Xue-Long; Angewandte Chemie - International Edition; vol. 44; nb. 40; (2005); p. 6544 - 6546, View in Reaxys; Horiuchi, Yoshihiro; Gnanadesikan, Vijay; Ohshima, Takashi; Masu, Hyuma; Katagiri, Kosuke; Sei, Yoshihisa; Yamaguchi, Kentaro; Shibasaki, Masakatsu; Chemistry - A European Journal; vol. 11; nb. 18; (2005); p. 5195 - 5204, View in Reaxys; Zheng, Wen-Hua; Zheng, Bao-Hui; Zhang, Yan; Hou, Xue-Long; Journal of the American Chemical Society; vol. 129; nb. 25; (2007); p. 7718 - 7719, View in Reaxys; Berke,

5/126

2018-07-03 19:01:53

Duan; Jakubec, Pavol; Winklerova, Dagmar; Povaanec, Frantiek; Daich, Adam; Organic and Biomolecular Chemistry; vol. 5; nb. 1; (2007); p. 121 - 124, View in Reaxys; Jiang, Jian-An; Du, Cai-Yan; Gu, Chun-Hui; Ji, Ya-Fei; Synlett; vol. 23; nb. 20; (2012); p. 2965 - 2968, View in Reaxys; Jiang, Jian-An; Huang, Wei-Bin; Zhai, Jiao-Jiao; Liu, Hong-Wei; Cai, Qi; Xu, Liu-Xin; Wang, Wei; Ji, Ya-Fei; Tetrahedron; vol. 69; nb. 2; (2013); p. 627 - 635, View in Reaxys; Yang, Yuzhu; Yao, Jinzhong; Zhang, Yuhong; Organic Letters; vol. 15; nb. 13; (2013); p. 3206 3209, View in Reaxys; Lim, Young Jo; Kim, Dae Young; Bulletin of the Korean Chemical Society; vol. 34; nb. 7; (2013); p. 1955 - 1956, View in Reaxys; Wei, Yu; Tang, Jinghua; Cong, Xuefeng; Zeng, Xiaoming; Green Chemistry; vol. 15; nb. 11; (2013); p. 3165 - 3169, View in Reaxys; Jiang, Qing; Xu, Bin; Zhao, An; Jia, Jing; Liu, Tian; Guo, Cancheng; Journal of Organic Chemistry; vol. 79; nb. 18; (2014); p. 8750 - 8756, View in Reaxys; Ghosh, Monoranjan; Mishra, Subhajit; Monir, Kamarul; Hajra, Alakananda; Organic and Biomolecular Chemistry; vol. 13; nb. 1; (2015); p. 309 - 314, View in Reaxys; Zhu, Cuiju; Zhang, Yuanfei; Zhao, Huaiqing; Huang, Shijun; Zhang, Min; Su, Weiping; Advanced Synthesis and Catalysis; vol. 357; nb. 2-3; (2015); p. 331 - 338, View in Reaxys; Moriuchi, Toshiyuki; Fukui, Yasuhiro; Kato, Satoshi; Kajikawa, Tomomi; Hirao, Toshikazu; Journal of Inorganic Biochemistry; vol. 147; (2015); p. 177 - 180, View in Reaxys; Du, Juan; Zhang, Xiuli; Sun, Xi; Wang, Lei; Chemical Communications; vol. 51; nb. 21; (2015); p. 4372 - 4375, View in Reaxys; Liang, Yu-Feng; Wu, Kai; Song, Song; Li, Xinyao; Huang, Xiaoqiang; Jiao, Ning; Organic Letters; vol. 17; nb. 4; (2015); p. 876 - 879, View in Reaxys; Grigalunas, Michael; Ankner, Tobias; Norrby, Per-Ola; Wiest, Olaf; Helquist, Paul; Journal of the American Chemical Society; vol. 137; nb. 22; (2015); p. 7019 - 7022, View in Reaxys; Siddaraju, Yogesh; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 13; nb. 24; (2015); p. 6749 - 6753, View in Reaxys; Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.; Organic Letters; vol. 17; nb. 13; (2015); p. 3222 - 3225, 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; Liu, Chunli; Wei, Wei; Yang, Daoshan; Zheng, Yuanyuan; Bi, Yanshuai; Chen, Min; Wang, Hua; Tetrahedron; vol. 71; nb. 38; (2015); p. 6901 - 6906, View in Reaxys; Siddaraju, Yogesh; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 13; nb. 48; (2015); p. 11651 - 11656, View in Reaxys; Jie, Xiaoming; Shang, Yaping; Zhang, Xiaofeng; Su, Weiping; Journal of the American Chemical Society; vol. 138; nb. 17; (2016); p. 5623 - 5633, View in Reaxys; Cinar, M. Emin; Engelen, Bernward; Panthöfer, Martin; Deiseroth, Hans-Jörg; Schlirf, Jens; Schmittel, Michael; Beilstein Journal of Organic Chemistry; vol. 12; (2016); p. 813 - 824, View in Reaxys; Dighe, Shashikant U.; Mukhopadhyay, Sushobhan; Priyanka, Kumari; Batra, Sanjay; Organic Letters; vol. 18; nb. 17; (2016); p. 4190 - 4193, View in Reaxys; Yang, Zhao; Liu, Chengkou; Zeng, Yu; Zhang, Jingming; Wang, Zhixiang; Fang, Zheng; Guo, Kai; RSC Advances; vol. 6; nb. 92; (2016); p. 89181 - 89184, View in Reaxys; Liang, Sen; Zeng, Cheng-Chu; Tian, Hong-Yu; Sun, Bao-Guo; Luo, Xu-Gang; Ren, Fa-Zheng; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11565 - 11573, View in Reaxys; Liu, Weibing; Chen, Cui; Zhou, Peng; Journal of Organic Chemistry; vol. 82; nb. 4; (2017); p. 2219 - 2222, View in Reaxys; Peng, Youbin; Liu, Juan; Qi, Chaorong; Yuan, Gaoqing; Li, Jiawei; Jiang, Huanfeng; Chemical Communications; vol. 53; nb. 18; (2017); p. 2665 - 2668, View in Reaxys; Liu, Weibing; Tan, Hua; Chen, Cui; Pan, Yupeng; Advanced Synthesis and Catalysis; vol. 359; nb. 9; (2017); p. 1594 - 1598, View in Reaxys; Dey, Amrita; Ali, Md Ashif; Jana, Sourav; Hajra, Alakananda; Journal of Organic Chemistry; vol. 82; nb. 9; (2017); p. 4812 - 4818, View in Reaxys; Tiweri, Dipak Kumar; Phanindrudu, Mandalaparthi; Wakade, Sandip Balasaheb; Nanubolu, Jagadeesh Babu; Tiwari, Dharmendra Kumar; Chemical Communications; vol. 53; nb. 38; (2017); p. 5302 - 5305, View in Reaxys; Tian, Miaomiao; Shi, Xiaonan; Zhang, Xinying; Fan, Xuesen; Journal of Organic Chemistry; vol. 82; nb. 14; (2017); p. 7363 - 7372, View in Reaxys; Patent; Henan Normal University; Fan Xuesen; Tian Miaomiao; Zhang Xinying; Shi Xiaonan; (15 pag.); CN107089950; (2017); (A) Chinese, View in Reaxys; Patent; Henan Normal University; Zhang Xinying; Wang Qianqian; Fan Xuesen; Wang Zhangxin; (12 pag.); CN107141209; (2017); (A) Chinese, View in Reaxys; Patent; Henan Normal University; Zhang Xinying; Fan Xuesen; Tian Miaomiao; Shi Xiaonan; (14 pag.); CN107141258; (2017); (A) Chinese, View in Reaxys; Chen, Guang; Wang, Ze; Zhang, Xinying; Fan, Xuesen; Journal of Organic Chemistry; vol. 82; nb. 20; (2017); p. 11230 - 11237, View in Reaxys; Liang, Sen; Zeng, Cheng-Chu; Tian, Hong-Yu; Sun, Bao-Guo; Luo, Xu-Gang; Ren, Fa-Zheng; Advanced Synthesis and Catalysis; vol. 360; nb. 7; (2018); p. 1444 - 1452, View in Reaxys; Li, Jiao; Yang, Zan; Yang, Tao; Yi, Jianmin; Zhou, Congshan; New Journal of Chemistry; vol. 42; nb. 3; (2018); p. 1581 - 1584, View in Reaxys; Patent; Henan Normal University; Fan Xuesen; Chen Guang; Zhang Xinying; Wang Ze; (12 pag.); CN107739332; (2018); (A) Chinese, View in Reaxys; Li, Hongyi; Jiang, Quandi; Jie, Xiaoming; Shang, Yaping; Zhang, Yuanfei; Goossen, Lukas J.; Su, Weiping; ACS Catalysis; vol. 8; nb. 6; (2018); p. 4777 - 4782, View in Reaxys 4b

Miyamoto, Hisakazu; Kanetaka, Shotaro; Tanaka, Koichi; Yoshizawa, Kazuhiro; Toyota, Shinji; Toda, Fumio; Chemistry Letters; nb. 8; (2000); p. 888 - 889, View in Reaxys; Vinogradov; Gorshkova; Chel'tsova; Pavlov; Razmanov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 52; nb. 2; (2003); p. 471 - 479, View in Reaxys; Reetz, Manfred T.; Guo, Hongchao; Synlett; nb. 13; (2006); p. 2127 - 2129, View in Reaxys; Sani Souna Sido, Abdelkarim; Chassaing, Stefan; Kumarraja, Mayilvasagam; Pale, Patrick; Sommer, Jean; Tetrahedron Letters; vol. 48; nb. 33; (2007); p. 5911 - 5914, 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; Ríos-Lombardía, Nicolás; Vidal, Cristian; Cocina, María; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Chemical Communications; vol. 51; nb. 54; (2015); p. 10937 - 10940, View in Reaxys; Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko; Journal of Organic Chemistry; vol. 81; nb. 12; (2016); p. 5101 - 5119, 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; 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; Hu,

6/126

2018-07-03 19:01:53

Yongke; Chen, Lei; Li, Bindong; Catalysis Communications; vol. 103; (2018); p. 42 - 46, View in Reaxys; Yang, Yiwen; Zhong, Wei; Nie, Binmei; Chen, Jiangmin; Wei, Zhenhong; Liu, Xiaoming; Journal of Organometallic Chemistry; vol. 853; (2017); p. 136 - 142, View in Reaxys; González Miera, Greco; Martínez-Castro, Elisa; Martín-Matute, Belén; Organometallics; vol. 37; nb. 5; (2018); p. 636 - 644, View in Reaxys 7

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; Dixon, Darren J.; Guarna, Antonio; Ley, Steven V.; Polara, Alessandra; Rodriguez, Felix; Synthesis; nb. 14; (2002); p. 1973 - 1978, View in Reaxys; Eames, Jason; Coumbarides, Gregory S.; Suggate, Michael J.; Weerasooriya, Neluka; European Journal of Organic Chemistry; nb. 4; (2003); p. 634 - 641, View in Reaxys; Wiedemann, Stefan; Frank, Daniel; Winsel, Harald; De Meijere, Armin; Organic Letters; vol. 5; nb. 5; (2003); p. 753 - 755, View in Reaxys; Deng, ChenLiang; Song, Ren-Jie; Guo, Sheng-Mei; Wang, Zhi-Qiang; Li, Jin-Heng; Organic Letters; vol. 9; nb. 24; (2007); p. 5111 - 5114, View in Reaxys; Wang, Wengui; Shen, Haiming; Wan, Xiao-Long; Chen, Qing-Yun; Guo, Yong; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6347 - 6353, View in Reaxys; Abdellatif, Khaled R. A.; Lamie, Phoebe F.; Omar, Hany A.; Journal of Enzyme Inhibition and Medicinal Chemistry; vol. 31; nb. 2; (2016); p. 318 324, View in Reaxys; Campbell, McKenzie L.; Sulejmanovic, Dino; Schiller, Jacqueline B.; Turner, Emily M.; Hwu, Shiou-Jyh; Whitehead, Daniel C.; Catalysis Science and Technology; vol. 6; nb. 9; (2016); p. 3208 - 3213, View in Reaxys; Campbell, McKenzie L.; Sulejmanovic, Dino; Schiller, Jacqueline B.; Turner, Emily M.; Hwu, Shiou-Jyh; Whitehead, Daniel C.; Helvetica Chimica Acta; vol. 100; nb. 3; (2017), View in Reaxys; Chen, Xiu-Wen; Zhao, He; Chen, Chun-Lian; Jiang, Huan-Feng; Zhang, Min; Angewandte Chemie - International Edition; vol. 56; nb. 45; (2017); p. 14232 - 14236; Angew. Chem.; vol. 129; (2017); p. 14420 - 14424,5, View in Reaxys; Cao, Xiao-Niu; Wan, Xiao-Min; Yang, Fa-Liu; Li, Ke; Hao, Xin-Qi; Shao, Tian; Zhu, Xinju; Song, Mao-Ping; Journal of Organic Chemistry; vol. 83; nb. 7; (2018); p. 3657 - 3668, View in Reaxys

Peng, Weimin; Shreeve, Jean'ne M.; Journal of Organic Chemistry; vol. 70; nb. 14; (2005); p. 5760 - 5763, View in Reaxys; Mori, Yoshikazu; Seki, Masahiko; Advanced Synthesis and Catalysis; vol. 349; nb. 11-12; (2007); p. 2027 - 2038, View in Reaxys; Wang, Yuanyuan; Wu, Yuetong; Wang; Dai, Liyi; Chinese Journal of Chemistry; vol. 30; nb. 8; (2012); p. 1709 - 1714, View in Reaxys; Ma, Ran; He, Liang-Nian; Liu, An-Hua; Song, Qing-Wen; Chemical Communications; vol. 52; nb. 10; (2016); p. 2145 - 2148, View in Reaxys; Khalili, Dariush; New Journal of Chemistry; vol. 40; nb. 3; (2016); p. 2547 - 2553, View in Reaxys; Kollár, László; Pongrácz, Péter; Journal of Organometallic Chemistry; vol. 866; (2018); p. 184 - 188, View in Reaxys

Pravst, Igor; Zupan, Marko; Stavber, Stojan; Tetrahedron Letters; vol. 47; nb. 27; (2006); p. 4707 - 4710, 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; Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul; Synthesis; nb. 24; (2007); p. 3877 - 3885, View in Reaxys; Madumo, Gilbert K.; Moshapo, Paseka T.; Kinfe, Henok H.; Medicinal Chemistry Research; vol. 27; nb. 3; (2018); p. 817 - 833, View in Reaxys

Ghosh, Rina; Maiti, Swarupananda; Chakraborty, Arijit; Synlett; nb. 1; (2005); p. 115 - 118; Art.No: G32904ST, View in Reaxys; Matsukawa, Yohei; Isobe, Minoru; Kotsuki, Hiyoshizo; Ichikawa, Yoshiyasu; Journal of Organic Chemistry; vol. 70; nb. 13; (2005); p. 5339 - 5341, 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; Consiglio, Gabriella Barozzino; Mordini, Alessandro; Letters in Organic Chemistry; vol. 15; nb. 5; (2018); p. 447 - 454, View in Reaxys

Park, Jungmin; Yeon, Jihee; Lee, Phil Ho; Lee, Kooyeon; Tetrahedron Letters; vol. 54; nb. 33; (2013); p. 4414 4417, View in Reaxys; Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei; Organic Letters; vol. 17; nb. 6; (2015); p. 1469 - 1472, View in Reaxys; Huo, Congde; Wu, Mingxia; Chen, Fengjuan; Jia, Xiaodong; Yuan, Yong; Xie, Haisheng; Chemical Communications; vol. 51; nb. 22; (2015); p. 4708 - 4711, View in Reaxys; Wang, Rongzhou; Fan, Hongjun; Zhao, Wei; Li, Feng; Organic Letters; vol. 18; nb. 15; (2016); p. 3558 - 3561, View in Reaxys; Li, Kangnan; Shao, Xinxin; Tseng, Luke; Malcolmson, Steven J.; Journal of the American Chemical Society; vol. 140; nb. 2; (2018); p. 598 - 601, View in Reaxys

Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng; Organic Letters; vol. 17; nb. 6; (2015); p. 1521 - 1524, View in Reaxys; Jia, Zhifang; Wang, Kewei; Tan, Bien; Gu, Yanlong; Advanced Synthesis and Catalysis; vol. 359; nb. 1; (2017); p. 78 - 88, View in Reaxys; Bao, Yishu; Yang, Xiuqin; Zhou, Qingfa; Yang, Fulai; Organic Letters; vol. 20; nb. 7; (2018); p. 1966 - 1969, View in Reaxys

Lou, Zhen-Bang; Pang, Xin-Long; Chen, Chao; Wen, Li-Rong; Li, Ming; Chinese Chemical Letters; vol. 26; nb. 10; (2015); p. 1231 - 1235, View in Reaxys; Patent; CÓRDOVA, Armando; PALO-NIETO, Carlos; AFEWERKI, Samson; (46 pag.); WO2016/96905; (2016); (A1) English, View in Reaxys; Palo-Nieto, Carlos; Afewerki, Samson; Anderson, Mattias; Tai, Cheuk-Wai; Berglund, Per; Córdova, Armando; ACS Catalysis; vol. 6; nb. 6; (2016); p. 3932 3940, View in Reaxys; Xu, Jiancong; Liu, Yang; Wang, Ying; Li, Yajuan; Xu, Xiaohua; Jin, Zhong; Organic Letters; vol. 19; nb. 7; (2017); p. 1562 - 1565, View in Reaxys; Qin, Chao; Hou, Chuan-Jin; Liu, Hongzhu; Liu, YanJun; Huang, De-Zhi; Hu, Xiang-Ping; Tetrahedron Letters; vol. 59; nb. 8; (2018); p. 719 - 722, View in Reaxys

Yang, Xiaodong; She, Yue; Chong, Ya; Zhai, Huichun; Zhu, He; Chen, Baohua; Huang, Guosheng; Yan, Rulong; Advanced Synthesis and Catalysis; vol. 358; nb. 19; (2016); p. 3130 - 3134, View in Reaxys; Patent; Shandong University; Li Mingli; Zhang Na; (9 pag.); CN105198841; (2017); (B) Chinese, View in Reaxys; Jiang, He-Yan; Xu, Jie; Sun, Bin; Applied Organometallic Chemistry; vol. 32; nb. 4; (2018); Art.No: E4260, View in Reaxys

7/126

2018-07-03 19:01:53

Morozzi, Chiara; Rosati, Ornelio; Curini, Massimo; Lanari, Daniela; Synlett; vol. 29; nb. 1; (2018); p. 126 - 130; Art.No: ST-2017-B0386-L, View in Reaxys

Parua, Seuli; Sikari, Rina; Sinha, Suman; Das, Siuli; Chakraborty, Gargi; Paul, Nanda D.; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 274 - 284, 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

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

Tan, Xuefeng; Gao, Shuang; Zeng, Weijun; Xin, Shan; Yin, Qin; Zhang, Xumu; Journal of the American Chemical Society; vol. 140; nb. 6; (2018); p. 2024 - 2027, 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

14b

Wang, Qingfu; Chai, Huining; Yu, Zhengkun; Organometallics; vol. 37; nb. 4; (2018); p. 584 - 591, View in Reaxys

a13

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

Noland, Wayland E.; Brown, Christopher D.; Zabronsky, Abigail E.; Tritch, Kenneth J.; Tetrahedron; vol. 74; nb. 19; (2018); p. 2391 - 2404, View in Reaxys

A%4&

Wisser, Florian M.; Mohr, Yorck; Quadrelli, Elsje Alessandra; Farrusseng, David; Canivet, Jérôme; ChemCatChem; vol. 10; nb. 8; (2018); p. 1778 - 1782, View in Reaxys

Martínez-Montero, Lía; Gotor, Vicente; Gotor-Fernández, Vicente; Lavandera, Iván; ACS Catalysis; vol. 8; nb. 3; (2018); p. 2413 - 2419, View in Reaxys

T5-3

Meng, Mengting; Yang, Liangfeng; Cheng, Kai; Qi, Chenze; Journal of Organic Chemistry; vol. 83; nb. 6; (2018); p. 3275 - 3284, 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

23a

Nakamura; Matsuda; Journal of Organic Chemistry; vol. 63; nb. 24; (1998); p. 8957 - 8964, View in Reaxys; Chen, Ming; Zhao, Xinxin; Yang, Chao; Xia, Wujiong; Organic Letters; vol. 19; nb. 14; (2017); p. 3807 - 3810, View in Reaxys

Firouzabadi, Habib; Karimi, Babak; Abbassi, Mohammad; Journal of Chemical Research - Part S; nb. 3; (1999); p. 236 - 237, View in Reaxys; Kase, Koichiro; Katayama, Mitsuhiro; Konno, Tsutomu; Ishihara, Takashi; Yamanaka, Hiroki; Gupton, John T.; Journal of Fluorine Chemistry; vol. 120; nb. 1; (2003); p. 33 - 39, View in Reaxys; Cho, Chan Sik; Seok, Hyo Jin; Shim, Sang Chul; Journal of Heterocyclic Chemistry; vol. 42; nb. 6; (2005); p. 1219 - 1222, View in Reaxys; Tani, Yosuke; Yamaguchi, Tatsuya; Fujihara, Tetsuaki; Terao, Jun; Tsuji, Yasushi; Chemistry Letters; vol. 44; nb. 3; (2015); p. 271 - 273, View in Reaxys; Mayo, Muhammad Shareef; Yu, Xiaoqiang; Feng, Xiujuan; Yamamoto, Yoshinori; Bao, Ming; Journal of Organic Chemistry; vol. 80; nb. 8; (2015); p. 3998 - 4002, View in Reaxys; Erbing, Elis; Vázquez-Romero, Ana; Bermejo Gómez, Antonio; Platero-Prats, Ana E.; Carson, Fabian; Zou, Xiaodong; Tolstoy, Päivi; Martín-Matute, Belén; Chemistry - A European Journal; vol. 22; nb. 44; (2016); p. 15659 - 15663, View in Reaxys; Yang, Kai; Dang, Qun; Cai, Pei-Jun; Gao, Yang; Yu, Zhi-Xiang; Bai, Xu; Journal of Organic Chemistry; vol. 82; nb. 5; (2017); p. 2336 - 2344, View in Reaxys

Tsuchimoto; Joya; Shirakawa; Kawakami; Synlett; nb. 12; (2000); p. 1777 - 1778, View in Reaxys; Wu, Yi-Lung; Chuang, Che-Ping; Lin, Pi-Yun; Tetrahedron; vol. 57; nb. 26; (2001); p. 5543 - 5549, View in Reaxys; Tokunaga, Makoto; Shirogane, Yuki; Aoyama, Hiroshi; Obora, Yasushi; Tsuji, Yasushi; Journal of Organometallic Chemistry; vol. 690; nb. 23; (2005); p. 5378 - 5382, View in Reaxys; 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; Liu, Xigong; Sun, Bin; Xie, Zhiyu; Qin, Xiaojun; Liu, Lei; Lou, Hongxiang; Journal of Organic Chemistry; vol. 78; nb. 7; (2013); p. 3104 - 3112, View in Reaxys; Singh, Kamal Nain; Singh, Paramjit; Singh, Pushpinder; Maheshwary, Yogita; Kessar, Satinder V.; Batra, Aanchal; Synlett; vol. 24; nb. 15; (2013); p. 1963 1967; Art.No: ST-2013-B0357-L, View in Reaxys; Ma, Xiaofeng; Zhang, Jichao; Tang, Qin; Ke, Jun; Zou, Wei; Shao, Huawu; Chemical Communications; vol. 50; nb. 26; (2014); p. 3505 - 3508, View in Reaxys; Zhu, Yanfang; Cai, Chun; RSC Advances; vol. 4; nb. 95; (2014); p. 52911 - 52914, View in Reaxys; Wusiman, Abudureheman; Lu, Chong-Dao; Applied Organometallic Chemistry; vol. 29; nb. 4; (2015); p. 254 - 258, View in Reaxys; Aegurla, Balakrishna; Peddinti, Rama Krishna; Organic and Biomolecular Chemistry; vol. 15; nb. 45; (2017); p. 9643 - 9652, View in Reaxys

Hon, Yung-Son; Hsu, Tzyy-Rong; Chen, Chun-Yan; Lin, Yi-Hui; Chang, Fong-Jong; Hsieh, Cheng-Han; Szu, Ping-Hui; Tetrahedron; vol. 59; nb. 9; (2003); p. 1509 - 1520, View in Reaxys; Ma, Yaping; Liu, Hui; Chen, Li; Cui, Xin; Zhu, Jin; Deng, Jingen; Organic Letters; vol. 5; nb. 12; (2003); p. 2103 - 2106, View in Reaxys; Eustache, Florence; Dalko, Peter I.; Cossy, Janine; Tetrahedron Letters; vol. 44; nb. 49; (2003); p. 8823 - 8826, View in Reaxys; Hayes, Aidan M.; Morris, David J.; Clarkson, Guy J.; Wills, Martin; Journal of the American Chemical Society;

8/126

2018-07-03 19:01:53

vol. 127; nb. 20; (2005); p. 7318 - 7319, View in Reaxys; Dohi, Toshifumi; Maruyama, Akinobu; Yoshimura, Misaki; Morimoto, Koji; Tohma, Hirofumi; Shiro, Motoo; Kita, Yasuyuki; Chemical Communications; nb. 17; (2005); p. 2205 - 2207, View in Reaxys; Vaestilae, Patrik; Wettergren, Jenny; Adolfsson, Hans; Chemical Communications; nb. 32; (2005); p. 4039 - 4041, View in Reaxys; Pandit, Rameshwar Prasad; Lee, Yong Rok; Bulletin of the Korean Chemical Society; vol. 33; nb. 11; (2012); p. 3559 - 3564, View in Reaxys; Pieri, Cyril; Brunel, Jean Michel; Letters in Drug Design and Discovery; vol. 12; nb. 6; (2015); p. 448 - 456, View in Reaxys; Teng, Bo; Chen, Wenchao; Dong, Shen; Kee, Choon Wee; Gandamana, Dhika Aditya; Zong, Lili; Tan, Choon-Hong; Journal of the American Chemical Society; vol. 138; nb. 31; (2016); p. 9935 - 9940, View in Reaxys; Obermayer, David; Znidar, Desiree; Glotz, Gabriel; Stadler, Alexander; Dallinger, Doris; Oliver Kappe; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11788 - 11801, View in Reaxys; Orr, Robert K.; Campeau, Louis-Charles; Chobanian, Harry R.; McCabe Dunn, Jamie M.; Pio, Barbara; Plummer, Christopher W.; Nolting, Andrew; Ruck, Rebecca T.; Synthesis (Germany); vol. 49; nb. 3; (2017); p. 657 - 666; Art.No: SS-2016-M0494-OP, View in Reaxys; Ismalaj, Ermal; Glenadel, Quentin; Billard, Thierry; European Journal of Organic Chemistry; vol. 2017; nb. 14; (2017); p. 1911 - 1914, View in Reaxys 32

Dieter, R. Karl; Sharma, Ram R.; Yu, Huayun; Gore, Vinayak K.; Tetrahedron; vol. 59; nb. 7; (2003); p. 1083 1094, 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; Tanemura, Kiyoshi; Suzuki, Tsuneo; Tetrahedron Letters; vol. 58; nb. 10; (2017); p. 955 - 958, View in Reaxys

Basavaiah, Deevi; Reddy, Gone Jayapal; Chandrashekar, Vanampally; Tetrahedron Asymmetry; vol. 15; nb. 1; (2004); p. 47 - 52, View in Reaxys; Reetz, Manfred T.; Li, Xiaoguang; Journal of the American Chemical Society; vol. 128; nb. 4; (2006); p. 1044 - 1045, View in Reaxys; Zhang, Jinli; Han, Zixing; Li, Junmiao; Wu, Yangjie; Arkivoc; vol. 2013; nb. 4; (2013); p. 251 - 271, View in Reaxys; Bouhachicha; Ngo Ndimba; Roisnel; Lalli; Argouarch; New Journal of Chemistry; vol. 41; nb. 12; (2017); p. 4767 - 4770, View in Reaxys

Gnanadesikan, Vijay; Horiuchi, Yoshihiro; Ohshima, Takashi; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 126; nb. 25; (2004); p. 7782 - 7783, View in Reaxys; Ito, Masato; Kitahara, Sachiko; Ikariya, Takao; Journal of the American Chemical Society; vol. 127; nb. 17; (2005); p. 6172 - 6173, View in Reaxys; Tesevic, Verona; Gladysz; Journal of Organic Chemistry; vol. 71; nb. 19; (2006); p. 7433 - 7440, View in Reaxys; Lamani, Manjunath; Prabhu, Kandikere Ramaiah; Chemistry - A European Journal; vol. 18; nb. 46; (2012); p. 14638 - 14642, 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; Gandeepan, Parthasarathy; Rajamalli; Cheng, Chien-Hong; ACS Catalysis; vol. 4; nb. 12; (2014); p. 4485 - 4489, View in Reaxys; Sathyanarayana, Pochampalli; Ravi, Owk; Muktapuram, Prathap Reddy; Bathula, Surendar Reddy; Organic and Biomolecular Chemistry; vol. 13; nb. 37; (2015); p. 9681 - 9685, View in Reaxys; Yousuf, Md; Das, Tuluma; Adhikari, Susanta; New Journal of Chemistry; vol. 39; nb. 11; (2015); p. 8763 - 8770, View in Reaxys; Ravi, Owk; Shaikh, Altab; Upare, Atul; Singarapu, Kiran Kumar; Bathula, Surendar Reddy; Journal of Organic Chemistry; vol. 82; nb. 8; (2017); p. 4422 - 4428, View in Reaxys; Suchand, Basuli; Satyanarayana, Gedu; European Journal of Organic Chemistry; vol. 2017; nb. 26; (2017); p. 3886 - 3895, View in Reaxys; Han, Jianwei; Guo, Xin; Liu, Yafeng; Fu, Yajie; Yan, Rulong; Chen, Baohua; Advanced Synthesis and Catalysis; vol. 359; nb. 15; (2017); p. 2676 - 2681, View in Reaxys

Hou; Wang; Huang; Chen; Organic Preparations and Procedures International; vol. 36; nb. 5; (2004); p. 491 - 494, View in Reaxys; Oisaki, Kounosuke; Zhao, Dongbo; Kanai, Motomu; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 128; nb. 22; (2006); p. 7164 - 7165, View in Reaxys; Zhou, Zhong Shi; Li, Li; He, Xue Han; Chinese Chemical Letters; vol. 23; nb. 11; (2012); p. 1213 - 1216,4, View in Reaxys; Zhou, Zhong-Shi; Li, Li; He, Xue-Han; Journal of Chemical Research; vol. 37; nb. 10; (2013); p. 633 - 635, View in Reaxys; Wang, Ying-Chun; Wang, Heng-Shan; Huang, Guo-Bao; Huang, Fu-Ping; Hu, Kun; Pan, Ying-Ming; Tetrahedron; vol. 70; nb. 8; (2014); p. 1621 - 1628, View in Reaxys; Grigalunas, Michael; Wiest, Olaf; Helquist, Paul; Organic Letters; vol. 18; nb. 21; (2016); p. 5724 - 5727, View in Reaxys; Tan, Liquan; Chen, Cui; Liu, Weibing; Beilstein Journal of Organic Chemistry; vol. 13; (2017); p. 1079 - 1084, View in Reaxys; Chaiseeda, Kittichai; Chavasiri, Warinthorn; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 192; nb. 9; (2017); p. 1034 - 1039, View in Reaxys; Shang, Ming; Cao, Min; Wang, Qifan; Wasa, Masayuki; Angewandte Chemie - International Edition; vol. 56; nb. 43; (2017); p. 13338 - 13341; Angew. Chem.; vol. 129; (2017); p. 13523 - 13526,4, View in Reaxys

Moreau, Xavier; Bazan-Tejeda, Belen; Campagne, Jean-Marc; Journal of the American Chemical Society; vol. 127; nb. 20; (2005); p. 7288 - 7289, View in Reaxys; Gore, Sangram; Baskaran, Sundarababu; König, Burkhard; Organic Letters; vol. 14; nb. 17; (2012); p. 4568 - 4571, View in Reaxys; Nguyen, Quynh Pham Bao; Kim, Taek Hyeon; Tetrahedron; vol. 69; nb. 24; (2013); p. 4938 - 4943, 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

Ghosh, Rina; Maiti, Swarupananda; Chakraborty, Arijit; Chakraborty, Santu; Mukherjee, Alok K.; Tetrahedron; vol. 62; nb. 17; (2006); p. 4059 - 4064, View in Reaxys; Guilbault, Audrey-Anne; Basdevant, Benoit; Wanie, Vincent; Legault, Claude Y.; Journal of Organic Chemistry; vol. 77; nb. 24; (2012); p. 11283 - 11295, 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; Yang, Dongmei; Wang, Hui; Yuan, Haijian; Li, Shujun; Molecules; vol. 21; nb. 11; (2016); Art.No: 1563, View in Reaxys; Read, Jacquelyne A.; Yang, Yingying; Woerpel; Organic Letters; vol. 19; nb. 13; (2017); p. 3346 - 3349, View in Reaxys

9/126

2018-07-03 19:01:53

S10

Hawkins, Michael J.; Powell, Eugene T.; Leo, Gregory C.; Gauthier, Diane A.; Greco, Michael N.; Maryanoff, Bruce; Organic Letters; vol. 8; nb. 16; (2006); p. 3429 - 3431, View in Reaxys; Coll, Mercedes; Pamies, Oscar; Adolfsson, Hans; Dieguez, Montserrat; ChemCatChem; vol. 5; nb. 12; (2013); p. 3821 - 3828, View in Reaxys; McDonald, Ivar M.; Peese, Kevin M.; Organic Letters; vol. 17; nb. 24; (2015); p. 6002 - 6005, View in Reaxys; Zhang, Changhe; Lupton, David W.; Organic Letters; vol. 19; nb. 17; (2017); p. 4456 - 4459, View in Reaxys

Wu, Xiaofeng; Vinci, Daniele; Ikariya, Takao; Xiao, Jiangliang; Chemical Communications; nb. 35; (2005); p. 4447 - 4449, View in Reaxys; Baumann, Thomas; Vogt, Henning; Braese, Stefan; European Journal of Organic Chemistry; nb. 2; (2007); p. 266 - 282, 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; 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; Thomas, Joice; Jana, Sampad; Liekens, Sandra; Dehaen, Wim; Chemical Communications; vol. 52; nb. 59; (2016); p. 9236 - 9239, View in Reaxys; Sun, Kai; Lv, Yunhe; Chen, Yao; Zhou, Tingting; Xing, Yanyan; Wang, Xin; Organic and Biomolecular Chemistry; vol. 15; nb. 20; (2017); p. 4464 - 4467, View in Reaxys; Wagh, Ganesh D.; Akamanchi, Krishnacharya G.; Tetrahedron Letters; vol. 58; nb. 31; (2017); p. 3032 - 3036, View in Reaxys; Tang, Shi-Zhong; Zhao, Wenshuang; Chen, Tao; Liu, Yang; Zhang, Xiao-Ming; Zhang, Fu-Min; Advanced Synthesis and Catalysis; vol. 359; nb. 23; (2017); p. 4177 - 4183, View in Reaxys

Ackermann, Lutz; Spatz, Julia H.; Gschrei, Christian J.; Born, Robert; Althammer, Andreas; Angewandte Chemie - International Edition; vol. 45; nb. 45; (2006); p. 7627 - 7630, View in Reaxys; Titova, Ekaterina M.; Rahaman, S.M. Wahidur; Shubina, Elena S.; Poli, Rinaldo; Belkova, Natalia V.; Manoury, Eric; Journal of Molecular Catalysis A: Chemical; vol. 426; (2017); p. 376 - 380, View in Reaxys

Clerici, Angelo; Pastori, Nadia; Porta, Ombretta; European Journal of Organic Chemistry; nb. 19; (2002); p. 3326 3335, View in Reaxys; Zhang, Jitan; Qian, Hongsheng; Liu, Zhanxiang; Xiong, Chunhua; Zhang, Yuhong; European Journal of Organic Chemistry; vol. 2014; nb. 36; (2014); p. 8110 - 8118, View in Reaxys; Liu, Zhenghui; Yang, Zhenzhen; Yu, Xiaoxiao; Zhang, Hongye; Yu, Bo; Zhao, Yanfei; Liu, Zhimin; Organic Letters; vol. 19; nb. 19; (2017); p. 5228 - 5231, View in Reaxys

16b

Gaunt; Yu; Spencer; Chemical Communications; nb. 18; (2001); p. 1844 - 1845, 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

Chen, Fu-Xue; Zhou, Hui; Liu, Xiaohua; Qin, Bo; Feng, Xiaoming; Zhang, Guolin; Jiang, Yaozhong; Chemistry A European Journal; vol. 10; nb. 19; (2004); p. 4790 - 4797, View in Reaxys; Das, Biswanath; Reddy, Kongara Ravinder; Helvetica Chimica Acta; vol. 89; nb. 12; (2006); p. 3109 - 3111, View in Reaxys; Wu, Yile; Shan, Changkai; Ying, Jianxi; Su, Jue; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen; Green Chemistry; vol. 19; nb. 17; (2017); p. 4169 4175, 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; Gomtsyan, Arthur; Bayburt, Erol K.; Keddy, Ryan; Turner, Sean C.; Jinkerson, Tammie K.; Didomenico, Stanley; Perner, Richard J.; Koenig, John R.; Drizin, Irene; McDonald, Heath A.; Surowy, Carol S.; Honore, Prisca; Mikusa, Joe; Marsh, Kennan C.; Wetter, Jill M.; Faltynek, Connie R.; Lee, Chih-Hung; Bioorganic and Medicinal Chemistry Letters; vol. 17; nb. 14; (2007); p. 3894 - 3899, 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; Devari, Shekaraiah; Rizvi, Masood Ahmad; Shah, Bhahwal Ali; Tetrahedron Letters; vol. 57; nb. 30; (2016); p. 3294 - 3297, View in Reaxys; Wei, Xiao-Feng; Xie, Xiao-Wei; Shimizu, Yohei; Kanai, Motomu; Journal of the American Chemical Society; vol. 139; nb. 13; (2017); p. 4647 - 4650, View in Reaxys; El-Sepelgy, Osama; Brzozowska, Aleksandra; Rueping, Magnus; ChemSusChem; vol. 10; nb. 8; (2017); p. 1664 - 1668, View in Reaxys

Chandrasekhar, Sosale; Gopalaiah, Kovuru; Tetrahedron Letters; vol. 44; nb. 40; (2003); p. 7437 - 7439, View in Reaxys; Su; Zhuang; Wu; Zhong; Organic Preparations and Procedures International; vol. 39; nb. 2; (2007); p. 195 - 199, View in Reaxys; Asokan; Anabha; Thomas, Ajith Dain; Jose, Ann Maria; Lethesh; Prasanth; Krishanraj; Tetrahedron Letters; vol. 48; nb. 32; (2007); p. 5641 - 5643, View in Reaxys; Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 - 4254; Art.No: 26677, View in Reaxys; Schmidt, Elena Yu.; Tatarinova, Inna V.; Protsuk, Nadezhda I.; Ushakov, Igor A.; Trofimov, Boris A.; Journal of Organic Chemistry; vol. 82; nb. 1; (2017); p. 119 - 125, View in Reaxys

Demir, Ayhan S.; Camkerten, Nurettin; Gercek, Zuhal; Duygu, Nese; Reis, Omer; Arikan, Elif; Tetrahedron; vol. 55; nb. 8; (1999); p. 2441 - 2448, View in Reaxys; Fukuzawa, Shin-Ichi; Nakano, Narihito; Saitoh, Takahide; European Journal of Organic Chemistry; nb. 13; (2004); p. 2863 - 2867, View in Reaxys; Saitoh, Toshiaki; Abe, Kenji; Ishikawa, Masami; Nakatani, Masanao; Shimazu, Seiichiro; Satoh, Noriyuki; Yoneda, Fumio; Taguchi, Kyoji; Horiguchi, Yoshie; European Journal of Medicinal Chemistry; vol. 41; nb. 2; (2006); p. 241 - 252, 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; Sabot, Cyrille; Kumar, Kanduluru Ananda; Antheaume, Cyril; Mioskowski, Charles; Journal of Organic Chemistry; vol. 72; nb. 13; (2007); p. 5001 - 5004, View in Reaxys; Babu, Srinivasarao Arulananda; Yasuda, Makoto; Baba, Akio; Journal of Organic Chemistry; vol. 72; nb. 26; (2007); p. 10264 - 10267, View in Reaxys; Saito, Akio; Hyodo, Nao; Hanzawa, Yuji; Molecules; vol. 17; nb. 9; (2012); p. 11046 - 11055, View in Reaxys; Oudeyer, Sylvain; Leonel, Eric; Paugam, Jean Paul; Nedelec, Jean-Yves; Tetrahedron; vol. 70; nb. 4; (2014); p. 919 - 923, View in Reaxys; Wang,

10/126

2018-07-03 19:01:53

Dong; Deraedt, Christophe; Ruiz, Jaime; Astruc, Didier; Journal of Molecular Catalysis A: Chemical; vol. 400; (2015); p. 14 - 21, View in Reaxys; 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 10

Molinari, Francesco; Gandolfi, Raffaella; Villa, Raffaella; Occhiato, Ernesto G.; Tetrahedron Asymmetry; vol. 10; nb. 18; (1999); p. 3515 - 3520, View in Reaxys; Kennedy, Andrew; Nelson, Adam; Perry, Alexis; Synlett; nb. 6; (2004); p. 967 - 970, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6765 6768, View in Reaxys; Saitoh, Terunobu; Yoshida, Suguru; Ichikawa, Junji; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6414 - 6419, View in Reaxys; Li, An-Hu; Ahmed, Eilaf; Chen, Xin; Cox, Matthew; Crew, Andrew P.; Dong, Han-Qing; Jin, Meizhong; Ma, Lifu; Panicker, Bijoy; Siu, Kam W.; Steinig, Arno G.; Stolz, Kathryn M.; Tavares, Paula A. R.; Volk, Brian; Weng, Qinghua; Werner, Doug; Mulvihill, Mark J.; Organic and Biomolecular Chemistry; vol. 5; nb. 1; (2007); p. 61 - 64, 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; Jung, Michael E.; Zhang, Ting-Hu; Organic Letters; vol. 10; nb. 1; (2008); p. 137 - 140, View in Reaxys; Xu, Ze-Feng; Cai, Chen-Xin; Liu, Jin-Tao; Organic Letters; vol. 15; nb. 9; (2013); p. 2096 - 2099, View in Reaxys; Coverdale, James P. C.; Sanchez-Cano, 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; Zhang, Yuecheng; Zhao, Liyuan; Zhang, Hongyu; Huang, Rong; Zhao, Jiquan; Applied Organometallic Chemistry; vol. 31; nb. 9; (2017); Art.No: E3709, View in Reaxys; Karanfil, Abdullah; Eskici, Mustafa; Synthetic Communications; vol. 47; nb. 24; (2017); p. 2342 - 2351, View in Reaxys; Liu, Jiawang; Zheng, Shilong; Guo, Shanchun; Zhang, Changde; Zhong, Qiu; Zhang, Qiang; Ma, Peng; Skripnikova, Elena V.; Bratton, Melyssa R.; Wiese, Thomas E.; Wang, Guangdi; ACS Medicinal Chemistry Letters; vol. 8; nb. 1; (2017); p. 102 - 106, View in Reaxys

Crotti, Paolo; Di Bussolo, Valeria; Favero, Lucilla; Macchia, Franco; Pineschi, Mauro; Napolitano, Elio; Tetrahedron; vol. 55; nb. 18; (1999); p. 5853 - 5866, View in Reaxys; Ford, Alan; Woodward, Simon; Angewandte Chemie International Edition; vol. 38; nb. 3; (1999); p. 335 - 336, View in Reaxys; Habermann, Joerg; Ley, Steven V.; Smits, Rene; Journal of the Chemical Society - Perkin Transactions 1; nb. 17; (1999); p. 2421 - 2423, 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; 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; Cho, Chan Sik; Kim, Bok Tae; Lee, Myung Jin; Kim, Tae-Jeong; Shim, Sang Chul; Angewandte Chemie, International Edition; vol. 40; nb. 5; (2001); p. 958 - 960; Angewandte Chemie; vol. 113; (2001); p. 984 - 986, View in Reaxys; Salvi; Chattopadhyay; Tetrahedron; vol. 57; nb. 14; (2001); p. 2833 - 2839, View in Reaxys; Sirol, Sabine; Courmarcel, James; Mostefai, Naouel; Riant, Olivier; Organic Letters; vol. 3; nb. 25; (2001); p. 4111 - 4113, 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; Grant, Anya A.; Allukian, Myron; Fry, Albert J.; Tetrahedron Letters; vol. 43; nb. 24; (2002); p. 4391 - 4393, View in Reaxys; Chi, Yongxiang; Zhou, Yong-Gui; Zhang, Xumu; Journal of Organic Chemistry; vol. 68; nb. 10; (2003); p. 4120 - 4122, View in Reaxys; Ishimoto, Keiko; Mitoma, Yoshiharu; Nagashima, Satoko; Tashiro, Hideki; Prakash, G. K. Surya; Olah, George A.; Tashiro, Masashi; Chemical Communications; nb. 4; (2003); p. 514 - 515, View in Reaxys; Jung, Jae-Chul; Lee, Ji-Ho; Oh, Seikwan; Lee, Jae-Gon; Park, Oee-Sook; Bioorganic and Medicinal Chemistry Letters; vol. 14; nb. 22; (2004); p. 5527 - 5531, View in Reaxys; Yasuda, Makoto; Shigeyoshi, Yusuke; Shibata, Ikuya; Baba, Akio; Synthesis; nb. 2; (2005); p. 233 - 239; Art.No: F12104SS, View in Reaxys; Wang, Boyuan; Zhang, Wei; Zhang, Leilei; Du, Da-Ming; Liu, Gang; Xu, Jiaxi; European Journal of Organic Chemistry; nb. 2; (2008); p. 350 - 355, View in Reaxys; Zhang, Min; Fang, Xianjie; Neumann, Helfried; Beller, Matthias; Journal of the American Chemical Society; vol. 135; nb. 30; (2013); p. 11384 - 11388, View in Reaxys; Cazares-Marinero, Jose De Jesus; Top, Siden; Vessieres, Anne; Jaouen, Gerard; Dalton Transactions; vol. 43; nb. 2; (2014); p. 817 - 830, View in Reaxys; Feurer, Markus; Frey, Georg; Luu, Hieu-Trinh; Kratzert, Daniel; Streuff, Jan; Chemical Communications; vol. 50; nb. 40; (2014); p. 5370 - 5372, View in Reaxys; Chandrasekhar, Srivari; Patro, Vidyavathi; Chavan, Lahu N.; Chegondi, Rambabu; Gre, Ren; Tetrahedron Letters; vol. 55; nb. 43; (2014); p. 5932 - 5935, View in Reaxys; Nikam; Kappe; Journal of Heterocyclic Chemistry; vol. 52; nb. 1; (2015); p. 215 - 220, 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; Kaldun, Johannes; Krimalowski, Alexander; Breuning, Matthias; Tetrahedron Letters; vol. 57; nb. 23; (2016); p. 2492 - 2495, View in Reaxys; Dang, Tuan Thanh; Seayad, Abdul Majeed; Advanced Synthesis and Catalysis; vol. 358; nb. 21; (2016); p. 3373 - 3380, View in Reaxys; Huang, Xiao; Chen, Lin; Ren, Fengying; Yang, Chen; Li, Jianghong; Shi, Kejin; Gou, Xiaojun; Wang, Wei; Synlett; vol. 28; nb. 4; (2017); p. 439 - 444; Art.No: ST-2016-U0636-L, View in Reaxys; Hopgood, Heather; Mack, James; Molecules; vol. 22; nb. 5; (2017); Art.No: 696, View in Reaxys; Li, Guangyue; Maria-Solano, Miguel A.; Romero-Rivera, Adrian; Osuna, Sílvia; Reetz, Manfred T.; Chemical Communications; vol. 53; nb. 68; (2017); p. 9454 - 9457, View in Reaxys; Gundala, Trivikram Reddy; Godugu, Kumar; Nallagondu, Chinna Gangi Reddy; Journal of the Chinese Chemical Society; vol. 64; nb. 12; (2017); p. 1408 - 1416, View in Reaxys

Hojo, Makoto; Yoshizawa, Junji; Funahashi, Yoshihiro; Okada, Ryo; Nakamura, Shin-Ya; Tateiwa, Jun-Ichi; Hosomi, Akira; Heterocycles; vol. 49; nb. 1; (1998); p. 85 - 88, View in Reaxys; Maj, Anna M.; Pietrusiewicz; Suisse, Isabelle; Agbossou, Francine; Mortreux, Andre; Journal of Organometallic Chemistry; vol. 626; nb. 1-2; (2001); p.

