9H-Fluoren-9-one (9-Fluorenone) [C13H8O] by Asch

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2018-06-21 20h:36m:51s (UTC)

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Search as: As drawn ) AND (IDE.XRN=1636531)))

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Reaxys ID 1636531 View in Reaxys

1/1 CAS Registry Number: 486-25-9 Chemical Name: 9-fluorenone; fluorenone Linear Structure Formula: OCC12H8 Molecular Formula: C13H8O Molecular Weight: 180.206 Type of Substance: isocyclic InChI Key: YLQWCDOCJODRMT-UHFFFAOYSA-N Note:

Substance Label (230) Label References I

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14b

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2{12}

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26a

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3al

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27a

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pr15

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compound F10

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10a

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VPC-3002

Li, Huifang; Hassona, Mohamed D.H.; Lack, Nathan A.; Axerio-Cilies, Peter; Leblanc, Eric; Tavassoli, Peyman; Kanaan, Natalia; Frewin, Kate; Singh, Kriti; Adomat, Hans; Boehm, Konrad J.; Prinz, Helge; Guns, Emma Tomlinson; Rennie, Paul S.; Cherkasov, Artem; Molecular Cancer Therapeutics; vol. 12; nb. 11; (2013); p. 2425 2435, View in Reaxys

Andrievskii; Gorelik; Linko; Grachev; Russian Journal of Organic Chemistry; vol. 49; nb. 10; (2013); p. 1474 - 1481; Zhurnal Organicheskoi Khimii; vol. 49; nb. 10; (2013); p. 1496 - 1502,7, View in Reaxys

Hou; Koizumi; Fujita; Yamazaki; Wakatsuki; Journal of the American Chemical Society; vol. 123; nb. 24; (2001); p. 5812 - 5813, View in Reaxys; Hesse, Nadine; Froehlich, Roland; Wibbeling, Birgit; Wuerthwein, Ernst-Ulrich; European Journal of Organic Chemistry; nb. 17; (2006); p. 3923 - 3937, View in Reaxys; Wiedemann, Sean H.; Bio, Matthew M.; Brown, Liane M.; Hansen, Karl B.; Langille, Neil F.; Synlett; vol. 23; nb. 15; (2012); p. 2231 - 2236, View in Reaxys

Gholap, Atul R.; Paul, Vincent; Srinivasan, Kumar V.; Synthetic Communications; vol. 38; nb. 17; (2008); p. 2967 2982, View in Reaxys; Cui, Hua; Li, Ying; Zhang, Songlin; Organic and Biomolecular Chemistry; vol. 10; nb. 14; (2012); p. 2862 - 2869, View in Reaxys

Balkrishna, Shah Jaimin; Prasad, Ch Durga; Panini, Piyush; Chopra, Deepak; Kumar, Sangit; Detty, Michael R.; Journal of Organic Chemistry; vol. 77; nb. 21; (2012); p. 9541 - 9552,12, View in Reaxys

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys

13a

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

E4; D12

Patent; CANON KABUSHIKI KAISHA; NISHIDE, Yosuke; MIYASHITA, Hirokazu; KAMATANI, Jun; SAITOH, Akihito; WO2011/96272; (2011); (A1) English, View in Reaxys

Flu

Ohura, Takeshi; Amagai, Takashi; Makino, Masakazu; Chemosphere; vol. 70; nb. 11; (2008); p. 2110 - 2117, View in Reaxys

Schank, Kurt; Beck, Horst; Buschlinger, Michael; Eder, Joerg; Heisel, Thomas; Pistorius, Susanne; Wagner, Christiane; Helvetica Chimica Acta; vol. 83; nb. 4; (2000); p. 801 - 826, View in Reaxys; Kommreddy, Amitha; Bowsher, Michael S.; Gunna, Meena R.; Botha, Kirankumar; Vinod, Thottumkara K.; Tetrahedron Letters; vol. 49; nb. 28; (2008); p. 4378 - 4382, View in Reaxys

12a

Zarudnitskii, Evgenij V.; Pervak, Igor I.; Merkulov, Anatolij S.; Yurchenko, Aleksandr A.; Tolmachev, Andrej A.; Tetrahedron; vol. 64; nb. 45; (2008); p. 10431 - 10442, View in Reaxys

Xiao, Xiangshu; Antony, Smitha; Kohlhagen, Glenda; Pommier, Yves; Cushman, Mark; Journal of Organic Chemistry; vol. 69; nb. 22; (2004); p. 7495 - 7501, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys

educt to L

Zhou, Hong-ping; Li, Dong-mei; Wang, Peng; Cheng, Le-hua; Gao, Yuan-hao; Zhu, Yong-min; Wu, Jie-ying; Tian, Yu-peng; Tao, Xu-tang; Jiang, Min-hua; Fun, Hoong-Kun; Journal of Molecular Structure; vol. 826; nb. 2-3; (2007); p. 205 - 210, View in Reaxys

starting to 7

Hua, Guoxiong; Li, Yang; Slawin, Alexandra M. Z.; Woollins, J. Derek; Dalton Transactions; nb. 15; (2007); p. 1477 - 1480, View in Reaxys

9-FLUO; (3)

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb. 2; (2007); p. 279 - 286, View in Reaxys

Albrecht, Uwe; Langer, Peter; Tetrahedron; vol. 63; nb. 22; (2007); p. 4648 - 4654, View in Reaxys

educt tab. 3, entr.18

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

table 1, entry 10

Sadeghi; Mohammadpoor-Baltork; Azarm; Mazidi; Synthetic Communications; vol. 31; nb. 3; (2001); p. 435 - 438, View in Reaxys; 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

9Fl

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys; Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

9/144

2018-06-21 20:37:19

FLO

Misaki, Kentaro; Kawami, Hirofumi; Tanaka, Tota; Handa, Yoji; Nakamura, Masafumi; Matsui, Saburo; Matsuda, Tomonari; Environmental Toxicology and Chemistry; vol. 26; nb. 7; (2007); p. 1370 - 1379, View in Reaxys

starting to 1

Hubert, Cecile; Tran, Khoa; Hauquier, Fanny; Cougnon, Charles; Pilard, Jean-Francois; Gosselin, Pascal; RaultBerthelot, Joelle; Raoult, Eugene; New Journal of Chemistry; vol. 31; nb. 10; (2007); p. 1730 - 1737, View in Reaxys

educt to 7b

Mlostoń, Grzegorz; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 90; nb. 9; (2007); p. 1758 - 1764, View in Reaxys

1e; 1f

Hatano, Manabu; Takagi, Eri; Ishihara, Kazuaki; Organic Letters; vol. 9; nb. 22; (2007); p. 4527 - 4530, View in Reaxys

Tab.1.run3

Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys

Table 1; Entry 5

Nakanishi, Masafumi; Bolm, Carsten; Advanced Synthesis and Catalysis; vol. 349; nb. 6; (2007); p. 861 - 864, View in Reaxys

IVa

Chaikovskii; Filimonov; Skorokhodov; Ogorodnikov; Russian Journal of Organic Chemistry; vol. 43; nb. 9; (2007); p. 1278 - 1281, View in Reaxys

3a-Fl

Moorthy, Jarugu Narasimha; Samanta, Subhas; Journal of Organic Chemistry; vol. 72; nb. 25; (2007); p. 9786 9789, View in Reaxys

Blagoev, Milen; Linden, Anthony; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 82; nb. 12; (1999); p. 2316 2335, View in Reaxys; Shing, Tony K. M.; Yeung, Ying-Yeung; Su, Pak L.; Organic Letters; vol. 8; nb. 14; (2006); p. 3149 - 3151, View in Reaxys

starting to 9b

Mloston, Grzegorz; Celeda, Malgorzata; Linden, Anthony; Heimgartner, Heinz; Heterocycles; vol. 68; nb. 1; (2006); p. 33 - 45, View in Reaxys

T.I, Entry 11, Product

Badri, Rashid; Mostoufi, Azar; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 181; nb. 7; (2006); p. 1513 - 1519, View in Reaxys

educt to 6a

Jones, David J.; Gibson, Vernon C.; Heterocycles; vol. 68; nb. 6; (2006); p. 1121 - 1138, View in Reaxys

product, tab 1/24

Hajipour; Bagheri; Ruoho; Russian Journal of Organic Chemistry; vol. 42; nb. 6; (2006); p. 844 - 848, View in Reaxys

8IIg

Pesquet, Anthony; Daich, Adam; Van Hijfte, Luc; Journal of Organic Chemistry; vol. 71; nb. 14; (2006); p. 5303 5311, View in Reaxys

product, tab 3/37

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

Li; Zhang; Petersen; Wang; Journal of Organic Chemistry; vol. 66; nb. 20; (2001); p. 6662 - 6668, View in Reaxys; Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys

product T. 1, E. 22

Hajipour, Abdol R.; Guo, Lian-Wang; Ruoho, Arnold E.; Molecular Crystals and Liquid Crystals; vol. 456; nb. 1; (2006); p. 85 - 93, View in Reaxys

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys

prod., Tab. 2, entry 1

Park, Kwanghee Koh; Tsou, Lun K.; Hamilton, Andrew D.; Synthesis; nb. 21; (2006); p. 3617 - 3620, View in Reaxys

subst., Tab.3, entry 10

Setamdideh, Davood; Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 61; nb. 10; (2006); p. 1275 - 1281, View in Reaxys

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb. 17; (2005); p. 6609 - 6615, View in Reaxys; Chen, Xudong; Lemal, David M.; Journal of Fluorine Chemistry; vol. 127; nb. 9; (2006); p. 1158 - 1167, View in Reaxys

Hatano, Bunpei; Kubo, Daisuke; Tagaya, Hideyuki; Chemical and Pharmaceutical Bulletin; vol. 54; nb. 9; (2006); p. 1304 - 1307, View in Reaxys

Kolyadina; Soldatenkov; Gridunova; Prostakov; Chemistry of Heterocyclic Compounds; vol. 34; nb. 7; (1998); p. 833 - 836, View in Reaxys; Ohura, Takeshi; Kitazawa, Atsushi; Amagai, Takashi; Makino, Masakazu; Environmental Science and Technology; vol. 39; nb. 1; (2005); p. 85 - 91, View in Reaxys

Olah, George A.; Mathew, Thomas; Farnia, Morteza; Prakash, G. K. Surya; Katherine; Donald; Synlett; nb. 7; (1999); p. 1067 - 1068, View in Reaxys; Ali, Mohammed Hashmat; Gomes, Maria Goretti; Synthesis; nb. 8; (2005); p. 1326 - 1332; Art.No: M05004SS, View in Reaxys

tab1, col2, entry4

Hunsen, Mo; Tetrahedron Letters; vol. 46; nb. 10; (2005); p. 1651 - 1653, View in Reaxys

10/144

2018-06-21 20:37:19

educt of tab.2, entr.21

Firouzabadi, Habib; Iranpoor, Nasser; Jafari, Abbas Ali; Journal of Organometallic Chemistry; vol. 690; nb. 6; (2005); p. 1556 - 1559, View in Reaxys

21b

Nair, Vijay; Suja; Mohanan, Kishor; Tetrahedron Letters; vol. 46; nb. 18; (2005); p. 3217 - 3219, View in Reaxys

7-1d0

Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys

Tab 2/1 Substrate

Zaccheria, Federica; Ravasio, Nicoletta; Ercoli, Mauro; Allegrini, Pietro; Tetrahedron Letters; vol. 46; nb. 45; (2005); p. 7743 - 7745, View in Reaxys

tab.4, entry 5, prod.

Wang, Jia-Rui; Liu, Lei; Wang, Ye-Feng; Zhang, Ying; Deng, Wei; Guo, Qing-Xiang; Tetrahedron Letters; vol. 46; nb. 27; (2005); p. 4647 - 4651, View in Reaxys

VIII

Krasnokutskaya; Trusova; Filimonov; Russian Journal of Organic Chemistry; vol. 41; nb. 12; (2005); p. 1750 - 1751, View in Reaxys

educt to 18b

Yamaguchi, Shigehiro; Xu, Caihong; Yamada, Hiroshi; Wakamiya, Atsushi; Journal of Organometallic Chemistry; vol. 690; nb. 23; (2005); p. 5365 - 5377, View in Reaxys

Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys

Tab. 1, entry 3, prod.

Hunsen, Mo; Journal of Fluorine Chemistry; vol. 126; nb. 9-10; (2005); p. 1356 - 1360, View in Reaxys

product tab. 3, entry Li, Shi-Jun; Wang, Yan-Guang; Tetrahedron Letters; vol. 46; nb. 46; (2005); p. 8013 - 8015, View in Reaxys 7 subst., Tab.2, entry 7

Zeynizadeh, Behzad; Behyar, Tarifen; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 60; nb. 4; (2005); p. 453 - 457, View in Reaxys

unsubst. fluorenone Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol. 75; nb. 2; (2005); p. 272 - 277, View in Reaxys A

Patent; Cephalon, Inc.; US2005/234040; (2005); (A1) English, View in Reaxys

Table 1., substrate 5.