11/126

2018-07-03 19:01:53

157 - 160, View in Reaxys; Chiba, Shunsuke; Cao, Zhengyan; El Bialy, Serry Atta Atta; Narasaka, Koichi; Chemistry Letters; vol. 35; nb. 1; (2006); p. 18 - 19, View in Reaxys; Das, Biswanath; Majhi, Anjoy; Chowdhury, Nikhil; Reddy, Kongara Ravinder; Ravikanth, Bommena; Chemistry Letters; vol. 36; nb. 9; (2007); p. 1106 - 1107, View in Reaxys; Salmi, Chanaz; Loncle, Celine; Letourneux, Yves; Brunel, Jean Michel; Tetrahedron; vol. 64; nb. 19; (2008); p. 4453 - 4459, View in Reaxys; Naveen, Togati; Kancherla, Rajesh; Maiti, Debabrata; Organic Letters; vol. 16; nb. 20; (2014); p. 5446 - 5449, 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; Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei; Organic Letters; vol. 17; nb. 16; (2015); p. 3998 4001, View in Reaxys; Wei, Simin; Feng, Xiangqing; Du, Haifeng; Organic and Biomolecular Chemistry; vol. 14; nb. 34; (2016); p. 8026 - 8029, View in Reaxys; Csimbók, Ervin; Takács, Daniella; Balog, József A.; Egyed, Orsolya; May-Nagy, Nóra V.; Keserű, György Miklós; Tetrahedron Letters; vol. 57; nb. 39; (2016); p. 4401 - 4404, View in Reaxys; Zhou, Yulu; Lin, Shasha; Bian, Yinghui; Xia, Daohong; Xiang, Yuzhi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 55B; nb. 5; (2016); p. 624 - 628, View in Reaxys; Koppolu, Srinivasa Rao; Balamurugan, Rengarajan; New Journal of Chemistry; vol. 41; nb. 3; (2017); p. 1186 - 1192, View in Reaxys; Marelli, Enrico; Renault, Yohann; Sharma, Sunil V.; Nolan, Steven P.; Goss, Rebecca J. M.; Chemistry - A European Journal; vol. 23; nb. 16; (2017); p. 3832 - 3836, View in Reaxys; Patent; THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; ALCHEM LABORATORIES CORPORATION; LIU, Paul S.; DENYSENKO, Sergiy M.; HUANG, Guangfei; (27 pag.); WO2017/70651; (2017); (A1) English, View in Reaxys; Yang, Yongkang; Qu, Chen; Chen, Xiaolan; Sun, Kai; Qu, Lingbo; Bi, Wenzhu; Hu, Hao; Li, Rui; Jing, Chunfeng; Wei, Donghui; Wei, Shengkai; Sun, Yuanqiang; Liu, Hui; Zhao, Yufen; Organic Letters; vol. 19; nb. 21; (2017); p. 5864 - 5867, View in Reaxys 1l

Su, Weike; Can, Jin; Journal of Chemical Research; nb. 2; (2005); p. 88 - 90, View in Reaxys; Kathiravan; Shishoo; Chitre; Mahadik; Jain; Synthetic Communications; vol. 37; nb. 23; (2007); p. 4273 - 4279, View in Reaxys; Kerr, William J.; Watson, Allan J. B.; Hayes, Douglas; Chemical Communications; nb. 47; (2007); p. 5049 - 5051, View in Reaxys; Yadav; Reddy, B.V. Subba; Reddy, U.V. Subba; Praneeth; Tetrahedron Letters; vol. 49; nb. 32; (2008); p. 4742 - 4745, View in Reaxys; Huang, Xing-Fen; Salman, Muhammad; Huang, Zhi-Zhen; Chemistry - A European Journal; vol. 20; nb. 22; (2014); p. 6618 - 6621, View in Reaxys; Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko; Tetrahedron; vol. 73; nb. 8; (2017); p. 1143 - 1156, View in Reaxys; Yang, Kai; Dang, Qun; Bai, Xu; European Journal of Organic Chemistry; vol. 2017; nb. 14; (2017); p. 1922 - 1925, View in Reaxys

Elinson, Michail N.; Feducovich, Sergey K.; Dorofeev, Alexander S.; Vereshchagin, Anatolii N.; Nikishin, Gennady I.; Tetrahedron; vol. 56; nb. 51; (2000); p. 9999 - 10003, View in Reaxys; 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; Hamamoto, Hiromi; Suzuki, Yachiyo; Yamada, Yoichi M. A.; Tabata, Hidetsugu; Takahashi, Hideyo; Ikegami, Shiro; Angewandte Chemie - International Edition; vol. 44; nb. 29; (2005); p. 4536 - 4538, View in Reaxys; Salvi, Neeta A.; Chattopadhyay, Subrata; Tetrahedron Asymmetry; vol. 19; nb. 16; (2008); p. 1992 - 1997, View in Reaxys; Iida, Kazuki; Miura, Takashi; Ando, Junki; Saito, Susumu; Organic Letters; vol. 15; nb. 7; (2013); p. 1436 - 1439, View in Reaxys; Kuroboshi, Manabu; Shiba, Takuya; Tanaka, Hideo; Tetrahedron Letters; vol. 54; nb. 28; (2013); p. 3666 - 3668, View in Reaxys; Brenet, Simon; Berthiol, Florian; Einhorn, Jacques; European Journal of Organic Chemistry; nb. 36; (2013); p. 8094 - 8096, 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; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, 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; Xu, Bin; Jiang, Qing; Zhao, An; Jia, Jing; Liu, Qiang; Luo, Weiping; Guo, Cancheng; Chemical Communications; vol. 51; nb. 56; (2015); p. 11264 - 11267, View in Reaxys; Jiang, Lei; Guo, Fang; Shi, Zhenghai; Li, Yang; Hou, Zhaomin; ChemCatChem; vol. 9; nb. 20; (2017); p. 3827 - 3832, View in Reaxys

Selva, Maurizio; Bomben, Andrea; Tundo, Pietro; Synthetic Communications; vol. 29; nb. 9; (1999); p. 1561 - 1569, View in Reaxys; Tajbakhsh; Bakooie; Ghassemzadeh; Beheshtiha; Heravi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 40; nb. 12; (2001); p. 1232 - 1233, View in Reaxys; Xie, Linfeng; Vanlandeghem, Keith; Isenberger, Kurt M.; Bernier, Carolyn; Journal of Organic Chemistry; vol. 68; nb. 2; (2003); p. 641 643, View in Reaxys; Li, Lian-Sheng; Das, Sanjib; Sinha, Subhash C.; Organic Letters; vol. 6; nb. 1; (2004); p. 127 130, 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; Barba, Fructuoso; Recio, Javier; Batanero, Belen; Tetrahedron Letters; vol. 54; nb. 14; (2013); p. 1835 - 1838, View in Reaxys; Zheng, Qing-Zhong; Liang, Yu-Feng; Qin, Chong; Jiao, Ning; Chemical Communications; vol. 49; nb. 50; (2013); p. 5654 - 5656, View in Reaxys; Schmidt, Elena Yu.; Zorina, Nadezhda V.; Tarasova, Olga A.; Ushakov, Igor A.; Trofimov, Boris A.; Mendeleev Communications; vol. 23; nb. 4; (2013); p. 204 - 205, View in Reaxys; Chaouni, Wafaa; Aadil, Mina; Djellal, Ahmed; Kirsch, Gilbert; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 69; nb. 5; (2014); p. 509 - 518, View in Reaxys; Manna, Kuntal; Zhang, Teng; Greene, Francis X.; Lin, Wenbin; Journal of the American Chemical Society; vol. 137; nb. 7; (2015); p. 2665 - 2673, View in Reaxys; Schlepphorst, Christoph; Maji, Biplab; Glorius, Frank; ACS Catalysis; vol. 6; nb. 7; (2016); p. 4184 - 4188, View in Reaxys; Shang, Ming; Wang, Xiaoxu; Koo, Seung Moh; Youn, Jennifer; Chan, Jessica Z.; Yao, Wenzhi; Hastings, Brian T.; Wasa, Masayuki; Journal of the American Chemical Society; vol. 139; nb. 1; (2017); p. 95 - 98, View in Reaxys; Hattori, Tomohiro; Okami, Hiroki; Ichikawa, Tomohiro; Mori, Shigeki; Sawama, Yoshinari; Monguchi, Yasunari; Sajiki, Hironao; Advanced Synthesis and Catalysis; vol. 359; nb. 20; (2017); p. 3490 - 3495, View in Reaxys

Allan; Carnell; Journal of Organic Chemistry; vol. 66; nb. 19; (2001); p. 6495 - 6497, View in Reaxys; Denmark, Scott E.; Fan, Yu; Journal of the American Chemical Society; vol. 124; nb. 16; (2002); p. 4233 - 4235, View in Reaxys;

12/126

2018-07-03 19:01:53

Hosseinzadeh, Rahman; Sharifi, Ali; Tabar-Heydar, Kourosh; Mohsenzadeh, Farshid; Monatshefte fur Chemie; vol. 133; nb. 11; (2002); p. 1413 - 1415, View in Reaxys; Hosseinzadeh, Rahmam; Sharifi, Ali; Mirzaei, Mojtaba; Tabar Heydar, Kourosh; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 57; nb. 8; (2002); p. 961 - 962, View in Reaxys; Zhang, Hui; Yang, Chuan-Bo; Li, Yan-Yun; Donga, Zhen-Rong; Gao, JingXing; Nakamura, Hideaki; Murata, Kunihiko; Ikariya, Takao; Chemical Communications; nb. 1; (2003); p. 142 143, View in Reaxys; Taguchi, Kazuhiko; Sakaguchi, Satoshi; Ishii, Yasutaka; Tetrahedron Letters; vol. 46; nb. 27; (2005); p. 4539 - 4542, View in Reaxys; Liu, Qiang; Han, Bing; Liu, Zhengang; Yang, Li; Liu, Zhong-Li; Yu, Wei; Tetrahedron Letters; vol. 47; nb. 11; (2006); p. 1805 - 1807, View in Reaxys; Denmark, Scott E.; Fan, Yu; Eastgate, Martin D.; Journal of Organic Chemistry; vol. 70; nb. 13; (2005); p. 5235 - 5248, View in Reaxys; Zhang, Yuhua; Li, Chao-Jun; Journal of the American Chemical Society; vol. 128; nb. 13; (2006); p. 4242 - 4243, 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; Liu, Tian-Yu; Cui, Hai-Lei; Zhang, Yan; Jiang, Kun; Du, Wei; He, Zhao-Quan; Chen, Ying-Chun; Organic Letters; vol. 9; nb. 18; (2007); p. 3671 - 3674, View in Reaxys; Yang, Min; Yip, Kai-Tai; Pan, Jie-Hui; Chen, Ying-Chun; Zhu, Nian-Yong; Yang, Dan; Synlett; nb. 18; (2006); p. 3057 - 3060, View in Reaxys; Patent; THE HONG KONG POLYTECHNIC UNIVERSITY; US2008/269490; (2008); (A1) English, View in Reaxys; Cui, Yi; Yamashita, Yasuhiro; Kobayashi, Shu; Chemical Communications; vol. 48; nb. 83; (2012); p. 10319 - 10321, View in Reaxys; Liao, Yunfeng; Qi, Hongrui; Chen, Shanping; Jiang, Pengcheng; Zhou, Wang; Deng, Guo-Jun; Organic Letters; vol. 14; nb. 23; (2012); p. 6004 - 6007, View in Reaxys; Endo, Kohei; Sakamoto, Akira; Ohkubo, Takahiro; Shibata, Takanori; Chemistry Letters; vol. 40; nb. 12; (2011); p. 1440 - 1442, 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; Meng, Xu; Li, Xiaolong; Chen, Wenlin; Zhang, Yuanqing; Wang, Wen; Chen, Jinying; Song, Jinli; Feng, Huijie; Chen, Baohua; Journal of Heterocyclic Chemistry; vol. 51; nb. 2; (2014); p. 349 - 356, View in Reaxys; Liu, Yangyang; Xie, Aming; Cao, Meiping; Feng, Liandong; Wang, Boliang; Asian Journal of Chemistry; vol. 27; nb. 2; (2015); p. 587 - 590, View in Reaxys; Luo, Jian; Zhang, Xiang; Zhang, Jian; ACS Catalysis; vol. 5; nb. 4; (2015); p. 2250 - 2254, View in Reaxys; VázquezRomero, Ana; Gómez, Antonio Bermejo; Martín-Matute, Belén; ACS Catalysis; vol. 5; nb. 2; (2015); p. 708 - 714, View in Reaxys; Cai, Yujuan; Tang, Xinjun; Ma, Shengming; Chemistry - A European Journal; vol. 22; nb. 7; (2016); p. 2266 - 2269, View in Reaxys; Tanaka, Shinji; Kon, Yoshihiro; Ogawa, Atsuko; Uesaka, Yumiko; Tamura, Masanori; Sato, Kazuhiko; ChemCatChem; vol. 8; nb. 18; (2016); p. 2930 - 2938, View in Reaxys; Zhao, Lei-Min; Meng, Qing-Yuan; Fan, Xiang-Bing; Ye, Chen; Li, Xu-Bing; Chen, Bin; Ramamurthy, Vaidhyanathan; Tung, Chen-Ho; Wu, Li-Zhu; Angewandte Chemie - International Edition; vol. 56; nb. 11; (2017); p. 3020 - 3024; Angew. Chem.; vol. 129; nb. 11; (2017); p. 3066 - 3070,5, View in Reaxys; Tan, Jiajing; Zheng, Tianyu; Yu, Yuqi; Xu, Kun; RSC Advances; vol. 7; nb. 25; (2017); p. 15176 - 15180, View in Reaxys; Shankar, Ravi; Rawal, Ravindra K.; Singh, Uma S.; Chaudhary, Preeti; Konwar, Rituraj; Hajela, Kanchan; Medicinal Chemistry Research; vol. 26; nb. 7; (2017); p. 1459 - 1468, View in Reaxys 5

Terao, Yoshito; Kametani, Yoko; Wakui, Hiroyuki; Satoh, Tetsuya; Miura, Masahiro; Nomura, Masakatsu; Tetrahedron; vol. 57; nb. 28; (2001); p. 5967 - 5974, View in Reaxys; Fan, Xuesen; Zhang, Yongmin; Tetrahedron Letters; vol. 43; nb. 10; (2002); p. 1863 - 1865, View in Reaxys; Mohammed, Abdulkarim H.A.; Nagendrappa, Gopalpur; Tetrahedron Letters; vol. 44; nb. 13; (2003); p. 2753 - 2755, View in Reaxys; Li, Hui-Jing; Tian, Hong-Yu; Wu, YanChao; Chen, Yong-Jun; Liu, Li; Wang, Dong; Li, Chao-Jun; Advanced Synthesis and Catalysis; vol. 347; nb. 9; (2005); p. 1247 - 1256, View in Reaxys; Fan, Xuesen; Zhang, Xinying; Zhang, Yongmin; Journal of Chemical Research; nb. 11; (2005); p. 750 - 752, View in Reaxys; Naud, Frederic; Malan, Christophe; Spindler, Felix; Rueggeberg, Carsten; Schmidt, Andreas T.; Blaser, Hans-Ulrich; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 47 - 50, View in Reaxys; Trost, Barry M.; Xu, Jiayi; Journal of the American Chemical Society; vol. 127; nb. 49; (2005); p. 17180 - 17181, View in Reaxys; Murru, Siva; Kavala, Veerababurao; Singh; Patel, Bhisma K.; Tetrahedron Letters; vol. 48; nb. 6; (2007); p. 1007 - 1011, View in Reaxys; Patent; SOLVIAS AG; WO2004/50585; (2004); (A1) English, View in Reaxys; Chen, Huoji; Huang, Li; Fu, Wei; Liu, Xiaohang; Jiang, Huanfeng; Chemistry - A European Journal; vol. 18; nb. 34; (2012); p. 10497 - 10500, View in Reaxys; Trost, Barry M.; Bringley, Dustin A.; Angewandte Chemie - International Edition; vol. 52; nb. 16; (2013); p. 4466 - 4469; Angew. Chem.; vol. 125; nb. 16; (2013); p. 4562 - 4565, View in Reaxys; Cochrane, Alison R.; Irvine, Stephanie; Kerr, William J.; Reid, Marc; Andersson, Shalini; Nilsson, Goeran N.; Journal of Labelled Compounds and Radiopharmaceuticals; vol. 56; nb. 9-10; (2013); p. 451 - 454, View in Reaxys; Lex, Timothy R.; Swasy, Maria I.; Whitehead, Daniel C.; Journal of Organic Chemistry; vol. 80; nb. 24; (2015); p. 12234 - 12243, View in Reaxys; Dragan, Andrei; Jones, D. Heulyn; Kennedy, Alan R.; Tomkinson, Nicholas C. O.; Organic Letters; vol. 18; nb. 13; (2016); p. 3086 - 3089, View in Reaxys; Xiong, Heng -Ying; Bayle, Alexandre; Pannecoucke, Xavier; Besset, Tatiana; Angewandte Chemie - International Edition; vol. 55; nb. 43; (2016); p. 13490 - 13494; Angew. Chem.; vol. 128; nb. 43; (2016); p. 13688 - 13692,5, View in Reaxys; Chen, Xiu-Wen; Zhao, He; Xiong, Biao; Jiang, Huan-Feng; Dixneuf, Pierre. H.; Zhang, Min; Organic and Biomolecular Chemistry; vol. 15; nb. 29; (2017); p. 6093 - 6097, View in Reaxys; Smith, Craig R.; Zhang, Aibin; Mans, Daniel J.; RajanBabu; Organic Syntheses; vol. 85; (2008); p. 248 - 266, View in Reaxys; Zhang, Sheng; Lian, Fei; Xue, Mengyu; Qin, Tengteng; Li, Lijun; Zhang, Xu; Xu, Kun; Organic Letters; vol. 19; nb. 24; (2017); p. 6622 6625, View in Reaxys

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; Giardina, Giuseppe A. M.; Raveglia, Luca F.; Grugni, Mario; Sarau, Henry M.; Farina, Carlo; Medhurst, Andrew D.; Graziani, Davide; Schmidt, Dulcie B.; Rigolio, Roberto; Luttmann, Mark; Cavagnera, Stefano; Foley, James J.; Vecchietti, Vittorio; Hay, Douglas W. P.; Journal of Medicinal Chemistry; vol. 42; nb. 6; (1999); p. 1053 - 1065, View in Reaxys; Asahara, Motoki; Katayama, Taku; Tohda, Yasuo; Nishiwaki, Nagatoshi; Ariga, Masahiro; Chemical and Pharmaceutical Bulletin; vol. 52; nb. 11;

13/126

2018-07-03 19:01:53

(2004); p. 1334 - 1338, View in Reaxys; Patent; RESEARCH TRIANGLE INSTITUTE; CARROLL, Frank Ivy; BLOUGH, Bruce; ABRAHAM, Philip; WO2010/121022; (2010); (A1) English, View in Reaxys; Verbelen, Bram; Dehaen, Wim; Organic Letters; vol. 18; nb. 24; (2016); p. 6412 - 6415, View in Reaxys; Call, Arnau; Casadevall, Carla; Acuña-Parés, Ferran; Casitas, Alicia; Lloret-Fillol, Julio; Chemical Science; vol. 8; nb. 7; (2017); p. 4739 4749, View in Reaxys 1n

Huang, Huawen; Ji, Xiaochen; Wu, Wanqing; Jiang, Huanfeng; Advanced Synthesis and Catalysis; vol. 355; nb. 1; (2013); p. 170 - 180, View in Reaxys; Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun; Advanced Synthesis and Catalysis; vol. 355; nb. 13; (2013); p. 2686 - 2692, View in Reaxys; Zheng, Zubiao; Han, Bingbing; Cheng, Peng; Niu, Jiangxiu; Wang, Aidong; Tetrahedron; vol. 70; nb. 52; (2014); p. 9814 - 9818, View in Reaxys; Imai, Sho; Kikui, Hiroki; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 71; nb. 33; (2015); p. 5267 - 5274, View in Reaxys; Rekunge, Deelip S.; Khatri, Chetan K.; Chaturbhuj, Ganesh U.; Monatshefte fur Chemie; vol. 148; nb. 12; (2017); p. 2091 - 2095, View in Reaxys

Tang, Dong; Li, Xiao-Long; Guo, Xin; Wu, Ping; Li, Ji-Hui; Wang, Kai; Jing, Huan-Wang; Chen, Bao-Hua; Tetrahedron; vol. 70; nb. 26; (2014); p. 4038 - 4042, 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; Porcheddu, Andrea; Colacino, Evelina; Cravotto, Giancarlo; Delogu, Francesco; De Luca, Lidia; Beilstein Journal of Organic Chemistry; vol. 13; (2017); p. 2049 2055, View in Reaxys

Smith, Samantha A.M.; Morris, Robert H.; Synthesis (Germany); vol. 47; nb. 12; (2015); p. 1775 - 1779; Art.No: SS-2014-C0753-ST, View in Reaxys; Smith, Samantha A. M.; Prokopchuk, Demyan E.; Morris, Robert H.; Israel Journal of Chemistry; vol. 57; nb. 12; (2017); p. 1204 - 1215, View in Reaxys

Wang, Zhiwei; Fan, Wenyou; Deng, Guo-Jun; Zhou, Wang; Tetrahedron Letters; vol. 56; nb. 40; (2015); p. 5449 5452, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 4016, View in Reaxys

Trifonov, Alexey L.; Zemtsov, Artem A.; Levin, Vitalij V.; Struchkova, Marina I.; Dilman, Alexander D.; Organic Letters; vol. 18; nb. 14; (2016); p. 3458 - 3461, View in Reaxys; Ma, Jiaqi; Hong, Chao; Wan, Yan; Li, Meichao; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Jin, Liqun; Shen, Zhenlu; Tetrahedron Letters; vol. 58; nb. 7; (2017); p. 652 - 657, View in Reaxys

a20

Bruneau-Voisine, Antoine; Wang, Ding; Roisnel, Thierry; Darcel, Christophe; Sortais, Jean-Baptiste; Catalysis Communications; vol. 92; (2017); p. 1 - 4, View in Reaxys

a15

Wei, Duo; Roisnel, Thierry; Darcel, Christophe; Clot, Eric; Sortais, Jean-Baptiste; ChemCatChem; vol. 9; nb. 1; (2017); p. 80 - 83, View in Reaxys

Tan, Da-Wei; Li, Hong-Xi; Zhang, Meng-Juan; Yao, Jian-Lin; Lang, Jian-Ping; ChemCatChem; vol. 9; nb. 6; (2017); p. 1113 - 1118, View in Reaxys

Wang, Ming-Hui; Chen, Ling-Yan; Tetrahedron Letters; vol. 58; nb. 8; (2017); p. 732 - 735, View in Reaxys

Lei, Chuanhu; Yip, Yong Jie; Zhou, Jianrong Steve; Journal of the American Chemical Society; vol. 139; nb. 17; (2017); p. 6086 - 6089, View in Reaxys

3Oa

Halima, Taoufik Ben; Zhang, Wanying; Yalaoui, Imane; Hong, Xin; Yang, Yun-Fang; Houk, Kendall N.; Newman, Stephen G.; Journal of the American Chemical Society; vol. 139; nb. 3; (2017); p. 1311 - 1318, View in Reaxys

Matsuda, Atsushi; Ushimaru, Tomoya; Kobayashi, Yusuke; Harada, Toshiro; Chemistry - A European Journal; vol. 23; nb. 36; (2017); p. 8605 - 8609, View in Reaxys

S9u

Yang, Bin; Chansaenpak, Kantapat; Wu, Hongmiao; Zhu, Lin; Wang, Mengzhe; Li, Zibo; Lu, Hongjian; Chemical Communications; vol. 53; nb. 24; (2017); p. 3497 - 3500, View in Reaxys

S13

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

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

II-c

Patent; Chinese Academy Of Sciences Chemical Institute; Wang Congyang; Hu Yuanyuan; Zhou Bingwei; Liu Ting; (9 pag.); CN106967055; (2017); (A) Chinese, View in Reaxys

Gaspa, Silvia; Porcheddu, Andrea; Valentoni, Antonio; Garroni, Sebastiano; Enzo, Stefano; De Luca, Lidia; European Journal of Organic Chemistry; vol. 2017; nb. 37; (2017); p. 5519 - 5526, View in Reaxys

Gómez, José Enrique; Guo, Wusheng; Gaspa, Silvia; Kleij, Arjan W.; Angewandte Chemie - International Edition; vol. 56; nb. 47; (2017); p. 15035 - 15038; Angew. Chem.; vol. 129; nb. 47; (2017); p. 15231 - 15234,4, View in Reaxys

Ni, Penghui; Li, Bin; Huang, Huawen; Xiao, Fuhong; Deng, Guo-Jun; Green Chemistry; vol. 19; nb. 23; (2017); p. 5553 - 5558, View in Reaxys

1c(Me)

Berton, Mateo; Mello, Rossella; Williard, Paul G.; González-Núñez, María Elena; Journal of the American Chemical Society; vol. 139; nb. 48; (2017); p. 17414 - 17420, View in Reaxys

14/126

2018-07-03 19:01:53

c1h

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

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

13A

Patent; BIOMARIN PHARMACEUTICAL INC.; WANG, Bing; (552 pag.); WO2017/214505; (2017); (A1) English, View in Reaxys

Sielemann, Dirk; Keuper, Ralf; Risch, Nikolaus; Advanced Synthesis and Catalysis; vol. 341; nb. 5; (1999); p. 487 491, View in Reaxys; Oisaki, Kounosuke; Suto, Yutaka; Kanai, Motomu; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 125; nb. 19; (2003); p. 5644 - 5645, View in Reaxys; Ichibakase, Tomonori; Nakajima, Makoto; Synthesis (Germany); vol. 44; nb. 20; (2012); p. 3145 - 3151, View in Reaxys; Matsubara, Hiroshi; Niwa, Yuki; Matake, Ryosuke; Synlett; vol. 26; nb. 9; (2015); p. 1276 - 1280, View in Reaxys; Monteiro, Julia L.; Pieber, Bartholomäus; Corrêa, Arlene G.; Kappe, C. Oliver; Synlett; vol. 27; nb. 1; (2016); p. 83 - 87; Art.No: ST-2015D0549-L, View in Reaxys

Hamada, Hiroki; Tanaka, Toshinori; Furuya, Tsutomu; Takahata, Hiroki; Nemoto, Hideo; Tetrahedron Letters; vol. 42; nb. 5; (2001); p. 909 - 911, View in Reaxys; Cherkaoui, Hassan; Soufiaoui, Mohammed; Gree, Rene; Tetrahedron; vol. 57; nb. 12; (2001); p. 2379 - 2383, 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; Ackermann, Lutz; Born, Robert; Angewandte Chemie - International Edition; vol. 44; nb. 16; (2005); p. 2444 - 2447, View in Reaxys; Basdevant, Benoit; Legault, Claude Y.; Organic Letters; vol. 17; nb. 19; (2015); p. 4918 - 4921, View in Reaxys; Yang, Junjuan; Shi, Daxin; Zhang, Kai; Zhao, Zhangtao; Qiu, Fadong; Bi, Yujiao; Zhang, Qi; Li, Jiarong; Heterocycles; vol. 92; nb. 5; (2016); p. 866 - 885, View in Reaxys

Yadav, Ashok K.; Singh, Arpita; Bulletin of the Chemical Society of Japan; vol. 75; nb. 3; (2002); p. 587 - 588, View in Reaxys; Patent; Yin, Qiang; (8 pag.); CN105111072; (2016); (B) Chinese, View in Reaxys

Levin, Vitalij V.; Dilman, Alexander D.; Belyakov, Pavel A.; Korlyukov, Alexander A.; Struchkova, Marina I.; Tartakovsky, Vladimir A.; European Journal of Organic Chemistry; nb. 24; (2004); p. 5141 - 5148, View in Reaxys; Liu, Jie; Li, Xing; Wang, Jun; Feng, Xiaoming; Advanced Synthesis and Catalysis; vol. 348; nb. 7-8; (2006); p. 939 944, View in Reaxys; Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys; Cui, Yi; Li, Wei; Sato, Takehiro; Yamashita, Yasuhiro; Kobayashi, Shu; Advanced Synthesis and Catalysis; vol. 355; nb. 6; (2013); p. 1193 - 1205, View in Reaxys; Liang, Shengzong; Hammond, Gerald B.; Xu, Bo; Chemical Communications; vol. 51; nb. 5; (2015); p. 903 - 906, View in Reaxys; Varun, Begur Vasanthkumar; Gadde, Karthik; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 14; nb. 32; (2016); p. 7665 - 7670, View in Reaxys

Delbos-Krampe, Jeanne; Risch, Nikolaus; Floerke, Ulrich; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 59; nb. 4; (2004); p. 414 - 423, View in Reaxys; Sun, Tian; Zhang, Xumu; Advanced Synthesis and Catalysis; vol. 354; nb. 17; (2012); p. 3211 - 3215, View in Reaxys; Kuroboshi, Manabu; Yamamoto, Takashi; Tanaka, Hideo; Synlett; vol. 24; nb. 2; (2013); p. 197 - 200; Art.No: ST-2012-U0872-L, 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; Christodoulou, Michael S.; Zarate, Mikel; Ricci, Francesca; Damia, Giovanna; Pieraccini, Stefano; Dapiaggi, Federico; Sironi, Maurizio; Lo Presti, Leonardo; García-Argáez, Aída Nelly; Dalla Via, Lisa; Passarella, Daniele; European Journal of Medicinal Chemistry; vol. 118; (2016); p. 79 - 89, View in Reaxys; Zhu, Minghui; Wei, Wei; Yang, Daoshan; Cui, Hong; Cui, Huanhuan; Sun, Xuejun; Wang, Hua; Organic and Biomolecular Chemistry; vol. 14; nb. 46; (2016); p. 10998 - 11001, View in Reaxys

Uchida, Tetsuro; Kita, Yoshio; Maekawa, Hirofumi; Nishiguchi, Ikuzo; Tetrahedron; vol. 62; nb. 13; (2006); p. 3103 - 3111, View in Reaxys; Fedorov, Oleg V.; Kosobokov, Mikhail D.; Levin, Vitalij V.; Struchkova, Marina I.; Dilman, Alexander D.; Journal of Organic Chemistry; vol. 80; nb. 11; (2015); p. 5870 - 5876, View in Reaxys; Wang, Jianqiang; Wang, Xiaolei; Niu, Zong-Qiang; Wang, Jian; Zhang, Man; Li, Jing-Hua; Synthetic Communications; vol. 46; nb. 2; (2016); p. 165 - 168, View in Reaxys; Ortiz, Pablo; Collados, Juan F.; Harutyunyan, Syuzanna R.; European Journal of Organic Chemistry; vol. 2016; nb. 7; (2016); p. 1247 - 1250, View in Reaxys

Ueura, Kenji; Miyamura, Sawako; Satoh, Tetsuya; Miura, Masahiro; Journal of Organometallic Chemistry; vol. 691; nb. 12; (2006); p. 2821 - 2826, View in Reaxys; Okumura, Shogo; Tang, Shuwei; Saito, Teruhiko; Semba, Kazuhiko; Sakaki, Shigeyoshi; Nakao, Yoshiaki; Journal of the American Chemical Society; vol. 138; nb. 44; (2016); p. 14699 - 14704, 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; Hale, Karl J.; Grabski, Milosz; Flasz, Jakub T.; Organic Letters; vol. 15; nb. 2; (2013); p. 370 - 373, View in Reaxys; Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys; Zhao, Li-Ming; Jin, Hai-Shan; Liu, Jinzhong; Skaar, Todd C.; Ipe, Joseph; Lv, Wei; Flockhart, David A.; Cushman, Mark; Bioorganic and Medicinal Chemistry; vol. 24; nb. 21; (2016); p. 5400 - 5409, View in Reaxys

15/126

2018-07-03 19:01:53

He, Zhi; Yudin, Andrei K.; Organic Letters; vol. 8; nb. 25; (2006); p. 5829 - 5832, View in Reaxys; Patent; JOHNSON MATTHEY PUBLIC LIMITED COMPANY; BALDINO, Salvatore; BARATTA, Walter; BLACKABY, Andrew; BRYAN, Richard, Charles; FACCHETTI, Sarah; JURCIK, Vaclav; NEDDEN, Hans, Guenter; (112 pag.); WO2016/193761; (2016); (A1) English, View in Reaxys

Zaitsev, Alexey B.; Adolfsson, Hans; Organic Letters; vol. 8; nb. 22; (2006); p. 5129 - 5132, View in Reaxys; Sasaki, Shigeru; Suzuki, Tatuo; Uchiya, Toshihiro; Toyota, Shigenobu; Hirano, Akira; Tanemura, Mao; Teramoto, Hiroyoshi; Yamauchi, Takayasu; Higashiyama, Kimio; Journal of Fluorine Chemistry; vol. 192; (2016); p. 78 - 85, View in Reaxys

Moriuchi-Kawakami, Takayo; Matsuda, Haruo; Shibata, Ikuya; Miyatake, Masato; Suwa, Toshihiro; Baba, Akio; Bulletin of the Chemical Society of Japan; vol. 72; nb. 3; (1999); p. 465 - 470, View in Reaxys; 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; Shimada, Tomohiro; Yamamoto, Yoshinori; Journal of the American Chemical Society; vol. 124; nb. 43; (2002); p. 12670 - 12671, 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; Wang, Hu; Zhang, Jin; Cui, Yu-Ming; Yang, KeFang; Zheng, Zhan-Jiang; Xu, Li-Wen; RSC Advances; vol. 4; nb. 65; (2014); p. 34681 - 34686, 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

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; Lee, Yoon Joo; Chan, Tak Hang; Canadian Journal of Chemistry; vol. 82; nb. 2; (2004); p. 71 - 74, View in Reaxys; Gu, Chunhui; Zhai, Jiaojiao; Jiang, Jianan; Liu, Hongwei; Wang, Lei; Zhu, Dunru; Ji, Yafei; Chinese Journal of Chemistry; vol. 32; nb. 2; (2014); p. 179 - 190, 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; Yu, Jing-Bo; Peng, Gang; Jiang, Zhi-Jiang; Hong, Zi-Kun; Su, Wei-Ke; European Journal of Organic Chemistry; vol. 2016; nb. 32; (2016); p. 5340 - 5344, View in Reaxys

Usui, Satoshi; Matsumoto, Takeshi; Ohkubo, Katsutoshi; Tetrahedron Letters; vol. 39; nb. 52; (1998); p. 9755 9758, View in Reaxys; Zhuo, Jin-Cong; Schenk, Kurt; Helvetica Chimica Acta; vol. 85; nb. 5; (2002); p. 1276 - 1283, View in Reaxys; Moldvai, Istvan; Temesvari-Major, Eszter; Incze, Maria; Platthy, Tuende; Gacs-Baitz, Eszter; Szantay, Csaba; Heterocycles; vol. 60; nb. 2; (2003); p. 309 - 319, View in Reaxys; Alexakis, Alexandre; Gille, Segolene; Prian, Fabrice; Rosset, Stephane; Ditrich, Klaus; Tetrahedron Letters; vol. 45; nb. 7; (2004); p. 1449 - 1451, View in Reaxys; Ohno, Kouji; Kataoka, Yasutaka; Mashima, Kazushi; Organic Letters; vol. 6; nb. 25; (2004); p. 4695 - 4697, 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; Payra, Soumen; Saha, Arijit; Banerjee, Subhash; RSC Advances; vol. 6; nb. 57; (2016); p. 52495 - 52499, View in Reaxys; Pieterse, Tanya; Visser, Melanie; Marais, Charlene; Bezuidenhoudt, Barend C. B.; Synlett; vol. 27; nb. 10; (2016); p. 1541 - 1546; Art.No: ST-2015-D0886-L, View in Reaxys; Chan, Chun-Ming; Zhou, Zhongyuan; Yu, Wing-Yiu; Advanced Synthesis and Catalysis; vol. 358; nb. 24; (2016); p. 4067 - 4074, View in Reaxys

Nakajin, Shizuo; Tamura, Fumihiro; Takase, Noriko; Toyoshima, Satoshi; Biological and Pharmaceutical Bulletin; vol. 20; nb. 11; (1997); p. 1215 - 1218, View in Reaxys; Zhang, Yanfei; Shen, Zongxuan; Tang, Jingting; Zhang, Yan; Kong, Lichun; Zhang, Yawen; Organic and Biomolecular Chemistry; vol. 4; nb. 8; (2006); p. 1478 - 1482, View in Reaxys; Facchetti, Sarah; Jurcik, Vaclav; Baldino, Salvatore; Giboulot, Steven; Nedden, Hans Günter; Zanotti-Gerosa, Antonio; Blackaby, Andrew; Bryan, Richard; Boogaard, Adrian; McLaren, David B.; Moya, Eduardo; Reynolds, Steven; Sandham, Karl S.; Martinuzzi, Paolo; Baratta, Walter; Organometallics; vol. 35; nb. 2; (2016); p. 277 - 287, View in Reaxys

Ganesh; Harish Kumar; David Krupadanam; Synthetic Communications; vol. 29; nb. 12; (1999); p. 2069 - 2078, View in Reaxys; Siqueira Filho, Ezequias P.; Rodrigues, J.Augusto R.; Moran, Paulo J.S.; Tetrahedron Asymmetry; vol. 12; nb. 6; (2001); p. 847 - 852, View in Reaxys; Xie, Yuan-Yuan; Chen, Zhen-Chu; Synthetic Communications; vol. 32; nb. 12; (2002); p. 1875 - 1879, View in Reaxys; Sheng, Shou-Ri; Zhong, Ming-Hua; Liu, Xiao-Ling; Luo, Qiu-Yan; Chen, Hui-Zong; Journal of Chemical Research; nb. 6; (2004); p. 392 - 393, View in Reaxys; Mizuta, Satoshi; Shibata, Norio; Akiti, Surendar; Fujimoto, Hiroyuki; Nakamura, Shuichi; Toru, Takeshi; Organic Letters; vol. 9; nb. 18; (2007); p. 3707 - 3710, View in Reaxys; Pu, Ye; Fang, Yingguo; Yan, Jie; Letters in Organic Chemistry; vol. 9; nb. 7; (2012); p. 522 - 525, View in Reaxys; Saito, Akira; Kumagai, Naoya; Shibasaki, Masakatsu; Tetrahedron Letters; vol. 55; nb. 20; (2014); p. 3167 - 3171, View in Reaxys; Grigalunas, Michael; Norrby, Per-Ola; Wiest, Olaf; Helquist, Paul; Angewandte Chemie - International Edition; vol. 54; nb. 40; (2015); p. 11822 - 11825; Angew. Chem.; vol. 54; nb. 40; (2015); p. 11822 - 11825,4, 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

Caposcialli, Nadia; Dell'Erba, Carlo; Novi, Marino; Petrillo, Giovanni; Tavani, Cinzia; Tetrahedron; vol. 54; nb. 20; (1998); p. 5315 - 5324, 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; Li, Jian; Ye, Deju; Liu, Hong; Luo, Xiaoming; Jiang, Hualiang; Synthetic Communications; vol. 38; nb. 4; (2008); p. 567 - 575, View in Reaxys; Liu, Saiwen; Chen, Ru;

16/126

2018-07-03 19:01:53

Chen, Hui; Deng, Guo-Jun; Tetrahedron Letters; vol. 54; nb. 29; (2013); p. 3838 - 3841, View in Reaxys; Yamashita, Yasuhiro; Cui, Yi; Xie, Peizhong; Kobayashi, Shu; Organic Letters; vol. 17; nb. 24; (2015); p. 6042 - 6045, View in Reaxys; Zhang, Qing-Bao; Jia, Wen-Liang; Ban, Yong-Liang; Zheng, Yong; Liu, Qiang; Wu, Li-Zhu; Chemistry - A European Journal; vol. 22; nb. 8; (2016); p. 2595 - 2598, View in Reaxys 3l

Bhati, Nishi; Sarma, Kuladip; Goswami, Amrit; Chemistry Letters; vol. 37; nb. 5; (2008); p. 496 - 497, 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; La Sorella, Giorgio; Sperni, Laura; Ballester, Pablo; Strukul, Giorgio; Scarso, Alessandro; Catalysis Science and Technology; vol. 6; nb. 15; (2016); p. 6031 6036, View in Reaxys

Morandi, Bill; Wickens, Zachary K.; Grubbs, Robert H.; Angewandte Chemie - International Edition; vol. 52; nb. 10; (2013); p. 2944 - 2948; Angew. Chem.; (2013); p. 3016 - 3020, View in Reaxys; Patent; CALIFORNIA INSTITUTE OF TECHNOLOGY; MORANDI, Bill; GRUBBS, Robert H.; WICKENS, Zachary K.; US2014/194604; (2014); (A1) English, View in Reaxys; Zohreh, Nasrin; Tavakolizadeh, Maryam; Hosseini, Seyed Hassan; Jahani, Mahboobeh; Pourjavadi, Ali; Bennett, Craig; New Journal of Chemistry; vol. 40; nb. 12; (2016); p. 10325 - 10332, View in Reaxys

Gao, Qi; Li, Shenyan; Pan, Yingming; Xu, Yanli; Wang, Hengshan; Tetrahedron; vol. 69; nb. 19; (2013); p. 3775 3781, View in Reaxys; Chen, Zheng-Wang; Ye, Dong-Nai; Qian, Yi-Ping; Ye, Min; Liu, Liang-Xian; Tetrahedron; vol. 69; nb. 30; (2013); p. 6116 - 6120, View in Reaxys; Talwar, Dinesh; Salguero, Noemi Poyatos; Robertson, Craig M.; Xiao, Jianliang; Chemistry - A European Journal; vol. 20; nb. 1; (2014); p. 245 - 252, View in Reaxys; Anand, Namrata; Chanda, Tanmoy; Koley, Suvajit; Chowdhury, Sushobhan; Singh, Maya Shankar; RSC Advances; vol. 5; nb. 10; (2015); p. 7654 - 7660, View in Reaxys; Chen, Shu-Jie; Lu, Guo-Ping; Cai, Chun; RSC Advances; vol. 5; nb. 17; (2015); p. 13208 - 13211, View in Reaxys; Martinez-Erro, Samuel; Sanz-Marco, Amparo; Bermejo Gómez, Antonio; Vázquez-Romero, Ana; Ahlquist, Mårten S. G.; Martín-Matute, Belén; Journal of the American Chemical Society; vol. 138; nb. 40; (2016); p. 13408 - 13414, View in Reaxys