Aceves; Arroyo; Vargas; Miranda; Cabrera; Delgado; Heteroatom Chemistry; vol. 15; nb. 1; (2004); p. 71 - 76, View in Reaxys

2l'

Mohammadpoor-Baltork, Iraj; Memarian, Hamid Reza; Bahrami, Kiumars; Monatshefte fur Chemie; vol. 135; nb. 4; (2004); p. 411 - 418, View in Reaxys

Nicolaou; Mathison, Casey J. N.; Montagnon, Tamsyn; Journal of the American Chemical Society; vol. 126; nb. 16; (2004); p. 5192 - 5201, View in Reaxys

Table 1, entry 10

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

6 (R1 = R2 = H)

Epperson, James R.; Bruce, Marc A.; Catt, John D.; Deskus, Jeffrey A.; Hodges, Donald B.; Karageorge, George N.; Keavy, Daniel J.; Mahle, Cathy D.; Mattson, Ronald J.; Ortiz, Astrid A.; Parker, Michael F.; Takaki, Katherine S.; Watson, Brett T.; Yevich, Joseph P.; Bioorganic and Medicinal Chemistry; vol. 12; nb. 17; (2004); p. 4601 4611, View in Reaxys

11b

Bei, Xiaohong; Hagemeyer, Alfred; Volpe, Anthony; Saxton, Robert; Turner, Howard; Guram, Anil S.; Journal of Organic Chemistry; vol. 69; nb. 25; (2004); p. 8626 - 8633, View in Reaxys

C6H4COC6H4

Zheng, Guorong; Li, Wei; Wang, Zixing; Lu, Ping; Australian Journal of Chemistry; vol. 57; nb. 8; (2004); p. 811 814, View in Reaxys

6h; 9b

Tanaka, Hirotaka; Hashimoto, Kentaro; Suzuki, Kyosuke; Kitaichi, Yasunori; Sato, Mitsuo; Ikeno, Taketo; Yamada, Tohru; Bulletin of the Chemical Society of Japan; vol. 77; nb. 10; (2004); p. 1905 - 1914, View in Reaxys

subs., Tab. 2, entry 4

Zeynizadeh, Behzad; Yahyaei, Saiedeh; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 59; nb. 6; (2004); p. 704 - 710, View in Reaxys

Product, Tab.2, run 5

Moorthy, Jarugu Narasimha; Singhal, Nidhi; Venkatakrishnan; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5419 - 5424, View in Reaxys

9-fluorenyl-C=O

Blake, Jessie A.; Ingold, Keith U.; Lin, Shuqiong; Mulder, Peter; Pratt, Derek A.; Sheeller, Brad; Walton, John C.; Organic and Biomolecular Chemistry; vol. 2; nb. 3; (2004); p. 415 - 420, View in Reaxys

Tab. 1, entry 1

Guram, Anil; Hagemeyer, Alfred; Lugmair, Claus G.; Turner, Howard W.; Volpe Jr., Anthony F.; Weinberg, W. Henry; Yaccato, Karin; Advanced Synthesis and Catalysis; vol. 346; nb. 2-3; (2004); p. 215 - 230, View in Reaxys

Tab.1. product

Kawabata, Hirotoshi; Hayashi, Masahiko; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5457 - 5459, View in Reaxys

11/144

2018-06-21 20:37:19

Hajipour, Abdol R.; Mallakpour, Shadpour E.; Mohammadpoor-Baltork, Iraj; Adibi, Hadi; Monatshefte fur Chemie; vol. 134; nb. 1; (2003); p. 45 - 49, View in Reaxys

Product, Tab.1, run 37

Mohammadpoor-Baltork, Iraj; Khodaei, Mohammad Mehdi; Nikoofar, Kobra; Tetrahedron Letters; vol. 44; nb. 3; (2003); p. 591 - 594, View in Reaxys

product, tab 2, e 4

Das, Sasmita; Panigrahi; Maikap, Golak C.; Tetrahedron Letters; vol. 44; nb. 7; (2003); p. 1375 - 1377, View in Reaxys

9-F

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Tab2.run3

Jablonski, Lukas; Billard, Thierry; Langlois, Bernard R.; Tetrahedron Letters; vol. 44; nb. 5; (2003); p. 1055 - 1057, View in Reaxys

FLU

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Pierres, Camille; George, Pascal; Van Hijfte, Luc; Ducep, Jean-Bernard; Hibert, Marcel; Mann, Andre; Tetrahedron Letters; vol. 44; nb. 18; (2003); p. 3645 - 3647, View in Reaxys

T. 2., prod. 7

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

Nair, Vijay; Bindu; Sreekumar; Balagopal, Lakshmi; Synthesis; nb. 9; (2003); p. 1446 - 1456, View in Reaxys

Tab.2, prod., entry 7

Kim, Sung Soo; Kim, Dong Won; Synlett; nb. 10; (2003); p. 1391 - 1394, View in Reaxys

Product, Tab.2, run 4

Jurado-Gonzalez, Magdalena; Sullivan, Alice C.; Wilson, John R. H.; Tetrahedron Letters; vol. 44; nb. 22; (2003); p. 4283 - 4286, View in Reaxys

Zhang, Baolian; Zhu, Xiao-Qing; Lu, Jin-Yong; He, Jiaqi; Wang, Peng G.; Cheng, Jin-Pei; Journal of Organic Chemistry; vol. 68; nb. 8; (2003); p. 3295 - 3298, View in Reaxys

Jacques; Allonas; Sarbach; Haselbach; Vauthey; Chemical Physics Letters; vol. 378; nb. 1-2; (2003); p. 185 - 191, View in Reaxys; Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys

T. 2-10, product

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

Korotchenko; Shastin; Nenaidenko; Balenkova; Russian Chemical Bulletin; vol. 52; nb. 2; (2003); p. 492 - 497, View in Reaxys

Bertini, Vincenzo; Lucchesini, Francesco; Pocci, Marco; Alfei, Silvana; De Munno, Angela; Synlett; nb. 8; (2003); p. 1201 - 1203, View in Reaxys

subst., Tab.2, entry 4

Zeynizadeh, Behzad; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 58; nb. 12; (2003); p. 1220 - 1226, View in Reaxys

25c

Kauffman, Joel M.; Moyna, Guillermo; Journal of Organic Chemistry; vol. 68; nb. 3; (2003); p. 839 - 853, View in Reaxys

Hanson, Peter; Rowell, Simon C.; Taylor, Alec B.; Walton, Paul H.; Timms, Allan W.; Journal of the Chemical Society. Perkin Transactions 2; nb. 6; (2002); p. 1126 - 1134, View in Reaxys; Yang, Yonghong; Petersen, Jeffrey L.; Wang, Kung K.; Journal of Organic Chemistry; vol. 68; nb. 22; (2003); p. 8545 - 8549, View in Reaxys