Atobe, Masakazu; Naganuma, Kenji; Kawanishi, Masashi; Morimoto, Akifumi; Kasahara, Ken-Ichi; Ohashi, Shigeki; Suzuki, Hiroko; Hayashi, Takahiko; Miyoshi, Shiro; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 22; (2013); p. 6064 - 6067, View in Reaxys; Hering, Thea; Mühldorf, Bernd; Wolf, Robert; König, Burkhard; Angewandte Chemie - International Edition; vol. 55; nb. 17; (2016); p. 5342 - 5345; Angew. Chem.; vol. 128; (2016); p. 5428 - 5431,4, 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; Wen, Genfa; Su, Yingpeng; Zhang, Guoxiang; Lin, Qiqiao; Zhu, Yujin; Zhang, Qianqian; Fang, Xinqiang; Organic Letters; vol. 18; nb. 16; (2016); p. 3980 3983, View in Reaxys

Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 - 8456, View in Reaxys; Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung; Chemical Communications; vol. 51; nb. 65; (2015); p. 13004 - 13007, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys

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

Sun, Kai; Zhu, Zhonghong; Sun, Jingjing; Liu, Lulu; Wang, Xin; Journal of Organic Chemistry; vol. 81; nb. 4; (2016); p. 1476 - 1483, View in Reaxys

Kumar, Prashant; Irrgang, Torsten; Kostakis, George E.; Kempe, Rhett; RSC Advances; vol. 6; nb. 45; (2016); p. 39335 - 39342, View in Reaxys

PEK

Zirakzadeh, Afrooz; de Aguiar, Sara R.M.M.; Widhalm, Michael; Mereiter, Kurt; Kirchner, Karl; Journal of Organometallic Chemistry; vol. 819; (2016); p. 260 - 265, View in Reaxys

II-21

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

Kiyokawa, Kensuke; Nagata, Takaya; Minakata, Satoshi; Angewandte Chemie - International Edition; vol. 55; nb. 35; (2016); p. 10458 - 10462; Angew. Chem.; vol. 128; nb. 35; (2016); p. 10614 - 10618,5, View in Reaxys

Zheng, Zubiao; Han, Bingbing; Wu, Fang; Shi, Tengfei; Liu, Jie; Zhang, Yong; Hao, Jialong; Tetrahedron; vol. 72; nb. 48; (2016); p. 7738 - 7743, View in Reaxys

10t

Bigler, Raphael; Huber, Raffael; Stöckli, Marco; Mezzetti, Antonio; ACS Catalysis; vol. 6; nb. 10; (2016); p. 6455 6464, View in Reaxys

Wu, Yile; Shan, Changkai; Sun, Ying; Chen, Peng; Ying, Jianxi; Zhu, Jun; Liu, Liu; Zhao, Yufen; Chemical Communications; vol. 52; nb. 95; (2016); p. 13799 - 13802, View in Reaxys

Ota, Yosuke; Itoh, Yukihiro; Kaise, Asako; Ohta, Kiminori; Endo, Yasuyuki; Masuda, Mitsuharu; Sowa, Yoshihiro; Sakai, Toshiyuki; Suzuki, Takayoshi; Angewandte Chemie - International Edition; vol. 55; nb. 52; (2016); p. 16115 - 16118; Angew. Chem.; nb. 128; (2016); p. 16349 - 16352,4, View in Reaxys

17/126

2018-07-03 19:01:53

S19

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

17b

Kim, Kil Joong; Kim, Kyongtae; Heterocycles; vol. 50; nb. 1; (1999); p. 147 - 157, View in Reaxys; Singh, Swastika; Saquib, Mohammad; Singh, Shyam Babu; Singh, Mandavi; Singh, Jagdamba; RSC Advances; vol. 5; nb. 56; (2015); p. 45152 - 45157, View in Reaxys

Napieraj, Anna; Zawadzki, Stefan; Zwierzak, Andrzej; Tetrahedron; vol. 56; nb. 34; (2000); p. 6299 - 6305, View in Reaxys; Suto, Yutaka; Kumagai, Naoya; Matsunaga, Shigeki; Kanai, Motomu; Shibasaki, Masakatsu; Organic Letters; vol. 5; nb. 17; (2003); p. 3147 - 3150, View in Reaxys; Kise, Naoki; Sueyoshi, Akinori; Takeuchi, ShinIchirou; Sakurai, Toshihiko; Organic Letters; vol. 15; nb. 11; (2013); p. 2746 - 2749, View in Reaxys; Pan, Xinhui; Hu, Qingwen; Chen, Wenfang; Liu, Xigong; Sun, Bin; Huang, Zhouli; Zeng, Ziyu; Wang, Liguo; Zhao, Dan; Ji, Mei; Liu, Lei; Lou, Hongxiang; Tetrahedron; vol. 70; nb. 21; (2014); p. 3447 - 3451, View in Reaxys; Crisenza, Giacomo E. M.; McCreanor, Niall G.; Bower, John F.; Journal of the American Chemical Society; vol. 136; nb. 29; (2014); p. 10258 - 10261, View in Reaxys; Pathe, Gulab Khushalrao; Konduru, Naveen K.; Parveen, Iram; Ahmed, Naseem; RSC Advances; vol. 5; nb. 101; (2015); p. 83512 - 83521, View in Reaxys

Lin, Yang-Miin; Fu, I-Pin; Uang, Biing-Jiun; Tetrahedron Asymmetry; vol. 12; nb. 23; (2001); p. 3217 - 3221, View in Reaxys; Uddin, Md. Jashim; Rao, P.N. Praveen; Knaus, Edward E.; Bioorganic and Medicinal Chemistry; vol. 13; nb. 2; (2005); p. 417 - 424, View in Reaxys; Martin-Matute, Belen; Bogar, Krisztian; Edin, Michaela; Kaynak, F. Betuel; Baeckvall, Jan-E.; Chemistry - A European Journal; vol. 11; nb. 20; (2005); p. 5832 - 5842, View in Reaxys; 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; Kise, Naoki; Miyamoto, Hiroyuki; Hamada, Yusuke; Sakurai, Toshihiko; Tetrahedron Letters; vol. 56; nb. 31; (2015); p. 4599 - 4602, View in Reaxys

Cheng, Xiaohui; Horton, Peter N.; Hursthouse, Michael B.; Hii, King Kuok; Tetrahedron Asymmetry; vol. 15; nb. 14; (2004); p. 2241 - 2246, View in Reaxys; Zhu, Feng; Wang, Zhong-Xia; Tetrahedron; vol. 70; nb. 52; (2014); p. 9819 - 9827, View in Reaxys; Jiang, He-Yan; Zheng, Xu-Xu; Catalysis Science and Technology; vol. 5; nb. 7; (2015); p. 3728 - 3734, View in Reaxys

Kromm, Klemenz; Eichenseher, Sandra; Prommesberger, Markus; Hampel, Frank; Gladysz; European Journal of Inorganic Chemistry; nb. 15; (2005); p. 2983 - 2998, View in Reaxys; Berkessel, Albrecht; Sebastian-Ibarz, M. Luisa; Mueller, Thomas N.; Angewandte Chemie - International Edition; vol. 45; nb. 39; (2006); p. 6567 - 6570, View in Reaxys; Prek, Benjamin; Bezensek, Jure; Kasunic, Marta; Groselj, Uros; Svete, Jurij; Stanovnik, Branko; Tetrahedron; vol. 70; nb. 14; (2014); p. 2359 - 2369, View in Reaxys; Ueda, Tohru; Inada, Mitsuhide; Morita, Nobuyoshi; Tamura, Osamu; Heterocycles; vol. 90; nb. 2; (2015); p. 1179 - 1195, View in Reaxys

Nicolaou; Montagnon; Ulven; Baran; Zhong; Sarabiat; Journal of the American Chemical Society; vol. 124; nb. 20; (2002); p. 5718 - 5728, View in Reaxys; Racine, Sophie; Denanteuil, Florian; Serrano, Eloisa; Waser, Jerome; Angewandte Chemie - International Edition; vol. 53; nb. 32; (2014); p. 8484 - 8487; Angew. Chem.; vol. 126; nb. 32; (2014); p. 8624 - 8627,4, View in Reaxys; Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys

Masumoto, Shuji; Suzuki, Masato; Kanai, Motomu; Shibasaki, Masakatsu; Tetrahedron; vol. 60; nb. 46 SPEC. ISS.; (2004); p. 10497 - 10504, View in Reaxys; Lou, Sha; Moquist, Philip N.; Schaus, Scott E.; Journal of the American Chemical Society; vol. 128; nb. 39; (2006); p. 12660 - 12661, View in Reaxys; Wang, Dong; Deraedt, Christophe; Salmon, Lionel; Labrugère, Christine; Etienne, Laetitia; Ruiz, Jaime; Astruc, Didier; Chemistry - A European Journal; vol. 21; nb. 17; (2015); p. 6501 - 6510, View in Reaxys

Burk, Mark J.; Hems, William; Herzberg, Daniela; Malan, Christophe; Zanotti-Gerosa, Antonio; Organic Letters; vol. 2; nb. 26; (2000); p. 4173 - 4175, View in Reaxys; Ma, Yuan; Heteroatom Chemistry; vol. 13; nb. 4; (2002); p. 310 - 315, View in Reaxys; Chandrasekhar; Raji Reddy, Ch.; Nagendra Babu; Journal of Organic Chemistry; vol. 67; nb. 25; (2002); p. 9080 - 9082, View in Reaxys; Uddin, Md. Jashim; Rao, P. N. Praveen; McDonald, Robert; Knaus, Edward E.; Journal of Medicinal Chemistry; vol. 47; nb. 24; (2004); p. 6108 - 6111, View in Reaxys; Dong, ZhenRong; 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; Goel, Atul; Singh, Fateh Veer; Tetrahedron Letters; vol. 46; nb. 33; (2005); p. 5585 - 5587, 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; Shen, Mei-Hua; Lu, Xiao-Long; Xu, Hua-Dong; RSC Advances; vol. 5; nb. 120; (2015); p. 98757 - 98761, View in Reaxys; Brenet, Simon; Minozzi, Clémentine; Clarens, Bastien; Amiri, Lilia; Berthiol, Florian; Synthesis (Germany); vol. 47; nb. 24; (2015); p. 3859 - 3873; Art.No: SS-2015-Z0445-OP, View in Reaxys

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys; Kafka, Frantisek; Holan, Martin; Hidasova, Denisa; Pohl, Radek; Klepetarova, Blanka; Jahn, Ullrich; Cisarova, Ivana; Angewandte Chemie, International Edition; vol. 53; nb. 37; (2014); p. 9944 - 9948,5; Angewandte Chemie; vol. 126; nb. 37; (2014); p. 10102 10106,5, View in Reaxys; Uchimoto, Hitomi; Tsuji, Tomoko; Kawasaki, Ikuo; Arimitsu, Kenji; Yasui, Hiroyuki; Yamashita, Masayuki; Ohta, Shunsaku; Nishide, Kiyoharu; Chemical and Pharmaceutical Bulletin; vol. 63; nb. 3; (2015); p. 200 - 209, View in Reaxys; Li, Aipeng; Ye, Lidan; Wu, Hongping; Yang, Xiaohong; Yu, Hongwei; Journal of Molecular Catalysis B: Enzymatic; vol. 122; (2015); p. 179 - 187, View in Reaxys

18/126

2018-07-03 19:01:53

Liang, Yu-Feng; Zhou, Xin-Feng; Tang, Shi-Ya; Huang, Yao-Bing; Feng, Yi-Si; Xu, Hua-Jian; RSC Advances; vol. 3; nb. 21; (2013); p. 7739 - 7742, View in Reaxys; Liu, Cong; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei; Organic Letters; vol. 16; nb. 20; (2014); p. 5458 - 5461, View in Reaxys; Huang, Xing-Fen; Wu, Qing-Lai; He, Jian-Shi; Huang, Zhi-Zhen; Organic and Biomolecular Chemistry; vol. 13; nb. 15; (2015); p. 4466 - 4472, View in Reaxys

Lou, Zhenbang; Zhang, Shu; Chen, Chao; Pang, Xinlong; Li, Ming; Wen, Lirong; Advanced Synthesis and Catalysis; vol. 356; nb. 1; (2014); p. 153 - 159, View in Reaxys; Xie, Yanjun; Cheng, Xiufang; Liu, Saiwen; Chen, Hui; Zhou, Wang; Yang, Luo; Deng, Guo-Jun; Green Chemistry; vol. 17; nb. 1; (2015); p. 209 - 213, View in Reaxys

PhCOCH&2%CH &3%

Denizalti, Serpil; Mercan, Deniz; A en, BetA l; GA kA e, AytaA GA rhan; A etinkaya, Bekir; Journal of Organometallic Chemistry; vol. 779; (2015); p. 62 - 66, View in Reaxys

24e

Waser, Jerome; Perrotta, Daniele; Racine, Sophie; Vuilleumier, Jeremy; De Nanteuil, Florian; Organic Letters; vol. 17; nb. 4; (2015); p. 1030 - 1033, 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

2aa

Guo, Jun; Chen, Jianhui; Lu, Zhan; Chemical Communications; vol. 51; nb. 26; (2015); p. 5725 - 5727, View in Reaxys

Song, Xiaoning; Chang, Jian; Zhu, Dongsheng; Li, Jiaheng; Xu, Cong; Liu, Qun; Wang, Mang; Organic Letters; vol. 17; nb. 7; (2015); p. 1712 - 1715, View in Reaxys; Sun, Kai; Wang, Xin; Jiang, Yongqing; Lv, Yunhe; Zhang, Liping; Xiao, Beibei; Li, Donghui; Zhu, Zhonghong; Liu, Lin; Chemistry - An Asian Journal; vol. 10; nb. 3; (2015); p. 536 - 539, View in Reaxys

2ab

Chen, Shu-Jie; Lu, Guo-Ping; Cai, Chun; Synthesis (Germany); vol. 47; nb. 7; (2015); p. 976 - 984, View in Reaxys

Feng, Xun; Xu, Chen; Wang, Zhi-Qiang; Tang, Si-Fu; Fu, Wei-Jun; Ji, Bao-Ming; Wang, Li-Ya; Inorganic Chemistry; vol. 54; nb. 5; (2015); p. 2088 - 2090, View in Reaxys

De La Campa, Raquel; Ortín, Irene; Dixon, Darren J.; Angewandte Chemie - International Edition; vol. 54; nb. 16; (2015); p. 4895 - 4898; Angew. Chem.; vol. 127; nb. 16; (2015); p. 4977 - 4980,4, View in Reaxys

Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Sun, Hui-Ying; Wang, Mei; Wu, An-Xin; Organic Letters; vol. 17; nb. 8; (2015); p. 1914 - 1917, View in Reaxys; Nakajima, Masaki; Fava, Eleonora; Loescher, Sebastian; Jiang, Zhen; Rueping, Magnus; Angewandte Chemie - International Edition; vol. 54; nb. 30; (2015); p. 8828 - 8832; Angew. Chem.; vol. 127; nb. 30; (2015); p. 8952 - 8956,5, View in Reaxys

IIo

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

2; 10; 5b

Pathe, Gulab Khushalrao; Ahmed, Naseem; Tetrahedron Letters; vol. 56; nb. 12; (2015); p. 1555 - 1561, View in Reaxys

10a

Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys

Facchetti, Giorgio; Gandolfi, Raffaella; Fusè, Marco; Zerla, Daniele; Cesarotti, Edoardo; Pellizzoni, Michela; Rimoldi, Isabella; New Journal of Chemistry; vol. 39; nb. 5; (2015); p. 3792 - 3800, View in Reaxys

Davis, Dexter C.; Mohammad, Haroon; Kyei-Baffour, Kwaku; Younis, Waleed; Creemer, Cassidy Noel; Seleem, Mohamed N.; Dai, Mingji; European Journal of Medicinal Chemistry; vol. 101; (2015); p. 384 - 390, View in Reaxys

1-1m

Hu, Naifu; Zhao, Guoqing; Zhang, Yuanyuan; Liu, Xiangqian; Li, Guangyu; Tang, Wenjun; Journal of the American Chemical Society; vol. 137; nb. 21; (2015); p. 6746 - 6749, View in Reaxys

Komkov, Alexander V.; Komendantova, Anna S.; Menchikov, Leonid G.; Chernoburova, Elena I.; Volkova, Yulia A.; Zavarzin, Igor V.; Organic Letters; vol. 17; nb. 15; (2015); p. 3734 - 3737, View in Reaxys

Kišic, Andrea; Stephan, Michel; Mohar, Barbara; Advanced Synthesis and Catalysis; vol. 357; nb. 11; (2015); p. 2540 - 2546, View in Reaxys

S-1b

Yang, Kai; Yang, Zhen; Dang, Qun; Bai, Xu; European Journal of Organic Chemistry; vol. 2015; nb. 20; (2015); p. 4344 - 4347, View in Reaxys

en 1 t3 sm

Pan, Xiaojun; Liu, Qiao; Chang, Liming; Yuan, Gaoqing; RSC Advances; vol. 5; nb. 63; (2015); p. 51183 - 51187, View in Reaxys

19/126

2018-07-03 19:01:53

18b

Dethe, Dattatraya H.; Murhade, Ganesh M.; Ghosh, Sourav; Journal of Organic Chemistry; vol. 80; nb. 16; (2015); p. 8367 - 8376, View in Reaxys

Garel, Claire; Renard, Brice-Loc; Escande, Vincent; Galtayries, Anouk; Hesemann, Peter; Grison, Claude; Applied Catalysis A: General; vol. 504; (2015); p. 272 - 286, View in Reaxys

Dong, Qizhi; Li, Ningbo; Qiu, Renhua; Wang, Jinying; Guo, Cancheng; Xu, Xinhua; Journal of Organometallic Chemistry; vol. 799-800; (2015); p. 122 - 127, View in Reaxys

3aa

Aravinda Kumar; Venkateswarlu, Vunnam; Vishwakarma, Ram A.; Sawant, Sanghapal D.; Synthesis (Germany); vol. 47; nb. 20; (2015); p. 3161 - 3168; Art.No: SS-2015-T0238-OP, View in Reaxys

Peng, Dongjie; Zhang, Mintao; Huang, Zheng; Chemistry - A European Journal; vol. 21; nb. 42; (2015); p. 14737 14741, View in Reaxys

2; 2a

Chandra Mohan, Darapaneni; Ravi, Chitrakar; Pappula, Venkatanarayana; Adimurthy, Subbarayappa; Journal of Organic Chemistry; vol. 80; nb. 13; (2015); p. 6846 - 6855, View in Reaxys

6; 6b

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

Yabu; Masumoto; Yamasaki; Hamashima; Kanai; Du; Curran; Shibasaki; Journal of the American Chemical Society; vol. 123; nb. 40; (2001); p. 9908 - 9909, View in Reaxys; Munoz-Hernandez, Lorell; Seda, Luis A.; Wang, Bo; Soderquist, John A.; Organic Letters; vol. 16; nb. 15; (2014); p. 4052 - 4055, View in Reaxys

Jun, Chul-Ho; Moon, Choong Woon; Hong, Jun-Bae; Lim, Sung-Gon; Chung, Kwan-Yong; Kim, Yeon-Hee; Chemistry - A European Journal; vol. 8; nb. 2; (2002); p. 485 - 492, View in Reaxys; Chelucci, Giorgio; Manca, Ilaria; Pinna, Gerard A.; Tetrahedron Letters; vol. 46; nb. 5; (2005); p. 767 - 770, View in Reaxys; Miura, Katsukiyo; Nakagawa, Takahiro; Hosomi, Akira; Synlett; nb. 12; (2005); p. 1917 - 1921; Art.No: U14605ST, View in Reaxys; Miyamura, Hiroyuki; Yasukawa, Tomohiro; Kobayashi, Shu; Tetrahedron; vol. 70; nb. 36; (2014); p. 6039 - 6049, View in Reaxys

Yu, Ajuan; Li, Jingya; Cui, Mengjun; Wu, Yangjie; Synlett; nb. 19; (2007); p. 3063 - 3067, View in Reaxys; Piola, Lorenzo; Ferandez-Salas, Jos A.; Manzini, Simone; Nolan, Steven P.; Organic and Biomolecular Chemistry; vol. 12; nb. 43; (2014); p. 8683 - 8688, View in Reaxys

12b

Li, Xiaoguang; Chen, Weiping; Hems, William; King, Frank; Xiao, Jianliang; Organic Letters; vol. 5; nb. 24; (2003); p. 4559 - 4561, View in Reaxys; Hobuss, Dennis; Baro, Angelika; Laschat, Sabine; Frey, Wolfgang; Tetrahedron; vol. 64; nb. 8; (2008); p. 1635 - 1640, View in Reaxys; Ren, Kai; Hu, Bei; Zhao, Mengmeng; Tu, Yahui; Xie, Xiaomin; Zhang, Zhaoguo; Journal of Organic Chemistry; vol. 79; nb. 5; (2014); p. 2170 - 2177, View in Reaxys

Takeda, Norihiko; Miyata, Okiko; Naito, Takeaki; European Journal of Organic Chemistry; nb. 9; (2007); p. 1491 1509, 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

Shi, Yan; Zhu, Xuebin; Mao, Haibin; Hu, Hongwen; Zhu, Chengjian; Cheng, Yixiang; Chemistry - A European Journal; vol. 19; nb. 35; (2013); p. 11553 - 11557, View in Reaxys; Achar, Tapas Kumar; Maiti, Saikat; Mal, Prasenjit; RSC Advances; vol. 4; nb. 25; (2014); p. 12834 - 12839, View in Reaxys

Morcillo, Sara P.; Martinez-Peragon, Angela; Jakoby, Verena; Mota, Antonio J.; Kube, Christian; Justicia, Jose; Cuerva, Juan M.; Gansaeuer, Andreas; Chemical Communications; vol. 50; nb. 17; (2014); p. 2211 - 2213, View in Reaxys

Jiang, Jinju; Chen, Xi; Feng, Jinhui; Wu, Qiaqing; Zhu, Dunming; Journal of Molecular Catalysis B: Enzymatic; vol. 100; (2014); p. 32 - 39, View in Reaxys

7; PP

Kohtani, Shigeru; Kamoi, Yuna; Yoshioka, Eito; Miyabe, Hideto; Catalysis Science and Technology; vol. 4; nb. 4; (2014); p. 1084 - 1091, View in Reaxys

14g

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

2; 3

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

1ab

Zhou, Yuhan; Yang, Dongmei; Luo, Gen; Zhao, Yilong; Luo, Yi; Xue, Na; Qu, Jingping; Tetrahedron; vol. 70; nb. 31; (2014); p. 4668 - 4674, View in Reaxys

1'u

Huang, Xiaoqiang; Jiao, Ning; Organic and Biomolecular Chemistry; vol. 12; nb. 25; (2014); p. 4324 - 4328, View in Reaxys

1{5}

Mobaraki, Akbar; Movassagh, Barahman; Karimi, Babak; ACS Combinatorial Science; vol. 16; nb. 7; (2014); p. 352 - 358, View in Reaxys

20/126

2018-07-03 19:01:53

S11

Coll, Mercè; Pàmies, Oscar; Diéguez, Montserrat; Advanced Synthesis and Catalysis; vol. 356; nb. 10; (2014); p. 2293 - 2302, View in Reaxys

Takise, Ryosuke; Muto, Kei; Yamaguchi, Junichiro; Itami, Kenichiro; Angewandte Chemie - International Edition; vol. 53; nb. 26; (2014); p. 6791 - 6794; Angew. Chem.; vol. 126; nb. 26; (2014); p. 6909 - 6912,4, View in Reaxys

Moriyama, Katsuhiko; Nakamura, Yu; Togo, Hideo; Organic Letters; vol. 16; nb. 14; (2014); p. 3812 - 3815, View in Reaxys

Jiang, Heyan; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 410 - 413, View in Reaxys

Soheilizad, Mehdi; Adiba, Mehdi; Sajjadifarb, Sami; Journal of Chemical Research; vol. 38; nb. 9; (2014); p. 524 527, View in Reaxys

11b

Ghaffari, Behnaz; Preshlock, Sean M.; Plattner, Donald L.; Staples, Richard J.; Maligres, Peter E.; Krska, Shane W.; Maleczka, Robert E.; Smith, Milton R.; Journal of the American Chemical Society; vol. 136; nb. 41; (2014); p. 14345 - 14348, View in Reaxys

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

4eb

Skillinghaug, Bobo; Sköld, Christian; Rydfjord, Jonas; Svensson, Fredrik; Behrends, Malte; Sävmarker, Jonas; Sjöberg, Per J. R.; Larhed, Mats; Journal of Organic Chemistry; vol. 79; nb. 24; (2014); p. 12018 - 12032, View in Reaxys

Chaudhuri, Sangeeta Roy; Hartwig, Jan; Kupracz, Lukas; Kodanek, Torben; Wegner, Jens; Kirschning, Andreas; Advanced Synthesis and Catalysis; vol. 356; nb. 17; (2014); p. 3530 - 3538, View in Reaxys

(E)-2a

Zhang, De-Yang; Zhu, Fu-Lin; Wang, Ya-Hui; Hu, Xin-Hu; Chen, Song; Hou, Chuan-Jin; Hu, Xiang-Ping; Chemical Communications; vol. 50; nb. 92; (2014); p. 14459 - 14462, 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

Miyagawa, Michiyo; Satou, Tadaaki; Yukimune, Chihiro; Ishibashi, Ayumi; Seimiya, Haruna; Yamada, Hideo; Hasegawa, Toshio; Koike, Kazuo; Phytotherapy Research; vol. 28; nb. 11; (2014); p. 1710 - 1712, View in Reaxys

Giurg, Miroslaw; Mlochowski, Jacek; Synthetic Communications; vol. 29; nb. 24; (1999); p. 4307 - 4313, View in Reaxys; Wang, Jin-Xian; Jia, Xuefeng; Meng, Tuanjie; Xin, Li; Synthesis; nb. 17; (2005); p. 2838 - 2844; Art.No: F07505SS, 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

Hamashima, Yoshitaka; Kanai, Motomu; Shibasaki, Masakatsu; Tetrahedron Letters; vol. 42; nb. 4; (2001); p. 691 694, View in Reaxys; Xu, Qing-Long; Gao, Hongyin; Yousufuddin, Muhammed; Ess, Daniel H.; Kuerti, Laszlo; Journal of the American Chemical Society; vol. 135; nb. 38; (2013); p. 14048 - 14051, View in Reaxys

Goessnitzer, Edith; Feierl, Gebhard; Wagner, Ute; European Journal of Pharmaceutical Sciences; vol. 15; nb. 1; (2002); p. 49 - 61, View in Reaxys; Menendez-Rodriguez, Lucia; Crochet, Pascale; Cadierno, Victorio; Journal of Molecular Catalysis A: Chemical; vol. 366; (2013); p. 390 - 399, View in Reaxys

Xu, Jiaxi; Wei, Tiezheng; Zhang, Qihan; Journal of Organic Chemistry; vol. 69; nb. 20; (2004); p. 6860 - 6866, View in Reaxys; Tanaka, Ken; Otake, Yousuke; Wada, Azusa; Noguchi, Keiichi; Hirano, Masao; Organic Letters; vol. 9; nb. 11; (2007); p. 2203 - 2206, View in Reaxys; Wang, Lei; Huang, Jiayao; Gong, Xiaojie; Wang, Jian; Chemistry - A European Journal; vol. 19; nb. 23; (2013); p. 7555 - 7560, View in Reaxys

Ghorai, Manas K.; Halder, Sandipan; Samanta, Sauvik; Australian Journal of Chemistry; vol. 65; nb. 9; (2012); p. 1262 - 1270,9, View in Reaxys; Ghorai, Manas K.; Halder, Sandipan; Samanta, Sauvik; Australian Journal of Chemistry; vol. 65; nb. 9; (2012); p. 1262 - 1270, View in Reaxys; Zhou, Han; Huang, Hanmin; ChemCatChem; vol. 5; nb. 8; (2013); p. 2253 - 2257, View in Reaxys

tbl 4 ent 4

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

2c; 6a

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys

Ding, Song; Qiao, Xin; Kucera, Gregory L.; Bierbach, Ulrich; Chemical Communications; vol. 49; nb. 24; (2013); p. 2415 - 2417, View in Reaxys

Zahid, Muhammad; Iaroshenko, Viktor O.; Saghyan, Ashot S.; Fischer, Christine; Langer, Peter; Tetrahedron; vol. 69; nb. 16; (2013); p. 3451 - 3458, View in Reaxys

13d

Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 - 5935, View in Reaxys

21a

Di Nunno, Leonardo; Scilimati, Antonio; Vitale, Paola; Tetrahedron; vol. 61; nb. 10; (2005); p. 2623 - 2630, View in Reaxys; Gonzalez-Lopez De Turiso, Felix; Shin, Youngsook; Brown, Matthew; Cardozo, Mario; Chen, Yi; Fong, David; Hao, Xiaolin; He, Xiao; Henne, Kirk; Hu, Yi-Ling; Johnson, Michael G.; Kohn, Todd; Lohman, Ju-

21/126

2018-07-03 19:01:53

lia; McBride, Helen J.; McGee, Lawrence R.; Medina, Julio C.; Metz, Daniela; Miner, Kent; Mohn, Deanna; Pattaropong, Vatee; Seganish, Jennifer; Simard, Jillian L.; Wannberg, Sharon; Whittington, Douglas A.; Yu, Gang; Cushing, Timothy D.; Journal of Medicinal Chemistry; vol. 55; nb. 17; (2012); p. 7667 - 7685, View in Reaxys 11a

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; Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 - 4260, View in Reaxys

14h

Dinca, Emanuela; Hartmann, Philip; Smrcek, Jakub; Dix, Ina; Jones, Peter G.; Jahn, Ullrich; European Journal of Organic Chemistry; nb. 24; (2012); p. 4461 - 4482, View in Reaxys

14n

Xie, Ying; Pan, Hongjie; Xiao, Xiao; Li, Songlei; Shi, Yian; Organic and Biomolecular Chemistry; vol. 10; nb. 45; (2012); p. 8960 - 8962,3, View in Reaxys; Xie, Ying; Pan, Hongjie; Xiao, Xiao; Li, Songlei; Shi, Yian; Organic and Biomolecular Chemistry; vol. 10; nb. 45; (2012); p. 8960 - 8962, View in Reaxys

Table 2. ketone 2,7

Khan, Noor-ul H.; Agrawal, Santosh; Kureshy, Rukhsana I.; Abdi, Sayed H.R.; Singh, Surendra; Suresh, Eringathodi; Jasra, Raksh V.; Tetrahedron Letters; vol. 49; nb. 4; (2008); p. 640 - 644, View in Reaxys

Eisch, John J.; Gitua, John N.; Otieno, Peter O.; Shi, Xian; Journal of Organometallic Chemistry; vol. 624; nb. 1-2; (2001); p. 229 - 238, View in Reaxys; Deng, Hongbo; Isler, Markus P; Snapper, Marc L; Hoveyda, Amir H; Angewandte Chemie (International ed. in English); vol. 41; nb. 6; (2002); p. 1009 - 1012, View in Reaxys; Moskalev, Nikolai; Barbasiewicz, Michal; Makosza, Mieczyslaw; Tetrahedron; vol. 60; nb. 2; (2004); p. 347 - 358, View in Reaxys; Eisch, John J.; Adeosun, Adetenu A.; European Journal of Organic Chemistry; nb. 6; (2005); p. 993 - 997, View in Reaxys; Coyne, Anthony G.; Guiry, Patrick J.; Tetrahedron Letters; vol. 48; nb. 5; (2007); p. 747 - 750, View in Reaxys; Border, Zola-Michele; Marais, Charlene; Bezuidenhoudt, Barend C. B.; Steenkamp, Jacobus A.; Australian Journal of Chemistry; vol. 61; nb. 2; (2008); p. 122 - 130, View in Reaxys

Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys

10 (R2=H)

Watanabe, Kazutoshi; Morinaka, Yasuhiro; Hayashi, Yoshio; Shinoda, Masaki; Nishi, Hiroyoshi; Fukushima, Nobuko; Watanabe, Toshiaki; Ishibashi, Akira; Yuki, Satoshi; Tanaka, Masahiko; Bioorganic and Medicinal Chemistry Letters; vol. 18; nb. 4; (2008); p. 1478 - 1483, View in Reaxys

start to 1b,d,i,j

Murakami, Kei; Ohmiya, Hirohisa; Yorimitsu, Hideki; Oshima, Koichiro; Tetrahedron Letters; vol. 49; nb. 15; (2008); p. 2388 - 2390, View in Reaxys

Substrate,Tab.2, run Matsukawa, Satoru; Kitazaki, Eri; Tetrahedron Letters; vol. 49; nb. 18; (2008); p. 2982 - 2984, View in Reaxys 17 Ph-CO-Et

Minisci, Francesco; Recupero, Francesco; Fontana, Francesca; Bjorsvik, Hans-Rene; Liguori, Lucia; Synlett; nb. 4; (2002); p. 610 - 612, 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; 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

Ph-COCH2CH3

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

Tab.2, entry 3, subst.

Zhou, Wenjun; Yan, Wenjun; Wang, Jin-Xian; Wang, Kehu; Synlett; nb. 1; (2008); p. 137 - 141, View in Reaxys

C6H5COC2H5

Shen, Yongcun; Feng, Xiaoming; Li, Yan; Zhang, Guolin; Jiang, Yaozhong; Synlett; nb. 5; (2002); p. 793 - 795, View in Reaxys; Zhou, Jian-Feng; Tu, Shu-Jiang; Feng, Jun-Cai; Synthetic Communications; vol. 32; nb. 7; (2002); p. 959 - 962, View in Reaxys; Matsukawa, Satoru; Saijo, Marina; Tetrahedron Letters; vol. 49; nb. 31; (2008); p. 4655 - 4657, View in Reaxys

PhCOCH2Me

Xie, Yuan-Yuan; Chen, Zhen-Chu; Zheng, Qin-Guo; Synthesis; nb. 11; (2002); p. 1505 - 1508, View in Reaxys; Kraus, George A.; Choudhury, Prabir K.; Synlett; nb. 1; (2004); p. 97 - 98, View in Reaxys; Kawano, Yuhta; Togo, Hideo; Synlett; nb. 2; (2008); p. 217 - 220, View in Reaxys

Baumgartner, Maria T.; Jimenez, Liliana B.; Pierini, Adriana B.; Rossi, Roberto A.; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (2002); p. 1092 - 1097, View in Reaxys; Demizu, Yosuke; Shiigi, Hirofumi; Oda, Takahisa; Matsumura, Yoshihiro; Onomura, Osamu; Tetrahedron Letters; vol. 49; nb. 1; (2008); p. 48 - 52, View in Reaxys

educt of 6f

Lu, Jun; Liu, Feng; Zhou, Wei-Juan; Loh, Teck-Peng; Tetrahedron Letters; vol. 49; nb. 37; (2008); p. 5389 - 5392, View in Reaxys

19a

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

Xu, Hanhui; Ekoue-Kovi, Kekeli; Wolf, Christian; Journal of Organic Chemistry; vol. 73; nb. 19; (2008); p. 7638 7650, 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.

22/126

2018-07-03 19:01:53

Patent; STUDIENGESELLSCHAFT KOHLE MBH; US2008/255355; (2008); (A1) English, View in Reaxys

Table 1, entry 2

Anderson, Christopher D.; Shea, Kenneth J.; Rychnovsky, Scott D.; Organic Letters; vol. 7; nb. 22; (2005); p. 4879 4882, View in Reaxys; Comte, Virginie; Balan, Cedric; Le Gendre, Pierre; Moise, Claude; Chemical Communications; nb. 7; (2007); p. 713 - 715, View in Reaxys

carbonyl comp. tab 2/11

Kumar, Atul; Ahamd; Maurya; Tetrahedron Letters; vol. 48; nb. 8; (2007); p. 1399 - 1401, View in Reaxys

byprod. to 3a

Nomura, Kenichi; Matsubara, Seijiro; Chemistry Letters; vol. 36; nb. 1; (2007); p. 164 - 165, View in Reaxys

1a, R1=Ph R2=CH3

Su, Weike; Jin, Can; Organic Letters; vol. 9; nb. 6; (2007); p. 993 - 996, View in Reaxys

educt 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

10b

Gupton, John T.; Krumpe, Keith E.; Burnham, Bruce S.; Dwornik, Kate A.; Petrich, Scott A.; Du, Karen X.; Bruce, Marc A.; Vu, Phong; Vargas, Marian; Keertikar, Kartik M.; Hosein, Kirsten N.; Jones, Claude R.; Sikorski, James A.; Tetrahedron; vol. 54; nb. 20; (1998); p. 5075 - 5088, View in Reaxys; Kuwano; Uemura; Saitoh; Ito; Tetrahedron Letters; vol. 40; nb. 7; (1999); p. 1327 - 1330, View in Reaxys; 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; Musser; Richey Jr.; Journal of Organic Chemistry; vol. 65; nb. 23; (2000); p. 7750 - 7756, View in Reaxys; Vinogradov; Mikhalev; Pavlov; Ferapontov; Malyshev; Heise; Russian Chemical Bulletin; vol. 50; nb. 5; (2001); p. 843 - 845, View in Reaxys; Chen, Tao; Liu, Xu-Guang; Shi, Min; Tetrahedron; vol. 63; nb. 23; (2007); p. 4874 - 4880, View in Reaxys

1 (table 3, runs 1-3) Kise, Naoki; Shiozawa, Yousuke; Ueda, Nasuo; Tetrahedron; vol. 63; nb. 25; (2007); p. 5415 - 5426, View in Reaxys product, tab 2/11

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

Tab.1.run3

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

table 1, entry 2

Shaabani, Ahmad; Rahmati, Abbas; Sharifi, Masoumeh; Rad, Jafar Mogimi; Aghaaliakbari, Behnaz; Farhangi, Elham; Lee, Donald G.; Monatshefte fur Chemie; vol. 138; nb. 7; (2007); p. 649 - 651, View in Reaxys

ketone b

Cortez, Norma A.; Aguirre, Gerardo; Parra-Hake, Miguel; Somanathan, Ratnasamy; Tetrahedron Letters; vol. 48; nb. 25; (2007); p. 4335 - 4338, View in Reaxys

Imachi, Shohei; Mukaiyama, Teruaki; Chemistry Letters; vol. 36; nb. 6; (2007); p. 718 - 719, View in Reaxys

2; X = CH3; R2 = Ph

Kumari, N. Vijaya; Nagarapu, Lingaiah; Shivaraj; Synthetic Communications; vol. 37; nb. 14; (2007); p. 2325 2329, View in Reaxys

9 (Tab.2, run 1)

Justik, Michael W.; Tetrahedron Letters; vol. 48; nb. 17; (2007); p. 3003 - 3007, View in Reaxys

Table 1, entry 6

Habibi, Mohammad H.; Farhadi, Saeid; Journal of Chemical Research; nb. 4; (2004); p. 296 - 297, View in Reaxys; Shaabani, Ahmad; Rahmati, Abbas; Naderi, Soheila; Synthetic Communications; vol. 37; nb. 22; (2007); p. 4035 4042, View in Reaxys

T1, E1-2, P1

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

phenyl-COEt

Lee, Sung Il; Hwang, Geum-Sook; Ryu, Do Hyun; Synlett; nb. 1; (2007); p. 59 - 62, View in Reaxys

ketone Table 3 entry 11

Vander Mierde, Hans; Ledoux, Nele; Allaert, Bart; Van Der Voort, Pascal; Drozdzak, Renata; De Vos, Dirk; Verpoort, Francis; New Journal of Chemistry; vol. 31; nb. 9; (2007); p. 1572 - 1574, View in Reaxys

PhCOEt

Ubeda, J. Ignacio; Villacampa, Mercedes; Avendano, Carmen; Synthesis; nb. 8; (1999); p. 1335 - 1340, View in Reaxys; Vazquez-Garcia, Digna; Fernandez, Alberto; Fernandez, Jesus J.; Lopez-Torres, Margarita; Suarez, Antonio; Ortigueira, Juan M.; Vila, Jose M.; Adams, Harry; Journal of Organometallic Chemistry; vol. 595; nb. 2; (2000); p. 199 - 207, View in Reaxys; Yasuda, Makoto; Onishi, Yoshiyuki; Ito, Takeshi; Baba, Akio; Tetrahedron Letters; vol. 41; nb. 14; (2000); p. 2425 - 2428, View in Reaxys; Dell'erba, Carlo; Gruttadauria, Michelangelo; Mugnoli, Angelo; Noto, Renato; Novi, Marino; Occhiucci, Giorgio; Petrillo, Giovanni; Spinelli, Domenico; Tetrahedron; vol. 56; nb. 26; (2000); p. 4565 - 4573, View in Reaxys; Aitken; Ali; De Elena; Lightfoot; Tetrahedron Letters; vol. 41; nb. 41; (2000); p. 7965 - 7968, View in Reaxys; Cooper; Lucas; Taylor; Ward; Williamson; Synthesis; nb. 4; (2001); p. 621 - 625, View in Reaxys; Tanabe; Matsumoto; Funakoshi; Manta; Synlett; nb. 12; (2001); p. 1959 1961, View in Reaxys; Miura; Ootsuka; Suda; Nishikori; Hosomi; Synlett; nb. 10; (2001); p. 1617 - 1619, View in Reaxys; Samec, Joseph S. M.; Baeckvall, Jan-E.; Chemistry - A European Journal; vol. 8; nb. 13; (2002); p. 2955 - 2961, View in Reaxys; Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Tetrahedron Asymmetry; vol. 14; nb. 9; (2003); p. 1103 - 1114, View in Reaxys; Concellon, Jose M.; Bardales, Eva; Gomez, Cecilia; Tetrahedron Letters; vol. 44; nb. 28; (2003); p. 5323 - 5326, View in Reaxys; Bartnik, Romuald; Baylere, Patrick; Chrostowska, Anna; Galindo, Alberto; Lesniak, Stanislaw; Pfister-Guillouzo, Genevieve; European Journal of Organic Chemistry; nb. 13; (2003); p. 2475 - 2479, View in Reaxys; Cuervo, Dario; Gamasa, M. Pilar; Gimeno, Jose; Chemistry - A European Journal; vol. 10; nb. 2; (2004); p. 425 - 432, View in Reaxys; Pandey, Ghanshyam; Singh, Ravi P.; Garg, Ashish;

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.

23/126

2018-07-03 19:01:53

Singh, Vinod K.; Tetrahedron Letters; vol. 46; nb. 12; (2005); p. 2137 - 2140, View in Reaxys; Martinez, Ricardo; Brand, Gabriel J.; Ramon, Diego J.; Yus, Miguel; Tetrahedron Letters; vol. 46; nb. 21; (2005); p. 3683 - 3686, View in Reaxys; Chang, Hsu-Kai; Datta, Swarup; Das, Arindam; Odedra, Arjan; Liu, Rai-Shung; Angewandte Chemie - International Edition; vol. 46; nb. 25; (2007); p. 4744 - 4747, View in Reaxys; Chang, Chi-Tsing; Liao, BeiSih; Liu, Shiuh-Tzung; Tetrahedron Letters; vol. 47; nb. 52; (2006); p. 9257 - 9259, View in Reaxys; Akiike, Junnosuke; Yamamoto, Yukiharu; Togo, Hideo; Synlett; nb. 14; (2007); p. 2168 - 2172, View in Reaxys; Vatmurge, Namdev S.; Hazra, Braja G.; Pore, Vandana S.; Australian Journal of Chemistry; vol. 60; nb. 3; (2007); p. 196 - 204, View in Reaxys; Nagase, Ryohei; Matsumoto, Noriaki; Hosomi, Kohei; Higashi, Takahiro; Funakoshi, Syunsuke; Misaki, Tomonori; Tanabe, Yoo; Organic and Biomolecular Chemistry; vol. 5; nb. 1; (2007); p. 151 - 159, View in Reaxys 4.4a

Rao, Maddali L.N.; Venkatesh, Varadhachari; Banerjee, Debasis; Tetrahedron; vol. 63; nb. 52; (2007); p. 12917 12926, View in Reaxys

Tab 3/6 ketone

Eagon, Scott; Kim, Jinsoo; Yan, Katie; Haddenham, Dustin; Singaram, Bakthan; Tetrahedron Letters; vol. 48; nb. 51; (2007); p. 9025 - 9029, View in Reaxys

educt to 2a-b

Jachak, Madhukar N.; Avhale, Appasaheb B.; Toche, Ragunath B.; Sabnis, Ram W.; Journal of Heterocyclic Chemistry; vol. 44; nb. 2; (2007); p. 343 - 347, View in Reaxys

Tab.2.,Ent.1., product

Zhu, Mingxia; Wei, Xin; Li, Bodong; Yuan, Youzhu; Tetrahedron Letters; vol. 48; nb. 52; (2007); p. 9108 - 9111, View in Reaxys

Table 1, entry 12

Karimi, Babak; Biglari, Abbass; Clark, James H.; Budarin, Vitaly; Angewandte Chemie - International Edition; vol. 46; nb. 38; (2007); p. 7210 - 7213, View in Reaxys

Li, Xiaoguang; Chen, Weiping; Hems, William; King, Frank; Xiao, Jianliang; Tetrahedron Letters; vol. 45; nb. 5; (2004); p. 951 - 953, 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; Singh, Pradeep N. D.; Mandel, Sarah M.; Sankaranarayanan, Jagadis; Muthukrishnan, Sivaramakrishnan; Chang, Mingxin; Robinson, Rachel M.; Lahti, Paul M.; Ault, Bruce S.; Gudmundsdottir, Anna D.; Journal of the American Chemical Society; vol. 129; nb. 51; (2007); p. 16263 - 16272, View in Reaxys

Gazzard, Lewis J.; Motherwell, William B.; Sandham, David A.; Journal of the Chemical Society - Perkin Transactions 1; nb. 8; (1999); p. 979 - 993, View in Reaxys; Camacho, Drexel H; Nakamura, Itaru; Oh, Byoung Ho; Saito, Shinichi; Yamamoto, Yoshinori; Tetrahedron Letters; vol. 43; nb. 16; (2002); p. 2903 - 2907, View in Reaxys; Anwar, Shaik; Periasamy, Mariappan; Tetrahedron Asymmetry; vol. 17; nb. 23; (2006); p. 3244 - 3247, View in Reaxys

Migianu, Evelyne; Kirsch, Gilbert; Synthesis; nb. 8; (2002); p. 1096 - 1100, View in Reaxys; Donohue, Sean R.; Halldin, Christer; Pike, Victor W.; Bioorganic and Medicinal Chemistry; vol. 14; nb. 11; (2006); p. 3712 - 3720, View in Reaxys

22j

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; 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

C6H5COCH2CH3

Chen, Fuxue; Feng, Xiaoming; Qin, Bo; Zhang, Guolin; Jiang, Yaozhong; Synlett; nb. 4; (2003); p. 558 - 560, View in Reaxys; Oudeyer; Leonel; Paugam; Nedelec; Synthesis; nb. 3; (2004); p. 389 - 400, View in Reaxys; Zhou, Hui; Chen, Fu-Xue; Qin, Bo; Feng, Xiaoming; Zhang, Guolin; Synlett; nb. 6; (2004); p. 1077 - 1079, View in Reaxys; Tajbakhsh; Lakouraj; Fadavi; Synthetic Communications; vol. 34; nb. 7; (2004); p. 1173 - 1181, View in Reaxys; Yamamoto, Yukiharu; Togo, Hideo; Synlett; nb. 5; (2006); p. 798 - 800, View in Reaxys

Product, Tab.2, run 6

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

product 19

Farhadi, Saeid; Zaringhadam, Parisa; Sahamieh, Reza Zarei; Tetrahedron Letters; vol. 47; nb. 12; (2006); p. 1965 1968, View in Reaxys

Tab. 3, entry 4

Crochet, Pascale; Diez, Josefina; Fernandez-Zumel, Mariano A.; Gimeno, Jose; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 93 - 100, View in Reaxys; Zhang, Guofu; Liu, Renhua; Xu, Qing; Ma, Lixin; Liang, Xinmiao; Advanced Synthesis and Catalysis; vol. 348; nb. 7-8; (2006); p. 862 - 866, View in Reaxys

starting to 1

Chau, Felix H. V.; Corey; Tetrahedron Letters; vol. 47; nb. 15; (2006); p. 2581 - 2583, View in Reaxys

1f, R1=Ph R2=CH3 Prakash, Om; Pannu, Kamaljeet; Prakash, Richa; Batra, Anita; Molecules; vol. 11; nb. 7; (2006); p. 523 - 527, View in Reaxys entry 18

Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys

Substrate,Tab.1/2,run 2

Rao, Maddali L.N.; Jadhav, Deepak N.; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6883 - 6886, View in Reaxys

t.1, ketone, line 3

Hernandez, Eliud; Burgos, Carlos H.; Alicea, Eyleen; Soderquist, John A.; Organic Letters; vol. 8; nb. 18; (2006); p. 4089 - 4091, 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.