FLUO

Lund, Torben; Christensen, Peter; Wilbrandt, Robert; Organic and Biomolecular Chemistry; vol. 1; nb. 6; (2003); p. 1020 - 1025, View in Reaxys

educt to 5b-5d

Vougioukalakis, Georgios C.; Orfanopoulos, Michael; Tetrahedron Letters; vol. 44; nb. 48; (2003); p. 8649 - 8652, View in Reaxys

Hajipour; Mallakpour; Mohammadpoor-Baltork; Khoee; Synthetic Communications; vol. 31; nb. 8; (2001); p. 1187 - 1194, View in Reaxys; Hajipour; Mallakpour; Khoee; Synthetic Communications; vol. 32; nb. 1; (2002); p. 9 - 15, View in Reaxys

t.2, ketone, entry 7

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

Table 2, E1, Product

Hashimoto, Kentaro; Tanaka, Hirotaka; Ikeno, Taketo; Yamada, Tohru; Chemistry Letters; nb. 6; (2002); p. 582 583, View in Reaxys

prod., Table 2./2

Matsuo, Jun-ichi; Kawana, Asahi; Pudhom, Khanitha; Mukaiyama, Teruaki; Chemistry Letters; nb. 2; (2002); p. 250 - 251, View in Reaxys

13d

Giurg; Wojtowicz; Mlochowski; Polish Journal of Chemistry; vol. 76; nb. 4; (2002); p. 537 - 542, View in Reaxys

Prashad, Mahavir; Liu, Yugang; Mak, Xiao Yin; Har, Denis; Repic, Oljan; Blacklock, Thomas J.; Tetrahedron Letters; vol. 43; nb. 47; (2002); p. 8559 - 8562, View in Reaxys

12/144

2018-06-21 20:37:19

tab. 1, entry 18, prod.

Bisai, Alakesh; Chandrasekhar; Singh, Vinod K.; Tetrahedron Letters; vol. 43; nb. 46; (2002); p. 8355 - 8357, View in Reaxys

Product, Tab.2, run 20

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

product, T1, E12

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

16a

Weber, Edwin; Nitsche, Silke; Wierig, Andreas; Csoeregh, Ingeborg; European Journal of Organic Chemistry; nb. 5; (2002); p. 856 - 872, View in Reaxys

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

11a

De Lijser, H. J. Peter; Fardoun, Fadia H.; Sawyer, Jody R.; Quant, Michelle; Organic Letters; vol. 4; nb. 14; (2002); p. 2325 - 2328, View in Reaxys

Fl=O

Larsen, Anna S.; Wang, Kun; Lockwood, Mark A.; Rice, Gordon L.; Won, Tae-Jin; Lovell, Scott; Sadilek, Martin; Turecek, Frantisek; Mayer, James M.; Journal of the American Chemical Society; vol. 124; nb. 34; (2002); p. 10112 - 10123, View in Reaxys

(E)

Patent; Symyx Technologies, Inc.; US6350916; (2002); (B1) English, View in Reaxys

Miyashita, Kazuyuki; Minagawa, Masatoshi; Ueda, Yohko; Tada, Yukie; Hoshino, Nobuhiro; Imanishi, Takeshi; Tetrahedron; vol. 57; nb. 16; (2001); p. 3361 - 3367, View in Reaxys

educt of 2b

Billard, Thierry; Langlois, Bernard R.; Blond, Gaelle; European Journal of Organic Chemistry; nb. 8; (2001); p. 1467 - 1471, View in Reaxys

FLone

Sabate; Bayona; Solanas; Chemosphere; vol. 44; nb. 2; (2001); p. 119 - 124, View in Reaxys

product, Tab 2, entry 7

Hashimoto, Kentaro; Kitaichi, Yasunori; Tanaka, Hirotaka; Ikeno, Taketo; Yamada, Tohru; Chemistry Letters; nb. 9; (2001); p. 922 - 923, View in Reaxys

T.1. ketone 19

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

9c (tab VI)

Hajipour; Mallakpour; Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals; vol. 356; (2001); p. 371 - 387, View in Reaxys

Robarge; Husbands; Kieltyka; Brodbeck; Thurkauf; Newman; Journal of Medicinal Chemistry; vol. 44; nb. 19; (2001); p. 3175 - 3186, View in Reaxys

9-Fl-one

Garon; Krivobok; Seigle-Murandi; Chemosphere; vol. 40; nb. 1; (2000); p. 91 - 97, View in Reaxys

run 5, electrophile

O'Neil, Ian A.; Wynn, Duncan; Lai, Justine Y. Q.; Tetrahedron Letters; vol. 41; nb. 2; (2000); p. 271 - 274, View in Reaxys

educt comp. to 11

Liu, Kwang-Ting; Chang, Chih-Wei; Chen, Hung-I.; Chin, Chien-Pu; Duann, Yen-Fang; Journal of Physical Organic Chemistry; vol. 13; nb. 4; (2000); p. 203 - 207, View in Reaxys

9FL

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys

Tab.1. col. 1. run 1

Hicks; Han; Fry; Tetrahedron Letters; vol. 41; nb. 41; (2000); p. 7817 - 7820, View in Reaxys

Chaikovski; Filimonov; Yagovkin; Kharlova; Tetrahedron Letters; vol. 41; nb. 47; (2000); p. 9101 - 9104, View in Reaxys

product 1 (fig. 7.)

Nuechter, Matthias; Ondruschka, Bernd; Jungnickel, Anja; Mueller, Ute; Journal of Physical Organic Chemistry; vol. 13; nb. 10; (2000); p. 579 - 586, View in Reaxys

Large; Roques; Langlois; Journal of Organic Chemistry; vol. 65; nb. 26; (2000); p. 8848 - 8856, View in Reaxys

substrate for 4b

Billard; Bruns; Langlois; Organic Letters; vol. 2; nb. 14; (2000); p. 2101 - 2103, View in Reaxys

Table 2 Entry 4 Prod.

Matsunaka, Katsuhisa; Iwahama, Takahiro; Sakaguchi, Satoshi; Ishii, Yasutaka; Tetrahedron Letters; vol. 40; nb. 11; (1999); p. 2165 - 2168, View in Reaxys

precursor of 2i

Mloston, Grzegorz; Romanski, Jaroslaw; Swiatek, Anna; Heimgartner, Heinz; Helvetica Chimica Acta; vol. 82; nb. 6; (1999); p. 946 - 956, View in Reaxys

3c (Tab. 2)

Hajipour, Abdol Reza; Mohammadpoor-Baltork, Iraj; Niknam, Kurosh; Organic Preparations and Procedures International; vol. 31; nb. 3; (1999); p. 335 - 341, View in Reaxys

Table 3, entry 6

Yamazaki, Shigekazu; Organic Letters; vol. 1; nb. 13; (1999); p. 2129 - 2132, View in Reaxys

Table 3, Entry 10

Mohammadpoor-Baltork, Iraj; Hajipour, Abdol Reza; Mohammadi, Hasan; Bulletin of the Chemical Society of Japan; vol. 71; nb. 7; (1998); p. 1649 - 1653, View in Reaxys

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starting to int. to 1

Henkel, Bernd; Bayer, Ernst; Tetrahedron Letters; vol. 39; nb. 51; (1998); p. 9401 - 9402, View in Reaxys

Hajipour, Abdol Reza; Baltork, Iraj Mohammadpoor; Kianfar, Godaraz; Bulletin of the Chemical Society of Japan; vol. 71; nb. 11; (1998); p. 2655 - 2659, View in Reaxys

Banciu, Mircea D.; Draghici, Constantin; Popescu, Angela; Banciu, Anca; Simion, Alina; Revue Roumaine de Chimie; vol. 43; nb. 7; (1998); p. 649 - 660, View in Reaxys

entry 31, prod.