24/126

2018-07-03 19:01:53

Substrate, 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

Table 1, starting

Xing, Yan; Chen, Jian-Shan; Dong, Zhen-Rong; Li, Yan-Yun; Gao, Jing-Xing; Tetrahedron Letters; vol. 47; nb. 26; (2006); p. 4501 - 4503, View in Reaxys

Tab.2.col.4.r.38.

Rao, Maddali L.N.; Venkatesh, Varadhachari; Jadhav, Deepak N.; Tetrahedron Letters; vol. 47; nb. 39; (2006); p. 6975 - 6978, View in Reaxys

Tab. 2, entry 7

Diaz-Alvarez, Alba E.; Crochet, Pascale; Zablocka, Maria; Duhayon, Carine; Cadierno, Victorio; Gimeno, Jose; Majoral, Jean Pierre; Advanced Synthesis and Catalysis; vol. 348; nb. 12-13; (2006); p. 1671 - 1679, View in Reaxys

Tab. 4, entry 16

Lu, Gui; Li, Xingshu; Li, Yue-Ming; Kwong, Fuk Yee; Chan, Albert S. C.; Advanced Synthesis and Catalysis; vol. 348; nb. 14; (2006); p. 1926 - 1933, View in Reaxys

Park, Jung-Woo; Chang, Hoon-Jo; Jun, Chul-Ho; Synlett; nb. 5; (2006); p. 771 - 775, View in Reaxys

Tab 1/8-9 Educt

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

product, tab 3/25

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

18a

Bacherikov, Valeriy A.; Tsai, Tsong-Jen; Chang, Jang-Yang; Chou, Ting-Chao; Lee, Rong-Zau; Su, Tsann-Long; European Journal of Organic Chemistry; nb. 19; (2006); p. 4490 - 4499, View in Reaxys

3b, tab.1,entries 2,3,4

Zhang, Lirong; Chan, Kin Shing; Journal of Organometallic Chemistry; vol. 691; nb. 18; (2006); p. 3782 - 3787, 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

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

Zhao, Baowei; Lu, Xiyan; Organic Letters; vol. 8; nb. 26; (2006); p. 5987 - 5990, View in Reaxys

ketone, Tab. 3, entry 8

Li, Xiaohong; Blacker, John; Houson, Ian; Wu, Xiaofeng; Xiao, Jianliang; Synlett; nb. 8; (2006); p. 1155 - 1160, View in Reaxys

Nagaoka; Kayahara; Wakabayashi; Bioscience, biotechnology, and biochemistry; vol. 65; nb. 3; (2001); p. 634 - 637, View in Reaxys; Ishichi, Yuji; Ikeura, Yoshinori; Natsugari, Hideaki; Tetrahedron; vol. 60; nb. 20; (2004); p. 4481 4490, 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

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; Knudsen, Kristian Rahbek; Stepan, Antonia F.; Michel, Patrick; Ley, Steven V.; Organic and Biomolecular Chemistry; vol. 4; nb. 8; (2006); p. 1471 - 1473, View in Reaxys

T. S2 entry 1. product

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

2, R1=Ph, R2=Me

Das, Biswanath; Reddy, K. Ravinder; Ramu; Thirupathi; Ravikanth; Synlett; nb. 11; (2006); p. 1756 - 1758, View in Reaxys

Tab. 2, entry 10, prod.

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

12, R1=Ph, R2=Et

Forrat, Vicente J.; Prieto, Oscar; Ramon, Diego J.; Yus, Miguel; Chemistry - A European Journal; vol. 12; nb. 16; (2006); p. 4431 - 4445, View in Reaxys

Kotha; Tafesh; Davenport; Ortiz; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 40; nb. 12; (2001); p. 1166 - 1169, View in Reaxys; Carmeli, Mira; Rozen, Shlomo; Tetrahedron Letters; vol. 47; nb. 5; (2006); p. 763 - 766, View in Reaxys; Crich, David; Huang, Xianhai; Newcomb, Martin; Organic Letters; vol. 1; nb. 2; (1999); p. 225 - 227, View in Reaxys

PHCOEt

Perosa, Alvise; Tundo, Pietro; Selva, Maurizio; Canton, Patrizia; Chemical Communications; nb. 43; (2006); p. 4480 - 4482, View in Reaxys

13f

Hansen, Anne-Lene L.; Murray, Anthony; Tanner, David; Organic and Biomolecular Chemistry; vol. 4; nb. 24; (2006); p. 4497 - 4505, View in Reaxys

20; 10

Jing, Qing; Sandoval, Christian A.; Wang, Zheng; Ding, Kuiling; European Journal of Organic Chemistry; nb. 16; (2006); p. 3606 - 3616, 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.

25/126

2018-07-03 19:01:53

starting Tab. run 8

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

Tab. 2. Ent.2-3. ketone

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

3, 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

19b

Zhang, Yongda; Rovis, Tomislav; Journal of the American Chemical Society; vol. 126; nb. 49; (2004); p. 15964 15965, View in Reaxys; Farhadi, Saeid; Afshari, Mozhgan; Maleki, Mansoureh; Babazadeh, Zaynab; Tetrahedron Letters; vol. 46; nb. 49; (2005); p. 8483 - 8486, View in Reaxys; Yamaguchi, Kazuya; Koike, Takeshi; Kotani, Miyuki; Matsushita, Mitsunori; Shinachi, Satoshi; Mizuno, Noritaka; Chemistry - A European Journal; vol. 11; nb. 22; (2005); p. 6574 - 6582, View in Reaxys

educt to 5g

Bhat, Ramakrishna P.; Raje, Vivek P.; Alexander, Varughese M.; Patil, Sachin B.; Samant, Shriniwas D.; Tetrahedron Letters; vol. 46; nb. 28; (2005); p. 4801 - 4803, View in Reaxys

substrate, entry 6

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

4, R1 = Ph, R2 = Me

Xie, Yuan-Yuan; Synthetic Communications; vol. 35; nb. 13; (2005); p. 1741 - 1746, View in Reaxys

ketone from 1b

Verzijl, Gerard K.M.; De Vries, Johannes G.; Broxterman, Quirinus B.; Tetrahedron Asymmetry; vol. 16; nb. 9; (2005); p. 1603 - 1610, View in Reaxys

5, Table 2, entry 2

Hatano, Manabu; Matsumura, Tokihiko; Ishihara, Kazuaki; Organic Letters; vol. 7; nb. 4; (2005); p. 573 - 576, View in Reaxys

Product, T. 1, Entry Tajbakhsh, Mahmoud; Alimohammadi, Kamal; Behmadi, Hossein; Barghamadi, Mohammad; Journal of Chemi5 cal Research; nb. 1; (2005); p. 35 - 37, View in Reaxys educt to 8

Balog, Mirela; Ramondenc, Yvan; Oprean, Ioan; Grosu, Ion; Ple, Gerard; Heterocyclic Communications; vol. 11; nb. 5; (2005); p. 389 - 394, View in Reaxys

Table 4. Ketone 8

Matsumoto, Kiyoshi; Kim, Jong Chul; Iida, Hirokazu; Hamana, Hiroshi; Kumamoto, Koji; Kotsuki, Hiyoshizo; Jenner, Gerard; Helvetica Chimica Acta; vol. 88; nb. 7; (2005); p. 1734 - 1753, View in Reaxys

4, 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

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

10, R%1& = Et

Forrat, Vicente J.; Ramon, Diego J.; Yus, Miguel; Tetrahedron Asymmetry; vol. 16; nb. 20; (2005); p. 3341 - 3344, View in Reaxys

11e

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

Inoue, Kousuke; Makino, Yoshihide; Itoh, Nobuya; Tetrahedron Asymmetry; vol. 16; nb. 15; (2005); p. 2539 - 2549, View in Reaxys

Wiles, Charlotte; Watts, Paul; Haswell, Stephen J.; Pombo-Villar, Esteban; Tetrahedron; vol. 61; nb. 45; (2005); p. 10757 - 10773, View in Reaxys

2; R1=Ph, R2=Me

Cai, Xiao-hua; Yang, Hai-jun; Zhang, Guo-lin; Synthesis; nb. 10; (2005); p. 1569 - 1571, View in Reaxys

tab2, ketone, entry2 Krzeminski, Marek P.; Wojtczak, Andrzej; Tetrahedron Letters; vol. 46; nb. 48; (2005); p. 8299 - 8302, View in Reaxys 1 (Ar = Ph, R1 = C2H5)

Kise, Naoki; Agui, Syun; Morimoto, Shinji; Ueda, Nasuo; Journal of Organic Chemistry; vol. 70; nb. 23; (2005); p. 9407 - 9410, View in Reaxys

Xu, Jiaxi; Xia, Jiakun; Lan, Yu; Synthetic Communications; vol. 35; nb. 17; (2005); p. 2347 - 2353, View in Reaxys

T.1, 2 (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

ketone, Tab.1, entry Yu, Tao; Sun, Xiaohua; Wang, Congyang; Deng, Liang; Xi, Zhenfeng; Chemistry - A European Journal; vol. 11; nb. 4 6; (2005); p. 1895 - 1902, View in Reaxys ketone, Tab.3, entry Cesar, Vincent; Beliemin-Laponnaz, Stephane; Wadepohl, Hubert; Gade, Lutz H.; Chemistry - A European Jour5 nal; vol. 11; nb. 9; (2005); p. 2862 - 2873, View in Reaxys educt to 4

Li, Donghong; Zhang, Yongbin; Guo, Wei; Xia, Chizhong; Heterocycles; vol. 65; nb. 5; (2005); p. 1063 - 1069, 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.

26/126

2018-07-03 19:01:53

ketone, table 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

3, 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

starting Tab.3. run 2 Tyagarajan, Sriram; Chakravarty, Prasun K.; Tetrahedron Letters; vol. 46; nb. 46; (2005); p. 7889 - 7891, View in Reaxys product tab. 3, entr.11

Li, Shi-Jun; Wang, Yan-Guang; Tetrahedron Letters; vol. 46; nb. 46; (2005); p. 8013 - 8015, View in Reaxys

PhCOC2H5

Mlynarski, Jacek; Jankowska, Joanna; Rakiel, Bartosz; Chemical Communications; nb. 38; (2005); p. 4854 - 4856, View in Reaxys

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

PhCOCH2CH3

Ranu, Brindaban C.; Dutta, Pinak; Sarkar, Arunkanti; Journal of the Chemical Society - Perkin Transactions 1; nb. 9; (1999); p. 1139 - 1140, View in Reaxys; Loh, Teck-Peng; Wei, Lin-Li; Feng, Li-Chun; Synlett; nb. 7; (1999); p. 1059 - 1060, View in Reaxys; Curphey; Libby; Tetrahedron Letters; vol. 41; nb. 36; (2000); p. 6977 - 6980, View in Reaxys; Lee; Jin; Choi; Chemical Communications; nb. 11; (2001); p. 956 - 957, View in Reaxys; Firouzabadi; Fakoorpour; Hazarkhani; Synthetic Communications; vol. 31; nb. 24; (2001); p. 3859 - 3862, View in Reaxys; Schmittel; Ghorai; Synlett; nb. 12; (2001); p. 1992 - 1994, View in Reaxys; Alnajjar, Mikhail S.; Zhang, Xian-Man; Gleicher, Gerald J.; Truksa, Scott V.; Franz, James A.; Journal of Organic Chemistry; vol. 67; nb. 25; (2002); p. 9016 - 9022, View in Reaxys; Lee, Jong Chan; Bae, Yong Hun; Synlett; nb. 4; (2003); p. 507 - 508, View in Reaxys; Kim, Sung Soo; Jung, Hyun Chul; Synthesis; nb. 14; (2003); p. 2135 - 2137, View in Reaxys; Saito, Bunnai; Katsuki, Tsutomu; Synlett; nb. 9; (2004); p. 1557 - 1560, View in Reaxys; Rahman, Md. Taifur; Kamata, Naoya; Matsubara, Hiroshi; Ryu, Ilhyong; Synlett; nb. 17; (2005); p. 2664 - 2666; Art.No: U24305ST, View in Reaxys

4, R1=H, R2=Me, Note 5

Watanuki, Susumu; Sakamoto, Shuichi; Harada, Hironori; Kikuchi, Kazumi; Kuramochi, Takahiro; Kawaguchi, Ken-Ichi; Okazaki, Toshio; Tsukamoto, Shin-Ichi; Heterocycles; vol. 62; (2004); p. 127 - 130, View in Reaxys

9, R1=Me, R2=H

Li, Jin; Lundy DeMello, Kristin M.; Cheng, Henry; Sakya, Subas M.; Bronk, Brian S.; Rafka, Robert J.; Jaynes, Burton H.; Ziegler, Carl B.; Kilroy, Carolyn; Mann, Donald W.; Nimz, Eric L.; Lynch, Michael P.; Haven, Michelle L.; Kolosko, Nicole L.; Minich, Martha L.; Li, Chao; Dutra, Jason K.; Rast, Bryson; Crosson, Rhonda M.; Morton, Barry J.; Kirk, Glen W.; Callaghan, Kathleen M.; Koss, David A.; Shavnya, Andrei; Lund, Lisa A.; Seibel, Scott B.; Petras, Carol F.; Silvia, Annette; Bioorganic and Medicinal Chemistry Letters; vol. 14; nb. 1; (2004); p. 95 - 98, View in Reaxys

7 (R1=C6H5, R2=C2H5)

Vaghei, Ramin Ghorbani; Khazaei, Ardeshir; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 179; nb. 1; (2004); p. 55 - 59, View in Reaxys

4b, Tab. 2

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

educt T.3 col.1 run 1

Justik, Michael W.; Koser, Gerald F.; Tetrahedron Letters; vol. 45; nb. 32; (2004); p. 6159 - 6163, View in Reaxys

table 2, entries 15+16

Karimi, Babak; Rajabi, Jamshid; Organic Letters; vol. 6; nb. 17; (2004); p. 2841 - 2844, View in Reaxys

10e

Seppi, Michael; Kalkofen, Rainer; Reupohl, Jens; Froehlich, Roland; Hoppe, Dieter; Angewandte Chemie - International Edition; vol. 43; nb. 11; (2004); p. 1423 - 1427, View in Reaxys

Table 1, entry 7

Kim, Sung Soo; Rajagopal, Gurusamy; Synthetic Communications; vol. 34; nb. 12; (2004); p. 2237 - 2243, View in Reaxys

Table 1, entry 4

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

2, R1=Ph, R2=Et

Firouzabadi, Habib; Iranpoor, Nasser; Hassani, Hassan; Sobhani, Sara; Synthetic Communications; vol. 34; nb. 11; (2004); p. 1967 - 1972, View in Reaxys

4(R1=C6H5, R2=C2H5)

Ghorbani-Vaghei, Ramin; Khazaei, Ardeshir; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 179; nb. 6; (2004); p. 1169 - 1173, View in Reaxys

Entry 1

Chavan, Subhash P.; Shivasankar; Sivappa; Journal of Chemical Research; nb. 6; (2004); p. 406 - 407, View in Reaxys

prod., Tab. 2, entry 5

Cadierno, Victorio; Garcia-Garrido, Sergio E.; Gimeno, Jose; Chemical Communications; nb. 2; (2004); p. 232 233, View in Reaxys

1; R1=H, R2=C2H5

Tamura, Masanori; Matsukawa, Yasuhisa; Quan, Heng-Dao; Mizukado, Junji; Sekiya, Akira; Journal of Fluorine Chemistry; vol. 125; nb. 5; (2004); p. 705 - 709, 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.

27/126

2018-07-03 19:01:53

Table 4, entry 1

Adjabeng, George; Brenstrum, Tim; Frampton, Christopher S.; Robertson, Al J.; Hillhouse, John; McNulty, James; Capretta, Alfredo; Journal of Organic Chemistry; vol. 69; nb. 15; (2004); p. 5082 - 5086, 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.1, product, entry 2 Shaabani, Ahmad; Soleimani, Kamal; Bazgir, Ayoob; Synthetic Communications; vol. 34; nb. 18; (2004); p. 3303 3315, View in Reaxys Entry 6, Tab. I

Heravi, Majid M.; Ajami, Darush; Shoar, Rahim Hekmat; Sarmad, Nooshin; Faridbod, Farnoush; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 179; nb. 12; (2004); p. 2423 - 2427, View in Reaxys

ketone, Tab.1, entry Ueno, Makoto; Togo, Hideo; Synthesis; nb. 16; (2004); p. 2673 - 2677, View in Reaxys 17 Tab. 2, entry 13,ketone

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

ketone, Tab.2, entry Li, Yan; He, Bin; Feng, Xiaoming; Zhang, Guolin; Synlett; nb. 9; (2004); p. 1598 - 1600, View in Reaxys 3 MeCH2COPh

Concellon, Jose M.; Bernad, Pablo L.; Bardales, Eva; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2445 - 2450, View in Reaxys

substr., Tab.1, entry 2

Kerrigan, Nessan J.; Hutchison, Panee C.; Heightman, Tom D.; Procter, David J.; Organic and Biomolecular Chemistry; vol. 2; nb. 17; (2004); p. 2476 - 2482, View in Reaxys

Subtrate, Tab.1, run Lee, Dong-Won; Yun, Jaesook; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5415 - 5417, View in Reaxys 9 1 (Ar=Ph, R1=Et)

Maekawa, Hirofumi; Yamamoto, Yoshimasa; Shimada, Hisashi; Yonemura, Kazuaki; Nishiguchi, Ikuzo; Tetrahedron Letters; vol. 45; nb. 20; (2004); p. 3869 - 3872, View in Reaxys

Table 1 entry 5 substr.

Lee, Jong Chan; Park, Jin Young; Yoon, So Young; Bae, Yong Hun; Lee, Seung Jun; Tetrahedron Letters; vol. 45; nb. 1; (2004); p. 191 - 193, View in Reaxys

Adam, Waldemar; Mock-Knoblauch, Cordula; Saha-Moeller, Chantu R.; Journal of Organic Chemistry; vol. 64; nb. 13; (1999); p. 4834 - 4839, View in Reaxys; Yamasaki, Shingo; Fujii, Kunihiko; Wada, Reiko; Kanai, Motomu; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 124; nb. 23; (2002); p. 6536 - 6537, View in Reaxys; Mori, Yoshikazu; Seki, Masahiko; Tetrahedron Letters; vol. 45; nb. 39; (2004); p. 7343 - 7345, View in Reaxys

Table 1, entry 6, educt

Kraus, George A.; Choudhury, Prabir K.; European Journal of Organic Chemistry; nb. 10; (2004); p. 2193 - 2197, View in Reaxys

Substrate, Tab.1, run 8

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

PhC(O)Et

Bolm, Carsten; Derrien, Nadine; Seger, Andreas; Chemical Communications; nb. 20; (1999); p. 2087 - 2088, View in Reaxys; Lorber, Christian Y.; Smidt, Sebastian P.; Osborn, John A.; European Journal of Inorganic Chemistry; nb. 4; (2000); p. 655 - 658, View in Reaxys; Lee, Jong Chan; Choi, Hyun Jung; Lee, Yong Chan; Tetrahedron Letters; vol. 44; nb. 1; (2003); p. 123 - 125, View in Reaxys; Firouzabadi, Habib; Iranpoor, Nasser; Amani, Kamal; Synthesis; nb. 3; (2003); p. 408 - 412, View in Reaxys; Kerrigan, Nessan J.; Hutchison, Panee C.; Heightman, Tom D.; Procter, David J.; Chemical Communications; nb. 12; (2003); p. 1402 - 1403, View in Reaxys

table 1, entry 9

Sakuratani, Kenji; Togo, Hideo; Synthesis; nb. 1; (2003); p. 21 - 23, View in Reaxys

2, Table 1, entry 8

Hoener, Annabelle P. Frutos; Henkel, Bernd; Gauvin, Jean-Christophe; Synlett; nb. 1; (2003); p. 63 - 66, View in Reaxys

ketone, entry 9

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

T. 2., prod. 4

Fernandes, Rodney A.; Kumar, Pradeep; Tetrahedron Letters; vol. 44; nb. 6; (2003); p. 1275 - 1278, View in Reaxys

6ca

Grison, Claude; Thomas, Antoine; Coutrot, Frederic; Coutrot, Philippe; Tetrahedron; vol. 59; nb. 12; (2003); p. 2101 - 2123, View in Reaxys

Xie, Jian-Hua; Wang, Li-Xin; Fu, Yu; Zhu, Shuo-Fei; Fan, Bao-Min; Duan, Hai-Feng; Zhou, Qi-Lin; Journal of the American Chemical Society; vol. 125; nb. 15; (2003); p. 4404 - 4405, View in Reaxys

Uma, Ramalinga; Gouault, Nicolas; Crevisy, Christophe; Gree, Rene; Tetrahedron Letters; vol. 44; nb. 33; (2003); p. 6187 - 6190, View in Reaxys

Tab. col.2/3 run5

Huertas, Ramon E.; Corella, Joseph A.; Soderquist, John A.; Tetrahedron Letters; vol. 44; nb. 24; (2003); p. 4435 4437, 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.

28/126

2018-07-03 19:01:53

1, R1=Ph, R2=Me

Winter, Andreas; Risch, Nikolaus; Synlett; nb. 13; (2003); p. 1959 - 1964, View in Reaxys; Haeuseler, Andreas; Henn, Wolfgang; Schmittel, Michael; Synthesis; nb. 16; (2003); p. 2576 - 2589, View in Reaxys

starting to 5h

Panunzi, Barbara; Rotiroti, Lucia; Tingoli, Marco; Tetrahedron Letters; vol. 44; nb. 49; (2003); p. 8753 - 8756, View in Reaxys

2, table 1, entry 3

Matsumoto, Kiyoshi; Tanaka, Akinori; Yukio, Ikemi; Hayashi, Naoto; Toda, Mitsuo; Bulman, Robert A.; Heterocyclic Communications; vol. 9; nb. 1; (2003); p. 9 - 12, View in Reaxys

R1=Ph, R2=CH3

Lee, Jong Chan; Lee, Yong Chan; Synthetic Communications; vol. 33; nb. 22; (2003); p. 3943 - 3946, View in Reaxys

T. 2-8, product

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

Tab.1, entry 13, subst.

Karimi, Babak; Ma'mani, Leila; Synthesis; nb. 16; (2003); p. 2503 - 2506, View in Reaxys

product tab. 1. run 2

Arnold, Joshua N.; Hayes, Patrick D.; Kohaus, Robert L.; Mohan, Ram S.; Tetrahedron Letters; vol. 44; nb. 51; (2003); p. 9173 - 9176, View in Reaxys

Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys

35a

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

subs., 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

ketone, Tab.3, entry Pastor, Isidro M.; Vaestilae, Patrik; Adolfsson, Hans; Chemistry - A European Journal; vol. 9; nb. 17; (2003); p. 4031 14 - 4045, 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

Table 2, entry 8

Kabalka; Li; Tejedor; Malladi; Gao; Trotman; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2783 - 2787, View in Reaxys; Tao, Beata; Fu, Gregory C.; Angewandte Chemie - International Edition; vol. 41; nb. 20; (2002); p. 3892 - 3894, View in Reaxys

ketone, entry 1

Lee, Cheng Leng; Sim, Mui Mui; Tetrahedron Letters; vol. 41; nb. 30; (2000); p. 5729 - 5732, View in Reaxys; Lee, Jong Chan; Park, Hong-Jun; Park, Jin Young; Tetrahedron Letters; vol. 43; nb. 32; (2002); p. 5661 - 5664, View in Reaxys

entry 1, product

Moisan, Lionel; Hardouin, Christophe; Rousseau, Bernard; Doris, Eric; Tetrahedron Letters; vol. 43; nb. 11; (2002); p. 2013 - 2015, View in Reaxys

t.2, ketone, entry 6

Tangestaninejad; Habibi; Mirkhani; Moghadam; Molecules; vol. 7; nb. 2; (2002); p. 264 - 270, View in Reaxys

1, Ar = Ph, R = Me

Lopez-Alvarado; Avendano; Synthesis; nb. 1; (2002); p. 104 - 110, View in Reaxys

10, T.3, e.9

Itoh, Takashi; Nagata, Kazuhiro; Kurihara, Ayako; Miyazaki, Michiko; Ohsawa, Akio; Tetrahedron Letters; vol. 43; nb. 17; (2002); p. 3105 - 3108, View in Reaxys

7b, Ar=C6H5, R=C2H5

Maillard, David; Pozzi, Gianluca; Quici, Silvio; Sinou, Denis; Tetrahedron; vol. 58; nb. 20; (2002); p. 3971 - 3976, View in Reaxys

Tabl 2 run 4 educt

Cai, Dongwei; Larsen, Robert D; Reider, Paul J; Tetrahedron Letters; vol. 43; nb. 23; (2002); p. 4285 - 4287, View in Reaxys

11, R2=Et

Tice, Colin M.; Michelotti, Enrique L.; Mata, Ernesto G.; Nicolas, Ernesto; Garcia, Javier; Albericio, Fernando; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7491 - 7494, View in Reaxys

IIb

Dem'yanovich; Shishkina; Potekhin; Sosnina; Zefirov; Doklady Chemistry; vol. 386; nb. 4-6; (2002); p. 269 - 272, View in Reaxys

Product, Tab.2, run 23

Ganchegui, Benjamin; Bouquillon, Sandrine; Henin, Francoise; Muzart, Jacques; Tetrahedron Letters; vol. 43; nb. 37; (2002); p. 6641 - 6644, View in Reaxys

product, T1, E3

Shaabani, Ahmad; Bazgir, Ayoob; Teimouri, Fatemeh; Lee, Donald G; Tetrahedron Letters; vol. 43; nb. 29; (2002); p. 5165 - 5167, View in Reaxys

Nicolaou; Montagnon; Baran; Zhong; Journal of the American Chemical Society; vol. 124; nb. 10; (2002); p. 2245 2258, View in Reaxys

entry 4, table 3

Nishiyama, Yutaka; Kajimoto, Hiroyuki; Kotani, Kazuya; Nishida, Takuma; Sonoda, Noboru; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5696 - 5700, View in Reaxys

Table 3, R = Ph

Inoue, Tadashi; Liu, Ji-Feng; Buske, Dana C.; Abiko, Atsushi; Journal of Organic Chemistry; vol. 67; nb. 15; (2002); p. 5250 - 5256, View in Reaxys

ketone for 1m

Concellon, Jose M.; Bardales, Eva; Organic Letters; vol. 4; nb. 2; (2002); p. 189 - 191, 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.

29/126

2018-07-03 19:01:53

9 (Table 3, entry 11)

Huang, Zheng-Zheng; Tang, Yong; Journal of Organic Chemistry; vol. 67; nb. 15; (2002); p. 5320 - 5326, View in Reaxys

I-4

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

13a

Crevisy, Christophe; Wietrich, Marina; Le Boulaire, Virginie; Uma, Ramalinga; Gree, Rene; Tetrahedron Letters; vol. 42; nb. 3; (2001); p. 395 - 398, View in Reaxys

Substr., Tab., entry 4

Lee, Jong Chan; Choi, Ju-Hee; Synlett; nb. 2; (2001); p. 234 - 235, View in Reaxys

Tab 6. Entry 2, Prod.

Fernandez, Isabel; Pedro, Jose R.; Rosello, Antonio L.; Ruiz, Rafael; Castro, Isabel; Ottenwaelder, Xavier; Journaux, Yves; European Journal of Organic Chemistry; nb. 7; (2001); p. 1235 - 1247, View in Reaxys

substrate,t.1,entry 7 Matloubi Moghaddam; Ghaffarzadeh; Synthetic Communications; vol. 31; nb. 2; (2001); p. 317 - 321, View in Reaxys 3, Table 1, entry 1

Kodomari, Mitsuo; Nagaoka, Takashi; Furusawa, Yuhsuke; Tetrahedron Letters; vol. 42; nb. 17; (2001); p. 3105 3107, View in Reaxys

Table 2, entry 2

Liu; Zhu; Sun; Xu; Synthetic Communications; vol. 31; nb. 10; (2001); p. 1521 - 1526, View in Reaxys

20d

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

1 (R1=Ph,R2=Me)

Xie; Chen; Journal of Chemical Research - Part S; nb. 4; (2001); p. 156 - 157, View in Reaxys

EtCOPh

Lagu, Bharat; Pan, Meng; Wachter, Michael P; Tetrahedron Letters; vol. 42; nb. 35; (2001); p. 6027 - 6030, View in Reaxys

1, R1=Ph, R2=CH3 Zhang; Chen; Synthesis; nb. 14; (2001); p. 2075 - 2077, View in Reaxys 5l, Ph-CO-Et

Wang, Yanli; Zhu, Shizheng; Tetrahedron Letters; vol. 42; nb. 33; (2001); p. 5741 - 5744, View in Reaxys

T.1. ketone 2

Kamble, Rajesh M; Singh, Vinod K; Tetrahedron Letters; vol. 42; nb. 42; (2001); p. 7525 - 7526, View in Reaxys

1, R1=C6H5, R2=CH3

Xie; Chen; Synthetic Communications; vol. 31; nb. 20; (2001); p. 3145 - 3149, View in Reaxys

Table 2, Run 8, Ketone

Ozawa, Fumiyuki; Yamamoto, Shogo; Kawagishi, Seiji; Hiraoka, Masatomi; Ikeda, Shintaro; Minami, Tatsuya; Ito, Shigekazu; Yoshifuji, Masaaki; Chemistry Letters; nb. 10; (2001); p. 972 - 973, View in Reaxys

Tab.2.,entry 2A,ketone

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

1ii

Firouzabadi; Iranpoor; Hazarkhani; Journal of Organic Chemistry; vol. 66; nb. 22; (2001); p. 7527 - 7529, View in Reaxys

t.2, pr., entry 6

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

Ph-COEt

Cho, Chan Sik; Kim, Bok Tae; Kim, Tae-Jeong; Shim, Sang Chul; Chemical Communications (Cambridge, United Kingdom); nb. 24; (2001); p. 2576 - 2577, View in Reaxys

subst.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

from 25

Uma, Ramalinga; Davies, Maxwell K.; Crevisy, Christophe; Gree, Rene; European Journal of Organic Chemistry; nb. 16; (2001); p. 3141 - 3146, View in Reaxys

ketone 6

Heravi, Majid M.; Beheshtiha, Yahya S.; Ghasemzadeh, Mitra; Hekmatshoar, Rahim; Sarmad, Nooshin; Monatshefte fur Chemie; vol. 131; nb. 2; (2000); p. 187 - 190, View in Reaxys

Substrate, Tab.2, run 3

Armstrong, Alan; Atkin, Mark A.; Swallow, Steven; Tetrahedron Letters; vol. 41; nb. 13; (2000); p. 2247 - 2251, View in Reaxys

carbonyl compound Heravi, Majid M.; Ajami, Dariush; Hekmatshoar, Rahim; Beheshtiha, Yahya Sh.; Assadollah, Karim; Ghassem6 zadeh, Mitra; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 55; nb. 5; (2000); p. 431 433, View in Reaxys C6H54COCH2CH3 Reddy; Synthesis; nb. 9; (2000); p. 1217 - 1218, View in Reaxys educt, entry 3

Lee, Jong Chan; Song, In-Goul; Tetrahedron Letters; vol. 41; nb. 31; (2000); p. 5891 - 5894, View in Reaxys

educt, row 4

Clavel, Philippe; Biran, Claude; Bordeau, Michel; Roques, Nicolas; Trevinc, Stephane; Tetrahedron Letters; vol. 41; nb. 45; (2000); p. 8763 - 8767, View in Reaxys

30/126

2018-07-03 19:01:53

Table 2. ketone 12

Hamasaki; Chounan; Horino; Yamamoto; Tetrahedron Letters; vol. 41; nb. 50; (2000); p. 9883 - 9887, View in Reaxys

tab. 5, entry 2

Touchard, Francois; Fache, Fabienne; Lemaire, Marc; European Journal of Organic Chemistry; nb. 22; (2000); p. 3787 - 3792, View in Reaxys

substrate T5/enty 4

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

Hamashima, Yoshitaka; Kanai, Motomu; Shibasaki, Masakatsu; Journal of the American Chemical Society; vol. 122; nb. 30; (2000); p. 7412 - 7413, View in Reaxys

5, H

Togo; Nabana; Yamaguchi; Journal of Organic Chemistry; vol. 65; nb. 24; (2000); p. 8391 - 8394, View in Reaxys

23b

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

Tab.1, run 4-6, Substr.

Moughamir, Khadija; Mezgueldi, Bouchra; Atmani, Aziz; Mestdagh, Helene; Rolando, Christian; Tetrahedron Letters; vol. 40; nb. 1; (1999); p. 59 - 62, View in Reaxys

substr. Table 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

ketone, tab. 1, ent. 2 Flintoft, Rebecca J.; Buzby, Jennifer C.; Tucker, John A.; Tetrahedron Letters; vol. 40; nb. 24; (1999); p. 4485 4488, View in Reaxys 5 R1=Ph R2=C2H5 Enders, Dieter; Meyer, Ilka; Runsink, Jan; Raabe, Gerhard; Heterocycles; vol. 50; nb. 2; (1999); p. 995 - 1024, View in Reaxys t.1,pr.,entry 3

Shi, Qi-Zeng; Wang, Jian-Ge; Cai, Kun; Synthetic Communications; vol. 29; nb. 7; (1999); p. 1177 - 1181, View in Reaxys

Table 2, entry 7

Yamanoi, Yoshinori; Imamoto, Tsuneo; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 2988 - 2989, View in Reaxys

Tab 1 Ent 2 product 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 43

Lu, Ling; Chang, Hung-Yu; Fang, Jim-Min; Journal of Organic Chemistry; vol. 64; nb. 3; (1999); p. 843 - 853, View in Reaxys

entry 5

Lee, Jong Chan; Jin, Yong Suk; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2769 - 2774, View in Reaxys

propioph.

Aramendia, Maria Angeles; Borau, Victoriano; Jimenez, Cesar; Marinas, Jose Maria; Romero, Francisco Jose; Journal of Catalysis; vol. 183; nb. 1; (1999); p. 119 - 127, 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

educt of b

Vila, Jose M.; Pereira, Ma. Teresa; Ortigueira, Juan M.; Grana, Maria; Lata, Dario; Suarez, Antonio; Fernandez, Jesus J.; Fernandez, Alberto; Lopez-Torres, Margarita; Adams, Harry; Journal of the Chemical Society - Dalton Transactions; nb. 23; (1999); p. 4193 - 4201, View in Reaxys

starting to 1g

Halterman, Ronald L.; Zhu, Chengian; Tetrahedron Letters; vol. 40; nb. 42; (1999); p. 7445 - 7448, 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

C6H5COEt

Bhattacharyya, Sukanta; Neidigh, Kurt A.; Avery, Mitchell A.; Williamson, John S.; Synlett; nb. 11; (1999); p. 1781 - 1783, View in Reaxys

Tab.2, entry 1, prod.

Marko, Istvan E.; Gautier, Arnaud; Tsukazaki, Masao; Llobet, Antoni; Plantalech-Mir, Elena; Urch, Christopher J.; Brown, Stephen M.; Angewandte Chemie - International Edition; vol. 38; nb. 13-14; (1999); p. 1960 - 1962, View in Reaxys

to 21

Aftab, Tajassus; Carter, Christabel; Hart, Jennifer; Nelson, Adam; Tetrahedron Letters; vol. 40; nb. 49; (1999); p. 8679 - 8683, View in Reaxys

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

ketone 1c

Miura, Katsukiyo; Sato, Hiroshi; Tamaki, Kentaro; Ito, Hajime; Hosomi, Akira; Tetrahedron Letters; vol. 39; nb. 17; (1998); p. 2585 - 2588, View in Reaxys

Table 2 (entries 5/6) Jiang, Qiongzhong; Jiang, Yutong; Xiao, Dengming; Cao, Ping; Zhang, Xumu; Angewandte Chemie - International Edition; vol. 37; nb. 8; (1998); p. 1100 - 1103, 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.

31/126

2018-07-03 19:01:53

ketone entry 4

Mukaiyama, Teruaki; Kagayama, Akifumi; Shiina, Isamu; Chemistry Letters; nb. 11; (1998); p. 1107 - 1108, View in Reaxys

IIa

Pashkevich; Khomutov; Sevenard; Russian Journal of Organic Chemistry; vol. 34; nb. 12; (1998); p. 1727 - 1730, View in Reaxys

Patent-Specific Data (30) Prophetic ComLocation in Patent pound

References Patent; HINDUSTAN PETROLEUM CORPORATION LTD.; RAVISHANKAR, Raman; RAJU, Chinthalapati Siva Kesava; PRAMANIK, Bhaskar; CHALAPATHI RAO, Peddy Venkat; NETTEM, Venkateswarlu Choudary; SRIGANESH, Gandham; (25 pag.); WO2018/2947; (2018); (A1) English, View in Reaxys Patent; CHIBA UNIVERSITY; GODO SHIGEN COMPANY LIMITED; TOGO, HIDEO; IMAI, SHO; MIYAMOTO, MICHIHIKO; (10 pag.); JP2018/2680; (2018); (A) Japanese, View in Reaxys Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys Patent; Yuanjiang Hualong Catalyst Technology Co., Ltd.; Guo, Cancheng; Xu, Jingwen; Guo, Xin; (10 pag.); CN106349149; (2017); (A) Chinese, View in Reaxys Patent; Soochow University (Suzhou); Ji Shunjun; Chu Xueqiang; Xu Xiaoping; (20 pag.); CN106496127; (2017); (A) Chinese, View in Reaxys Patent; Anyang Normal University; Sun Kai; Du Weimin; Lv Yunhe; Wang Xin; (11 pag.); CN106699662; (2017); (A) Chinese, View in Reaxys Patent; Henan Normal University; Fan Xuesen; Wang Ze; Zhang Xinying; Chen Guang; (18 pag.); CN106749238; (2017); (A) Chinese, View in Reaxys Patent; Hunan Institute of Science and Technology; Zhou Congshan; Yang Zan; Yang Tao; Li Jiao; (11 pag.); CN107011162; (2017); (A) Chinese, View in Reaxys Patent; Henan Normal University; Fan Xuesen; Tian Miaomiao; Zhang Xinying; Shi Xiaonan; (15 pag.); CN107089950; (2017); (A) Chinese, View in Reaxys Patent; Henan Normal University; Zhang Xinying; Fan Xuesen; Tian Miaomiao; Shi Xiaonan; (14 pag.); CN107141258; (2017); (A) Chinese, View in Reaxys Patent; Shanghai University; Shen Subo; Zhang Jianmin; Fang Fang; Guo Yuwei; He Zhiqing; (11 pag.); CN104557670; (2017); (B) Chinese, View in Reaxys Patent; Nanjing University of Science and Technology; Li Feng; Wang Rongzhou; (15 pag.); CN107400084; (2017); (A) Chinese, View in Reaxys Patent; Henan Normal University; Zhang Xinying; Fan Xuesen; Wang Ze; Chen Guang; (12 pag.); CN106749020; (2017); (A) Chinese, View in Reaxys Patent; Nanyang Normal College; Zhang Xu; Xu Xuefeng; Wang Zhiqiang; Xu Kun; Yu Lintao; Zhao Qiang; Mao Wutao; Yan Yanlei; (10 pag.); CN105175328; (2017); (B) Chinese, View in Reaxys Patent; ERICA Industry-University Cooperation Foundation of Hanyang University; Lee Hak-jun; Go Seong-hyeon; Ahn Hyeon-seok; (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; Yuanjiang Hualong Catalyst Technology Co., Ltd.; Guo, Xin; Xu, Jingwen; Guo, Cancheng; (18 pag.); CN106220495; (2016); (A) Chinese, View in Reaxys Patent; ANHUI NORMAL UNIVERSITY; YAN, LIQIN; XIE, QIGUANG; PANG, SHUFEN; (8 pag.); CN105669441; (2016); (A) Chinese, View in Reaxys Patent; Hanyang University Erica Campus; Lee, Hak Jun; Koh, Sung Hyung; Ahn, Hyun Suk; (8 pag.); KR2016/119898; (2016); (A) Korean, View in Reaxys Patent; Yin, Qiang; (8 pag.); CN105111072; (2016); (B) Chinese, View in Reaxys

32/126

2018-07-03 19:01:53

Patent; Yuanjiang Hualong Catalysis Technology Co., Ltd.; Guo Xin; Xu Jingwen; Guo Cancheng; (19 pag.); CN106242968; (2016); (A) Chinese, View in Reaxys Patent; Yuanjiang Hualong Catalyst Technology Co., Ltd.; Guo, Xin; Xu, Jingwen; Guo, Cancheng; (18 pag.); CN106220496; (2016); (A) Chinese, View in Reaxys Patent; DPX HOLDINGS B.V.; SCHURMANN, Martin; PEETERS, Wijnand Peter Helena; SMEETS, Natascha Hubertina Johannes; SCHWAB, Helmut; STEINER, Kerstin; LYPETSKA, Kateryna Mykolayivna; STROHMEIER, Gernot; (55 pag.); US2016/32335; (2016); (A1) English, View in Reaxys Page/Page column

Patent; INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF MEDICAL SCIENCES; Shi, Jiangong; Zhang, Jianjun; Yue, Zhenggang; Li, Min; Zhu, Chenggen; Zhang, Ying; Zi, Jiachen; Wang, Yafang; Fan, Xiaona; Xu, Ruiming; Lin, Sheng; Li, Yan; Yang, Yongchun; Sheng, Li; US2013/45942; (2013); (A1) English, View in Reaxys; Patent; TAKASAGO INTERNATIONAL CORPORATION; Touge, Taichiro; Hakamata, Tomohiko; Nara, Hideki; US2014/51871; (2014); (A1) English, View in Reaxys; Patent; University of Tennessee Research Foundation; Bozell, Joseph J.; Chatterjee, Sabornie; US2014/249300; (2014); (A1) English, View in Reaxys; Patent; ZHEJIANG UNIVERSITY; Ma, Shengming; Lv, Bo; Fu, Chunling; US2014/309422; (2014); (A1) English, View in Reaxys

Page/Page column

Patent; NIPPON CHEMICAL INDUSTRIAL CO., LTD.; Zhang, Wanbin; Liu, Delong; Guo, Hui; Liu, Yangang; US2013/53574; (2013); (A1) English, View in Reaxys Patent; CENTAURUS BIOPHARMA CO., LTD.; XIAO, Dengming; ZHU, Li; HU, Yuandong; YU, Rong; HU, Wei; ZHAO, Na; PENG, Yong; LUO, Hong; HAN, Yongxin; WO2013/97773; (2013); (A1) English, View in Reaxys

prophetic product

Patent; Hoechst Aktiengesellschaft; US4266066; (1981); (A) English, View in Reaxys; Patent; BASF SE; US2010/267948; (2010); (A1) English, View in Reaxys Patent; Clariant Specialty Fine Chemicals (Deutschland); US2007/78282; (2007); (A1) English, View in Reaxys Patent; SOLVIAS AG; WO2004/50585; (2004); (A1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

2.152

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

17.07

Lipinski Number

Veber Number

Related Structure (1) Related Structure References Enol-Gehalt von unverduenntem Propiophenon. Derivative (45) Comment (Derivative)

Gero; Journal of Organic Chemistry; vol. 19; (1954); p. 1960,1962, View in Reaxys

Derivative

References

propiophenone((E)-2,4-dinitrophenylhydrazone)

Lue, Ping; Fan, Wei-Qiang; Zhou, Xun-Jun; Synthesis; nb. 9; (1989); p. 692 - 693, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 187-189grad, rot

Shalaby et al.; Croatica Chemica Acta; vol. 52; (1979); p. 353,359, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 189-190grad

Ishido,Y. et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1977); p. 521 - 530, View in Reaxys

2,4-Dinitrophenylhydrazon: F:186.5grad

Olah et al.; Synthesis; (1977); p. 677, View in Reaxys

33/126

2018-07-03 19:01:53

Semicarbazon: F: 179-180grad

Dorofeenko et al.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 2424,2476,2478, View in Reaxys

Komplex mit Br2: 81Br - NQR

Grechishkin; Gushchin; Journal of Structural Chemistry; vol. 15; (1974); p. 276; ; p. 302, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 187-189grad

Balachandran; George; Tetrahedron; vol. 29; (1973); p. 2119,2124, 2127, View in Reaxys

2,4-Dinitro-phenylhydrazon, F:188grad

Rachmankulow et al.; Neftekhimiya; vol. 13; (1973); p. 254; Chem.Abstr.; vol. 79; nb. 66270; (1973), View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 2(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 6(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 7(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 9(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 12(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 14(1:1): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Komplex m. Anthrachinon (Farbstoff EB) 3(1:1,1:2): Gleichgew.konst. ΕK(1) (Ε(K(2))

Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys

Propiophenon-hydrazon: NMR

Campbell,J.R. et al.; Australian Journal of Chemistry; vol. 24; (1971); p. 1425 - 1436, View in Reaxys

Semicarbazon: F: 190grad

Meyers; Smith; Journal of the American Chemical Society; vol. 92; (1970); p. 1084, View in Reaxys

2,4-Dinitrophenylhydrazon: F:191grad

Moussa; Abdalla; Journal of Applied Chemistry; vol. 20; (1970); p. 256, View in Reaxys

*BF3. IR, 1H-,19FNMR

Gates; Mooney; Journal of Inorganic and Nuclear Chemistry; vol. 30; (1968); p. 839,842,844-846, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 191 192grad

Gassman,P.G.; Richmond,G.D.; Journal of Organic Chemistry; vol. 31; (1966); p. 2355 - 2357, View in Reaxys

Semicarbazon: F: 177 - 178grad

Kossanyi,J.; Bulletin de la Societe Chimique de France; (1965); p. 714 - 722, View in Reaxys

34/126

2018-07-03 19:01:53

2,6-Dinitro-4-methyl-phenylhydrazon: F: 150grad

Gupta; Garg; Journal of the Indian Chemical Society; vol. 42; (1965); p. 728, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 197.5 - 198grad; S.721, 722

Kossanyi,J.; Bulletin de la Societe Chimique de France; (1965); p. 714 - 722, View in Reaxys

Dinitrophenylhydrazon: F: 193 195grad

Reinheckel; Jahnke; Chemische Berichte; vol. 97; (1964); p. 2661, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 193 193.8grad

Pasynkiewicz et al.; Roczniki Chemii; vol. 38; (1964); p. 67,77, View in Reaxys

Addukt mit Decachlor-octahydro-1.3.4-metheno-2H-cyclobuta<cd>pentalenon-(2): F:140-143grad; IR

Patent; Allied Chem.; NL6402964; (1964); Chem.Abstr.; vol. 62; nb. 7658; (1965), View in Reaxys

Das Anion bildet m. Azobenzol einen Charge-TransferKomplex; analoge Komplexe m. anderen ungesaettigten Verbindungen

Russel et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 1807,1812, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 191grad

Melson; Hofmann; Pharmazeutische Zentralhalle; vol. 102; (1963); p. 59,60, View in Reaxys

Tosylhydrazon: F: 122 - 125grad

Farnum; Journal of Organic Chemistry; vol. 28; (1963); p. 870, View in Reaxys

2,4-Dinitrophenylhydrazon : F: 194-195grad

Bertsch; Reinheckl; Fette, Seifen, Anstrichmittel; vol. 64; (1962); p. 881; Chem.Abstr.; vol. 58; nb. 6686f; (1963), View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 190 191grad (unkorr.)