Baltork, I. Mohammadpoor; Sadeghi, M. M.; Mahmoodi, N.; Kharamesh, B.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 36; nb. 5; (1997); p. 438 - 441, View in Reaxys

IIIa

Soldatenkov; Kolyadina; Kuleshova; Khrustalev; Chemistry of Heterocyclic Compounds; vol. 32; nb. 7; (1996); p. 817 - 821, View in Reaxys

124

Paxeus, Nicklas; Water Research; vol. 30; nb. 5; (1996); p. 1115 - 1122, View in Reaxys

Table 4; 37

Fobe, Bart O.; Vleugels, Greta J.; Roekens, Eddy J.; Grieken, Rene E. Van; Hermosin, Bernardo; et al.; Environmental Science & Technology; vol. 29; nb. 6; (1995); p. 1691 - 1701, View in Reaxys

Patent-Specific Data (9) Prophetic ComLocation in Patent pound

References Patent; NAGOYA INSTITUTE OF TECHNOLOGY; TOSOH F-TECH INCORPORATED; SHIBATA, NORIO; OKUSU, SATOSHI; KAGAWA, TAKUMI; (15 pag.); JP2016/204276; (2016); (A) Japanese, View in Reaxys Patent; TAOKA CHEMICAL COMPANY LIMITED; MATSUBARA, MASAAKI; KAWAMURA, YOSHINORI; FUJII, KATSUHIRO; (14 pag.); JP2016/3220; (2016); (A) Japanese, View in Reaxys Patent; Osaka Gas Chemical Co., Ltd.; Nishiyama, Yutaro; Kuratani, Yuji; Miyauchi, Shinsuke; (9 pag.); JP2016/196445; (2016); (A) Japanese, View in Reaxys

Page/Page column

Patent; Dickmeis, Marcus; Cinar, Hakan; Ritter, Helmut; US2013/18140; (2013); (A1) English, View in Reaxys; Patent; Martineau, Louis C.; US2014/135359; (2014); (A1) English, View in Reaxys; Patent; SOLVAY (SOCIETE ANONYME); Bascour, Dominique; Catinat, Jean-Pierre; US9076971; (2015); (B2) English, View in Reaxys Patent; CIBA HOLDING INC.; WO2009/47151; (2009); (A1) English, View in Reaxys Patent; Symyx Technologies, Inc.; US6350916; (2002); (B1) English, View in Reaxys Patent; Board of Regents, The University of Texas System; US6362200; (2002); (B1) English, View in Reaxys

prophetic product

Claim

prophetic product

Patent; Rhone-Poulenc Chimie; US5414153; (1995); (A) English, View in Reaxys; Patent; Rhone-Poulenc Chimie; US5434317; (1995); (A) English, View in Reaxys Patent; Hitachi Chemical Company, Ltd.; US5352834; (1994); (A) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

3.494

H Bond Donors

H Bond Acceptors

Rotatable Bonds

TPSA

17.07

Lipinski Number

Veber Number

Related Structure (1) Related Structure References Die frueher von Hey et al.; Journal of the Chemical Society; (1962); p. 4579,4581, View in Reaxys Finzi, Bellavita (s. E III 2331) unter dieser Konstitution beschriebene Verbindung ist als Benzo<#c!>chromen-6on zu formulieren. Derivative (71)

14/144

2018-06-21 20:37:19

Comment (Derivative)

Derivative

References

fluorenone-2,4-dinitrophenylhydrazone

Kuselan, P.; Venkatasubramanian, N.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 21; nb. 12; (1982); p. 1095 - 1097, View in Reaxys; Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 84.5grad

Olah et al.; Synthesis; (1979); p. 274, View in Reaxys

BCl3-Komplex: Abs.-Sp. (Fig. 3); Fluoreszenz (Fig. 4)

Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys

2,4-Dinitrophenylhydrazon; mp: 240grad

Olah,G.A.; Welch,J.; Journal of the American Chemical Society; vol. 100; (1978); p. 5396 5402, View in Reaxys

2,4-Dinitrophenylhydrazin: F: 285-287grad

Wittig; Schoch-Gruebler; Justus Liebigs Annalen der Chemie; (1978); p. 362,364,365,368, View in Reaxys

Hydrazon: Kinetik d. Wolff-KishnerReaktion, ΔH(excit.), ΔS(excit.)

Szmant; Alciaturi; Journal of Organic Chemistry; vol. 42; (1977); p. 1081, View in Reaxys

2,4-Dinitrophenylhydrazon: F:276-278grad(Zers .)

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 559 - 570, View in Reaxys

2,4-Dinitrophenylhydrazon: F:281-283grad(Zers .); F:291grad(Zers.)

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Oxim (Tab. 1)

Terent'eva; Petrenko; J. Anal. Chem. USSR (Engl. Transl.); vol. 31; (1976); p. 2452,1805, View in Reaxys

Komplex mi Phenol: Gleichgew.konst., IR (HBruecken)

Bostwick et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 1505,1506, 1508, View in Reaxys

39K-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

23Na-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

85Rb-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

87Rb-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

133Cs-Fl, 1/T(2)

Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys

Prot. Form: Abs. Sp. (Fig. 1); SCFCl-Lad.-Dichte (Fig. 3)

Filipescu et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 2276, View in Reaxys

Lu-Komplexes: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Eu-FluorenonKomplex: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Yb-FluorenonKomplex: NMR

Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys

Oxim: F: 194-195grad (Bzl.)

Troszkiewicz et al.; Roczniki Chemii; vol. 46; (1972); p. 399,403, 404, View in Reaxys

15/144

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2,4-Dinitrophenylhydrazon: F.: 284grad

Saxena; Kulshreshtha; Journal of the Indian Chemical Society; vol. 48; (1971); p. 137, View in Reaxys

Thiosemicarbazon, F: 172grad, aus Alkohol

Taha; Hassan; Journal of Chemistry of the United Arab Republic; vol. 14; (1971); p. 531, View in Reaxys

bei der Bildung entsteht bei laengerer Reaktionszeit ein DMSO-Addukt (X)

Rawson; Wynberg; Recueil des Travaux Chimiques des Pays-Bas; vol. 90; (1971); p. 39,43, 44, View in Reaxys

Na2(Fl)2

Norris; Weissman; Journal of Physical Chemistry; vol. 73; (1969); p. 3119, View in Reaxys

Na+ <C13H7O>- : 23Na-NMR

Canters et al.; Chemical Physics Letters; vol. 1; (1968); p. 627, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 282-284grad

Peddle; Ward; Journal of Organometallic Chemistry; vol. 14; (1968); p. 131,136, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 305grad

Rappoport,Z.; Sheradsky,T.; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 898 - 903, View in Reaxys

Fluorenonkalium: Temp.-Abhaengigk. der 13C-Aufspalt. des ESR-Spektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Fluorenonlithium: Temp.-Abhaengigk. der Li- u. 13C-Aufspalt. des ESRSpektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Fluorenoncaesium: Temp.-Abhaengigk. der Cs- u. der 13CAufspalt. des ESRSpektrums

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

K-Ketyl: Temp.-abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -70 - +60grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

Li-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -60 - +30grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

Fluorenonnatrium: ESR-Spektrum in 1,2-Dimethoxyethan u. in DMF (Temp.-Abhaengigk. der Na- u. 13C-Aufspalt.)

Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys

Cs-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in THF, -60 - +50grad, in 1,2-

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

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Dimethoxy-ethan, -90 - +50grad Na-Ketyl: Temp.abhaengigkeit der 13C-Aufspaltung (der Carbonylgruppe) in 1,2-Dimethoxy-ethan, -90 - +30grad, in THF, -60 - +20grad, in DMF -15 - +75grad

Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 282-283grad, orange

Chiba; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 1289,1292, View in Reaxys

Ketylradikal: B: elektrochem. Red. (nult-ionischer, semi-ionischer u. ionischer Rk.mechanismus), 38percentig. wss. A., 23grad; Dimerisierungskonst.; 929

Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys

Ketylradikal: B: elektrochem. Red. (nult-ionischer, semi-ionischer u. ionischer Rk.mechanismus), 38percentig. wss. A., 23grad; Geschwindigkeitskonst., Disproportionierung

Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys

Oxidations sowie Redox-Potential des bei der elektrochem. Red. gebildeten Ketylradikals (920): Geschwindigkeitskonst. der Dimerisierung des Ketyl-Radikals (921); Dissoziationsexponent pK (922)

Kalinowski et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 918, View in Reaxys

Ba-Verb.: Abs.Max. (in THF)

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Ca-Verb.: Abs.Max. (in THF); S.2539

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Mg-Verb.: Abs.Max. (in THF); S.2539

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Phenylhydrazon: F: 146 - 149grad

Nickon,A.; Hill,A.S.; Journal of the American Chemical Society; vol. 86; (1964); p. 1152 - 1159, View in Reaxys

Fluorenonketyle s. Syst. Nr. 540

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Radikalanion: ESRSpektrum des Radikal-Anions in Mischungen von Me. u.

Luckhurst; Orgel; Molecular Physics; vol. 8; (1964); p. 117,118, View in Reaxys

17/144

2018-06-21 20:37:19

N,N-Dimethyl-formamid Na-Verb.: Abs.Max. (in THF); Abs.-Sp. (in Me/ THF, THF, DME, bzw. Toluol) (S.2540, 2541); ESR-Sp. (in Me/ THF) (S.2541)

Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys

Radikal-Anion: ESR-Spektrum u. Daten

Dehl; Fraenkel; Journal of Chemical Physics; vol. 39; (1963); p. 1793, View in Reaxys

CT-Komlex m. 1 Ba: Abs.-Max. i. Lsg. (Dioxan)

Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys

CT-Komlex m. 1/2 Ba: Abs.-Max. i. Lsg. (Dioxan)

Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys

Kalium-Verb. C13H8*K: Elektronen paramangn. Resonaz. in THF

Kasakowa; Syrkin; Journal of Structural Chemistry; vol. 3; (1962); p. 518; Zhurnal Strukturnoi Khimii; vol. 3; (1962); p. 536, View in Reaxys

Zur RadikalanionB. i. Ggw. v. Fluorenol-(9) (1:), Ktert-butylat in tertButanol, Dimethylsulfoxid

Russel et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4155,4156, View in Reaxys

Kalium-Verb.: Spin-Spin-Aufspaltung d. paramagnet. Elektronenresonanz; B. v. Dimeren in 2-Methyl-tetrahydrofuran

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Lithium-Verb.: ESR-p. (2-Methyltetrahydrofuran bei 77K); Spin-SpinAufspaltung d. paramagnet. Elektronenresonanz; B. v. Dimeren (in 2Methyl-tetrahydrofuran)

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Natrium-Verb.: Abs.max. (2-Methyl-tetrahydrofuran bei 300K): 5200 A; Spin-Spin-Aufspaltung d. paramagnet. Elektronenresonanz; B. eines Dimeren (Abs.Max.: 4550 A)

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Phenylhydrazon: C20H14N2O4

Kuhn et al.; Chemische Berichte; vol. 94; (1961); p. 2252,2257, View in Reaxys

Komplex m. 1 K (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 K (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

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Komplex m. 1 Li (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 1 Na (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 Li (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. 2 Na (Dioxan): UV-Max.

Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys

Komplex m. Na (Dioxan): Kinetik der Rk. m. Methyliodid, 12 - 40grad

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Komplex m. Na (in Dioxan): Kinetik der Rk. m. Methyliodid; Kinetik der Rk. m. Propylbromid

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2-diphenylacetyl-3oxo-indan-1-ylidenehydrazone (mp: 282-283 degree )

Braun; Mosher; Journal of the American Chemical Society; vol. 80; (1958); p. 3048, View in Reaxys

4-nitro-phenylhydrazone (mp: 143-144 degree )

de Toma; Gazzetta Chimica Italiana; vol. 82; (1952); p. 40,44, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 302 degree )

Cavill; Robertson; Whalley; Journal of the Chemical Society; (1949); p. 1567,1570, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 299-301 degree )

Campbell; Wang; Journal of the Chemical Society; (1949); p. 2186, View in Reaxys

phenylhydrazone (mp: 151-152 degree )

Oliveri-Mandala; Deleo; Gazzetta Chimica Italiana; vol. 70; (1940); p. 186,189, View in Reaxys; Wislicenus; Densch; Chemische Berichte; vol. 35; (1902); p. 761, View in Reaxys; Wislicenus; Russ; Chemische Berichte; vol. 43; (1910); p. 2729, View in Reaxys

p-nitro-phenylhydrazone (mp: 269 degree )