Warner et al.; Journal of the Chemical Society; (1962); p. 1232, View in Reaxys

syn-2,4-Dinitrophenylhydrazon: F: 187 - 189grad (korr.)

Scoggins; Hancock; Journal of Organic Chemistry; vol. 26; (1961); p. 3490,3492, View in Reaxys

p-Nitro-phenylhydrazon: F: 149.4 151grad

Dahlig et al.; Roczniki Chemii; vol. 34; (1960); p. 401,409; Chem.Abstr.; nb. 361a; (1961), View in Reaxys

2,4-Dinitrophenylhydrazon: F: 193.6 - 194.5grad

Dahlig et al.; Roczniki Chemii; vol. 34; (1960); p. 401,409; Chem.Abstr.; nb. 361a; (1961), View in Reaxys

Papierchromatograph. Isolierung u. Identifizierung als 2,4-Dinitrophenylhydrazon

Breuer et al.; Bulletin of the Research Council of Israel, Section A: Chemistry; vol. 9; (1960); p. 43; Journal of Chromatographic Science; vol. 5; (1961); p. D8; Chem.Abstr.; nb. 3500; (1961), View in Reaxys

as 2,4-dinitro-phenylhydrazone (mp: 193-194 degree )

Johnson; Journal of the American Chemical Society; vol. 75; (1953); p. 2720,2721; Journal of the American Chemical Society; vol. 73; (1951); p. 5888, View in Reaxys

4-phenyl semicarbazone (mp: 159 degree )

Grammaticakis; Bulletin de la Societe Chimique de France; (1949); p. 410,414, 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.

35/126

2018-07-03 19:01:53

2.4-dinitro-phenylhydrazone (mp: 190 degree )

Shivers; Dillon; Hauser; Journal of the American Chemical Society; vol. 69; (1947); p. 119,120, View in Reaxys; Kharasch; Sternfeld; Mayo; Journal of Organic Chemistry; vol. 5; (1940); p. 362,375, View in Reaxys

4-carboxy-phenylhydrazone (mp: 193-194 degree )

Veibel; Acta Chemica Scandinavica (1947-1973); vol. 1; (1947); p. 54,63, View in Reaxys; Veibel; Blaaberg; Stevns; Dansk. Tidskr. Farm.; vol. 14; (1940); p. 184,188, View in Reaxys

azine (mp: 64,5-65,2 degree )

Blout; Eager; Gofstein; Journal of the American Chemical Society; vol. 68; (1946); p. 1983,1985, View in Reaxys

semicarbazone (mp: 180-181 degree )

Reichert; Posemann; Archiv der Pharmazie (Weinheim, Germany); vol. 281; (1943); p. 189, View in Reaxys

azine (mp: 68 degree )

v. Vargha; Kovacs; Chemische Berichte; vol. 75; (1942); p. 794,802, View in Reaxys

semicarbazone (mp: 178-179 degree )

Gilman; Nelson; Recueil des Travaux Chimiques des Pays-Bas; vol. 55; (1936); p. 518,528, 529; Journal of the American Chemical Society; vol. 61; (1939); p. 741, View in Reaxys

4-thiocyanato-phenylhydrazone (mp: 98 degree )

Horii; Kinouchi; Yakugaku Zasshi; vol. 56; (1936); p. 690,696; dtsch. Ref. S. 163, 166; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 2584, View in Reaxys

semicarbazone (mp: 174-175 degree )

McKenzie; Luis; Mitchell; Chemische Berichte; vol. 65; (1932); p. 798,803, View in Reaxys

Melting Point (8) 1 of 8

Melting Point [°C]

17 - 18

Shaabani, Ahmad; Farhangi, Elham; Rahmati, Abbas; Monatshefte fur Chemie; vol. 139; nb. 8; (2008); p. 905 - 908, View in Reaxys 2 of 8

Melting Point [°C]

Morley; Green; Chemische Berichte; vol. 17; (1884); p. 3016, View in Reaxys; Maruyama; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 105, View in Reaxys; Patent; Bombrini-Parodi-Delfino Soc. p. Azioni; IT660910; (1961); Chem.Abstr.; vol. 62; nb. 7693; (1965), View in Reaxys; Patent; Sionogi seiyaku k. k.; JP5128601; (1976); Ref. Zh., Khim.; vol. 10; nb. N129P; (1977), View in Reaxys; Caira; Nassimbeni; Scott; Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals; vol. 276-277; nb. pt 1-2; (1996); p. 113 - 120, View in Reaxys 3 of 8

Melting Point [°C]

19 - 20

Kishner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 45; (1913); p. 953; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 2129, View in Reaxys; Kossanyi; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 250; (1960); p. 3487, View in Reaxys 4 of 8

Melting Point [°C]

Jakowlew; Kreimer; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 3313; engl. Ausg. S. 3685, View in Reaxys 5 of 8

Melting Point [°C]

18.61

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 6 of 8

Melting Point [°C]

18.6

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys; Evans; Journal of the Chemical Society; (1936); p. 785,788, View in Reaxys 7 of 8

Melting Point [°C]

18.4 - 18.5

Zucker; Hammett; Journal of the American Chemical Society; vol. 61; (1939); p. 2779,2783, View in Reaxys 8 of 8

Melting Point [°C]

18.5

Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 325; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys Boiling Point (72) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

Location

References

36/126

2018-07-03 19:01:53

216

supporting informa- Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rotion sario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys

216

Lee, Jong Chan; Kim, Jimi; Lee, Seung Bae; Chang, Soon-Uk; Jeong, Yeon Jin; Synthetic Communications; vol. 41; nb. 13; (2011); p. 1947 1951, View in Reaxys

215 - 216

760

Shaabani, Ahmad; Soleimani, Kamal; Bazgir, Ayoob; Synthetic Communications; vol. 34; nb. 18; (2004); p. 3303 - 3315, View in Reaxys

82 - 84

0.010501

Zhou, Jian-Feng; Tu, Shu-Jiang; Feng, Jun-Cai; Synthetic Communications; vol. 32; nb. 7; (2002); p. 959 - 962, View in Reaxys

91 - 92

Yu, Yongping; Zhang, Yongmin; Synthetic Communications; vol. 29; nb. 2; (1999); p. 243 - 247, View in Reaxys

64 - 65

Varma, Rajender S.; Saini, Rajesh K.; Dahiya, Rajender; Journal of Chemical Research - Part S; nb. 3; (1998); p. 120 - 121, View in Reaxys

218

760

Iranpoor, Nasser; Firouzabadi, Habib; Zolfigol, Mohammad Ali; Bulletin of the Chemical Society of Japan; vol. 71; nb. 4; (1998); p. 905 - 908, View in Reaxys

218

Morley; Green; Chemische Berichte; vol. 17; (1884); p. 3016, View in Reaxys; Patent; Dow Chem.; US3280147; (1966); Chem.Abstr.; vol. 66; nb. 2372r; (1967), View in Reaxys; Patent; Sionogi seiyaku k. k.; JP5128601; (1976); Ref. Zh., Khim.; vol. 10; nb. N129P; (1977), View in Reaxys; Caira; Nassimbeni; Scott; Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals; vol. 276-277; nb. pt 1-2; (1996); p. 113 - 120, View in Reaxys; Sreekumar; Padmakumar, Raghavakaimal; Synthetic Communications; vol. 27; nb. 5; (1997); p. 777 - 780, View in Reaxys

89 - 90

Hirano, Masao; Ukawa, Ken; Yakabe, Sigetaka; Clark, James H.; Morimoto, Takashi; Synthesis; nb. 8; (1997); p. 858 - 860, View in Reaxys; Hirano, Masao; Ukawa, Ken; Yakabe, Shigetaka; Morimoto, Takashi; Organic Preparations and Procedures International; vol. 29; nb. 4; (1997); p. 480 - 484, View in Reaxys

Zhang; Yu; Bao; Synthetic Communications; vol. 25; nb. 12; (1995); p. 1825 - 1830, View in Reaxys

Yanlong, Qian; Guisheng, Li; Huang, Yao-Zeng; Journal of Organometallic Chemistry; vol. 381; nb. 1; (1990); p. 29 - 34, View in Reaxys

107 - 109

Guthrie, J. Peter; Cossar, John; Canadian Journal of Chemistry; vol. 68; nb. 11; (1990); p. 2060 - 2069, View in Reaxys

216 - 218

Lue, Ping; Fan, Wei-Qiang; Zhou, Xun-Jun; Synthesis; nb. 9; (1989); p. 692 - 693, View in Reaxys

110 - 115

24.8

Svoboda, Jiri; Palecek, Jaroslav; Dedek, Vaclav; Mostecky, Jiri; Collection of Czechoslovak Chemical Communications; vol. 49; nb. 6; (1984); p. 1515 - 1520, View in Reaxys

105

Ono; Tamura; Kaji; Journal of the American Chemical Society; vol. 105; nb. 12; (1983); p. 4017 - 4022, View in Reaxys

Lociuro, S.; Vecchi, E.; Zeuli, E.; Delfini, M.; Tetrahedron; vol. 38; nb. 22; (1982); p. 3339 - 3345, View in Reaxys

Duhamel, Lucette; Poirier, Jean-Marie; Bulletin de la Societe Chimique de France; vol. 2; nb. 9-10; (1982); p. 297 - 303, View in Reaxys

Stahl, Ingfried; Synthesis; nb. 2; (1981); p. 135 - 137, View in Reaxys

84 - 86

Perumal, P. Thirumalai; Bhatt, M. Vivekananda; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 20; nb. 2; (1981); p. 153 - 155, View in Reaxys

214

210

Olah et al.; Synthesis; (1979); p. 113, View in Reaxys

115 - 120

Olah et al.; Synthesis; (1977); p. 677, 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.

37/126

2018-07-03 19:01:53

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

125 - 130

Chauhan,S.M.S.; Junjappa,H.; Tetrahedron; vol. 32; (1976); p. 1911 1916, View in Reaxys

0.3

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys

65 - 66

Bratchanskii,P.E.; Komissarova,G.G.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1661 - 1665,1650 - 1654, View in Reaxys

104 - 105

Guyon,R.; Villa,P.; Bulletin de la Societe Chimique de France; (1975); p. 2593 - 2598, View in Reaxys

69 - 70

Bratchanskii; Komissarova; Sov. Prog. Chem. (Engl. Transl.); vol. 41; nb. 4; (1975); p. 409,72,73, View in Reaxys

114

Dorofeenko et al.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 2424,2476,2478, View in Reaxys

52 - 56

0.05

Brady; Ting; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1975); p. 456, View in Reaxys

Bauer; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 158; (1914); p. 1682, View in Reaxys; Rachmankulow et al.; Neftekhimiya; vol. 13; (1973); p. 254; Chem.Abstr.; vol. 79; nb. 66270; (1973), View in Reaxys

217

Moriconi,E.J.; Shimakawa,Y.; Journal of Organic Chemistry; vol. 37; (1972); p. 196 - 207, View in Reaxys

Rusakowicz et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 3263,3264, View in Reaxys

120

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

110

Lamm,B.; Samuelsson,B.; Acta Chemica Scandinavica (1947-1973); vol. 24; (1970); p. 561 - 568, View in Reaxys

95 - 103

Uemura; Nippon Kagaku Zasshi; vol. 89; (1968); p. 692,694; Chem.Abstr.; vol. 70; nb. 19678u, View in Reaxys

100

House,H.O.; Larson,J.K.; Journal of Organic Chemistry; vol. 33; (1968); p. 61 - 65, View in Reaxys

104

Jullien; Thoi-Lai; Bulletin de la Societe Chimique de France; (1968); p. 4669, View in Reaxys

0.1

Rouessac,F. et al.; Bulletin de la Societe Chimique de France; (1967); p. 818 - 822, View in Reaxys

101

Pines; Goetschel; Journal of Catalysis; vol. 6; (1966); p. 380,383, View in Reaxys

0.05

Asinger,F. et al.; Monatshefte fuer Chemie; vol. 97; (1966); p. 1510 - 1522, View in Reaxys

232 - 233

Tomson; Eesti NSV Teaduste Akadeemia Toimetised, Keemia, Geoloogia; (1966); p. 447,448-453; Chem.Abstr.; vol. 66; nb. 94734, View in Reaxys

62 - 66

1.5

Gassman,P.G.; Richmond,G.D.; Journal of Organic Chemistry; vol. 31; (1966); p. 2355 - 2357, View in Reaxys

214 - 215

760

Kupin; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1206,1217, View in Reaxys

0.4

Dhami,K.S.; Stothers,J.B.; Canadian Journal of Chemistry; vol. 43; (1965); p. 498 - 509, View in Reaxys

67 - 68

Kossanyi,J.; Bulletin de la Societe Chimique de France; (1965); p. 714 722, View in Reaxys; Kossanyi; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 250; (1960); p. 3487, View in Reaxys

38/126

2018-07-03 19:01:53

98 - 100

Reinheckel; Jahnke; Chemische Berichte; vol. 97; (1964); p. 2661, View in Reaxys

215 - 218

760

Reinheckel; Jahnke; Chemische Berichte; vol. 97; (1964); p. 2661, View in Reaxys

59 - 61

Pasynkiewicz et al.; Roczniki Chemii; vol. 38; (1964); p. 67,77, View in Reaxys

214 - 216

Konowalow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 25; (1893); p. 530; Chem. Zentralbl.; vol. 65; nb. I; (1894); p. 465, View in Reaxys; Warner et al.; Journal of the Chemical Society; (1962); p. 1232, View in Reaxys

Bertsch; Reinheckl; Fette, Seifen, Anstrichmittel; vol. 64; (1962); p. 881; Chem.Abstr.; vol. 58; nb. 6686f; (1963), View in Reaxys

103 - 105

Fel'dman et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 35; (1962); p. 1364,1309; Chem.Abstr.; vol. 57; nb. 11064; (1962), View in Reaxys

105

Maruyama; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p. 105, View in Reaxys

212 - 213

760

Kupin; Petrow; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2958,2758; Chem.Abstr.; vol. 57; nb. 2125; (1962), View in Reaxys

Dahlig et al.; Roczniki Chemii; vol. 34; (1960); p. 401,409; Chem.Abstr.; nb. 361a; (1961), View in Reaxys

88 - 92

Tscherkasowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 2846,2826, View in Reaxys

92 - 94

Tscherkasowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 2846,2826, View in Reaxys

105 - 105.5

Jurjew et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 415,439; Chem.Abstr.; nb. 24638; (1960), View in Reaxys

87.2

Wibaut; Paulis; Recueil des Travaux Chimiques des Pays-Bas; vol. 77; (1958); p. 792,798; Proceedings of the Koninklijke Nederlandse Akademie van Wetenschappen, Series B: Physical Sciences; vol. <B> 61; (1958); p. 103,105, View in Reaxys

114

Elving; Leone; Analytical Chemistry; vol. 29; (1957); p. 782, View in Reaxys

108 - 110

Schultz; Bicking; Journal of the American Chemical Society; vol. 75; (1955); p. 1128, View in Reaxys

215

763

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys

Zucker; Hammett; Journal of the American Chemical Society; vol. 61; (1939); p. 2779,2783, View in Reaxys

96.4 - 96.6

15.5

Kohlrausch; Pongratz; Monatshefte fuer Chemie; vol. 64; (1934); p. 374,382, View in Reaxys

217.7

760

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys

92.5 - 94.5

Thierfelder; Daiber; Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie; vol. 130; (1923); p. 380,383, 384, View in Reaxys

218

764

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

215

746

Senderens; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 313, View in Reaxys; Senderens; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 111,1336; Bulletin de la Societe Chimique de France; vol. <4> 7; (1910); p. 647, View in Reaxys

124

v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys

39/126

2018-07-03 19:01:53

217

765

Piutti; Chemische Berichte; vol. 39; (1906); p. 2771; Gazzetta Chimica Italiana; vol. 36 II; (1906); p. 370, View in Reaxys

218.3 - 218.8

760

Jawelow; Chemische Berichte; vol. 39; (1906); p. 1195, View in Reaxys

142 - 142.2

Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys

215.5

750

Wagner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 16; (1884); p. 325; Chemische Berichte; 17 Ref. <1884>, 317, View in Reaxys

Refractive Index (35) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

References

1.5245

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys; Moravkova; Wagner; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 7; (2005); p. 658 - 666, View in Reaxys

1.5241

589

Bratchanskii,P.E.; Komissarova,G.G.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1661 - 1665,1650 - 1654, View in Reaxys

1.528

589

Guyon,R.; Villa,P.; Bulletin de la Societe Chimique de France; (1975); p. 2593 - 2598, View in Reaxys

Bratchanskii; Komissarova; Sov. Prog. Chem. (Engl. Transl.); vol. 41; nb. 4; (1975); p. 409,72,73, View in Reaxys

1.5274 1.5259

589

Castelli,F.; Cannone,P.; Bulletin de la Societe Chimique de France; (1974); p. 317 - 330, View in Reaxys; Kupin; Petrow; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2958,2758; Chem.Abstr.; vol. 57; nb. 2125; (1962), View in Reaxys

1.5342

589

Rachmankulow et al.; Neftekhimiya; vol. 13; (1973); p. 254; Chem.Abstr.; vol. 79; nb. 66270; (1973), View in Reaxys

1.5262

589

Jullien; Thoi-Lai; Bulletin de la Societe Chimique de France; (1968); p. 4669, View in Reaxys

1.527

589

Wallach; Justus Liebigs Annalen der Chemie; vol. 332; (1904); p. 317, View in Reaxys; Frainnet et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 261; (1965); p. 1329, View in Reaxys

1.5239

589

Kupin; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1206,1217, View in Reaxys

1.526

589

Dhami,K.S.; Stothers,J.B.; Canadian Journal of Chemistry; vol. 43; (1965); p. 498 - 509, View in Reaxys

1.5267

589

1.5275

589

Frainnet et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 261; (1965); p. 1329, View in Reaxys

1.5266

589

Reinheckel; Jahnke; Chemische Berichte; vol. 97; (1964); p. 2661, View in Reaxys

1.5278

589

Bertsch; Reinheckl; Fette, Seifen, Anstrichmittel; vol. 64; (1962); p. 881; Chem.Abstr.; vol. 58; nb. 6686f; (1963), View in Reaxys

1.524

589

Jurjew et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 415,439; Chem.Abstr.; nb. 24638; (1960), View in Reaxys

1.5242

589

Jurjew et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 415,439; Chem.Abstr.; nb. 24638; (1960), View in Reaxys

1.515

589

Jakowlew; Kreimer; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 3313; engl. Ausg. S. 3685, View in Reaxys

1.5243

589

Schultz; Bicking; Journal of the American Chemical Society; vol. 75; (1955); p. 1128, View in Reaxys

40/126

2018-07-03 19:01:53

1.5212

589

Lagemann et al.; Journal of the American Chemical Society; vol. 74; (1952); p. 1602, View in Reaxys

1.5268

589

Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys

1.5269

589

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys; Evans; Journal of the Chemical Society; (1936); p. 785,788, View in Reaxys

1.5251

589

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys

1.5218

656.3

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys

1.52

656.3

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys

1.5294

546.1

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys

1.5401

486.1

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys

1.538

486.1

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys

1.549

435.8

Cherrier; Metzger; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 797, View in Reaxys

1.5511

434

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys

1.5279

589

1.5238

656.3

15.9

v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys

1.529

589

15.9

v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys

1.5422

486.1

15.9

v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys

1.554

434

15.9

v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys

1.52461

656.3

15.7

Eijkman; Chem. Zentralbl.; vol. 75; nb. I; (1904); p. 1259, View in Reaxys

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

Density (42) 1 of 42

Density [g·cm-3]

0.99826

Measurement Temperature 49.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys 2 of 42

Density [g·cm-3]

1.00422

Measurement Temperature 39.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys 3 of 42

Density [g·cm-3]

1.00584

Measurement Temperature 34.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

41/126

2018-07-03 19:01:53

4 of 42

Density [g·cm-3]

1.00653

Measurement Temperature 34.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys 5 of 42

Density [g·cm-3]

1.00724

Measurement Temperature 29.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys 6 of 42

Density [g·cm-3]

1.00564

Measurement Temperature 39.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys 7 of 42

Density [g·cm-3]

1.00653

Measurement Temperature 34.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys 8 of 42

Density [g·cm-3]

1.00725

Measurement Temperature 29.99 [°C] Comment (Density)

Press = 0.1 MPa; Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys 9 of 42

Density [g·cm-3]

1.00437

Measurement Temperature 29.99 [°C] Gowrisankar; Sivarambabu; Venkateswarlu; Kumar, K. Siva; Bulletin of the Korean Chemical Society; vol. 33; nb. 5; (2012); p. 1686 - 1692, View in Reaxys 10 of 42

Density [g·cm-3]

1.00896

Measurement Temperature 34.99 [°C] Gowrisankar; Sivarambabu; Venkateswarlu; Kumar, K. Siva; Bulletin of the Korean Chemical Society; vol. 33; nb. 5; (2012); p. 1686 - 1692, View in Reaxys 11 of 42

Density [g·cm-3]

1.0081

Measurement Temperature 24.99 [°C] Kumar, Harish; Chahal, Savita; Journal of Solution Chemistry; vol. 40; nb. 2; (2011); p. 165 - 181, View in Reaxys 12 of 42

Density [g·cm-3]

1.0006 - 1.0092

Measurement Temperature 24.99 - 34.99 [°C] Comment (Density)

in the presence of organic compounds

42/126

2018-07-03 19:01:53

Tangeda, Savitha Jyostna; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 3; (2006); p. 272 277, View in Reaxys 13 of 42

Density [g·cm-3]

1.0006 - 1.0092

Measurement Temperature 24.99 - 34.99 [°C] Tangeda, Savitha Jyostna; Boodida, Sathyanarayana; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 11; (2006); p. 1438 - 1442, View in Reaxys 14 of 42

Density [g·cm-3]

1.0092

Measurement Temperature 25 [°C] Tangeda, Savitha J.; Nallani, Satyanarayana; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 89 - 91, View in Reaxys; Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys 15 of 42

Density [g·cm-3]

1.0006

Measurement Temperature 35 [°C] Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys 16 of 42

Density [g·cm-3]

1.00526

Measurement Temperature 25 [°C] Moravkova; Wagner; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 7; (2005); p. 658 - 666, View in Reaxys 17 of 42

Density [g·cm-3]

1.0032 - 1.0053

Measurement Temperature 25 - 55 [°C] Comment (Density)

pressure dependence

Moravkova; Wagner; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 7; (2005); p. 658 - 666, View in Reaxys 18 of 42

Density [g·cm-3]

1.00579

Measurement Temperature 25 [°C] Dusart et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 832,833, View in Reaxys 19 of 42

Density [g·cm-3]

1.0121

Reference Temperature [°C]

Measurement Temperature 20 [°C] Bratchanskii,P.E.; Komissarova,G.G.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1661 - 1665,1650 - 1654, View in Reaxys 20 of 42

Density [g·cm-3]

1.011

Measurement Temperature 20 [°C] Bratchanskii; Komissarova; Sov. Prog. Chem. (Engl. Transl.); vol. 41; nb. 4; (1975); p. 409,72,73, View in Reaxys 21 of 42

Density [g·cm-3]

1.0115

Reference Temperature [°C]

Measurement Temperature 20 [°C] Kupin; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1206,1217, View in Reaxys 22 of 42

Density [g·cm-3]

1.0125

43/126

2018-07-03 19:01:53

Reference Temperature [°C]

Measurement Temperature 20 [°C] Kupin; Petrow; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2958,2758; Chem.Abstr.; vol. 57; nb. 2125; (1962), View in Reaxys 23 of 42

Density [g·cm-3]

1.0122

Reference Temperature [°C]

Measurement Temperature 20 [°C] Jurjew et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 30; (1960); p. 415,439; Chem.Abstr.; nb. 24638; (1960), View in Reaxys 24 of 42

Density [g·cm-3]

1.034

Reference Temperature [°C]

Measurement Temperature 24 [°C] Jakowlew; Kreimer; Zhurnal Obshchei Khimii; vol. 26; (1956); p. 3313; engl. Ausg. S. 3685, View in Reaxys 25 of 42

Density [g·cm-3]

1.0014

Reference Temperature [°C]

Measurement Temperature 30 [°C] Lagemann et al.; Journal of the American Chemical Society; vol. 73; (1951); p. 3213, View in Reaxys 26 of 42

Density [g·cm-3]

1.0096

Reference Temperature [°C]

Measurement Temperature 20 [°C] Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 27 of 42

Density [g·cm-3]

1.0053

Reference Temperature [°C]

Measurement Temperature 25 [°C] Dreisbach; Martin; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2876, View in Reaxys 28 of 42

Density [g·cm-3]

1.0139

Measurement Temperature 16 [°C] Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 1016, View in Reaxys 29 of 42

Density [g·cm-3]

1.0101

Reference Temperature [°C]

Measurement Temperature 20 [°C] Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys 30 of 42

Density [g·cm-3]

0.9934

44/126

2018-07-03 19:01:53

Reference Temperature [°C]

Measurement Temperature 41.8 [°C] Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys 31 of 42

Density [g·cm-3]

0.9776

Reference Temperature [°C]

Measurement Temperature 61.2 [°C] Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys 32 of 42

Density [g·cm-3]

0.9572

Reference Temperature [°C]

Measurement Temperature 85.5 [°C] Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys 33 of 42

Density [g·cm-3]

1.0105

Reference Temperature [°C]

Measurement Temperature 20 [°C] Evans; Journal of the Chemical Society; (1936); p. 785,788, View in Reaxys 34 of 42

Density [g·cm-3]

1.157

Reference Temperature [°C]

Measurement Temperature 0 [°C] Ziegler; Ditzel; Justus Liebigs Annalen der Chemie; vol. 473; (1929); p. 201, View in Reaxys 35 of 42

Density [g·cm-3]

1.0164

Reference Temperature [°C]

Measurement Temperature 15 [°C] Kishner; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 45; (1913); p. 953; Chem. Zentralbl.; vol. 84; nb. II; (1913); p. 2129, View in Reaxys 36 of 42

Density [g·cm-3]

1.0131

Reference Temperature [°C]

Measurement Temperature 16.3 [°C] v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys 37 of 42

Density [g·cm-3]

1.012

Measurement Temperature 20 [°C] Wallach; Justus Liebigs Annalen der Chemie; vol. 332; (1904); p. 317, View in Reaxys 38 of 42

Density [g·cm-3]

1.0133

45/126

2018-07-03 19:01:53

Measurement Temperature 15.7 [°C] Eijkman; Chem. Zentralbl.; vol. 75; nb. I; (1904); p. 1259, View in Reaxys 39 of 42

Density [g·cm-3]

1.0087

Reference Temperature [°C]

Measurement Temperature 25 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 40 of 42

Density [g·cm-3]

1.0118

Reference Temperature [°C]

Measurement Temperature 20 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 41 of 42

Density [g·cm-3]

1.015

Reference Temperature [°C]

Measurement Temperature 15 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 42 of 42

Density [g·cm-3]

1.0043

Reference Temperature [°C]

Measurement Temperature 23 [°C] Konowalow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 25; (1893); p. 530; Chem. Zentralbl.; vol. 65; nb. I; (1894); p. 465, View in Reaxys Adsorption (MCS) (3) 1 of 3

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

tetrahydrofuran; H2O

Partner (Adsorption (MCS))

toluene/ZrO2

Weber, Thomas P.; Jackson, Paul T.; Carr, Peter W.; Analytical Chemistry; vol. 67; nb. 17; (1995); p. 3042 - 3050, View in Reaxys 2 of 3

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

tetrahydrofuran; H2O

Partner (Adsorption (MCS))

hexane/ZrO2

Weber, Thomas P.; Jackson, Paul T.; Carr, Peter W.; Analytical Chemistry; vol. 67; nb. 17; (1995); p. 3042 - 3050, View in Reaxys 3 of 3

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

sodium dodecylsulfate

46/126

2018-07-03 19:01:53

Scaiano, J. C.; Selwyn, J.C.; Canadian Journal of Chemistry; vol. 59; (1981); p. 2368 - 2372, View in Reaxys Association (MCS) (7) 1 of 7

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

CD2Cl2

Temperature (Association (MCS)) [°C]

-78

Partner (Association (MCS))

TiCl4

Mohanta, Pramod K.; Davis, Todd A.; Gooch, Jeremy R.; Flowers II, Robert A.; Journal of the American Chemical Society; vol. 127; nb. 34; (2005); p. 11896 - 11897, View in Reaxys 2 of 7

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

solid

Partner (Association (MCS))

TiCl4

Maier, Guenther; Kalinowski, Hans-Otto; Weber, Claudia; Henrich, Markus; Magnetic Resonance in Chemistry; vol. 33; nb. 4; (1995); p. 290 - 296, View in Reaxys 3 of 7

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

acetonitrile; lithium dodecyl sulphate

Ahuja, Eric S.; Foley, Joe P.; Analytical Chemistry; vol. 67; nb. 14; (1995); p. 2315 - 2324, View in Reaxys 4 of 7

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

acetonitrile; sodium dodecyl-sulfate

Ahuja, Eric S.; Foley, Joe P.; Analytical Chemistry; vol. 67; nb. 14; (1995); p. 2315 - 2324, View in Reaxys 5 of 7

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methanol

Laurence, Christian; Berthelot, Michel; Helbert, Maryvonne; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 41; nb. 7; (1985); p. 883 - 892, View in Reaxys 6 of 7

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

diisopropyl-2,6-nitro-4-phenol-d1

47/126

2018-07-03 19:01:53

Laurence, Christian; Berthelot, Michel; Helbert, Maryvonne; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 41; nb. 7; (1985); p. 883 - 892, View in Reaxys 7 of 7

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

BF3

Berthelot, Michel; Gal, Jean-Francois; Helbert, Maryvonne; Laurence, Christian; Maria, Pierre-Charles; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 82; nb. 4; (1985); p. 427 - 432, View in Reaxys Azeotropes (MCS) (24) 1 of 24

Temperature (Azeotropes (MCS)) [°C]

218.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

m-cresol

Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 113, View in Reaxys 2 of 24

Temperature (Azeotropes (MCS)) [°C]

219.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

p-cresol

Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 113, View in Reaxys 3 of 24

Temperature (Azeotropes (MCS)) [°C]

204

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetamide

Lecat; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 4 of 24

Temperature (Azeotropes (MCS)) [°C]

223

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

tribromohydrin

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p. 112,151,155, View in Reaxys 5 of 24

Temperature (Azeotropes (MCS)) [°C]

216.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

succinic acid diethyl ester

Lecat; Ann. Soc. scient. Bruxelles; vol. 45 I; (1926); p. 290, View in Reaxys 6 of 24

Azeotropes

thymol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 7 of 24

Azeotropes

acetamide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 8 of 24

Azeotropes

propionamide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 9 of 24

Azeotropes

heptanoic acid

48/126

2018-07-03 19:01:53

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 10 of 24

Azeotropes

2-bromo-anisole

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 11 of 24

Azeotropes

ethylene glycol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 12 of 24

Azeotropes

4-chloro-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 13 of 24

Azeotropes

3-methyl-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 14 of 24

Azeotropes

4-ethyl-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 15 of 24

Azeotropes

4-methyl-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 16 of 24

Azeotropes

2-ethoxy-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 17 of 24

Azeotropes

2-methoxy-aniline

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 18 of 24

Azeotropes

2.4-dimethyl-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 19 of 24

Azeotropes

3.4-dimethyl-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 20 of 24

Azeotropes

#N.N!-diethyl-aniline

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 21 of 24

Azeotropes

1.3.5-triethyl-benzene

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 22 of 24

Azeotropes

fumaric acid diethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 23 of 24

Azeotropes

(+-)-2.3-dibromo-propanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 24 of 24

Azeotropes

succinic acid diethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys Chromatographic Data (9) Chromatographic Location data GC (Gas chromatography)

References

supporting informa- Jolley, Katherine E.; Zanotti-Gerosa, Antonio; Hancock, Fred; Dyke, Alan; Grainger, Damtion ian 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; Soni, Rina; Jolley, Katherine E.; Clarkson, Guy J.; Wills, Martin; Organic Letters; vol. 15; nb. 19; (2013); p. 5110 - 5113, View in Reaxys; Goek, Luetfiye; Tuerkmen, Hayati; Tetrahedron; vol. 69; nb. 49; (2013); p. 10669 - 10674, 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; 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; 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; Bigler, Raphael; Huber, Raffael; Mezzetti, Antonio; Angewandte Chemie - International Edition; vol.

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.

49/126

2018-07-03 19:01:53

54; nb. 17; (2014); p. 5171 - 5174; Angew. Chem.; vol. 127; nb. 17; (2014); p. 5260 - 5263,4, View in Reaxys; Coverdale, James P. C.; Sanchez-Cano, 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; Smith, Samantha A.M.; Morris, Robert H.; Synthesis (Germany); vol. 47; nb. 12; (2015); p. 1775 - 1779; Art.No: SS-2014-C0753-ST, 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; 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; Çalik, Hatice Selvi; Ispir, Esin; Karabuga, Şemistan; Aslantas, Mehtet; Journal of Organometallic Chemistry; vol. 801; (2016); p. 122 - 129, 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; Martínez-Montero, Lía; Gotor, Vicente; Gotor-Fernández, Vicente; Lavandera, Iván; Green Chemistry; vol. 19; nb. 2; (2017); p. 474 - 480, View in Reaxys; Li, Guangyue; Maria-Solano, Miguel A.; Romero-Rivera, Adrian; Osuna, Sílvia; Reetz, Manfred T.; Chemical Communications; vol. 53; nb. 68; (2017); p. 9454 - 9457, View in Reaxys; Zhang, Wuyuan; Burek, Bastien O.; Fernández-Fueyo, Elena; Alcalde, Miguel; Bloh, Jonathan Z.; Hollmann, Frank; Angewandte Chemie - International Edition; vol. 56; nb. 48; (2017); p. 15451 15455; Angew. Chem.; vol. 129; nb. 48; (2017); p. 15654 - 15658,5, View in Reaxys; Berton, Mateo; Mello, Rossella; Williard, Paul G.; González-Núñez, María Elena; Journal of the American Chemical Society; vol. 139; nb. 48; (2017); p. 17414 - 17420, 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; 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- Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; tion vol. 16; nb. 1; (2014); p. 66 - 69, View in Reaxys; Gaspa, Silvia; Porcheddu, Andrea; Valentoni, Antonio; Garroni, Sebastiano; Enzo, Stefano; De Luca, Lidia; European Journal of Organic Chemistry; vol. 2017; nb. 37; (2017); p. 5519 - 5526, View in Reaxys

GC (Gas chromatography)

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; Janeczko, Tomasz; Kostrzewa-Suslow, 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; Blažević, Ivica; De Nicola, Gina Rosalinda; Montaut, Sabine; Rollin, Patrick; Ruščić, Mirko; Croatica Chemica Acta; vol. 88; nb. 3; (2015); p. 307 - 314, 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; Liang, Sen; Zeng, Cheng-Chu; Tian, Hong-Yu; Sun, Bao-Guo; Luo, Xu-Gang; Ren, Fa-Zheng; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11565 11573, View in Reaxys

HPLC (High performance liquid chromatography)

supporting informa- Park, Eul-Soo; Park, Sae-Rom; Han, Sang-Woo; Dong, Joo-Young; Shin, Jong-Shik; Adtion vanced Synthesis and Catalysis; vol. 356; nb. 1; (2014); p. 212 - 220, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Cocina, María; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Chemical Communications; vol. 51; nb. 54; (2015); p. 10937 - 10940, View in Reaxys; Han, Sang-Woo; Park, Eul-Soo; Dong, Joo-Young; Shin, Jong-Shik; Advanced Synthesis and Catalysis; vol. 357; nb. 12; (2015); p. 2712 - 2720, View in Reaxys; RíosLombardía, 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

TLC (Thin layer chromatography)

Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, HansGünther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 - 7384, View in Reaxys

HPLC (High performance liquid chromatography)

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

GC (Gas chromatography)

Page/Page column 76

Patent; MCNEFF, Clayton, V.; MCNEFF, Larry, C.; NOWLAN, Daniel, Thomas; YAN, Bingwen; GREUEL, Peter, G.; WO2014/8355; (2014); (A1) English, View in Reaxys

HPLC (High performance liquid chromatography) LC (Liquid chromatography)

Tang, Tuo-Xian; Liu, Yan; Wu, Zhong-Liu; Journal of Molecular Catalysis B: Enzymatic; vol. 105; (2014); p. 82 - 88, View in Reaxys supporting informa- Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; tion vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys

50/126

2018-07-03 19:01:53

Compressibility (2) Description (Com- Comment (Compressibility) pressibility)

References

Isothermal compressibility

Moravkova; Wagner; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 7; (2005); p. 658 - 666, View in Reaxys

Adiabatic compres- (aus der SchallLagemann et al.; Journal of the American Chemical Society; vol. 73; (1951); p. 3213, sibility geschwindigkeit er- View in Reaxys mittelt) bei 30grad. Conformation (1) Object of Investiga- References tion Conformation

Solladie-Cavallo; Solladie; Organic Magnetic Resonance; vol. 10; (1977); p. 235, View in Reaxys; Zaitsev; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 23; (1974); p. 747,751; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 23; (1974); p. 780, View in Reaxys

Crystal Property Description (12) Colour & Other Location Properties

References

colourless

supporting informa- Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; tion Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys; Gao, Qi; Li, Shenyan; Pan, Yingming; Xu, Yanli; Wang, Hengshan; Tetrahedron; vol. 69; nb. 19; (2013); p. 3775 - 3781, View in Reaxys; Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; vol. 16; nb. 1; (2014); p. 66 - 69, View in Reaxys; Jiang, Jian-An; Du, Jia-Lei; Wang, Zhan-Guo; Zhang, Zhong-Nan; Xu, Xi; Zheng, Gan-Lin; Ji, Ya-Fei; Tetrahedron Letters; vol. 55; nb. 10; (2014); p. 1677 - 1681, View in Reaxys; Moriyama, Katsuhiko; Nakamura, Yu; Togo, Hideo; Organic Letters; vol. 16; nb. 14; (2014); p. 3812 - 3815, View in Reaxys; Wang, Yuanxun; Wang, Chao; Sun, Jian; Synthetic Communications; vol. 44; nb. 20; (2014); p. 2961 - 2965, View in Reaxys; Chaudhuri, Sangeeta Roy; Hartwig, Jan; Kupracz, Lukas; Kodanek, Torben; Wegner, Jens; Kirschning, Andreas; Advanced Synthesis and Catalysis; vol. 356; nb. 17; (2014); p. 3530 - 3538, View in Reaxys; Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei; Organic Letters; vol. 17; nb. 6; (2015); p. 1469 - 1472, View in Reaxys; Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 8218, View in Reaxys; Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, Hans-Günther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 7384, View in Reaxys; 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; Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys; Martinez-Erro, Samuel; Sanz-Marco, Amparo; Bermejo Gómez, Antonio; Vázquez-Romero, Ana; Ahlquist, Mårten S. G.; Martín-Matute, Belén; Journal of the American Chemical Society; vol. 138; nb. 40; (2016); p. 13408 - 13414, View in Reaxys; Erbing, Elis; Vázquez-Romero, Ana; Bermejo Gómez, Antonio; PlateroPrats, Ana E.; Carson, Fabian; Zou, Xiaodong; Tolstoy, Päivi; Martín-Matute, Belén; Chemistry - A European Journal; vol. 22; nb. 44; (2016); p. 15659 - 15663, View in Reaxys; Ma, Jiaqi; Hong, Chao; Wan, Yan; Li, Meichao; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Jin, Liqun; Shen, Zhenlu; Tetrahedron Letters; vol. 58; nb. 7; (2017); p. 652 - 657, View in Reaxys; Halima, Taoufik Ben; Zhang, Wanying; Yalaoui, Imane; Hong, Xin; Yang, Yun-Fang; Houk, Kendall N.; Newman, Stephen G.; Journal of the American Chemical Society; vol. 139; nb. 3; (2017); p. 1311 - 1318, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Gaspa, Silvia; Porcheddu, Andrea; Valentoni, Antonio; Garroni, Sebastiano; Enzo, Stefano; De Luca, Lidia; European Journal of Organic Chemistry; vol. 2017; nb. 37; (2017); p. 5519 - 5526, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24; (2017); p. 6760 - 6762, View in Reaxys; Wang, Qingfu; Chai, Huining; Yu, Zhengkun; Organometallics; vol. 37; nb. 4; (2018); p. 584 - 591, View in Reaxys

colourless

Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys; Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 - 5935, 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; Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 6104, View in Reaxys; Skillinghaug, Bobo; Sköld, Christian; Rydfjord, Jonas; Svensson, Fredrik; Behrends, Malte; Sävmarker, Jonas; Sjöberg, Per J. R.; Larhed, Mats; Journal of Organic Chemistry; vol. 79; nb. 24; (2014); p. 12018 - 12032, View in Reaxys; Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 4254; Art.No: 26677, View in Reaxys; Yousuf, Md; Das, Tuluma; Adhikari, Susanta; New