Schmidt,J.; Wagner; Chemische Berichte; vol. 43; (1910); p. 1800; Justus Liebigs Annalen der Chemie; vol. 387; (1912); p. 159, View in Reaxys

compound of fluorenone with 9oxy-9-p-diphenylyl-fluorene (mp: 123 degree , light yellow octahedrons); Further Data see Handbook (Preparation)

Schlenk; Herzenstein; Justus Liebigs Annalen der Chemie; vol. 372; (1910); p. 30, View in Reaxys

phenylhydrazone (mp: 151-151,5 degree )

Goldschmiedt; Schranzhofer; Monatshefte fuer Chemie; vol. 16; (1895); p. 812, View in Reaxys

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Melting Point [°C]

83 - 84

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Melting Point [°C]

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Melting Point [°C]

85 - 87

Location

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 6 of 96

Melting Point [°C]

79 - 80

Location

supporting information

Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys; Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 7 of 96

Melting Point [°C]

81 - 83

Location

supporting information

Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys 8 of 96

Melting Point [°C]

82 - 83

Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys 9 of 96

Melting Point [°C]

83 - 85

Location

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Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys 10 of 96

Melting Point [°C]

80 - 81

Location

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p. 4952 - 4961, View in Reaxys 11 of 96

Melting Point [°C]

Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys 12 of 96

Melting Point [°C]

79 - 81

Shaabani, Ahmad; Shaabani, Shabnam; Afaridoun, Hadi; RSC Advances; vol. 6; nb. 54; (2016); p. 48396 - 48404, View in Reaxys 13 of 96

Melting Point [°C]

84 - 85

Location

supporting information

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Melting Point [°C]

80 - 83

Location

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Melting Point [°C]

83 - 84

Location

Paragraph 0037; 0039; 0041; 0043

Patent; Zhongwei Lianjiao Technology National Engineering Research Center Co.,Ltd; Wang, Guang Xing; Wang, Shou Kai; Li, Qiang; CAI, Hong Tao; Jin, Dan; Wang, LiLi; (6 pag.); CN104230690; (2016); (B) Chinese, View in Reaxys 16 of 96

Melting Point [°C]

82 - 84

Location

Paragraph 0045; 0047

Melting Point [°C]

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys; Diehl, Fabrice; Barbier, Jacques; Duprez, Daniel; Guibard, Isabelle; Mabilon, Gil; Applied Catalysis A: General; vol. 504; (2015); p. 37 - 43, View in Reaxys 18 of 96

Melting Point [°C]

82 - 83

Location

supporting information

Wei, Peng; Zhang, Datong; Gao, Zhigang; Cai, Wenqing; Xu, Weiren; Tang, Lida; Zhao, Guilong; Synthetic Communications; vol. 45; nb. 12; (2015); p. 1457 - 1470, View in Reaxys 19 of 96

Melting Point [°C]

83 - 84

Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys 20 of 96

Melting Point [°C]

82 - 84

Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys; Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 21 of 96

Melting Point [°C]

80 - 82

Saluja, Pooja; Magoo, Devanshi; Khurana, Jitender M.; Synthetic Communications; vol. 44; nb. 6; (2014); p. 800 - 806, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 22 of 96

Melting Point [°C]

81 - 83

Location

supporting information

Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 3219, View in Reaxys 23 of 96

Melting Point [°C]

81 - 83

Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7220 - 7225, View in Reaxys 24 of 96

Melting Point [°C]

80 - 83

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 25 of 96

Melting Point [°C]

81 - 82

Location

supporting information

Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys 26 of 96

Melting Point [°C]

84 - 86

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 27 of 96

Melting Point [°C]

79 - 80

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

21/144

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28 of 96

Melting Point [°C]

82 - 84

Khurana, Jitender M.; Chaudhary, Ankita; Kumar, Sanjay; Organic Preparations and Procedures International; vol. 45; nb. 3; (2013); p. 241 - 245, View in Reaxys 29 of 96

Melting Point [°C]

Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys 30 of 96

Melting Point [°C]

82 - 84

Location

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 31 of 96

Melting Point [°C]

83 - 85

Li, Dan-Dan; Yuan, Ting-Ting; Wang, Guan-Wu; Journal of Organic Chemistry; vol. 77; nb. 7; (2012); p. 3341 - 3347, View in Reaxys 32 of 96

Melting Point [°C]

83 - 84

Bahrami, Kiumars; Khodaei, Mohammad M.; Shakibaian, Vida; Khaledian, Donya; Yousefi, Behrooz H.; Journal of Sulfur Chemistry; vol. 33; nb. 2; (2012); p. 155 - 163, View in Reaxys 33 of 96

Melting Point [°C]

79 - 80

Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 34 of 96

Melting Point [°C]

82 - 83

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 35 of 96

Melting Point [°C]

75 - 77

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; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys 36 of 96

Melting Point [°C]

84 - 86

Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys 37 of 96

Melting Point [°C]

78 - 80

Location

supporting information

Cosner, Casey C.; Cabrera, Pablo J.; Byrd, Katherine M.; Adams Thomas, Asia M.; Helquist, Paul; Organic Letters; vol. 13; nb. 8; (2011); p. 2071 - 2073, View in Reaxys 38 of 96

Melting Point [°C]

74.5 - 76.3

Location

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys 39 of 96

Melting Point [°C]

83 - 85

Solvent (Melting Point)

ethanol

Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys 40 of 96

Melting Point [°C]

75 - 77

Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, Xiao-Feng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys

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2018-06-21 20:37:19

41 of 96

Melting Point [°C]

80 - 82

Location

supporting information

Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys 42 of 96

Melting Point [°C]

81 - 82

Solvent (Melting Point)

dichloromethane; hexane

Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 43 of 96

Melting Point [°C]

83 - 84

Location

supporting information

Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 44 of 96

Melting Point [°C]

Bahrami, Kiumars; Khodaei, Mohammad M.; Farrokhi, Azita; Tetrahedron; vol. 65; nb. 36; (2009); p. 7658 - 7661, View in Reaxys; Bahrami, Kiumars; Khodaei, Mohammad Mehdi; Tajik, Maryam; Synthesis; nb. 24; (2010); p. 4282 4286; Art.No: Z21310SS, View in Reaxys 45 of 96

Melting Point [°C]

82 - 83

Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb. 3; (2009); p. 312 - 315, View in Reaxys 46 of 96

Melting Point [°C]

81 - 83

Hajipour, Abdol R.; Safaei, Somayeh; Ruoho, Arnold E.; Synthetic Communications; vol. 39; nb. 20; (2009); p. 3687 - 3692, View in Reaxys 47 of 96

Melting Point [°C]