51/126

2018-07-03 19:01:53

Journal of Chemistry; vol. 39; nb. 11; (2015); p. 8763 - 8770, View in Reaxys; Madumo, Gilbert K.; Moshapo, Paseka T.; Kinfe, Henok H.; Medicinal Chemistry Research; vol. 27; nb. 3; (2018); p. 817 - 833, View in Reaxys; Meng, Mengting; Yang, Liangfeng; Cheng, Kai; Qi, Chenze; Journal of Organic Chemistry; vol. 83; nb. 6; (2018); p. 3275 - 3284, View in Reaxys; Consiglio, Gabriella Barozzino; Mordini, Alessandro; Letters in Organic Chemistry; vol. 15; nb. 5; (2018); p. 447 - 454, View in Reaxys yellow

supporting informa- Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; tion vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys; Shen, Duyi; Miao, Chengxia; Wang, Shoufeng; Xia, Chungu; Sun, Wei; Organic Letters; vol. 16; nb. 4; (2014); p. 1108 - 1111, 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; Shen, Duyi; Miao, Chengxia; Xu, Daqian; Xia, Chungu; Sun, Wei; Organic Letters; vol. 17; nb. 1; (2015); p. 54 - 57, View in Reaxys; Chatupheeraphat, Adisak; Liao, Hsuan-Hung; Srimontree, Watchara; Guo, Lin; Minenkov, Yury; Poater, Albert; Cavallo, Luigi; Rueping, Magnus; Journal of the American Chemical Society; vol. 140; nb. 10; (2018); p. 3724 - 3735, View in Reaxys

white

Paragraph 0052; 0056; 0060

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys

yellow

Paragraph 0039

Patent; University of Science and Technology of China; Kang Yanbiao; Liu Jie; (15 pag.); CN107011133; (2017); (A) Chinese, View in Reaxys

yellow

Zhang, Jinli; Han, Zixing; Li, Junmiao; Wu, Yangjie; Arkivoc; vol. 2013; nb. 4; (2013); p. 251 - 271, View in Reaxys; Raeisaenen, Minna T.; Al-Hunaiti, Afnan; Atosuo, Elisa; Kemell, Marianna; Leskelae, Markku; Repo, Timo; Catalysis Science and Technology; vol. 4; nb. 8; (2014); p. 2564 - 2573, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Liu, Yangyang; Xie, Aming; Li, Junjian; Xu, Xiao; Dong, Wei; Wang, Boliang; Tetrahedron; vol. 70; nb. 52; (2014); p. 9791 9796, View in Reaxys; Obermayer, David; Znidar, Desiree; Glotz, Gabriel; Stadler, Alexander; Dallinger, Doris; Oliver Kappe; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11788 - 11801, View in Reaxys

white

supporting informa- Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; tion Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys

colourless

supporting informa- Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; tion Journal of Organic Chemistry; vol. 73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys; Munoz, Maria Paz; De La Torre, Maria C.; Sierra, Miguel A.; Advanced Synthesis and Catalysis; vol. 352; nb. 13; (2010); p. 2189 - 2194, View in Reaxys; Gowda, Maravanhalli Sidde; Pande, Sushanth Sudhir; Ramakrishna, Ramesha Andagar; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 9; nb. 15; (2011); p. 5365 - 5368, View in Reaxys; Lin, Riyuan; Chen, Feng; Jiao, Ning; Organic Letters; vol. 14; nb. 16; (2012); p. 4158 - 4161, View in Reaxys

colourless

Bouziane, Asmae; Carboni, Bertrand; Bruneau, Christian; Carreaux, Francois; Renaud, Jean-Luc; Tetrahedron; vol. 64; nb. 51; (2008); p. 11745 - 11750, View in Reaxys; Hachiya, Iwao; Inagaki, Takao; Ishihara, Yasuhisa; Shimizu, Makoto; Bulletin of the Chemical Society of Japan; vol. 84; nb. 4; (2011); p. 419 - 421, View in Reaxys; Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys; Tripathi, Chandra Bhushan; Mukherjee, Santanu; Journal of Organic Chemistry; vol. 77; nb. 3; (2012); p. 1592 - 1598, View in Reaxys

yellow

Landers, Brant; Berini, Christophe; Wang, Chao; Navarro, Oscar; Journal of Organic Chemistry; vol. 76; nb. 5; (2011); p. 1390 - 1397, View in Reaxys

yellow

supporting informa- Berini, Christophe; Brayton, Daniel F.; Mocka, Corey; Navarro, Oscar; Organic Letters; vol. tion 11; nb. 18; (2009); p. 4244 - 4247, View in Reaxys; Berini, Christophe; Winkelmann, Ole H.; Otten, Jennifer; Vicic, David A.; Navarro, Oscar; Chemistry - A European Journal; vol. 16; nb. 23; (2010); p. 6857 - 6860, View in Reaxys

Tafeln

Morley; Green; Chemische Berichte; vol. 17; (1884); p. 3016, View in Reaxys

Dielectric Constant (1) References Pinkus; Custard; Journal of Physical Chemistry; vol. 74; (1970); p. 1042, View in Reaxys Dissociation Energy (2) Dissociation Ener- Bond Type gy [Jmol-1]

References

52/126

2018-07-03 19:01:53

368324

C-H

Alnajjar, Mikhail S.; Zhang, Xian-Man; Gleicher, Gerald J.; Truksa, Scott V.; Franz, James A.; Journal of Organic Chemistry; vol. 67; nb. 25; (2002); p. 9016 - 9022, View in Reaxys

368438

Ε-C-H

Bordwell, F. G.; Harrelson, J. A.; Lynch, Tsuei-Yun; Journal of Organic Chemistry; vol. 55; nb. 10; (1990); p. 3337 - 3341, View in Reaxys

Dissociation Exponent (7) 1 of 7

Dissociation Exponent (pK)

-4.52

Temperature (Dissociation Exponent) [°C]

24.85

Solvent (Dissociation Exponent)

D2SO4; H2O

Method (Dissociation Exponent)

NMR

Type (Dissociation Exponent)

b1/apparent

Dell'erba, Carlo; Gruttadauria, Michelangelo; Mugnoli, Angelo; Noto, Renato; Novi, Marino; Occhiucci, Giorgio; Petrillo, Giovanni; Spinelli, Domenico; Tetrahedron; vol. 56; nb. 26; (2000); p. 4565 - 4573, View in Reaxys 2 of 7

Dissociation Exponent (pK)

17.56

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

H2O

Type (Dissociation Exponent)

a1/apparent

Guthrie, J. Peter; Cossar, John; Canadian Journal of Chemistry; vol. 68; nb. 11; (1990); p. 2060 - 2069, View in Reaxys 3 of 7

Dissociation Exponent (pK)

-1.36 - -1.37

Temperature (Dissociation Exponent) [°C]

Solvent (Dissociation Exponent)

tetrahydrofuran

Type (Dissociation Exponent)

a1/apparent

Kaufman, Michael J.; Streitwieser, Andrew; Journal of the American Chemical Society; vol. 109; nb. 20; (1987); p. 6092 6097, View in Reaxys 4 of 7

Comment (Dissociation Exponent)

(pk')pK

Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3095,3096, View in Reaxys 5 of 7

Comment (Dissociation Exponent)

(pk')pK: 24.40167

Bordwell et al.; Journal of Organic Chemistry; vol. 42; (1977); p. 326,331, View in Reaxys 6 of 7

Comment (Dissociation Exponent)

(pk')pK-Werte

Bordwell et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 1885, View in Reaxys 7 of 7

Comment (Dissociation Exponent)

(pk)absoluter pK(S)-Wert in DMSO

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys Dynamic Viscosity (14) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

Comment (Dynamic Viscosity)

References

53/126

2018-07-03 19:01:53

0.0124757

49.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.0144238

39.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.015389

34.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.015399

34.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.016224

29.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.0162606

29.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 91; nb. 6; (2017); p. 1037 - 1044, View in Reaxys

0.0144895

39.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

0.0153996

34.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

0.0162246

29.99

Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

0.01469

34.99

Gowrisankar; Sivarambabu; Venkateswarlu; Kumar, K. Siva; Bulletin of the Korean Chemical Society; vol. 33; nb. 5; (2012); p. 1686 - 1692, View in Reaxys

0.0151

29.99

Gowrisankar; Sivarambabu; Venkateswarlu; Kumar, K. Siva; Bulletin of the Korean Chemical Society; vol. 33; nb. 5; (2012); p. 1686 - 1692, View in Reaxys

0.01468

34.99

Tangeda, Savitha Jyostna; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 3; (2006); p. 272 - 277, View in Reaxys

0.015177

Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys

0.01765

Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys

Electrical Moment (3) 1 of 3

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

30grad, in C6H6

Pinkus; Custard; Journal of Physical Chemistry; vol. 74; (1970); p. 1042, View in Reaxys 2 of 3

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (unverduennt)

Vuks; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 1239; Zhurnal Fizicheskoi Khimii; vol. 43; (1969); p. 2208, View in Reaxys 3 of 3

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.88

Method (Electrical Moment)

Dielectric constant (Ε)

Solvent (Electrical Moment)

benzene

Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 225; (1947); p. 1306, View in Reaxys

54/126

2018-07-03 19:01:53

Electrical Polarizability (1) Description (Elec- References trical Polarizability) Polarizability

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Electrochemical Behaviour (7) Description (Elec- Comment (Electrotrochemical Behav- chemical Behaviour) iour) Acidity

References

Cumming; Kebarle; Canadian Journal of Chemistry; vol. 56; (1978); p. 1,5, View in Reaxys; Bordwell; Matthews; Journal of the American Chemical Society; vol. 96; (1974); p. 1216, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 1885, View in Reaxys; Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys; Alnajjar, Mikhail S.; Zhang, Xian-Man; Gleicher, Gerald J.; Truksa, Scott V.; Franz, James A.; Journal of Organic Chemistry; vol. 67; nb. 25; (2002); p. 9016 - 9022, View in Reaxys

Basicity

gas

Basicity

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Electrolytic dissociation / protonation equilibrium

Bordwell, Frederick G.; Harrelson, John A.; Canadian Journal of Chemistry; vol. 68; nb. 10; (1990); p. 1714 - 1718, View in Reaxys; Guthrie, J. Peter; Cossar, John; Canadian Journal of Chemistry; vol. 68; nb. 11; (1990); p. 2060 - 2069, View in Reaxys

Polarography

Zuman; Horak; Collection of Czechoslovak Chemical Communications; vol. 27; (1962); p. 187, View in Reaxys; Michel et al.; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 98; (1979); p. 319,321, View in Reaxys; Abrutskaya et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 25; (1970); p. 176,141, View in Reaxys; Molnar et al.; Chemicke Zvesti; vol. 14; (1960); p. 783,786,787; Chem.Abstr.; vol. 55; nb. 16221; (1961), View in Reaxys

Electrochemical properties

Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 33; (1971); p. 419,421, View in Reaxys

Basicity

spektrophotometrisch ermittelt.

Zucker; Hammett; Journal of the American Chemical Society; vol. 61; (1939); p. 2779,2783, View in Reaxys

Electrochemical Characteristics (6) 1 of 6

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Kohtani, Shigeru; Yoshioka, Eito; Saito, Kenji; Kudo, Akihiko; Miyabe, Hideto; Catalysis Communications; vol. 11; nb. 13; (2010); p. 1049 - 1053, View in Reaxys 2 of 6

Description (Electrochemical Characteristics)

oxidation potential

Bordwell; Zhang, Xian-Man; Alnajjar, Mikhail S.; Journal of the American Chemical Society; vol. 114; nb. 20; (1992); p. 7623 - 7629, View in Reaxys; Fukuzumi, Shunichi; Koumitsu, Shintaro; Hironaka, Katsuhiko; Tanaka, Toshio; Journal of the American Chemical Society; vol. 109; nb. 2; (1987); p. 305 - 316, View in Reaxys 3 of 6

Description (Electrochemical Characteristics)

redox potential

van Tilborg et al.; Recueil des Travaux Chimiques des Pays-Bas; vol. 97; (1978); p. 321,325, View in Reaxys; Fukuzumi, Shunichi; Hironaka, Katsuhiko; Nishizawa, Nobuaki; Tanaka, Toshio; Bulletin of the Chemical Society of Japan; vol. 56; nb. 8; (1983); p. 2220 - 2227, View in Reaxys 4 of 6

Description (Electrochemical Characteristics)

polarographic half-wave potential

Volke et al.; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 32; (1971); p. 445,449, View in Reaxys; Asano et al.; Chemistry Letters; (1974); p. 1149, View in Reaxys; Ganapathy; Ramanujam; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 16; (1978); p. 532, View in Reaxys 5 of 6

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

(wss.-aethanol. Loesungen vom pH 3.8-12.4).

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.

55/126

2018-07-03 19:01:53

Portillo; Varela; An. Bromatol.; vol. 2; (1950); p. 147,179, View in Reaxys; Elving; Leone; Analytical Chemistry; vol. 29; (1957); p. 782, View in Reaxys; Elving; Leone; Journal of the American Chemical Society; vol. 80; (1958); p. 1021,1022, View in Reaxys 6 of 6

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Davies; Evans; Journal of the Chemical Society; (1939); p. 546,547, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Wentworth et al.; Journal of Physical Chemistry; vol. 79; (1975); p. 1161,1163, 1165, View in Reaxys

Enthalpy of Combustion (1) References Colomina et al.; Pure and Applied Chemistry; vol. 2; (1961); p. 133,134, 135; Chem.Abstr.; vol. 55; nb. 26637; (1961), View in Reaxys Enthalpy of Formation (1) References McLoughlin; Traeger; Organic Mass Spectrometry; vol. 14; (1979); p. 434,436, View in Reaxys Enthalpy of Vaporization (1) Comment (Enthal- References py of Vaporization) Enthalpy of vaporization given

Ji, Chang; Day, Shannon E.; Ortega, Stephanie A.; Beall, Gary W.; Journal of Chemical and Engineering Data; vol. 53; nb. 5; (2008); p. 1093 - 1097, View in Reaxys

Further Information (29) Description (FurReferences ther Information) Further information Roth et al.; Journal of Chemical Physics; vol. 71; (1979); p. 610, View in Reaxys Further information Ganapathy; Ramanujam; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 16; (1978); p. 532, View in Reaxys Further information Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p. 2637,2638, View in Reaxys Further information Grechishkin; Gushchin; Journal of Structural Chemistry; vol. 15; (1974); p. 276; ; p. 302, View in Reaxys Further information Asano et al.; Chemistry Letters; (1974); p. 1149, View in Reaxys Further information Kitamura et al.; Nippon Kagaku Kaishi; (1973); p. 1970,1971, View in Reaxys Further information Gacoin; Leclercq; Journal of Chemical Physics; vol. 59; (1973); p. 4351, View in Reaxys Further information Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys Further information Volke et al.; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 32; (1971); p. 445,449, View in Reaxys Further information Ferretti; Flanagan; Journal of Agricultural and Food Chemistry; vol. 19; (1971); p. 245,247, View in Reaxys Further information Hertz et al.; Analytical Chemistry; vol. 43; (1971); p. 681,688, View in Reaxys Further information Beynon et al.; Organic Mass Spectrometry; vol. 5; (1971); p. 967,972, View in Reaxys Further information Sollenberger,P.Y.; Martin,R.B.; Journal of the American Chemical Society; vol. 92; (1970); p. 4261 - 4270, View in Reaxys Further information Dym; Hochstrasser; Journal of Chemical Physics; vol. 51; (1969); p. 2458,2464, View in Reaxys Further information Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys Further information Kraft; Spiteller; Organic Mass Spectrometry; vol. 1; (1968); p. 617,622,623,625, View in Reaxys Further information Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys Further information McFarland; Harris; Journal of Organic Chemistry; vol. 32; (1967); p. 1273, View in Reaxys Further information Gupta; Mital; Bulletin des Societes Chimiques Belges; vol. 76; (1967); p. 631,634, 636, View in Reaxys Further information Maroni-Barnaud; Gilard; Bulletin de la Societe Chimique de France; (1966); p. 125,131, View in Reaxys Further information Shida; Hamill; Journal of the American Chemical Society; vol. 88; (1966); p. 3683,3685, 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.

56/126

2018-07-03 19:01:53

Further information Pignataro et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 49; (1966); p. 291, View in Reaxys Further information Purrello,G.; Gazzetta Chimica Italiana; vol. 95; (1965); p. 1078 - 1088, View in Reaxys Further information Arai; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 1032, View in Reaxys Further information Patent; Allied Chem.; NL6402964; (1964); Chem.Abstr.; vol. 62; nb. 7658; (1965), View in Reaxys Further information Berton; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 679, View in Reaxys Further information Cox; Tetrahedron; vol. 18; (1962); p. 1337,1342, View in Reaxys Further information Foster; Mackie; Tetrahedron; vol. 18; (1962); p. 1131,1134, View in Reaxys Further information Kupin; Petrow; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2958,2758; Chem.Abstr.; vol. 57; nb. 2125; (1962), View in Reaxys Heat Capacity Cp (3) Heat Capacity Cp Temperature (Heat [Jmol-1K-1] Capacity Cp) [°C]

References

243.2

25.1

Fuchs, Richard; Canadian Journal of Chemistry; vol. 58; nb. 22; (1980); p. 2305 - 2306, View in Reaxys

243.8

25.1

Fuchs, Richard; Canadian Journal of Chemistry; vol. 58; nb. 22; (1980); p. 2305 - 2306, View in Reaxys

244

25.1

Fuchs, Richard; Canadian Journal of Chemistry; vol. 58; nb. 22; (1980); p. 2305 - 2306, View in Reaxys

Henry Constant (MCS) (1) 1 of 1

Comment (Henry Constant Henry constant given (MCS)) Ji, Chang; Day, Shannon E.; Ortega, Stephanie A.; Beall, Gary W.; Journal of Chemical and Engineering Data; vol. 53; nb. 5; (2008); p. 1093 - 1097, View in Reaxys

Ionization Potential (1) References Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p. 2637,2638, View in Reaxys; Pignataro et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 49; (1966); p. 291, View in Reaxys; McLoughlin; Traeger; Organic Mass Spectrometry; vol. 14; (1979); p. 434,436, View in Reaxys Liquid/Liquid Systems (MCS) (10) 1 of 10

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

26.85

Pressure (Liquid/Liquid Systems (MCS)) [Torr]

60004.8

Partner (Liquid/Liquid Systems (MCS))

carbon dioxide

Timko, Michael T.; Nicholson, Benjamin F.; Steinfeld, Jeffrey I.; Smith, Kenneth A.; Tester, Jefferson W.; Journal of Chemical and Engineering Data; vol. 49; nb. 4; (2004); p. 768 - 778, View in Reaxys 2 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

aq. phosphate buffer

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate; H2O

Khaledi; Kelly; Burns; Analytical Chemistry; vol. 73; nb. 24; (2001); p. 6057 - 6062, View in Reaxys 3 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS))

57/126

2018-07-03 19:01:53

Solvent (Liquid/Liquid Systems (MCS))

acetonitrile; various solvent(s)

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

immobilized artificial membrane (IAC)

Valko, Klara; Du, Chau My; Bevan, Christopher D.; Reynolds, Derek P.; Abraham, Michael H.; Journal of Pharmaceutical Sciences; vol. 89; nb. 8; (2000); p. 1085 - 1096, View in Reaxys 4 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

dibutyl ether; H2O

Pagliara, Alessandra; Caron, Giulia; Lisa, Giuseppe; Fan, Weizheng; Gaillard, Patrick; Carrupt, Pierre-Alain; Testa, Bernard; Abraham, Michael H.; Journal of the Chemical Society. Perkin Transactions 2; nb. 12; (1997); p. 2639 - 2643, View in Reaxys 5 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate; butan-1-ol; n-heptane; H2O

Ishihama, Yasushi; Oda, Yoshiya; Uchikawa, Kiyohiko; Asakawa, Naoki; Analytical Chemistry; vol. 67; nb. 9; (1995); p. 1588 - 1595, View in Reaxys 6 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

octanol; H2O

Ishihama, Yasushi; Oda, Yoshiya; Uchikawa, Kiyohiko; Asakawa, Naoki; Analytical Chemistry; vol. 67; nb. 9; (1995); p. 1588 - 1595, View in Reaxys 7 of 10

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

Partner (Liquid/Liquid Systems (MCS))

octanol / water

Ishihama; Oda; Uchikawa; Asakawa; Chemical and Pharmaceutical Bulletin; vol. 42; nb. 7; (1994); p. 1525 - 1527, View in Reaxys 8 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

octanol

Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys 9 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

Partner (Liquid/Liquid Systems (MCS))

octanol

58/126

2018-07-03 19:01:53

Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys 10 of 10

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Laub; Purnell; Analytical Chemistry; vol. 48; (1976); p. 799,800, View in Reaxys

Liquid/Vapour Systems (MCS) (18) 1 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

water

Grunbauer; Bultsma; Rekker; European Journal of Medicinal Chemistry; vol. 17; nb. 5; (1982); p. 421 - 428, View in Reaxys 2 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 3 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

chloroform

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 4 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

methyl iodide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 5 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 6 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

1,2-dichloro-ethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 7 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl bromide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 8 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl iodide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys

59/126

2018-07-03 19:01:53

9 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

acetone

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 10 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

1-Chloropropane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 11 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 12 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

tertiary butyl chloride

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 13 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

isoprene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 14 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

cyclopenta-1,3-diene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 15 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

benzene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 16 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 17 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

hexane

60/126

2018-07-03 19:01:53

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 18 of 18

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

di-isopropyl ether

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys Magnetic Susceptibility (1) Magnetic Suscepti- References bility [10-6cm3mol-1] -83.7

Angus; Llewelyn; Transactions of the Faraday Society; vol. 51; (1955); p. 245,246, View in Reaxys

Mechanical & Physical Properties (MCS) (10) 1 of 10

Description (Mechanical & Physical Properties (MCS))

Ultrasonic velocity

Temperature (Mechanical & Physical Properties (MCS)) [°C]

34.99

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

acetonitrile

Tangeda, Savitha Jyostna; Boodida, Sathyanarayana; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 11; (2006); p. 1438 - 1442, View in Reaxys 2 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

9.99

Comment (Mechanical & Physical Properties (MCS))

temperature dependence

Partner (Mechanical & Physical Properties (MCS))

toluene

Moravkova; Linek; Journal of Chemical Thermodynamics; vol. 38; nb. 10; (2006); p. 1240 - 1244, View in Reaxys 3 of 10

Description (Mechanical & Physical Properties (MCS))

Ultrasonic velocity

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

N-methyl-acetamide

Tangeda, Savitha J.; Nallani, Satyanarayana; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 89 - 91, View in Reaxys 4 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

61/126

2018-07-03 19:01:53

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

N-methyl-acetamide

Tangeda, Savitha J.; Nallani, Satyanarayana; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 89 - 91, View in Reaxys 5 of 10

Description (Mechanical & Physical Properties (MCS))

Adiabatic compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

N-methyl-acetamide

Tangeda, Savitha J.; Nallani, Satyanarayana; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 89 - 91, View in Reaxys 6 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

Partner (Mechanical & Physical Properties (MCS))

acetonitrile

Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys 7 of 10

Description (Mechanical & Physical Properties (MCS))

Isothermal compressibility

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 55

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

750.06 - 297174

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

toluene

Moravkova; Wagner; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 7; (2005); p. 658 - 666, View in Reaxys 8 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25 - 55

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

62/126

2018-07-03 19:01:53

Partner (Mechanical & Physical Properties (MCS))

benzene

Moravkova; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 9; (2005); p. 1023 - 1028, View in Reaxys 9 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [Â°C]

25 - 55

Comment (Mechanical & Physical Properties (MCS))

concentration dependence

Partner (Mechanical & Physical Properties (MCS))

ethylbenzene

Moravkova; Linek; Journal of Chemical Thermodynamics; vol. 37; nb. 9; (2005); p. 1023 - 1028, View in Reaxys 10 of 10

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Dusart et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 832,833, View in Reaxys Mechanical Properties (4) Description (MeComment (MeReferences chanical Properties) chanical Properties) Compressibility Molar volume

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys Liquid

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

Specific volume

Ishihama, Yasushi; Asakawa, Naoki; Journal of Pharmaceutical Sciences; vol. 88; nb. 12; (1999); p. 1305 - 1312, View in Reaxys

Molar volume

Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys; Taft; Abraham; Famini; Doherty; Abboud; Kamlet; Journal of Pharmaceutical Sciences; vol. 74; nb. 8; (1985); p. 807 - 814, View in Reaxys

Optics (1) Description (Optics) Magnetorotation

References Dawber, J. Graham; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 80; (1984); p. 2133 - 2144, View in Reaxys; Dawber, J. Graham; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 78; (1982); p. 2297 - 2302, View in Reaxys

Other Thermochemical Data (3) Description (Other References Thermochemical Data) Thermodynamic properties

Herkstroeter et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 4537,4539, View in Reaxys; Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Cumming; Kebarle; Journal of the American Chemical Society; vol. 100; (1978); p. 1835,1836, View in Reaxys; Guiheneuf et al.; Bulletin de la Societe Chimique de France; (1971); p. 1157,1160, 1162, View in Reaxys

Entropy

Guiheneuf et al.; Bulletin de la Societe Chimique de France; (1971); p. 1157,1160, 1162, View in Reaxys

Enthalpy

Guiheneuf et al.; Bulletin de la Societe Chimique de France; (1971); p. 1157,1160, 1162, View in Reaxys

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

log POW

2.19

Valko, Klara; Du, Chau My; Bevan, Christopher D.; Reynolds, Derek P.; Abraham, Michael H.; Journal of Pharmaceutical Sciences; vol. 89; nb. 8; (2000); p. 1085 - 1096, View in Reaxys; Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys; Kohtani, Shigeru; Kamoi, Yuna; Yoshioka, Eito; Miyabe, Hideto; Catalysis Science and Technology; vol. 4; nb. 4; (2014); p. 1084 - 1091, View in Reaxys Solubility (MCS) (4)

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.

63/126

2018-07-03 19:01:53

1 of 4

Comment (Solubility (MCS))

Soluble in 2-methyltetrahydrofuran; Insoluble in 2-propanol

Demmans; Ko; Morris; RSC Advances; vol. 6; nb. 91; (2016); p. 88580 - 88587, View in Reaxys 2 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 3 of 4

Saturation

in solution

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

various solvent(s)

Comment (Solubility (MCS))

Solubilty: 2 mol-percent

Workentin; Leigh; Jeffrey; Journal of the American Chemical Society; vol. 112; nb. 20; (1990); p. 7329 - 7336, View in Reaxys 4 of 4

Saturation

in solution

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

various solvent(s)

Comment (Solubility (MCS))

Solubilty: 0.8 mol-percent

Workentin; Leigh; Jeffrey; Journal of the American Chemical Society; vol. 112; nb. 20; (1990); p. 7329 - 7336, View in Reaxys Solution Behaviour (MCS) (5) 1 of 5

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

lithium perfluoro-1-octanesufonate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 2 of 5

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium cholate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 3 of 5

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium dodecyl-sulfate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 4 of 5

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Be- 19.4 - 90.5 haviour (MCS)) [°C]

64/126

2018-07-03 19:01:53

Partner (Solution Behaviour (MCS))

H2O

Stephenson; Journal of Chemical and Engineering Data; vol. 37; nb. 1; (1992); p. 80 - 95, View in Reaxys 5 of 5

Description (Solution Behaviour (MCS))

Dissolving capacity

Bikitimirov; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 1276; Zhurnal Fizicheskoi Khimii; p. 2356, View in Reaxys Sound Properties (2) Description (Sound Comment (Sound Properties) Properties) Ultrasonic velocity

Velocity of sound

References Tangeda, Savitha J.; Nallani, Satyanarayana; Journal of Chemical and Engineering Data; vol. 50; nb. 1; (2005); p. 89 - 91, View in Reaxys; Tangeda, Savitha Jyostna; Boodida, Sathyanarayana; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 11; (2006); p. 1438 - 1442, View in Reaxys

in Propiophenon bei 20grad: 1498 m/sec.

Surface Tension (4) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C]

Schaaffs; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 194; (1944); p. 28,33, 39, 48; Annalen der Physik (Weinheim, Germany); vol. <5> 40; (1941); p. 393,402, View in Reaxys

References

1.0957

39.99

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

1.2

34.99

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

1.2973

29.99

Bindhani; Roy; Mohanty; Kubendran; Russian Journal of Physical Chemistry A; vol. 89; nb. 10; (2015); p. 1828 - 1837, View in Reaxys

30.23 - 37.22

22.3 - 86.7

Vogel; Journal of the Chemical Society; (1948); p. 631, View in Reaxys

Transport Phenomena (MCS) (6) 1 of 6

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

34.99

Comment (Transport Phenomena (MCS))

concentration dependence

Partner (Transport Phenomena (MCS))

N-methyl-acetamide

Tangeda, Savitha Jyostna; Nallani, Satyanarayana; Journal of Chemical Thermodynamics; vol. 38; nb. 3; (2006); p. 272 277, View in Reaxys 2 of 6

Description (Transport Phenomena (MCS))

Dynamic viscosity

Temperature (Transport Phenomena (MCS)) [°C]

Partner (Transport Phenomena (MCS))

acetonitrile

Savitha Jyostna; Satyanarayana; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 44; nb. 7; (2005); p. 1365 - 1371, View in Reaxys 3 of 6

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25.1

Partner (Transport Phenomena (MCS))

ethanol

Chen, Nong; Chan; Chemical Communications; nb. 7; (1997); p. 719 - 720, View in Reaxys

65/126

2018-07-03 19:01:53

4 of 6

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25.1

Partner (Transport Phenomena (MCS))

acetone

Chan; Ma; Chen; Journal of Chemical Physics; vol. 107; nb. 6; (1997); p. 1890 - 1895, View in Reaxys 5 of 6

Description (Transport Phenomena (MCS))

Viscosity

Dusart et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 919,920, 921, 924, 926, View in Reaxys 6 of 6

Description (Transport Phenomena (MCS))

Diffusion

Grushka; Kikta; Journal of the American Chemical Society; vol. 98; (1976); p. 643,645, View in Reaxys Vapour Pressure (1) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C] 57.04 - 507.5

132.2 - 201.3

References Dreisbach; Shrader; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2879, View in Reaxys

NMR Spectroscopy (159) 1 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Zhang, Jinli; Han, Zixing; Li, Junmiao; Wu, Yangjie; Arkivoc; vol. 2013; nb. 4; (2013); p. 251 - 271, View in Reaxys; Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 - 4254; Art.No: 26677, View in Reaxys; Madumo, Gilbert K.; Moshapo, Paseka T.; Kinfe, Henok H.; Medicinal Chemistry Research; vol. 27; nb. 3; (2018); p. 817 - 833, View in Reaxys 2 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Shen, Duyi; Miao, Chengxia; Xu, Daqian; Xia, Chungu; Sun, Wei; Organic Letters; vol. 17; nb. 1; (2015); p. 54 - 57, View in Reaxys; Dong, Yanli; Zhao, Xiaomei; Liu, Renhua; Chinese Journal of Chemistry; vol. 33; nb. 9; (2015); p. 1019 1023, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; 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; Erbing, Elis; VázquezRomero, Ana; Bermejo Gómez, Antonio; Platero-Prats, Ana E.; Carson, Fabian; Zou, Xiaodong; Tolstoy, Päivi; MartínMatute, Belén; Chemistry - A European Journal; vol. 22; nb. 44; (2016); p. 15659 - 15663, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Halima, Taoufik Ben; Zhang, Wanying; Yalaoui, Imane; Hong, Xin; Yang, Yun-Fang; Houk, Kendall N.; Newman, Stephen G.; Journal of the American Chemical Society; vol. 139; nb. 3; (2017); p. 1311 - 1318, View in Reaxys; Toyomura, Kazuki; Fujita, Ken-Ichi; Chemistry Letters; vol. 46; nb. 6; (2017); p. 808 - 810, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Gaspa, Silvia; Porcheddu, Andrea; Valentoni, Antonio; Garroni, Sebastiano; Enzo, Stefano; De Luca, Lidia; European Journal of Organic Chemistry; vol. 2017; nb. 37; (2017); p. 5519 - 5526, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24;

66/126

2018-07-03 19:01:53

(2017); p. 6760 - 6762, View in Reaxys; Meng, Mengting; Yang, Liangfeng; Cheng, Kai; Qi, Chenze; Journal of Organic Chemistry; vol. 83; nb. 6; (2018); p. 3275 - 3284, View in Reaxys 3 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Dong, Yanli; Zhao, Xiaomei; Liu, Renhua; Chinese Journal of Chemistry; vol. 33; nb. 9; (2015); p. 1019 - 1023, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; 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; Erbing, Elis; VázquezRomero, Ana; Bermejo Gómez, Antonio; Platero-Prats, Ana E.; Carson, Fabian; Zou, Xiaodong; Tolstoy, Päivi; MartínMatute, Belén; Chemistry - A European Journal; vol. 22; nb. 44; (2016); p. 15659 - 15663, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Halima, Taoufik Ben; Zhang, Wanying; Yalaoui, Imane; Hong, Xin; Yang, Yun-Fang; Houk, Kendall N.; Newman, Stephen G.; Journal of the American Chemical Society; vol. 139; nb. 3; (2017); p. 1311 - 1318, View in Reaxys; Toyomura, Kazuki; Fujita, Ken-Ichi; Chemistry Letters; vol. 46; nb. 6; (2017); p. 808 - 810, View in Reaxys; Suchand, Basuli; Satyanarayana, Gedu; European Journal of Organic Chemistry; vol. 2017; nb. 26; (2017); p. 3886 - 3895, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Gaspa, Silvia; Porcheddu, Andrea; Valentoni, Antonio; Garroni, Sebastiano; Enzo, Stefano; De Luca, Lidia; European Journal of Organic Chemistry; vol. 2017; nb. 37; (2017); p. 5519 - 5526, View in Reaxys; Shipilovskikh, Sergei A.; Rubtsov, Aleksandr E.; Malkov, Andrei V.; Organic Letters; vol. 19; nb. 24; (2017); p. 6760 - 6762, View in Reaxys; Meng, Mengting; Yang, Liangfeng; Cheng, Kai; Qi, Chenze; Journal of Organic Chemistry; vol. 83; nb. 6; (2018); p. 3275 - 3284, View in Reaxys 4 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Zhou, Yulu; Lin, Shasha; Bian, Yinghui; Xia, Daohong; Xiang, Yuzhi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 55B; nb. 5; (2016); p. 624 - 628, View in Reaxys; Madumo, Gilbert K.; Moshapo, Paseka T.; Kinfe, Henok H.; Medicinal Chemistry Research; vol. 27; nb. 3; (2018); p. 817 - 833, View in Reaxys 5 of 159

Description (NMR Spectroscopy)

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 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

67/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Xia, Tian; Wei, Zhihong; Spiegelberg, Brian; Jiao, Haijun; Hinze, Sandra; de Vries, Johannes G.; Chemistry - A European Journal; vol. 24; nb. 16; (2018); p. 4043 - 4049, View in Reaxys; Sun, Jin-Shi; Jing, Li-Ping; Tian, Yuyang; Sun, Fuxing; Chen, Peng; Zhu, Guangshan; Chemical Communications; vol. 54; nb. 13; (2018); p. 1603 - 1606, View in Reaxys 7 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

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

supporting information

Wang, Qingfu; Chai, Huining; Yu, Zhengkun; Organometallics; vol. 37; nb. 4; (2018); p. 584 - 591, View in Reaxys 9 of 159

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

Wang, Qingfu; Chai, Huining; Yu, Zhengkun; Organometallics; vol. 37; nb. 4; (2018); p. 584 - 591, View in Reaxys 10 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz]

68/126

2018-07-03 19:01:53

Location

supporting information

Chatupheeraphat, Adisak; Liao, Hsuan-Hung; Srimontree, Watchara; Guo, Lin; Minenkov, Yury; Poater, Albert; Cavallo, Luigi; Rueping, Magnus; Journal of the American Chemical Society; vol. 140; nb. 10; (2018); p. 3724 - 3735, View in Reaxys 11 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

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

González Miera, Greco; Martínez-Castro, Elisa; Martín-Matute, Belén; Organometallics; vol. 37; nb. 5; (2018); p. 636 644, View in Reaxys 13 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectro- 200 scopy) [MHz] Consiglio, Gabriella Barozzino; Mordini, Alessandro; Letters in Organic Chemistry; vol. 15; nb. 5; (2018); p. 447 - 454, View in Reaxys 14 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0052; 0056; 0060

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys

69/126

2018-07-03 19:01:53

15 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0052; 0056; 0060

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 16 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

Gatto, Mattia; Baratta, Walter; Belanzoni, Paola; Belpassi, Leonardo; Del Zotto, Alessandro; Tarantelli, Francesco; Zuccaccia, Daniele; Green Chemistry; vol. 20; nb. 9; (2018); p. 2125 - 2134, View in Reaxys 17 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys; Chowdhury, Abhishek Dutta; Ray, Ritwika; Lahiri, Goutam Kumar; Chemical Communications; vol. 48; nb. 44; (2012); p. 5497 - 5499, View in Reaxys; Saisaha, Pattama; Buettner, Lea; Van Der Meer, Margarethe; Hage, Ronald; Feringa, Ben L.; Browne, Wesley R.; De Boer, Johannes W.; Advanced Synthesis and Catalysis; vol. 355; nb. 13; (2013); p. 2591 - 2603, View in Reaxys; Liang, Shengzong; Hammond, Gerald B.; Xu, Bo; Chemical Communications; vol. 51; nb. 5; (2015); p. 903 - 906, View in Reaxys; Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys; Yang, Yiwen; Zhong, Wei; Nie, Binmei; Chen, Jiangmin; Wei, Zhenhong; Liu, Xiaoming; Journal of Organometallic Chemistry; vol. 853; (2017); p. 136 - 142, View in Reaxys; Berton, Mateo; Mello, Rossella; Williard, Paul G.; González-Núñez, María Elena; Journal of the American Chemical Society; vol. 139; nb. 48; (2017); p. 17414 - 17420, View in Reaxys 18 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys; Nelson, David J.; Fernandez-Salas, Jose A.; Truscott, Byron J.; Nolan, Steven P.; Organic and Biomolecular Chemistry; vol. 12; nb. 34; (2014); p. 6672 - 6676, View in Reaxys;

70/126

2018-07-03 19:01:53

Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys; Yousuf, Md; Das, Tuluma; Adhikari, Susanta; New Journal of Chemistry; vol. 39; nb. 11; (2015); p. 8763 - 8770, View in Reaxys; Devari, Shekaraiah; Rizvi, Masood Ahmad; Shah, Bhahwal Ali; Tetrahedron Letters; vol. 57; nb. 30; (2016); p. 3294 - 3297, View in Reaxys; Ma, Jiaqi; Hong, Chao; Wan, Yan; Li, Meichao; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Jin, Liqun; Shen, Zhenlu; Tetrahedron Letters; vol. 58; nb. 7; (2017); p. 652 - 657, View in Reaxys; Porcheddu, Andrea; Colacino, Evelina; Cravotto, Giancarlo; Delogu, Francesco; De Luca, Lidia; Beilstein Journal of Organic Chemistry; vol. 13; (2017); p. 2049 - 2055, View in Reaxys 19 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wu, Ji-Cheng; Gong, Lu-Bing; Xia, Yuanzhi; Song, Ren-Jie; Xie, Ye-Xiang; Li, Jin-Heng; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9909 - 9913, View in Reaxys; Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys; Ma, Jiaqi; Hong, Chao; Wan, Yan; Li, Meichao; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Jin, Liqun; Shen, Zhenlu; Tetrahedron Letters; vol. 58; nb. 7; (2017); p. 652 - 657, View in Reaxys 20 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, Hans-Günther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 - 7384, View in Reaxys; 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 21 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0040

Patent; Soochow University; Li, Hongxi; Tan, Dawei; Li, Haiyan; Lang, Jianping; (15 pag.); CN106588957; (2017); (A) Chinese, View in Reaxys 22 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

Paragraph 0040

71/126

2018-07-03 19:01:53

Patent; Soochow University; Li, Hongxi; Tan, Dawei; Li, Haiyan; Lang, Jianping; (15 pag.); CN106588957; (2017); (A) Chinese, View in Reaxys 23 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Location

supporting information

Dip, Irene; Gethers, Christina; Rice, Tonya; Straub, Thomas S.; Tetrahedron Letters; vol. 58; nb. 28; (2017); p. 2720 - 2722, View in Reaxys 24 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.84

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

supporting information

Suchand, Basuli; Satyanarayana, Gedu; European Journal of Organic Chemistry; vol. 2017; nb. 26; (2017); p. 3886 - 3895, View in Reaxys 25 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0039

Patent; University of Science and Technology of China; Kang Yanbiao; Liu Jie; (15 pag.); CN107011133; (2017); (A) Chinese, View in Reaxys 26 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0039

Patent; University of Science and Technology of China; Kang Yanbiao; Liu Jie; (15 pag.); CN107011133; (2017); (A) Chinese, View in Reaxys 27 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

72/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Porcheddu, Andrea; Colacino, Evelina; Cravotto, Giancarlo; Delogu, Francesco; De Luca, Lidia; Beilstein Journal of Organic Chemistry; vol. 13; (2017); p. 2049 - 2055, View in Reaxys 28 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Berton, Mateo; Mello, Rossella; Williard, Paul G.; González-Núñez, María Elena; Journal of the American Chemical Society; vol. 139; nb. 48; (2017); p. 17414 - 17420, View in Reaxys 29 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys; Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys; Martinez-Erro, Samuel; Sanz-Marco, Amparo; Bermejo Gómez, Antonio; Vázquez-Romero, Ana; Ahlquist, Mårten S. G.; Martín-Matute, Belén; Journal of the American Chemical Society; vol. 138; nb. 40; (2016); p. 13408 - 13414, View in Reaxys 30 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Obermayer, David; Znidar, Desiree; Glotz, Gabriel; Stadler, Alexander; Dallinger, Doris; Oliver Kappe; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11788 - 11801, View in Reaxys 31 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Zhang, Yuecheng; Liu, Liu; Cao, Xiaohui; Zhao, Jiquan; Polyhedron; vol. 105; (2016); p. 170 - 177, View in Reaxys

73/126

2018-07-03 19:01:53

32 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0114

Patent; Zhejiang University; Zhang, Guofu; Li, Shasha; Ding, Chengrong; Zhang, Guihua; Xie, Xiaoqiang; Lei, Jie; (12 pag.); CN105294413; (2016); (A) Chinese, View in Reaxys 33 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0115

Patent; Zhejiang University; Zhang, Guofu; Li, Shasha; Ding, Chengrong; Zhang, Guihua; Xie, Xiaoqiang; Lei, Jie; (12 pag.); CN105294413; (2016); (A) Chinese, View in Reaxys 34 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20.84

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

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys 35 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.84

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

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys 36 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

74/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Martinez-Erro, Samuel; Sanz-Marco, Amparo; Bermejo Gómez, Antonio; Vázquez-Romero, Ana; Ahlquist, Mårten S. G.; Martín-Matute, Belén; Journal of the American Chemical Society; vol. 138; nb. 40; (2016); p. 13408 - 13414, View in Reaxys 37 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H NMR (400 MHz, CDCl3): Ε=1.23 (t, J=7.3 Hz, 3H), 3.02 (q, J=7.3 Hz, 2H), 7.46 (t, J=7.5 Hz, troscopy) 2H), 7.56 (t, J=7.5 Hz, 1H), 7.97 (d, J=7.5 Hz, 2H) Location

supporting information

Signals [ppm]

1.23; 3.02; 7.46; 7.56; 7.97

Kind of signal

t, J=7.3 Hz, 3H; q, J=7.3 Hz, 2H; t, J=7.5 Hz, 2H; t, J=7.5 Hz, 1H; d, J=7.5 Hz, 2H

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 38 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

8.19; 31.73; 127.92; 128.5; 132.83; 136.85; 200.82

NMR (100 MHz, CDCl3): Ε=8.19, 31.73, 127.92, 128.50, 132.83, 136.85, 200.82

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 39 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, Hans-Günther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 - 7384, View in Reaxys 40 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

75/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Munoz, Maria Paz; De La Torre, Maria C.; Sierra, Miguel A.; Advanced Synthesis and Catalysis; vol. 352; nb. 13; (2010); p. 2189 - 2194, View in Reaxys; Landers, Brant; Berini, Christophe; Wang, Chao; Navarro, Oscar; Journal of Organic Chemistry; vol. 76; nb. 5; (2011); p. 1390 - 1397, View in Reaxys; Ríos-Lombardía, Nicolás; Vidal, Cristian; Cocina, María; Morís, Francisco; García-Álvarez, Joaquín; González-Sabín, Javier; Chemical Communications; vol. 51; nb. 54; (2015); p. 10937 - 10940, View in Reaxys 41 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 8456, View in Reaxys; Zhao, Jinwu; Liu, Li; Xiang, Shijian; Liu, Qiang; Chen, Huoji; Organic and Biomolecular Chemistry; vol. 13; nb. 20; (2015); p. 5613 - 5616, View in Reaxys 42 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Wang, Peng; Cai, Jin; Yang, Jiabin; Sun, Chunlong; Li, Lushen; Hu, Huayou; Ji, Min; Tetrahedron Letters; vol. 54; nb. 6; (2013); p. 533 - 535, View in Reaxys; Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys 43 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys; Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 - 4254; Art.No: 26677, View in Reaxys 44 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 4260, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431,

76/126

2018-07-03 19:01:53

View in Reaxys; Liu, Yangyang; Xie, Aming; Cao, Meiping; Feng, Liandong; Wang, Boliang; Asian Journal of Chemistry; vol. 27; nb. 2; (2015); p. 587 - 590, View in Reaxys 45 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Shen, Duyi; Miao, Chengxia; Wang, Shoufeng; Xia, Chungu; Sun, Wei; Organic Letters; vol. 16; nb. 4; (2014); p. 1108 1111, View in Reaxys; Ren, Kai; Hu, Bei; Zhao, Mengmeng; Tu, Yahui; Xie, Xiaomin; Zhang, Zhaoguo; Journal of Organic Chemistry; vol. 79; nb. 5; (2014); p. 2170 - 2177, View in Reaxys; Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei; Organic Letters; vol. 17; nb. 6; (2015); p. 1469 - 1472, View in Reaxys; Shen, Duyi; Miao, Chengxia; Xu, Daqian; Xia, Chungu; Sun, Wei; Organic Letters; vol. 17; nb. 1; (2015); p. 54 - 57, View in Reaxys 46 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Liu, Yangyang; Xie, Aming; Cao, Meiping; Feng, Liandong; Wang, Boliang; Asian Journal of Chemistry; vol. 27; nb. 2; (2015); p. 587 - 590, View in Reaxys 47 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

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

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 - 4802, View in Reaxys 48 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

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

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 - 4802, View in Reaxys

77/126

2018-07-03 19:01:53

49 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Zhao, Jinwu; Liu, Li; Xiang, Shijian; Liu, Qiang; Chen, Huoji; Organic and Biomolecular Chemistry; vol. 13; nb. 20; (2015); p. 5613 - 5616, View in Reaxys 50 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Mameda, Naresh; Peraka, Swamy; Marri, Mahender Reddy; Kodumuri, Srujana; Chevella, Durgaiah; Gutta, Naresh; Nama, Narender; Applied Catalysis A: General; vol. 505; (2015); p. 213 - 216; Art.No: 15488, View in Reaxys 51 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Mameda, Naresh; Peraka, Swamy; Marri, Mahender Reddy; Kodumuri, Srujana; Chevella, Durgaiah; Gutta, Naresh; Nama, Narender; Applied Catalysis A: General; vol. 505; (2015); p. 213 - 216; Art.No: 15488, View in Reaxys 52 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- 1H NMR (400 MHz, CDCl3): Ε 7.95 (d, J = 7.6 Hz, 2H), 7.56-7.52 (m, 1H), 7.42 (t, J = 7.6 Hz, 2H), troscopy) 3.02-2.96 (m, 2H), 1.22 (t, J = 7.6 Hz, 3H) Location

supporting information

Signals [ppm]

7.95; 7.52 - 7.56; 7.42; 2.96 - 3.02; 1.22

Kind of signal

d, J = 7.6 Hz, 2H; m, 1H; t, J = 7.6 Hz, 2H; m, 2H; t, J = 7.6 Hz, 3H

Dong, Qizhi; Li, Ningbo; Qiu, Renhua; Wang, Jinying; Guo, Cancheng; Xu, Xinhua; Journal of Organometallic Chemistry; vol. 799-800; (2015); p. 122 - 127, View in Reaxys 53 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

78/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 100 scopy) [MHz] Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

201.05; 137.11; 133.09; 128.75; 128.17; 31.98; 8.44

NMR (100 MHz, CDCl3): Ε 201.05, 137.11, 133.09, 128.75, 128.17, 31.98, 8.44

Dong, Qizhi; Li, Ningbo; Qiu, Renhua; Wang, Jinying; Guo, Cancheng; Xu, Xinhua; Journal of Organometallic Chemistry; vol. 799-800; (2015); p. 122 - 127, View in Reaxys 54 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25.04

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

supporting information

Yousuf, Md; Das, Tuluma; Adhikari, Susanta; New Journal of Chemistry; vol. 39; nb. 11; (2015); p. 8763 - 8770, View in Reaxys 55 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 2685, View in Reaxys; Piola, Lorenzo; Ferandez-Salas, Jos A.; Manzini, Simone; Nolan, Steven P.; Organic and Biomolecular Chemistry; vol. 12; nb. 43; (2014); p. 8683 - 8688, View in Reaxys 56 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Bouziane, Asmae; Carboni, Bertrand; Bruneau, Christian; Carreaux, Francois; Renaud, Jean-Luc; Tetrahedron; vol. 64; nb. 51; (2008); p. 11745 - 11750, View in Reaxys; Cao, Hai Thuong; Gree, Rene; Tetrahedron Letters; vol. 50; nb. 13; (2009); p. 1493 - 1494, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 431, View in Reaxys 57 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

79/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; vol. 16; nb. 1; (2014); p. 66 69, View in Reaxys 58 of 159

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) Ε 8.00-7.94 (m, 4H), 7.59-7.53 (tt, J = 7.3, 1.4 Hz, 1H), 7.49-7.43 (tt, J troscopy) = 7.6, 1.6 Hz, 4H), 3.05-2.98 (q, J = 7.2 Hz, 0H), 1.26-1.20 (t, J = 7.2 Hz, 1H) 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 59 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101 scopy) [MHz] Original Text (NMR Spec- 13C NMR (101 MHz, CDCl3) Ε 201.01, 137.06, 133.03, 128.70 (overlap), 128.12 (overlap), 31.93, troscopy) 8.39 Signals [ppm]

201.01; 137.06; 133.03; 128.7; 128.12; 31.93; 8.39

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 60 of 159

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 61 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

19.84

80/126

2018-07-03 19:01:53

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

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 62 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

19.84

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

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 63 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

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 64 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Original Text (NMR Spec- 1H NMR: 7.98-7.94 (m, 2H), 7.57-7.52 (m, 1H), 7.48-7.43 (m, 2H), 3.00 (q, J=7.2 Hz, 2H), 1.22 (t, troscopy) J=7.2 Hz, 3H). Location

Paragraph 0129; 0130

Patent; CALIFORNIA INSTITUTE OF TECHNOLOGY; MORANDI, Bill; GRUBBS, Robert H.; WICKENS, Zachary K.; US2014/194604; (2014); (A1) English, View in Reaxys 65 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Original Text (NMR Spectroscopy)

13C

Location

Paragraph 0129; 0130

NMR: Ε 200.8, 136.9, 132.9, 128.5, 128.0, 31.8, 8.2.

Patent; CALIFORNIA INSTITUTE OF TECHNOLOGY; MORANDI, Bill; GRUBBS, Robert H.; WICKENS, Zachary K.; US2014/194604; (2014); (A1) English, View in Reaxys 66 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

81/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 300 scopy) [MHz] Raeisaenen, Minna T.; Al-Hunaiti, Afnan; Atosuo, Elisa; Kemell, Marianna; Leskelae, Markku; Repo, Timo; Catalysis Science and Technology; vol. 4; nb. 8; (2014); p. 2564 - 2573, View in Reaxys 67 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Original Text (NMR Spec- 1H NMR (300 MHz, CDCl3) Ε 8.01-7.90 (m, 2H), 7.55 (t, J=7.3 Hz, 1H), 7.45 (t, J=7.4 Hz, 2H), troscopy) 3.00 (q, J=7.2 Hz, 2H), 1.22 (t, J=7.2 Hz, 3H) Location

supporting information

Liu, Yangyang; Xie, Aming; Li, Junjian; Xu, Xiao; Dong, Wei; Wang, Boliang; Tetrahedron; vol. 70; nb. 52; (2014); p. 9791 - 9796, View in Reaxys 68 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

200.39; 136.52; 132.5; 128.18; 127.58; 31.38; 7.85

NMR (75 MHz, CDCl3) Ε 200.39, 136.52, 132.50, 128.18, 127.58, 31.38, 7.85

Liu, Yangyang; Xie, Aming; Li, Junjian; Xu, Xiao; Dong, Wei; Wang, Boliang; Tetrahedron; vol. 70; nb. 52; (2014); p. 9791 - 9796, View in Reaxys 69 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 101.5 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

82/126

2018-07-03 19:01:53

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Frequency (NMR Spectro- 300.1 scopy) [MHz] Location

supporting information

Kechaou-Perrot, Manel; Vendier, Laure; Bastin, Stphanie; Sotiropoulos, Jean-Marc; Miqueu, Karinne; Menndez-Rodrguez, Luca; Crochet, Pascale; Cadierno, Victorio; Igau, Alain; Organometallics; vol. 33; nb. 22; (2014); p. 6294 - 6297, View in Reaxys 71 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Coupling Nuclei

31P

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Hyder, Zeynab; Ruan, Jiwu; Xiao, Jianliang; Chemistry - A European Journal; vol. 14; nb. 18; (2008); p. 5555 - 5566, View in Reaxys; Li, Xiao-Qiang; Wang, Wei-Kun; Zhang, Chi; Advanced Synthesis and Catalysis; vol. 351; nb. 14-15; (2009); p. 2342 - 2350, View in Reaxys; Zhang, Jinli; Han, Zixing; Li, Junmiao; Wu, Yangjie; Arkivoc; vol. 2013; nb. 4; (2013); p. 251 - 271, View in Reaxys 73 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Shei, Chun-Tin; Chien, Hao-Lun; Sung, Kuangsen; Synlett; nb. 7; (2008); p. 1021 - 1026, View in Reaxys; Hyder, Zeynab; Ruan, Jiwu; Xiao, Jianliang; Chemistry - A European Journal; vol. 14; nb. 18; (2008); p. 5555 - 5566, View in Reaxys; Li, Xiao-Qiang; Wang, Wei-Kun; Zhang, Chi; Advanced Synthesis and Catalysis; vol. 351; nb. 14-15; (2009); p. 2342 - 2350, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 2970, View in Reaxys 74 of 159

Description (NMR Spectroscopy)

Chemical shifts

83/126

2018-07-03 19:01:53

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys; Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 - 5935, View in Reaxys 75 of 159

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)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Hachiya, Iwao; Inagaki, Takao; Ishihara, Yasuhisa; Shimizu, Makoto; Bulletin of the Chemical Society of Japan; vol. 84; nb. 4; (2011); p. 419 - 421, View in Reaxys; Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys 77 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 126 scopy) [MHz] Hachiya, Iwao; Inagaki, Takao; Ishihara, Yasuhisa; Shimizu, Makoto; Bulletin of the Chemical Society of Japan; vol. 84; nb. 4; (2011); p. 419 - 421, View in Reaxys; Kamimura, Akio; Nozaki, Yuichiro; Nishiyama, Mai; Nakayama, Masaharu; RSC Advances; vol. 3; nb. 2; (2013); p. 468 - 472, View in Reaxys 78 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Chowdhury, Abhishek Dutta; Ray, Ritwika; Lahiri, Goutam Kumar; Chemical Communications; vol. 48; nb. 44; (2012); p. 5497 - 5499, View in Reaxys; Wang, Peng; Cai, Jin; Yang, Jiabin; Sun, Chunlong; Li, Lushen; Hu, Huayou; Ji, Min; Tetrahedron Letters; vol. 54; nb. 6; (2013); p. 533 - 535, View in Reaxys 79 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

84/126

2018-07-03 19:01:53

Frequency (NMR Spectro- 125 scopy) [MHz] Xu, Yuan; Yang, Zhenping; Hu, Jiantao; Yan, Jie; Synthesis (Germany); vol. 45; nb. 3; (2013); p. 370 - 374; Art.No: SS-2012-F0873-OP, View in Reaxys 80 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Kamimura, Akio; Nozaki, Yuichiro; Nishiyama, Mai; Nakayama, Masaharu; RSC Advances; vol. 3; nb. 2; (2013); p. 468 472, View in Reaxys 81 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Original Text (NMR Spec- 1H NMR (500 MHz, CDCl3): Ε 7.99-7.94 (m, 2H), 7.58-7.51 (m, 1H), 7.48-7.42 (m, 2H), 3.00 (q, troscopy) J=7.2 Hz, 2H), 1.22 (t, J=7.2 Hz, 3H) Location

supporting information

Signals [ppm]

7.94 - 7.99; 7.51 - 7.58; 7.42 - 7.48; 3; 1.22

Kind of signal

m, 2H; m, 1H; m, 2H; q, J=7.2 Hz, 2H; t, J=7.2 Hz, 3H

Gao, Qi; Li, Shenyan; Pan, Yingming; Xu, Yanli; Wang, Hengshan; Tetrahedron; vol. 69; nb. 19; (2013); p. 3775 - 3781, View in Reaxys 84 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz]

85/126

2018-07-03 19:01:53

Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

200.8; 136.8; 132.8; 128.5; 127.9; 31.7; 8.2

NMR (125 MHz, CDCl3): Ε 200.8, 136.8, 132.8, 128.5, 127.9, 31.7, 8.2

Gao, Qi; Li, Shenyan; Pan, Yingming; Xu, Yanli; Wang, Hengshan; Tetrahedron; vol. 69; nb. 19; (2013); p. 3775 - 3781, View in Reaxys 85 of 159

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): Ε=7.93 (d, J=7.6 Hz, 2H), 7.49-7.52 (m, 1H), 7.41 (t, J=7.6 Hz, 2H), troscopy) 2.13-2.98 (m, 2H), 1.19 (t, J=7.6 Hz, 3H) Signals [ppm]

7.93; 7.49 - 7.52; 7.41; 2.13 - 2.98; 1.19

Kind of signal

d, J=7.6 Hz, 2H; m, 1H; t, J=7.6 Hz, 2H; m, 2H; t, J=7.6 Hz, 3H

Chen, Zheng-Wang; Ye, Dong-Nai; Qian, Yi-Ping; Ye, Min; Liu, Liang-Xian; Tetrahedron; vol. 69; nb. 30; (2013); p. 6116 6120, View in Reaxys 86 of 159

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]

200.7; 136.9; 132.8; 128.5; 127.9; 31.7; 8.2

NMR (100 MHz, CDCl3): Ε=200.7, 136.9, 132.8, 128.5, 127.9, 31.7, 8.2

Chen, Zheng-Wang; Ye, Dong-Nai; Qian, Yi-Ping; Ye, Min; Liu, Liang-Xian; Tetrahedron; vol. 69; nb. 30; (2013); p. 6116 6120, View in Reaxys 87 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013U0386-L, View in Reaxys 88 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz]

86/126

2018-07-03 19:01:53

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013U0386-L, View in Reaxys 89 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

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

supporting information

Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys 92 of 159

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

Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys 93 of 159

Description (NMR Spectroscopy)

Spectrum

87/126

2018-07-03 19:01:53

Nucleus (NMR Spectroscopy)

Location

supporting information

Hyder, Zeynab; Ruan, Jiwu; Xiao, Jianliang; Chemistry - A European Journal; vol. 14; nb. 18; (2008); p. 5555 - 5566, View in Reaxys; Guo, Hui; Liu, Delong; Butt, Nicholas A.; Liu, Yangang; Zhang, Wanbin; Tetrahedron; vol. 68; nb. 16; (2012); p. 3295 - 3299, View in Reaxys 94 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Shei, Chun-Tin; Chien, Hao-Lun; Sung, Kuangsen; Synlett; nb. 7; (2008); p. 1021 - 1026, View in Reaxys; Bouziane, Asmae; Carboni, Bertrand; Bruneau, Christian; Carreaux, Francois; Renaud, Jean-Luc; Tetrahedron; vol. 64; nb. 51; (2008); p. 11745 - 11750, View in Reaxys; Cao, Hai Thuong; Gree, Rene; Tetrahedron Letters; vol. 50; nb. 13; (2009); p. 1493 - 1494, View in Reaxys; Lee, Jong Chan; Kim, Jimi; Lee, Seung Bae; Chang, Soon-Uk; Jeong, Yeon Jin; Synthetic Communications; vol. 41; nb. 13; (2011); p. 1947 - 1951, View in Reaxys; Han, Mikyoung; Jeong, Ku Sun; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 7; (2012); p. 2405 - 2406, View in Reaxys 95 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Li, Mingzong; Wang, Cong; Ge, Haibo; Organic Letters; vol. 13; nb. 8; (2011); p. 2062 - 2064, View in Reaxys; Zhang, Guofu; Wen, Xin; Wang, Yong; Mo, Weimin; Ding, Chengrong; Journal of Organic Chemistry; vol. 76; nb. 11; (2011); p. 4665 4668, View in Reaxys; Zhang, Guofu; Wang, Yong; Wen, Xin; Ding, Chengrong; Li, Ying; Chemical Communications; vol. 48; nb. 24; (2012); p. 2979 - 2981, View in Reaxys 96 of 159

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

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz]

88/126

2018-07-03 19:01:53

Location

supporting information

Berini, Christophe; Winkelmann, Ole H.; Otten, Jennifer; Vicic, David A.; Navarro, Oscar; Chemistry - A European Journal; vol. 16; nb. 23; (2010); p. 6857 - 6860, View in Reaxys; Urgoitia, Garazi; Sanmartin, Raul; Herrero, Maria Teresa; Dominguez, Esther; Green Chemistry; vol. 13; nb. 8; (2011); p. 2161 - 2166, View in Reaxys; Cabrero-Antonino, Jose R.; Leyva-Perez, Antonio; Corma, Avelino; Chemistry - A European Journal; vol. 18; nb. 35; (2012); p. 11107 - 11114, View in Reaxys 98 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 2685, View in Reaxys; Liu, Pei Nian; Ju, Kun Dong; Lau, Chak Po; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 275 - 280, View in Reaxys; Gowda, Maravanhalli Sidde; Pande, Sushanth Sudhir; Ramakrishna, Ramesha Andagar; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 9; nb. 15; (2011); p. 5365 - 5368, View in Reaxys; Tsuchiya, Daisuke; Moriyama, Katsuhiko; Togo, Hideo; Synlett; nb. 18; (2011); p. 2701 - 2704, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 99 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 2685, View in Reaxys; Gowda, Maravanhalli Sidde; Pande, Sushanth Sudhir; Ramakrishna, Ramesha Andagar; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 9; nb. 15; (2011); p. 5365 - 5368, View in Reaxys; Tsuchiya, Daisuke; Moriyama, Katsuhiko; Togo, Hideo; Synlett; nb. 18; (2011); p. 2701 - 2704, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 100 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Hamasaki, Akiyuki; Kuwada, Hideyuki; Tokunaga, Makoto; Tetrahedron Letters; vol. 53; nb. 7; (2012); p. 811 - 814, View in Reaxys 101 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

89/126

2018-07-03 19:01:53

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Hamasaki, Akiyuki; Kuwada, Hideyuki; Tokunaga, Makoto; Tetrahedron Letters; vol. 53; nb. 7; (2012); p. 811 - 814, View in Reaxys 102 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Havare, Nizam; Plattner, Dietmar A.; Organic Letters; vol. 14; nb. 19; (2012); p. 5078 - 5081,4, View in Reaxys; Jurcik, Vaclav; Schmid, Thibault E.; Dumont, Quentin; Slawin, Alexandra M. Z.; Cazin, Catherine S. J.; Dalton Transactions; vol. 41; nb. 40; (2012); p. 12619 - 12623,5, View in Reaxys 103 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

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

supporting information

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 90 scopy) [MHz] Location

supporting information

Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Mohammadpoor-baltork, Iraj; Sirjanian, Narges; Parand, Somayeh; Bioorganic and Medicinal Chemistry; vol. 17; nb. 9; (2009); p. 3394 - 3398, View in Reaxys 106 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

90/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 2685, View in Reaxys; Berini, Christophe; Brayton, Daniel F.; Mocka, Corey; Navarro, Oscar; Organic Letters; vol. 11; nb. 18; (2009); p. 4244 - 4247, View in Reaxys 107 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Moriuchi-Kawakami, Takayo; Matsuda, Haruo; Shibata, Ikuya; Miyatake, Masato; Suwa, Toshihiro; Baba, Akio; Bulletin of the Chemical Society of Japan; vol. 72; nb. 3; (1999); p. 465 - 470, View in Reaxys; Mino, Takashi; Hirota, Tatsuya; Fujita, Noriko; Yamashita, Masakazu; Synthesis; nb. 12; (1999); p. 2024 - 2026, View in Reaxys; Fan, Xuesen; Zhang, Xinying; Zhang, Yongmin; Journal of Chemical Research; nb. 11; (2005); p. 750 - 752, View in Reaxys; He, Zhi; Yudin, Andrei K.; Organic Letters; vol. 8; nb. 25; (2006); p. 5829 - 5832, View in Reaxys; Rao, Maddali L.N.; Venkatesh, Varadhachari; Banerjee, Debasis; Tetrahedron; vol. 63; nb. 52; (2007); p. 12917 - 12926, View in Reaxys; Zhu, Mingxia; Wei, Xin; Li, Bodong; Yuan, Youzhu; Tetrahedron Letters; vol. 48; nb. 52; (2007); p. 9108 - 9111, View in Reaxys; Mori, Yoshikazu; Seki, Masahiko; Advanced Synthesis and Catalysis; vol. 349; nb. 11-12; (2007); p. 2027 - 2038, View in Reaxys; Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys; Xu, Hanhui; Ekoue-Kovi, Kekeli; Wolf, Christian; Journal of Organic Chemistry; vol. 73; nb. 19; (2008); p. 7638 - 7650, View in Reaxys 108 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys; Xu, Hanhui; Ekoue-Kovi, Kekeli; Wolf, Christian; Journal of Organic Chemistry; vol. 73; nb. 19; (2008); p. 7638 - 7650, View in Reaxys 109 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys; Xu, Hanhui; Ekoue-Kovi, Kekeli; Wolf, Christian; Journal of Organic Chemistry; vol. 73; nb. 19; (2008); p. 7638 - 7650, View in Reaxys 110 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz]

91/126

2018-07-03 19:01:53

Moriuchi-Kawakami, Takayo; Matsuda, Haruo; Shibata, Ikuya; Miyatake, Masato; Suwa, Toshihiro; Baba, Akio; Bulletin of the Chemical Society of Japan; vol. 72; nb. 3; (1999); p. 465 - 470, View in Reaxys; He, Zhi; Yudin, Andrei K.; Organic Letters; vol. 8; nb. 25; (2006); p. 5829 - 5832, View in Reaxys; Rao, Maddali L.N.; Venkatesh, Varadhachari; Banerjee, Debasis; Tetrahedron; vol. 63; nb. 52; (2007); p. 12917 - 12926, View in Reaxys; Zhu, Mingxia; Wei, Xin; Li, Bodong; Yuan, Youzhu; Tetrahedron Letters; vol. 48; nb. 52; (2007); p. 9108 - 9111, View in Reaxys; Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys; Xu, Hanhui; Ekoue-Kovi, Kekeli; Wolf, Christian; Journal of Organic Chemistry; vol. 73; nb. 19; (2008); p. 7638 - 7650, View in Reaxys 111 of 159

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20.7

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

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol. 73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys 112 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Fujita, Ken-Ichi; Tanino, Nobuhide; Yamaguchi, Ryohei; Organic Letters; vol. 9; nb. 1; (2007); p. 109 - 111, View in Reaxys 113 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Fujita, Ken-Ichi; Tanino, Nobuhide; Yamaguchi, Ryohei; Organic Letters; vol. 9; nb. 1; (2007); p. 109 - 111, View in Reaxys 114 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 270 scopy) [MHz] Fujita, Ken-Ichi; Tanino, Nobuhide; Yamaguchi, Ryohei; Organic Letters; vol. 9; nb. 1; (2007); p. 109 - 111, View in Reaxys 115 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

92/126

2018-07-03 19:01:53

Frequency (NMR Spectro- 67.8 scopy) [MHz] Fujita, Ken-Ichi; Tanino, Nobuhide; Yamaguchi, Ryohei; Organic Letters; vol. 9; nb. 1; (2007); p. 109 - 111, View in Reaxys 116 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 67.8 scopy) [MHz] Fujita, Ken-Ichi; Tanino, Nobuhide; Yamaguchi, Ryohei; Organic Letters; vol. 9; nb. 1; (2007); p. 109 - 111, View in Reaxys 117 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Gompper, Rudolf; Vogt, Hans-Hubert; Chemische Berichte; vol. 114; nb. 8; (1981); p. 2866 - 2883, View in Reaxys; Lue, Ping; Fan, Wei-Qiang; Zhou, Xun-Jun; Synthesis; nb. 9; (1989); p. 692 - 693, View in Reaxys; Katritzky, Alan R.; Lang, Hengyuan; Wang, Zuoquan; Zhang, Zhongxing; Song, Huimin; Journal of Organic Chemistry; vol. 60; nb. 23; (1995); p. 7619 - 7624, View in Reaxys; Wang, Junquan; Zhang, Yongmin; Synthetic Communications; vol. 26; nb. 10; (1996); p. 1931 1934, View in Reaxys; Hong, Jong Eoun; Shin, Won Suk; Jang, Won Bum; Oh, Dong Young; Journal of Organic Chemistry; vol. 61; nb. 6; (1996); p. 2199 - 2201, View in Reaxys; Jang, Won Bum; Shin, Won Suk; Hong, Jong Eun; Lee, Shi Yong; Oh, Dong Young; Synthetic Communications; vol. 27; nb. 19; (1997); p. 3333 - 3339, View in Reaxys; Matano, Yoshihiro; Suzuki, Takeshi; Shinokura, Tomonori; Imahori, Hiroshi; Tetrahedron Letters; vol. 48; nb. 16; (2007); p. 2885 - 2888, View in Reaxys 118 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Zhao, Baowei; Lu, Xiyan; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6765 - 6768, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Organic Letters; vol. 8; nb. 26; (2006); p. 5987 - 5990, View in Reaxys 120 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

93/126

2018-07-03 19:01:53

Frequency (NMR Spectro- 300.08 scopy) [MHz] Cruz, Alejandro; Contreras, Rosalinda; Padilla-Martinez, Itzia I.; Juarez-Juarez, Minerva; Tetrahedron Asymmetry; vol. 17; nb. 10; (2006); p. 1499 - 1505, View in Reaxys 121 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectro- 75.46 scopy) [MHz] Cruz, Alejandro; Contreras, Rosalinda; Padilla-Martinez, Itzia I.; Juarez-Juarez, Minerva; Tetrahedron Asymmetry; vol. 17; nb. 10; (2006); p. 1499 - 1505, View in Reaxys 122 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

D2O; acetonitrile

Hawkins, Michael J.; Powell, Eugene T.; Leo, Gregory C.; Gauthier, Diane A.; Greco, Michael N.; Maryanoff, Bruce; Organic Letters; vol. 8; nb. 16; (2006); p. 3429 - 3431, View in Reaxys 123 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

D2O; acetonitrile

Hawkins, Michael J.; Powell, Eugene T.; Leo, Gregory C.; Gauthier, Diane A.; Greco, Michael N.; Maryanoff, Bruce; Organic Letters; vol. 8; nb. 16; (2006); p. 3429 - 3431, View in Reaxys 124 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

toluene-d8

Temperature (NMR Spectroscopy) [°C]

-86

He, Xuyang; Morris, J. Jacob; Noll, Bruce C.; Brown, Seth N.; Henderson, Kenneth W.; Journal of the American Chemical Society; vol. 128; nb. 41; (2006); p. 13599 - 13610, View in Reaxys 125 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

toluene-d8

Temperature (NMR Spectroscopy) [°C]

-86

He, Xuyang; Morris, J. Jacob; Noll, Bruce C.; Brown, Seth N.; Henderson, Kenneth W.; Journal of the American Chemical Society; vol. 128; nb. 41; (2006); p. 13599 - 13610, View in Reaxys 126 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

94/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

CD2Cl2

Temperature (NMR Spectroscopy) [°C]

-86

He, Xuyang; Morris, J. Jacob; Noll, Bruce C.; Brown, Seth N.; Henderson, Kenneth W.; Journal of the American Chemical Society; vol. 128; nb. 41; (2006); p. 13599 - 13610, View in Reaxys 127 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Huang, Zheng-Zheng; Tang, Yong; Journal of Organic Chemistry; vol. 67; nb. 15; (2002); p. 5320 - 5326, View in Reaxys; Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys; Ito, Masato; Kitahara, Sachiko; Ikariya, Takao; Journal of the American Chemical Society; vol. 127; nb. 17; (2005); p. 6172 - 6173, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6765 - 6768, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Organic Letters; vol. 8; nb. 26; (2006); p. 5987 - 5990, View in Reaxys 128 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

26.85

Frequency (NMR Spectro- 400.13 scopy) [MHz] Anderson, Christopher D.; Shea, Kenneth J.; Rychnovsky, Scott D.; Organic Letters; vol. 7; nb. 22; (2005); p. 4879 - 4882, View in Reaxys 130 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CD2Cl2

Mohanta, Pramod K.; Davis, Todd A.; Gooch, Jeremy R.; Flowers II, Robert A.; Journal of the American Chemical Society; vol. 127; nb. 34; (2005); p. 11896 - 11897, View in Reaxys 131 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

95/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

CD2Cl2

Mohanta, Pramod K.; Davis, Todd A.; Gooch, Jeremy R.; Flowers II, Robert A.; Journal of the American Chemical Society; vol. 127; nb. 34; (2005); p. 11896 - 11897, View in Reaxys 132 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CD2Cl2

Mohanta, Pramod K.; Davis, Todd A.; Gooch, Jeremy R.; Flowers II, Robert A.; Journal of the American Chemical Society; vol. 127; nb. 34; (2005); p. 11896 - 11897, View in Reaxys 133 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Duhamel, Lucette; Poirier, Jean-Marie; Bulletin de la Societe Chimique de France; vol. 2; nb. 9-10; (1982); p. 297 - 303, View in Reaxys; Zhang; Yu; Bao; Synthetic Communications; vol. 25; nb. 12; (1995); p. 1825 - 1830, View in Reaxys; Guo, Hongyun; Zhang, Yongmin; Synthetic Communications; vol. 30; nb. 14; (2000); p. 2559 - 2564, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys 134 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 11420, View in Reaxys 135 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys 136 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75.4 scopy) [MHz] Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys 137 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75.4 scopy) [MHz] Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys

96/126

2018-07-03 19:01:53

138 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 48.8 scopy) [MHz] Zhuo, Jin-Cong; Schenk, Kurt; Helvetica Chimica Acta; vol. 85; nb. 5; (2002); p. 1276 - 1283, View in Reaxys 139 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300.4 scopy) [MHz] Shimada, Tomohiro; Yamamoto, Yoshinori; Journal of the American Chemical Society; vol. 124; nb. 43; (2002); p. 12670 12671, View in Reaxys 140 of 159

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300.4 scopy) [MHz] Shimada, Tomohiro; Yamamoto, Yoshinori; Journal of the American Chemical Society; vol. 124; nb. 43; (2002); p. 12670 12671, View in Reaxys 141 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75.45 scopy) [MHz] Shimada, Tomohiro; Yamamoto, Yoshinori; Journal of the American Chemical Society; vol. 124; nb. 43; (2002); p. 12670 12671, View in Reaxys 142 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Gazzard, Lewis J.; Motherwell, William B.; Sandham, David A.; Journal of the Chemical Society - Perkin Transactions 1; nb. 8; (1999); p. 979 - 993, View in Reaxys 143 of 159

Description (NMR Spectroscopy)

Chemical shifts

97/126

2018-07-03 19:01:53

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Maruoka, Keiji; Nagahara, Shigeru; Yamamoto, Hisashi; Tetrahedron Letters; vol. 31; nb. 38; (1990); p. 5475 - 5478, View in Reaxys; Olivato, Paulo R.; Filho, Rubens R.; Lopes, Julio C. D.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 92; nb. 1-4; (1994); p. 109 - 128, View in Reaxys; Katritzky, Alan R.; Lang, Hengyuan; Wang, Zuoquan; Zhang, Zhongxing; Song, Huimin; Journal of Organic Chemistry; vol. 60; nb. 23; (1995); p. 7619 - 7624, View in Reaxys; Hong, Jong Eoun; Shin, Won Suk; Jang, Won Bum; Oh, Dong Young; Journal of Organic Chemistry; vol. 61; nb. 6; (1996); p. 2199 - 2201, View in Reaxys; Jang, Won Bum; Shin, Won Suk; Hong, Jong Eun; Lee, Shi Yong; Oh, Dong Young; Synthetic Communications; vol. 27; nb. 19; (1997); p. 3333 - 3339, View in Reaxys 144 of 159

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Lue, Ping; Fan, Wei-Qiang; Zhou, Xun-Jun; Synthesis; nb. 9; (1989); p. 692 - 693, View in Reaxys; Katritzky, Alan R.; Lang, Hengyuan; Wang, Zuoquan; Zhang, Zhongxing; Song, Huimin; Journal of Organic Chemistry; vol. 60; nb. 23; (1995); p. 7619 - 7624, View in Reaxys; Hong, Jong Eoun; Shin, Won Suk; Jang, Won Bum; Oh, Dong Young; Journal of Organic Chemistry; vol. 61; nb. 6; (1996); p. 2199 - 2201, View in Reaxys; Jang, Won Bum; Shin, Won Suk; Hong, Jong Eun; Lee, Shi Yong; Oh, Dong Young; Synthetic Communications; vol. 27; nb. 19; (1997); p. 3333 - 3339, View in Reaxys 145 of 159

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

tetrahydrofuran; hexane

Temperature (NMR Spectroscopy) [°C]

-78

Bernardi, Anna; Cavicchioli; Marchionni, Chiara; Potenza, Donatella; Scolastico, Carlo; Journal of Organic Chemistry; vol. 59; nb. 13; (1994); p. 3690 - 3694, View in Reaxys 146 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CCl4

Yanlong, Qian; Guisheng, Li; Huang, Yao-Zeng; Journal of Organometallic Chemistry; vol. 381; nb. 1; (1990); p. 29 - 34, View in Reaxys; Ono; Tamura; Kaji; Journal of the American Chemical Society; vol. 105; nb. 12; (1983); p. 4017 - 4022, View in Reaxys; Bergmark, William R.; Barnes, Curtis; Clark, Jeffrey; Paparian, Seth; Marynowski, Susan; Journal of Organic Chemistry; vol. 50; nb. 26; (1985); p. 5612 - 5615, View in Reaxys 147 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

acetonitrile

Temperature (NMR Spectroscopy) [°C]

Boykin, D. W.; Balakrishnan, P.; Baumstark, A. L.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 248 - 250, View in Reaxys 148 of 159

Description (NMR Spectroscopy)

Spin-spin coupling constants

98/126

2018-07-03 19:01:53

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Krivdin, L. B.; Shcherbakov, V. V.; Korostova, S. E.; Shevchenko, S. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 36; nb. 4; (1987); p. 694 - 697; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 4; (1987); p. 766 - 769, View in Reaxys 149 of 159

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CCl4

Comment (NMR Spectroscopy)

1H-1H

Ono; Tamura; Kaji; Journal of the American Chemical Society; vol. 105; nb. 12; (1983); p. 4017 - 4022, View in Reaxys 150 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

hexamethylphosphoric acid triamide

Vogt, Hans-Hubert; Gompper, Rudolf; Chemische Berichte; vol. 114; nb. 8; (1981); p. 2884 - 2897, View in Reaxys 151 of 159

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

various solvent(s); fluorosulfonic acid

Temperature (NMR Spectroscopy) [°C]

-70

Drakenberg, Torbjoern; Sommer, Jean; Jost, Roland; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 363 - 369, View in Reaxys 152 of 159

Description (NMR Spectroscopy)

CIDNP

Maurer; Bargon; Journal of the American Chemical Society; vol. 101; (1979); p. 6865,6867, View in Reaxys 153 of 159

Description (NMR Spectroscopy)

Spin-lattice relaxation time (T1)

Sterk et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 118; (1979); p. 151,155, View in Reaxys 154 of 159

Description (NMR Spectroscopy)

NMR

Deuchert,K. et al.; Chemische Berichte; vol. 112; (1979); p. 2045 - 2061, View in Reaxys; Sato,S.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1440 - 1444, View in Reaxys; Castelli,F.; Cannone,P.; Bulletin de la Societe Chimique de France; (1974); p. 317 - 330, View in Reaxys; Ng,S.; Ong,S.H.; Journal of Organic Chemistry; vol. 35; (1970); p. 354 - 355, View in Reaxys; Tyman,J.H.P.; Najam,A.A.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 33; (1977); p. 479 - 485, View in Reaxys; Yalpani,M.; Modarai,B.; Khoshdel,E.; Organic Magnetic Resonance; vol. 12; (1979); p. 254, View in Reaxys; Sheehan; Umezawa; Journal of Organic Chemistry; vol. 38; (1973); p. 3771,3773, View in Reaxys; Solladie-Cavallo; Solladie; Organic Magnetic Resonance; vol. 10; (1977); p. 235, View in Reaxys; Venien; Lefeuvre; Organic Magnetic Resonance; vol. 5; (1973); p. 113,114, View in Reaxys; Alper; Prickett; Inorganic Chemistry; vol. 16; (1977); p. 67,71, View in Reaxys; Ng; Organic Magnetic Resonance; vol. 2; (1970); p. 283, View in Reaxys; Hassner et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 1672,1674, View in Reaxys; Kupin; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1206,1217, View in Reaxys; Miyajima et al.; Chemical and Pharmaceutical Bulletin; vol. 19; (1971); p. 2301,2305, View in Reaxys; Gates; Mooney; Journal of Inorganic and Nuclear Chemistry; vol. 30; (1968); p. 839,842,844-846, View in Reaxys; Haynes; Sazavsky; Applied Spectroscopy; vol. 24; (1970); p. 452, View in Reaxys; Engel; Nathan; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3844, View in Reaxys; Leibfritz; Chemische Berichte; vol. 108; (1975); p. 3014,3019, View in Reaxys; Maurer; Bargon; Journal of the American Chemical Society; vol. 101; (1979); p. 6865,6867, View in Reaxys; Dimmel et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 3092, View in Reaxys; Alper; Keung; Journal

99/126

2018-07-03 19:01:53

of Organic Chemistry; vol. 37; (1972); p. 2566,2568,2571, View in Reaxys; Jaeckel; Hanack; Chemische Berichte; vol. 110; (1977); p. 199,207, View in Reaxys 155 of 159

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

Baba; Kawai; Yakugaku Zasshi; vol. 94; (1974); p. 783,785; Chem.Abstr.; vol. 81; nb. 37514; (1974), View in Reaxys 156 of 159

Description (NMR Spectroscopy)

NMR with shift reagents

Mackie; Shepherd; Organic Magnetic Resonance; vol. 4; (1972); p. 557,560,562, View in Reaxys 157 of 159

Description (NMR Spectroscopy)

Chemical shifts

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys; Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys 158 of 159

Description (NMR Spectroscopy)

Spin-spin coupling constants

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys 159 of 159

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-NMR: S.500, 501

Dhami,K.S.; Stothers,J.B.; Canadian Journal of Chemistry; vol. 43; (1965); p. 498 - 509, View in Reaxys IR Spectroscopy (41) 1 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Moriyama, Katsuhiko; Nakamura, Yu; Togo, Hideo; Organic Letters; vol. 16; nb. 14; (2014); p. 3812 - 3815, View in Reaxys; Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys 2 of 41

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Location

supporting information

Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 8218, View in Reaxys; Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, Hans-Günther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 - 7384, View in Reaxys 3 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Original Text (IR Spectroscopy)

IR (neat): 1684 cm-1

Imai, Sho; Togo, Hideo; Tetrahedron; vol. 72; nb. 44; (2016); p. 6948 - 6954, View in Reaxys 4 of 41

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

film

Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 - 5935, View in Reaxys; Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 - 4254; Art.No: 26677, View in Reaxys 5 of 41

Description (IR Spectroscopy)

Bands

100/126

2018-07-03 19:01:53

Laurence et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 4793,4795, View in Reaxys; Pasynkiewicz; Zeszyty Naukowe Politechniki Slaskiej, Chemia; vol. 21; (1964); p. 1,66, View in Reaxys; Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys; Guo, Hongyun; Zhang, Yongmin; Synthetic Communications; vol. 30; nb. 14; (2000); p. 2559 - 2564, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys; Rao, Maddali L.N.; Venkatesh, Varadhachari; Banerjee, Debasis; Tetrahedron; vol. 63; nb. 52; (2007); p. 12917 - 12926, View in Reaxys; Mori, Yoshikazu; Seki, Masahiko; Advanced Synthesis and Catalysis; vol. 349; nb. 11-12; (2007); p. 2027 2038, View in Reaxys; Ruan, Jiwu; Li, Xinming; Saidi, Ourida; Xiao, Jianliang; Journal of the American Chemical Society; vol. 130; nb. 8; (2008); p. 2424 - 2425, View in Reaxys; Raeisaenen, Minna T.; Al-Hunaiti, Afnan; Atosuo, Elisa; Kemell, Marianna; Leskelae, Markku; Repo, Timo; Catalysis Science and Technology; vol. 4; nb. 8; (2014); p. 2564 - 2573, View in Reaxys; Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 - 8456, View in Reaxys 6 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013-U0386-L, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys 7 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

sodium chloride; dichloromethane

Location

supporting information

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 8 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; vol. 16; nb. 1; (2014); p. 66 69, View in Reaxys 9 of 41

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat liquid

Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 6104, View in Reaxys 10 of 41

Description (IR Spectroscopy)

Bands

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 11 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 8456, View in Reaxys 12 of 41

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys

101/126

2018-07-03 19:01:53

13 of 41

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat liquid

Gowda, Maravanhalli Sidde; Pande, Sushanth Sudhir; Ramakrishna, Ramesha Andagar; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 9; nb. 15; (2011); p. 5365 - 5368, View in Reaxys; Tsuchiya, Daisuke; Moriyama, Katsuhiko; Togo, Hideo; Synlett; nb. 18; (2011); p. 2701 - 2704, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 14 of 41

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat liquid

Hachiya, Iwao; Inagaki, Takao; Ishihara, Yasuhisa; Shimizu, Makoto; Bulletin of the Chemical Society of Japan; vol. 84; nb. 4; (2011); p. 419 - 421, View in Reaxys 15 of 41

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

chloroform-d1

Shei, Chun-Tin; Chien, Hao-Lun; Sung, Kuangsen; Synlett; nb. 7; (2008); p. 1021 - 1026, View in Reaxys 17 of 41

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Dohi, Toshifumi; Takenaga, Naoko; Goto, Akihiro; Fujioka, Hiromichi; Kita, Yasuyuki; Journal of Organic Chemistry; vol. 73; nb. 18; (2008); p. 7365 - 7368, View in Reaxys 18 of 41

Description (IR Spectroscopy)

Reflection spectrum

Mori, Yoshikazu; Seki, Masahiko; Advanced Synthesis and Catalysis; vol. 349; nb. 11-12; (2007); p. 2027 - 2038, View in Reaxys 19 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys; Fan, Xuesen; Zhang, Xinying; Zhang, Yongmin; Journal of Chemical Research; nb. 11; (2005); p. 750 - 752, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Tetrahedron Letters; vol. 47; nb. 38; (2006); p. 6765 - 6768, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Organic Letters; vol. 8; nb. 26; (2006); p. 5987 - 5990, View in Reaxys 20 of 41

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1670 cm**(-1)

Varma, Rajender S.; Dahiya, Rajender; Tetrahedron Letters; vol. 38; nb. 12; (1997); p. 2043 - 2044, View in Reaxys 21 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

102/126

2018-07-03 19:01:53

Comment (IR Spectroscopy)

1684 cm**(-1)

Dyall, Leonard K.; Ferguson, John A.; Jarman, Tony B.; Australian Journal of Chemistry; vol. 49; nb. 11; (1996); p. 1197 1202, View in Reaxys 22 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1690 cm**(-1)

Dyall, Leonard K.; Ferguson, John A.; Jarman, Tony B.; Australian Journal of Chemistry; vol. 49; nb. 11; (1996); p. 1197 1202, View in Reaxys 23 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

hexane

Comment (IR Spectroscopy)

1700 cm**(-1)

Olivato, Paulo R.; Filho, Rubens R.; Lopes, Julio C. D.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 92; nb. 1-4; (1994); p. 109 - 128, View in Reaxys 24 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

1689 cm**(-1)

Olivato, Paulo R.; Filho, Rubens R.; Lopes, Julio C. D.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 92; nb. 1-4; (1994); p. 109 - 128, View in Reaxys 25 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1694 cm**(-1)

Olivato, Paulo R.; Filho, Rubens R.; Lopes, Julio C. D.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 92; nb. 1-4; (1994); p. 109 - 128, View in Reaxys 26 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1688 cm**(-1)

Kolb, Vera M.; Stupar, Joseph W.; Janota, Timothy E.; Duax, William L.; Journal of Organic Chemistry; vol. 54; nb. 10; (1989); p. 2341 - 2346, View in Reaxys 27 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3074 - 690 cm**(-1)

Barbero, Margherita; Cadamuro, Silvano; Ceruti, Maurizio; Degani, Iacapo; Fochi, Rita; Regondi, Valeria; Gazzetta Chimica Italiana; vol. 117; nb. 4; (1987); p. 227 - 236, View in Reaxys 28 of 41

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1735 cm**(-1)

103/126

2018-07-03 19:01:53

Bergmark, William R.; Barnes, Curtis; Clark, Jeffrey; Paparian, Seth; Marynowski, Susan; Journal of Organic Chemistry; vol. 50; nb. 26; (1985); p. 5612 - 5615, View in Reaxys 29 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1685 cm**(-1)

Ono; Tamura; Kaji; Journal of the American Chemical Society; vol. 105; nb. 12; (1983); p. 4017 - 4022, View in Reaxys 30 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1695 cm**(-1)

Duhamel, Lucette; Poirier, Jean-Marie; Bulletin de la Societe Chimique de France; vol. 2; nb. 9-10; (1982); p. 297 - 303, View in Reaxys 31 of 41

Description (IR Spectroscopy)

Sekiya,M.; Terao,Y.; Chemical and Pharmaceutical Bulletin; vol. 18; (1970); p. 947 - 956, View in Reaxys; Castelli,F.; Cannone,P.; Bulletin de la Societe Chimique de France; (1974); p. 317 - 330, View in Reaxys; Guyon,R.; Villa,P.; Bulletin de la Societe Chimique de France; (1975); p. 2593 - 2598, View in Reaxys; Bratchanskii,P.E.; Komissarova,G.G.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1661 - 1665,1650 - 1654, View in Reaxys; Sheehan; Umezawa; Journal of Organic Chemistry; vol. 38; (1973); p. 3771,3773, View in Reaxys; Alper; Prickett; Inorganic Chemistry; vol. 16; (1977); p. 67,71, View in Reaxys; Kabiel; Tera; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 232; (1966); p. 402, View in Reaxys; Rentea et al.; Tetrahedron; vol. 22; (1966); p. 3501,3503, View in Reaxys; Welti; Stephany; Applied Spectroscopy; vol. 22; (1968); p. 678,686, View in Reaxys; Borisov et al.; Zhurnal Organicheskoi Khimii; vol. 4; (1968); p. 2034,1962, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Osipow; Gaiworonskii; J. Gen. Chem. USSR (Engl. Transl.); vol. 33; (1963); p. 1346,1315, View in Reaxys; House et al.; Journal of the American Chemical Society; vol. 82; (1960); p. 4099,4104, View in Reaxys; Katritzky et al.; Tetrahedron; vol. 28; (1972); p. 3449,3451, 3453,3456,3463, View in Reaxys; Katritzky et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 6861,6863, View in Reaxys; Gates; Mooney; Journal of Inorganic and Nuclear Chemistry; vol. 30; (1968); p. 839,842,844-846, View in Reaxys; Dimmel et al.; Journal of Organic Chemistry; vol. 41; (1976); p. 3092, View in Reaxys; Jaeckel; Hanack; Chemische Berichte; vol. 110; (1977); p. 199,207, View in Reaxys; Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 63; (1967); p. 639,640-660, View in Reaxys; Lebedeva et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 770; ; p. 1380, View in Reaxys; Guiheneuf et al.; Bulletin de la Societe Chimique de France; (1971); p. 1157,1160, 1162, View in Reaxys; Morcillo et al.; Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica; vol. 60; (1964); p. 199,203, View in Reaxys 32 of 41

Description (IR Spectroscopy)

Intensity of IR bands

Seth-Paul,W.A.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 30; (1974); p. 1817 - 1833, View in Reaxys; Dusart et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 73; (1976); p. 832,833, View in Reaxys 33 of 41

Description (IR Spectroscopy)

Spectrum

Kupin; Petrow; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2958,2758; Chem.Abstr.; vol. 57; nb. 2125; (1962), View in Reaxys; Baba; Kawai; Yakugaku Zasshi; vol. 94; (1974); p. 783,785; Chem.Abstr.; vol. 81; nb. 37514; (1974), View in Reaxys 34 of 41

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

Intensitaet und Halbwertsbreite der CO-Valenzschwingungsbande bei 1686 cmE-1 (CCl4) und 1694 cmE-1 (CCl4).

Morcillo et al.; Spectrochimica Acta; vol. 15; (1959); p. 497,498, 503, 506, View in Reaxys; Thompson et al.; Spectrochimica Acta; vol. 9; (1957); p. 208,210, View in Reaxys 35 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

104/126

2018-07-03 19:01:53

Comment (IR Spectroscopy)

CO-Valenzschwingungsbande.

Depireux; Bulletin des Societes Chimiques Belges; vol. 66; (1957); p. 218,221, View in Reaxys; Lascombe et al.; Bulletin de la Societe Chimique de France; (1957); p. 773, View in Reaxys 36 of 41

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

CO-Valenzschwingungsbande.

Depireux; Bulletin des Societes Chimiques Belges; vol. 66; (1957); p. 218,221, View in Reaxys; Lascombe et al.; Bulletin de la Societe Chimique de France; (1957); p. 773, View in Reaxys 37 of 41

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1695 cm**(-1); Feinstruktur der CO-Bande.

Gray; Mangin; Journal de Physique et le Radium; vol. <8> 15; (1954); p. 9, View in Reaxys 38 of 41

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1695 - 847 cm**(-1)

Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 228; (1949); p. 379; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 225; (1947); p. 997, View in Reaxys 39 of 41

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1695 - 741 cm**(-1)

Thompson; Torkington; Journal of the Chemical Society; (1945); p. 645, View in Reaxys 40 of 41

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

4000 cm**(-1)

Ellis; Journal of the American Chemical Society; vol. 51; (1929); p. 1386; Physical Review; vol. <2>32; (1928); p. 906; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1419, View in Reaxys 41 of 41

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

3367 - 1255 cm**(-1)

Lecomte; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 180; (1925); p. 1482; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 178; (1924); p. 1699, View in Reaxys Mass Spectrometry (45) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

Peak

electron impact (EI); spectrum

References Wang, Donghui; Zhang, Zhaoguo; Organic Letters; vol. 5; nb. 24; (2003); p. 4645 - 4648, View in Reaxys; Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 - 8456, View in Reaxys; Consiglio, Gabriella Barozzino; Mordini, Alessandro; Letters in Organic Chemistry; vol. 15; nb. 5; (2018); p. 447 - 454, View in Reaxys

supporting information

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.

105/126

2018-07-03 19:01:53

Huoji; Organic and Biomolecular Chemistry; vol. 13; nb. 20; (2015); p. 5613 - 5616, View in Reaxys; Chatupheeraphat, Adisak; Liao, Hsuan-Hung; Srimontree, Watchara; Guo, Lin; Minenkov, Yury; Poater, Albert; Cavallo, Luigi; Rueping, Magnus; Journal of the American Chemical Society; vol. 140; nb. 10; (2018); p. 3724 - 3735, View in Reaxys high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); spectrum

supporting information

Saisaha, Pattama; Buettner, Lea; Van Der Meer, Margarethe; Hage, Ronald; Feringa, Ben L.; Browne, Wesley R.; De Boer, Johannes W.; Advanced Synthesis and Catalysis; vol. 355; nb. 13; (2013); p. 2591 - 2603, View in Reaxys; Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 - 5701, View in Reaxys; Li, Yang; Xue, Dong; Lu, Wei; Wang, Chao; Liu, Zhao-Tie; Xiao, Jianliang; Organic Letters; vol. 16; nb. 1; (2014); p. 66 - 69, View in Reaxys; Xia, Tian; Wei, Zhihong; Spiegelberg, Brian; Jiao, Haijun; Hinze, Sandra; de Vries, Johannes G.; Chemistry - A European Journal; vol. 24; nb. 16; (2018); p. 4043 - 4049, View in Reaxys

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

Meng, Mengting; Yang, Liangfeng; Cheng, Kai; Qi, Chenze; Journal of Organic Chemistry; vol. 83; nb. 6; (2018); p. 3275 - 3284, View in Reaxys

gas chromatograParagraph 0052; phy mass spectrom- 0056; 0060 etry (GCMS); electron impact (EI); spectrum

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, 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

electron impact (EI); gas chromatography mass spectrometry (GCMS); spectrum

supporting information

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; Berton, Mateo; Mello, Rossella; Williard, Paul G.; González-Núñez, María Elena; Journal of the American Chemical Society; vol. 139; nb. 48; (2017); p. 17414 - 17420, View in Reaxys

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

Wang, Jian-Cheng; Ding, Feng-Wen; Ma, JianPing; Liu, Qi-Kui; Cheng, Jun-Yan; Dong, Yu-Bin; Inorganic Chemistry; vol. 54; nb. 22; (2015); p. 10865 - 10872, View in Reaxys; Movahhed, Sohajl; Westphal, Julia; Dindaroǧlu, Mehmet; Falk, Anna; Schmalz, Hans-Günther; Chemistry - A European Journal; vol. 22; nb. 22; (2016); p. 7381 - 7384, View in Reaxys

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

supporting information

Erbing, Elis; Vázquez-Romero, Ana; Bermejo Gómez, Antonio; Platero-Prats, Ana E.; Carson, Fabian; Zou, Xiaodong; Tolstoy, Päivi; Martín-Matute, Belén; Chemistry - A European Journal; vol. 22; nb. 44; (2016); p. 15659 - 15663, View in Reaxys

spectrum

supporting information

Urgoitia; Sanmartin; Herrero; Domínguez; Chemical Communications; vol. 51; nb. 23; (2015); p. 4799 4802, View in Reaxys

106/126

2018-07-03 19:01:53

electrospray ionisation (ESI); liquid chromatography mass spectrometry (LCMS); spectrum high resolution mass spectrometry (HRMS); CI (Chemical ionization); spectrum

Huang, Pei-Qiang; Wang, Yu; Xiao, Kai-Jiong; Huang, Ying-Hong; Tetrahedron; vol. 71; nb. 24; (2015); p. 4248 - 4254; Art.No: 26677, View in Reaxys supporting information

spectrum

Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys

134.1 m/z

Dong, Qizhi; Li, Ningbo; Qiu, Renhua; Wang, Jinying; Guo, Cancheng; Xu, Xinhua; Journal of Organometallic Chemistry; vol. 799-800; (2015); p. 122 - 127, View in Reaxys

high resolution supporting informamass spectrometry tion (HRMS); electron impact (EI); timeof-flight mass spectra (TOFMS); spectrum

Jiang, Jian-An; Du, Jia-Lei; Wang, Zhan-Guo; Zhang, Zhong-Nan; Xu, Xi; Zheng, Gan-Lin; Ji, Ya-Fei; Tetrahedron Letters; vol. 55; nb. 10; (2014); p. 1677 - 1681, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); timeof-flight mass spectra (TOFMS); electrospray ionisation (ESI); spectrum

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

high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); time-offlight mass spectra (TOFMS); spectrum

Gu, Lijun; Jin, Cheng; Zhang, Hongtao; Zhang, Lizhu; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8453 - 8456, View in Reaxys

spectrum

Shurukhin, Yu. V.; Klyuev, N. A.; Grandberg, I. I.; Journal of Organic Chemistry USSR (English Translation); vol. 23; nb. 5; (1987); p. 960 - 965; Zhurnal Organicheskoi Khimii; vol. 23; nb. 5; (1987); p. 1063 1069, View in Reaxys; Hanack, Michael; Weber, Erhard; Chemische Berichte; vol. 116; nb. 2; (1983); p. 777 - 797, View in Reaxys; 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; Mino, Takashi; Hirota, Tatsuya; Fujita, Noriko; Yamashita, Masakazu; Synthesis; nb. 12; (1999); p. 2024 - 2026, View in Reaxys; Wiles, Charlotte; Watts, Paul; Haswell, Stephen J.; Tetrahedron Letters; vol. 47; nb. 30; (2006); p. 5261 - 5264, View in Reaxys; Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 - 4260, View in Reaxys; Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 5935, View in Reaxys

spectrum

supporting information

gas chromatography mass spectrometry (GCMS); elec-

135 m/z

Gao, Qi; Li, Shenyan; Pan, Yingming; Xu, Yanli; Wang, Hengshan; Tetrahedron; vol. 69; nb. 19; (2013); p. 3775 - 3781, View in Reaxys

134 m/z; 105 m/z; 77 m/z; 51 m/z

Chen, Zheng-Wang; Ye, Dong-Nai; Qian, Yi-Ping; Ye, Min; Liu, Liang-Xian; Tetrahedron; vol. 69; nb. 30; (2013); p. 6116 - 6120, View in Reaxys

107/126

2018-07-03 19:01:53

tron impact (EI); spectrum high resolution mass spectrometry (HRMS); spectrum

Jones, Raymond C. F.; Nichols, John R.; Organic and Biomolecular Chemistry; vol. 11; nb. 35; (2013); p. 5926 - 5935, View in Reaxys

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

Zhang, Fang; Liang, Chao; Chen, Mingzheng; Guo, Haibing; Jiang, Huangyong; Li, Hexing; Green Chemistry; vol. 15; nb. 10; (2013); p. 2865 2871, View in Reaxys; Chorghade, Rajeev; Battilocchio, Claudio; Hawkins, Joel M.; Ley, Steven V.; Organic Letters; vol. 15; nb. 22; (2013); p. 5698 5701, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

Althaus, Martin; Togni, Antonio; Mezzetti, Antonio; Journal of Fluorine Chemistry; vol. 130; nb. 8; (2009); p. 702 - 707, View in Reaxys; 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

HRMS (High resolution mass spectrometry); ESI (Electrospray ionisation); TOFMS (Time of flight mass spectrum); Spectrum

supporting information

Gowda, Maravanhalli Sidde; Pande, Sushanth Sudhir; Ramakrishna, Ramesha Andagar; Prabhu, Kandikere Ramaiah; Organic and Biomolecular Chemistry; vol. 9; nb. 15; (2011); p. 5365 - 5368, View in Reaxys; Chowdhury, Abhishek Dutta; Ray, Ritwika; Lahiri, Goutam Kumar; Chemical Communications; vol. 48; nb. 44; (2012); p. 5497 - 5499, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

supporting information

Yang, Xiu-Li; Xie, Ming-Hua; Zou, Chao; He, Yabing; Chen, Banglin; O'Keeffe, Michael; Wu, Chuan-De; Journal of the American Chemical Society; vol. 134; nb. 25; (2012); p. 10638 - 10645, View in Reaxys; Cabrero-Antonino, Jose R.; LeyvaPerez, Antonio; Corma, Avelino; Chemistry - A European Journal; vol. 18; nb. 35; (2012); p. 11107 11114, View in Reaxys; Yin, Lixia; Wu, Jingjing; Xiao, Juan; Cao, Song; Tetrahedron Letters; vol. 53; nb. 33; (2012); p. 4418 - 4421, View in Reaxys

EI (Electron impact); Spectrum

supporting information

Lin, Riyuan; Chen, Feng; Jiao, Ning; Organic Letters; vol. 14; nb. 16; (2012); p. 4158 - 4161, 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

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

Durchschein, Katharina; Fabian, Walter M. F.; MacHeroux, Peter; Zangger, Klaus; Trimmel, Gregor; Faber, Kurt; Organic and Biomolecular Chemistry; vol. 9; nb. 9; (2011); p. 3364 - 3369, View in Reaxys

Spectrum

Lee, Jong Chan; Kim, Jimi; Lee, Seung Bae; Chang, Soon-Uk; Jeong, Yeon Jin; Synthetic Communications; vol. 41; nb. 13; (2011); p. 1947 - 1951, View in Reaxys

HRMS (High resolution mass spectrometry); EI (Electron impact); Spectrum

Hachiya, Iwao; Inagaki, Takao; Ishihara, Yasuhisa; Shimizu, Makoto; Bulletin of the Chemical Society of Japan; vol. 84; nb. 4; (2011); p. 419 - 421, View in Reaxys

ESI (Electrospray ionisation); HRMS

supporting informa- mol peak tion

Bartoszewicz, Agnieszka; Martin-Matute, Belen; Organic Letters; vol. 11; nb. 8; (2009); p. 1749 - 1752, View in Reaxys

108/126

2018-07-03 19:01:53

(High resolution mass spectrometry) CI (Chemical ionization)

mol peak

Hyder, Zeynab; Ruan, Jiwu; Xiao, Jianliang; Chemistry - A European Journal; vol. 14; nb. 18; (2008); p. 5555 - 5566, View in Reaxys

HRMS (High resolution mass spectrometry)

mol peak

Hyder, Zeynab; Ruan, Jiwu; Xiao, Jianliang; Chemistry - A European Journal; vol. 14; nb. 18; (2008); p. 5555 - 5566, View in Reaxys

spectrum; electron impact (EI)

Agafonov, N. E.; Sedishev, I. P.; Dudin, A. V.; Kutin, A. A.; Stashina, G. A.; Zhulin, V. M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 40; nb. 2.2; (1991); p. 366 - 372; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 2; (1991); p. 426 433, View in Reaxys; Zhao, Baowei; Lu, Xiyan; Organic Letters; vol. 8; nb. 26; (2006); p. 5987 - 5990, View in Reaxys

spectrum; chemical ionization (CI)

metastable ions

Cheung; Harrison; Journal of Mass Spectrometry; vol. 30; nb. 9; (1995); p. 1267 - 1272, View in Reaxys

spectrum; chemical ionization (CI)

collisional activation

Cheung; Harrison; Journal of Mass Spectrometry; vol. 30; nb. 9; (1995); p. 1267 - 1272, View in Reaxys

spectrum

collisional activation; charge exchange with positive ions

Kingston, E. E.; Beynon, J. H.; Ast, T.; Flammang, R.; Maquestiau, A.; Organic Mass Spectrometry; vol. 20; nb. 9; (1985); p. 546 - 555, View in Reaxys

chemical ionization (CI); spectrum

Chai, Rosalind; Harrison, Alex. G.; Analytical Chemistry; vol. 55; nb. 6; (1983); p. 969 - 971, View in Reaxys

negative ion spectroscopy

Vaglio; Annali di Chimica (Rome, Italy); vol. 69; (1979); p. 139, View in Reaxys; Vaglio, Gian Angelo; Volpe, Paolo; Operti, Lorensa; Organic Mass Spectrometry; vol. 17; nb. 12; (1982); p. 617 - 619, View in Reaxys

fragmentation pattern

Audier, H.E.; Moustapha, C.; Denhez, J.P.; Tetrahedron Letters; vol. 23; nb. 24; (1982); p. 2443 - 2444, View in Reaxys

chemical ionization (CI)

Vaglio, Gian Angelo; Volpe, Paolo; Operti, Lorensa; Organic Mass Spectrometry; vol. 17; nb. 12; (1982); p. 617 - 619, View in Reaxys

fragmentation pattern; electron impact (EI); spectrum

Teleshefsky, L. A.; Jones, B. E.; Abbey, L. E.; Bostwick, D. E.; Burgess, E. M; Moran T. F.; Organic Mass Spectrometry; vol. 17; nb. 10; (1982); p. 481 492, View in Reaxys

spectrum

MIKE (mass ion kinetic energy)

Audier, Henri-Edouard; Bouchoux, Guy; Milliet, Arielle; Denhez, Jean-Pierre; Maquestiau, Andre; Flammang, Robert; Journal of Chemical Research, Miniprint; nb. 3; (1982); p. 943 - 963, View in Reaxys

spectrum; chemical ionization (CI); electron impact (EI)

Audier, Henri-Edouard; Bouchoux, Guy; Milliet, Arielle; Denhez, Jean-Pierre; Maquestiau, Andre; Flammang, Robert; Journal of Chemical Research, Miniprint; nb. 3; (1982); p. 943 - 963, View in Reaxys Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys; Lee et al.; Journal of Agricultural and Food Chemistry; vol. 23; (1975); p. 1195,1196, View in Reaxys; Ferretti; Flanagan; Journal of Agricultural and Food Chemistry; vol. 19; (1971); p. 245,247, View in Reaxys; Hertz et al.; Analytical Chemistry; vol. 43; (1971); p. 681,688, View in Reaxys; Sigsby et al.; Organic Mass Spectrometry; vol. 14; (1979); p. 273,276, View in Reaxys; Dimmel et al.; Journal of

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.

109/126

2018-07-03 19:01:53

Organic Chemistry; vol. 41; (1976); p. 3092, View in Reaxys; Cooks; Williams; Chemical Communications (London); (1968); p. 627, View in Reaxys; Kraft; Spiteller; Organic Mass Spectrometry; vol. 1; (1968); p. 617,622,623,625, View in Reaxys; Bursey; Wolfe; Organic Mass Spectrometry; vol. 1; (1968); p. 543, View in Reaxys; Dimmel; Gharpure; Journal of the American Chemical Society; vol. 93; (1971); p. 3991,3994, View in Reaxys; Michnowicz; Munson; Organic Mass Spectrometry; vol. 6; (1972); p. 283,287, View in Reaxys; Baba; Kawai; Yakugaku Zasshi; vol. 94; (1974); p. 783,785; Chem.Abstr.; vol. 81; nb. 37514; (1974), View in Reaxys; Rjabinkin et al.; Zhurnal Organicheskoi Khimii; vol. 3; (1967); p. 216,206, View in Reaxys appearance potentials

Tajima et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 3687, View in Reaxys

UV/VIS Spectroscopy (18) 1 of 18

Absorption Maxima (UV/ VIS) [nm]

244

Ext./Abs. Coefficient [l·mol-1cm-1]

10300

Backstrom, Nicholas; Burton, Neil A.; Turega, Simon; Watt, C. Ian F.; Journal of Physical Organic Chemistry; vol. 21; nb. 7-8; (2008); p. 603 - 613, View in Reaxys 2 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

315; 321

Ext./Abs. Coefficient [l·mol-1cm-1]

17; 17

Olivato, Paulo R.; Filho, Rubens R.; Lopes, Julio C. D.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 92; nb. 1-4; (1994); p. 109 - 128, View in Reaxys 3 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

H2O

Absorption Maxima (UV/ VIS) [nm]

244

Ext./Abs. Coefficient [l·mol-1cm-1]

12000

Guthrie, J. Peter; Cossar, John; Canadian Journal of Chemistry; vol. 68; nb. 11; (1990); p. 2060 - 2069, View in Reaxys 4 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

benzene

Comment (UV/VIS Spectroscopy)

295 - 370 nm

Wismontski-Knittel, T.; Kilp, T.; Journal of Physical Chemistry; vol. 88; nb. 1; (1984); p. 110 - 115, View in Reaxys 5 of 18

Description (UV/VIS Spectroscopy)

UV/VIS

Sekiya,M.; Terao,Y.; Chemical and Pharmaceutical Bulletin; vol. 18; (1970); p. 947 - 956, View in Reaxys; McKinney,M.A.; So,E.C.; Journal of Organic Chemistry; vol. 37; nb. 18; (1972); p. 2818 - 2822, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Katritzky et al.; Tetrahedron; vol. 28; (1972); p. 3449,3451, 3453,3456,3463, View in Reaxys; Hashimoto; Tetrahedron; vol. 28; (1972); p. 217,218, 221, 225,

110/126

2018-07-03 19:01:53

View in Reaxys; Seth-Paul; Vermylen-De Winter; Journal of Molecular Structure; vol. 4; (1969); p. 303,304, View in Reaxys; Sahini; Butucelea; Revue Roumaine de Chimie; vol. 14; (1969); p. 981, View in Reaxys; Guiheneuf et al.; Bulletin de la Societe Chimique de France; (1971); p. 1157,1160, 1162, View in Reaxys 6 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Baly; Collie; Journal of the Chemical Society; vol. 87; (1905); p. 1342, View in Reaxys; Dombrowskii; Schewtschuk; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 192,190, View in Reaxys 7 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Spinner; Burawoy; Spectrochimica Acta; vol. 17; (1961); p. 558,560, View in Reaxys 8 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Grewe; Winter; Chemische Berichte; vol. 92; (1959); p. 1092,1100, View in Reaxys 9 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ VIS) [nm]

240

Kwart; Keen; Journal of the American Chemical Society; vol. 81; (1959); p. 943,945, View in Reaxys 10 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

242

Braude; Sondheimer; Journal of the Chemical Society; (1955); p. 3754,3765, View in Reaxys 11 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

240; 276

Forbes; Mueller; Canadian Journal of Chemistry; vol. 33; (1955); p. 1145,1153, View in Reaxys 12 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

220 - 350 nm

Grammaticakis; Bulletin de la Societe Chimique de France; (1953); p. 865,866, View in Reaxys 13 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

220 - 350 nm

Grammaticakis; Bulletin de la Societe Chimique de France; (1953); p. 865,866, View in Reaxys 14 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

111/126

2018-07-03 19:01:53

Comment (UV/VIS Spectroscopy)

Extinktionskoeffizient.

Absorption Maxima (UV/ VIS) [nm]

236.97; 277.01; 285.71

Hedden; Brown; Journal of the American Chemical Society; vol. 75; (1953); p. 3744,3745, View in Reaxys 15 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

diethyl ether

Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 226; (1948); p. 1016, View in Reaxys; Kato; Scientific Papers of the Institute of Physical and Chemical Research (Japan); vol. 23; (1934); p. 256,260, 262 Abb. LIX/3; Chem. Zentralbl.; vol. 105; nb. II; (1934); p. 2179, View in Reaxys 16 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Biquard; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 55,67, View in Reaxys 17 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ramart-Lucas; Guerlain; Bulletin de la Societe Chimique de France; vol. <4> 49; (1931); p. 1860,1867, View in Reaxys; Biquard; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 55,67, View in Reaxys 18 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Ramart-Lucas; Salmon-Legagneur; Bulletin de la Societe Chimique de France; vol. <4> 51; (1932); p. 1069,1083, View in Reaxys; Ramart-Lucas; Guerlain; Bulletin de la Societe Chimique de France; vol. <4> 49; (1931); p. 1860,1867, View in Reaxys Raman Spectroscopy (1) Description (Ram- References an Spectroscopy) Spectrum

Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 225; (1947); p. 930, View in Reaxys; Cherrier; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 228; (1949); p. 307, View in Reaxys; Gray; Annales de Chimie (Cachan, France); vol. <12> 3; (1948); p. 355,387, View in Reaxys; Biquard; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 55,67, View in Reaxys; Kohlrausch; Pongratz; Monatshefte fuer Chemie; vol. 64; (1934); p. 374,382, View in Reaxys; Schmidt; Brova; Berichte der BunsenGesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys

Luminescence Spectroscopy (4) Description (Lumi- Comment (Luminescence Spectronescence Spectroscopy) scopy)

References

Luminescence quantum yield

Rusakowicz et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 3263,3264, View in Reaxys; Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Catalani, Luiz H.; Wilson, Therese; Journal of the American Chemical Society; vol. 109; nb. 24; (1987); p. 7458 - 7462, View in Reaxys

Luminescence lifetime

Harbaugh et al.; Analytical Chemistry; vol. 45; (1973); p. 381,382, View in Reaxys; Rusakowicz et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 3263,3264, View in Reaxys; Kanamara et al.; Chemical Physics Letters; vol. 26; (1974); p. 1,4, View in Reaxys; Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Wagner; Journal of the American Chemical Society; vol. 89; (1967); p. 2820,2822, View in Reaxys; Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys

Luminescence quenching

Quenching with dit-butyl peroxide

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys

112/126

2018-07-03 19:01:53

Luminescence quenching

Cosandey; Lerch; Helvetica Chimica Acta; vol. 50; (1967); p. 2215, View in Reaxys; Kochevar; Wagner; Journal of the American Chemical Society; vol. 94; (1972); p. 3859,3861, View in Reaxys; Encinas; Scaiano; Journal of Photochemistry; vol. 11; (1979); p. 241,243, 244, View in Reaxys

Fluorescence Spectroscopy (1) Description (Fluo- References rescence Spectroscopy) Fluorescence

Rusakowicz et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 3263,3264, View in Reaxys

Phosphorescence Spectroscopy (4) Description (Phos- Solvent (Phosphorphorescence Spec- escence Spectrotroscopy) scopy)

Comment (Phosphorescence Spectroscopy)

Phosphorescence

References

Harbaugh et al.; Analytical Chemistry; vol. 45; (1973); p. 381,382, View in Reaxys; Kanamara et al.; Chemical Physics Letters; vol. 26; (1974); p. 1,4, View in Reaxys; Shimada; Goodman; Journal of Chemical Physics; vol. 43; (1965); p. 2027,2030, 2033, View in Reaxys

Maxima

light petroleum

untersucht wurde die Abklingkeit bei -195grad.

Ermolaew; Optika i Spektroskopiya; vol. 1; (1956); p. 523,528; Chem.Abstr.; (1957); p. 5568, View in Reaxys

Maxima

ethanol; diethyl ether

untersucht wurde die Quantenausbeute bei -195grad.

Ermolaew; Optika i Spektroskopiya; vol. 1; (1956); p. 523,528; Chem.Abstr.; (1957); p. 5568, View in Reaxys

Maxima

ethanol; diethyl ether

untersucht wurde die Abklingzeit bei -195grad.

Ermolaew; Optika i Spektroskopiya; vol. 1; (1956); p. 523,528; Chem.Abstr.; (1957); p. 5568, View in Reaxys

Use (3) Laboratory Use and Use Pattern Handling

References

process for preparing furanopyrimidine compounds

Patent; XENTION DISCOVERY LIMITED; WO2005/121149; (2005); (A1) English, View in Reaxys

starting material

Patent; XENTION DISCOVERY LIMITED; WO2005/121149; (2005); (A1) English, View in Reaxys

Startsubstanz zur Radikalerzeugung

Paul; Fischer; Helvetica Chimica Acta; vol. 56; (1973); p. 1575,1584, View in Reaxys

Isolation from Natural Product (1) Isolation from Nat- References ural Product aus Kaffeearoma

Stoll et al.; Helvetica Chimica Acta; vol. 50; (1967); p. 628,635, View in Reaxys

Quantum Chemical Calculations (1) Calculated Proper- Method (Quantum ties Chemical Calculations) Potential energy function, potential curve

References

DFT - density func- Kohtani, Shigeru; Kamoi, Yuna; Yoshioka, Eito; Miyabe, Hideto; Catalysis Science and Techtional methods nology; vol. 4; nb. 4; (2014); p. 1084 - 1091, View in Reaxys

Medchem (32) 1 of 32

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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.

113/126

2018-07-03 19:01:53

2 of 32

Bioassay Details

Effect : |enzyme; examination of Bioassay : APA: amine:pyruvate aminotransferase; 1 APA unit: amount catalyzed 1 μmol/l acetophenone formation in 1 min at 50 mmol/l (S)-A1; LP: large pocket; SP: small pocket; A1: PhCH(CH3)NH2; D1: pyruvate APA active site model on basis of substrate structure - reactivity relationship; 5 mmol/l title comp., 5 mmol/l (S)-A1, 0.75 unit/ml APA incub. at 37 deg C, 10 min; reaction stopped by 75 μl HClO4 (16% (v/v)); analyzed by HPLC

Substance RN

606215View in Reaxys

Substance Name

1430915

Qualitative Results

title comp. reactivity < 1 %, compared with D1 (100%); two-binding site model for test ensyme proposed; dual substrate recognition mode for both hydrophobic and carboxyl groups in LP, acidic group repulsion and steric constraint in SP proposed

Measurement Parameter

qualitative

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |enzyme; examination of Bioassay : in vitro; carbonyl reductase activity determined spectrophotometrically by measuring oxidation rate of NADPH; 80 mM NADPH; potassium phosphate buffer, pH 6.5; 37 deg C

Substance RN

606215View in Reaxys

Substance Name

1430915

Substance Dose

0.300000 µM

Qualitative Results

exhibited carbonyl reductase activity with Km of 0.228 mM and Vmax of 14.8 nmol/min/mg (Vmax/Km: 64.3)

Measurement Parameter

qualitative

Nakajin, Shizuo; Tamura, Fumihiro; Takase, Noriko; Toyoshima, Satoshi; Biological and Pharmaceutical Bulletin; vol. 20; nb. 11; (1997); p. 1215 - 1218, View in Reaxys 3 of 32

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Tetrahymena pyriformis GL-C, protozoaBioassay : controls: 1) no title comp., no T. pyriformis; 2) inoculated with T. pyriformis without title comp. population growth impairment testing; 40-h TETRATOX assay; population density quantitated spectrophotometrically at 540 nm

Substance RN

606215View in Reaxys

Substance Name

1430915

Measurement Parameter

pGI50

Quantitative value

0.05

Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys 4 of 32

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose in rat

Biological Species/NCBI ID

rat

Substance RN

606215View in Reaxys

Measurement Parameter

LD50

Unit

µL/kg

114/126

2018-07-03 19:01:53

Qualitative value

Quantitative value

4490

Material Safety Data Sheet, View in Reaxys 5 of 32

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose in rabbit

Biological Species/NCBI ID

Leporidae

Substance RN

606215View in Reaxys

Measurement Parameter

LD50

Unit

µL/kg

Qualitative value

Quantitative value

4490

Material Safety Data Sheet, View in Reaxys 6 of 32

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose in Mouse

Biological Species/NCBI ID

mouse

Substance RN

606215View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

100

Material Safety Data Sheet, View in Reaxys 7 of 32

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose in Mouse

Biological Species/NCBI ID

mouse

Substance RN

606215View in Reaxys

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

Quantitative value

2250

Material Safety Data Sheet, View in Reaxys 8 of 32

Target Name

L-xylulose reductase [guinea pig]

Target Synonyms

dcxr; dicarbonyl/l-xylulose reductase; glb; l-xylulose reductase; protein p26h; xr

Target Uniprot ID

q920n9

Target, Subunit, Species

L-xylulose reductase [guinea pig]

Target Mutant/Chimera Details

L-xylulose reductase [guinea pig]:Wild

Target Species (Bioactivity)

guinea pig

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Michaelis-menten constant of the compound against guinea pig liver Carbonyl reductase 2 upon incubation in 80 mM sodium citrate buffer, pH 5.2

115/126

2018-07-03 19:01:53

9 of 32

10 of 32

Biological Species/NCBI ID

guinea pig

Substance RN

606215View in Reaxys

Measurement Parameter

Km (Michaelis constant)

Unit

Measurement Object

Michaelis-menten constant

Qualitative value

Quantitative value

1.4

Measurement pX

2.85

Target Name

Carbonyl reductase [NADPH] 1 [guinea pig]

Target Synonyms

carbonyl reductase

Target, Subunit, Species

Carbonyl reductase [NADPH] 1 [guinea pig]

Target Mutant/Chimera Details

Carbonyl reductase [NADPH] 1 [guinea pig]:Wild

Target Species (Bioactivity)

guinea pig

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent relative maximum velocity of the compound towards guinea pig liver Carbonyl reductase 1 upon incubation in 80 mM potassium phosphate buffer, pH 6.3 along with pyridine-4-aldehyde

Biological Species/NCBI ID

guinea pig

Substance RN

606215View in Reaxys

Unit

Measurement Object

Maximum velocity

Qualitative value

Quantitative value

Concomitants: Compound name

pyridine-4-aldehyde

Concomitants: Compound role

COM

Target Name

L-xylulose reductase [guinea pig]

Target Synonyms

dcxr; dicarbonyl/l-xylulose reductase; glb; l-xylulose reductase; protein p26h; xr

Target Uniprot ID

q920n9

Target, Subunit, Species

L-xylulose reductase [guinea pig]

Target Mutant/Chimera Details

L-xylulose reductase [guinea pig]:Wild

Target Species (Bioactivity)

guinea pig

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent relative maximum velocity of the compound towards guinea pig liver Carbonyl reductase 2 upon incubation in 80 mM potassium phosphate buffer, pH 6.3 along with pyridine-4-aldehyde

Biological Species/NCBI ID

guinea pig

Substance RN

606215View in Reaxys

Unit

Measurement Object

Percent relative maximum velocity

Qualitative value

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.

116/126

2018-07-03 19:01:53

11 of 32

12 of 32

Quantitative value

103

Concomitants: Compound name

pyridine-4-aldehyde

Concomitants: Compound role

COM

Target Name

Carbonyl reductase [NADPH] 1 [guinea pig]

Target Synonyms

carbonyl reductase

Target, Subunit, Species

Carbonyl reductase [NADPH] 1 [guinea pig]

Target Mutant/Chimera Details

Carbonyl reductase [NADPH] 1 [guinea pig]:Wild

Target Species (Bioactivity)

guinea pig

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Michaelis-menten constant of the compound against guinea pig liver Carbonyl reductase 1 upon incubation in 80 mM potassium phosphate buffer, pH 6.3

Biological Species/NCBI ID

guinea pig

Substance RN

606215View in Reaxys

Qualitative Results

ND = Not determined

Measurement Parameter

Km (Michaelis constant)

Measurement Object

Michaelis-menten constant

Qualitative value

Target Name

Estradiol 17-beta-dehydrogenase 1 [rat]

Target Synonyms

17-beta-hsd 1; 17-beta-hydroxysteroid dehydrogenase type 1; edh17b1; estradiol 17-beta-dehydrogenase 1; hsd17b1

Target Uniprot ID

p51657

Target, Subunit, Species

Estradiol 17-beta-dehydrogenase 1 [rat]

Target Mutant/Chimera Details

Estradiol 17-beta-dehydrogenase 1 [rat]:Wild

Target Species (Bioactivity)

rat

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent inhibition of 17-beta-hydroxysteroid dehydrogenase 1 from rat testicular microsomes using estrone (E1) (5 uM) as substrate upon incubation in phosphate buffer, pH 7.4 at 37 degree C for 90 min at concentration 100 uM

Biological Species/NCBI ID

rat

Cells/Cell Lines

testis cell

Substance RN

606215View in Reaxys

Measurement Parameter

inhibition rate

Unit

Measurement Object

Percent inhibition of 17-beta-hydroxysteroid dehydrogenase 1 from rat testicular microsomes

Qualitative value

Quantitative value

5.09

Deviation

3.9

Concomitants: Compound name

Estrone (E1) (5 uM)

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.

117/126

2018-07-03 19:01:53

13 of 32

14 of 32

Concomitants: Compound role

COM

Target Name

Testosterone 17-beta-dehydrogenase 3 [rat]

Target Synonyms

17-beta-hsd 3; 17-beta-hydroxysteroid dehydrogenase type 3; edh17b3; hsd17b3; testicular 17-beta-hydroxysteroid dehydrogenase; testosterone 17-beta-dehydrogenase 3

Target Uniprot ID

o54939

Target, Subunit, Species

Testosterone 17-beta-dehydrogenase 3 [rat]

Target Mutant/Chimera Details

Testosterone 17-beta-dehydrogenase 3 [rat]:Wild

Target Species (Bioactivity)

rat

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent inhibition of 17-beta-hydroxysteroid dehydrogenase 3 from rat testicular microsomes using [1,2,6,7-3H]AD (1.5 uM) as substrate upon incubation in phosphate buffer, pH 7.4 at 37 degree C for 30 min at concentration 100 uM

Biological Species/NCBI ID

rat

Cells/Cell Lines

testis cell

Substance RN

606215View in Reaxys

Measurement Parameter

inhibition rate

Unit

Qualitative value

Quantitative value

16.33

Deviation

1.39

Target Name

Hydroxy-Delta-5-Steroid Dehydrogenase, 3 Beta- Steroid Delta-Isomerase 1 [rat]

Target Synonyms

hydroxy-delta-5-steroid dehydrogenase, 3 beta- steroid delta-isomerase 1

Target, Subunit, Species

Hydroxy-Delta-5-Steroid Dehydrogenase, 3 Beta- Steroid Delta-Isomerase 1 [rat]

Target Mutant/Chimera Details

Hydroxy-Delta-5-Steroid Dehydrogenase, 3 Beta- Steroid Delta-Isomerase 1 [rat]:Wild

Target Species (Bioactivity)

rat

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent inhibition of 3-beta-hydroxysteroid dehydrogenase from rat testicular microsomes using [1,2,6,7-3H]DHEA (15 uM) as substrate upon incubation in Tris-HCl buffer, pH 8.4 at 37 degree C for 40 min at concentration 100 uM

Biological Species/NCBI ID

rat

Cells/Cell Lines

testis cell

Substance RN

606215View in Reaxys

Measurement Parameter

inhibition rate

Unit

Measurement Object

Percent inhibition

Qualitative value

Quantitative value

Concomitants: Compound name

2; 6; 7-3H]DHEA (15 uM); [1

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.

118/126

2018-07-03 19:01:53

15 of 32

Concomitants: Compound role

COM; COM; COM; COM

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

alcohol dehydrogenase; alcohol dehydrogenase adhp; putative iron-containing nadph-dependent propanol dehydrogenase; sorbitol dehydrogenase; zinc-dependent alcohol dehydrogenase; zn-dependent alcohol dehydrogenase

Target Uniprot ID

a0a0c1m2w0; a0a0c1m6a3; a0a0c1m9u4; a0a0c1mb50; a0a0c1mcc6; a0a0c1pyk8; a0a0c1q6j3; a0a0c1q768; a0a0c1q8w1; a0a0d0fez9; a0a0d0grx3; a0a0d0gvr2; a0a0d0gyb5; a0a1w6n751; a0a1w6n8l3; a0a1w6nch5; a0a1w6nfb7; a0a1w6nhm6; a0a1w6njv8; a0a1x0xpd6; a0a1x0xty0

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent bioreduction of compound catalyzed by Lactobacillus brevis Alcohol dehydrogenase upon incubation in 50 mM Tris-HCl buffer, pH 7.5 at 30 degree C for 48 hr in presence of 2.5 eq. of isopropanol and 1 mM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

qualitative

Unit

Qualitative value

Quantitative value

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

Target Uniprot ID

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Catalytic constant of the compound (dissolved in DMSO) towards Lactobacillus brevis Alcohol dehydrogenase upon incubation in 50 mM Tris-HCl buffer, pH 7.5 in presence of 100 uM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

qualitative

Unit

s-1

Qualitative value

Quantitative value

6.5

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.

119/126

2018-07-03 19:01:53

17 of 32

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

Target Uniprot ID

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Michaelis Menten constant of the compound (dissolved in DMSO) towards Lactobacillus brevis Alcohol dehydrogenase upon incubation in 50 mM Tris-HCl buffer, pH 7.5 in presence of 100 uM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

qualitative

Unit

Qualitative value

Quantitative value

1.4

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

Target Uniprot ID

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Catalytic constant of the compound (dissolved in DMSO) towards Lactobacillus brevis Alcohol dehydrogenase to that of michaelis menten constant upon incubation in 50 mM Tris-HCl buffer, pH 7.5 in presence of 100 uM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

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.

120/126

2018-07-03 19:01:53

Target Uniprot ID

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent bioreduction of compound catalyzed by Lactobacillus brevis Alcohol dehydrogenase upon incubation in 50 mM Tris-HCl buffer, pH 7.5 at 30 degree C for 48 hr in presence of 5 v/v of isopropanol and 1 mM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

percentage

Unit

Measurement Object

Reduction activity

Qualitative value

Quantitative value

Target Name

Alcohol dehydrogenase [Lactobacillus brevis]

Target Synonyms

Target Uniprot ID

Target, Subunit, Species

Alcohol dehydrogenase [Lactobacillus brevis]

Target Mutant/Chimera Details

Alcohol dehydrogenase [Lactobacillus brevis]:Wild

Target Species (Bioactivity)

Lactobacillus brevis

Substance Effect

catalytic activity

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent relative activity of Lactobacillus brevis Alcohol dehydrogenase towards compound reduction upon incubation in 50 mM Tris-HCl buffer, pH 7.5 in presence of 100 uM NADPH

Substance RN

606215View in Reaxys

Measurement Parameter

qualitative

Unit

Qualitative value

Quantitative value

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]: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.

121/126

2018-07-03 19:01:53

22 of 32

23 of 32

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

89.3

Measurement pX

1.05

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]:Wild

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

Measurement Parameter

Vmax

Unit

U/mg

Quantitative value

0.545

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]:Wild

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

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.

122/126

2018-07-03 19:01:53

24 of 32

25 of 32

26 of 32

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

4.38

Measurement pX

2.36

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]:Wild

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

Measurement Parameter

Km (Michaelis constant)

Unit

Quantitative value

5.28

Measurement pX

2.28

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]:Wild

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

Measurement Parameter

Vmax

Unit

U/mg

Quantitative value

0.086

Target Name

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Synonyms

aldo-keto reductase

Target, Subunit, Species

Aldo-keto reductase [Lodderomyces elongisporus LH703]

Target Mutant/Chimera Details

Aldo-keto reductase [Lodderomyces elongisporus LH703]: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.

123/126

2018-07-03 19:01:53

27 of 32

Target Species (Bioactivity)

Lodderomyces elongisporus LH703

Target Transfection

Transfected

Substance Action on Target

Substrate

Bioassay Category

In Vitro (Efficacy)

Biological Species/NCBI ID

Escherichia coli BL21 (DE3)

Substance RN

606215View in Reaxys

Substance Name

propiophenone

Measurement Parameter

Vmax

Unit

U/mg

Quantitative value

0.033

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent relative reduction of compound (1 mM, dissolved in dimethyl sulfoxide) by Escherichia coli HB 101 (pNTOM3) in presence of NADPH (0.25 mM) upon incubation in 100 mM phosphate buffer, pH 6.5 for 1 min at 30 degree C when compared to control (CBPB)=100

Biological Species/NCBI ID

Escherichia coli HB101

Substance RN

606215View in Reaxys

Measurement Parameter

Activity

Unit

Measurement Object

relative activity

Qualitative value

Quantitative value

183

Patent; Kaneka Corporation; US7794993; (2010); (B2) English, View in Reaxys 28 of 32

Target Name

carbonyl reductase (NADPH)

Target Synonyms

carbonyl reductase; carbonyl reductase (nadph); carbonyl reductase (nadph) activity; nadph-dependent carbonyl reductase; nadph2-dependent carbonyl reductase; nonspecific nadph-dependent carbonyl reductase; secondary-alcohol:nadp+ oxidoreductase

Target, Subunit, Species

carbonyl reductase (NADPH)

Target Mutant/Chimera Details

carbonyl reductase (NADPH):Wild

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Activity of the compound against Carbonyl reductase

Substance RN

606215View in Reaxys

Qualitative Results

Not Published

Measurement Parameter

qualitative

Qualitative value

Not Published

Patent; Kaneka Corporation; US7794993; (2010); (B2) English, View in Reaxys 29 of 32

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Percent relative reduction of compound (1 mM, dissolved in dimethyl sulfoxide) by Escherichia coli HB 101 (pNTOM4) in presence of NADPH (0.25 mM) upon incubation in 100 mM phosphate buffer, pH 6.5 for 1 min at 30 degree C when compared to control (CBPB)=100

Biological Species/NCBI ID

Escherichia coli HB101

Substance RN

606215View 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.

124/126

2018-07-03 19:01:53

Measurement Parameter

Activity

Unit

Measurement Object

relative activity

Qualitative value

Quantitative value

Patent; Kaneka Corporation; US7794993; (2010); (B2) English, View in Reaxys 30 of 32

Target Name

carbonyl reductase (NADPH)

Target Synonyms

Target, Subunit, Species

carbonyl reductase (NADPH)

Target Mutant/Chimera Details

carbonyl reductase (NADPH):Wild

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Activity of the compound against Carbonyl reductase

Substance RN

606215View in Reaxys

Qualitative Results

Not Published

Measurement Parameter

qualitative

Qualitative value

Not Published

Patent; SOUICHI MORIKAWA; NORIYUKI KIZAKI; MIHO YANO; MASAHIRO FUNAKI; TERUAKI TAKESUE; YOSHIHIKO YASOHARA; TAKAHISA NAKAI; MICHIHIKO KATAOKA; SAKAYU SHIMIZU; US2010/317075; (A1); (2010), View in Reaxys 31 of 32

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Biological Species/NCBI ID

Escherichia coli HB101

Substance RN

606215View in Reaxys

Measurement Parameter

Activity

Unit

Measurement Object

relative activity

Qualitative value

Quantitative value

183

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Biological Species/NCBI ID

Escherichia coli HB101

Substance RN

606215View in Reaxys

Measurement Parameter

Activity

Unit

Measurement Object

relative activity

Qualitative value

125/126

2018-07-03 19:01:53

Quantitative value

126/126

2018-07-03 19:01:53