Habibzadeh, Setareh; Tajbakhsh, Mahmood; Journal of Chemical Research; nb. 11; (2009); p. 696 - 698, View in Reaxys 48 of 96

Melting Point [°C]

80 - 81

Shaabani, Ahmad; Farhangi, Elham; Rahmati, Abbas; Monatshefte fur Chemie; vol. 139; nb. 8; (2008); p. 905 - 908, View in Reaxys 49 of 96

Melting Point [°C]

Batterbee; Bailey; Journal of Organic Chemistry; vol. 32; (1967); p. 3899,3902, View in Reaxys; Davies; Waring; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2332, View in Reaxys; Oae, Shigeru; Inubushi, Yoichi; Yoshihara, Masakuni; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 103; nb. 1-4; (1995); p. 101 - 110, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys 50 of 96

Melting Point [°C]

82 - 83

Melting Point [°C]

82 - 84

Solvent (Melting Point)

methanol

Patent; Humanetics Corporation; US6384251; (2002); (B1) English, View in Reaxys 52 of 96

Melting Point [°C]

Solvent (Melting Point)

ethanol

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys; Schank, Kurt; Beck, Horst; Buschlinger, Michael; Eder, Joerg; Heisel, Thomas; Pistorius, Susanne; Wagner, Christiane; Helvetica Chimica Acta; vol. 83; nb. 4; (2000); p. 801 - 826, View in Reaxys 53 of 96

Melting Point [°C]

82 - 84

Solvent (Melting Point)

hexane

Mirafzal, Gholam A.; Lozeva, Albena M.; Tetrahedron Letters; vol. 39; nb. 40; (1998); p. 7263 - 7266, View in Reaxys 54 of 96

Melting Point [°C]

83 - 85

23/144

2018-06-21 20:37:19

Abramovitch; Robson; Journal of the Chemical Society [Section] C: Organic; (1967); p. 1101, View in Reaxys; Nicolaides, Demetrios N.; Awad, R. Wajih; Papageorgiou, Georgios K.; Kojanni, Efthalia; Tsoleridis, Constantinos A.; Journal of Heterocyclic Chemistry; vol. 34; nb. 6; (1997); p. 1651 - 1656, View in Reaxys 55 of 96

Melting Point [°C]

78 - 79

Sanabria, R.; Castaneda, P.; Miranda, R.; Tobon, A.; Delgado, F.; Velasco, L.; Organic Preparations and Procedures International; vol. 27; nb. 4; (1995); p. 480 - 482, View in Reaxys 56 of 96

Melting Point [°C]

76 - 80

Braven, J.; Hanson, R. W.; Smith, N. G.; Journal of Heterocyclic Chemistry; vol. 32; nb. 3; (1995); p. 1051 - 1056, View in Reaxys 57 of 96

Melting Point [°C]

Comment (Melting Point)

Method: distilled sample

Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys 58 of 96

Melting Point [°C]

Abdou, Wafaa M.; Elkhoshnieh, Yehia O.; Sidky, Mahmoud M.; Tetrahedron; vol. 50; nb. 11; (1994); p. 3595 - 3602, View in Reaxys 59 of 96

Melting Point [°C]

83.5 - 84

Solvent (Melting Point)

cyclohexane

Brown, Eric; Leze, Antoine; Touet, Joel; Tetrahedron Letters; vol. 32; nb. 34; (1991); p. 4309 - 4310, View in Reaxys 60 of 96

Melting Point [°C]

83 - 84

Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Brown,P.M. et al.; Journal of the Chemical Society [Section] C: Organic; (1968); p. 842 - 848, View in Reaxys; Battaglia,A. et al.; Synthesis; (1971); p. 378 - 379, View in Reaxys; Fridman,A.L. et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 1126 - 1128,1154 1156, View in Reaxys; Fridman,A.L. et al.; Zhurnal Organicheskoi Khimii; vol. 8; nb. 12; (1972); p. 2457 - 2462,2505 - 2509, View in Reaxys; Stobbe; Chemische Berichte; vol. 44; (1911); p. 1481, View in Reaxys; Soboleva et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1787,1799,1800,1801, View in Reaxys; Futami; Hishino; Kurosawa; Bulletin of the Chemical Society of Japan; vol. 62; nb. 11; (1989); p. 3567 - 3571, View in Reaxys 61 of 96

Melting Point [°C]

77 - 79

Suzuki,K. et al.; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 2217 - 2222, View in Reaxys; Hendrickson, James B.; Hussoin, Md. Sajjat; Journal of Organic Chemistry; vol. 54; nb. 5; (1989); p. 1144 - 1149, View in Reaxys 62 of 96

Melting Point [°C]

78 - 82

Solvent (Melting Point)

hexane; toluene

Rich, Jonathan D.; Journal of the American Chemical Society; vol. 111; nb. 15; (1989); p. 5886 - 5893, View in Reaxys 63 of 96

Melting Point [°C]

80 - 81

Minabe,M. et al.; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1614 - 1619, View in Reaxys; DiBiase,S.A. et al.; Journal of Organic Chemistry; vol. 44; nb. 25; (1979); p. 4640 - 4649, View in Reaxys; Otsuka et al.; Justus Liebigs Annalen der Chemie; (1975); p. 626,635, View in Reaxys; Anjaneyulu, P. S. R.; Lala, Anil K.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 23; nb. 9; (1984); p. 802 - 807, View in Reaxys; Chidambaram, Nallaperumal; Chandrasekaran, Srinivasan; Journal of Organic Chemistry; vol. 52; nb. 22; (1987); p. 5048 - 5051, View in Reaxys 64 of 96

Melting Point [°C]

81 - 83

Ratusky; Collection of Czechoslovak Chemical Communications; vol. 37; (1972); p. 2436,2448, View in Reaxys; Tamarkin, Dov; Rabinovitz, Mordecai; Journal of Organic Chemistry; vol. 52; nb. 15; (1987); p. 3472 - 3474, View in Reaxys 65 of 96

Melting Point [°C]

75 - 80

Solvent (Melting Point)

petroleum ether; CH2Cl2

Lianis, Pygmalion S.; Rodios, Nestor A.; Alexandrou, Nicholas E.; Liebigs Annalen der Chemie; (1987); p. 537 - 540, View in Reaxys 66 of 96

Melting Point [°C]

Kappe et al.; Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie; vol. 34; (1979); p. 716, View in Reaxys; Cardillo et al.; Synthesis; (1976); p. 394, View in Reaxys; Parsons; Cohen; Journal of the American Chemical Society; vol. 96; (1974); p. 2948,2950,2951, View in Reaxys; Ogata et al.; Journal of Organic Chemistry; vol. 40; (1975); p.

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2018-06-21 20:37:19

615,618, View in Reaxys; Kajigaeshi; Nippon Kagaku Zasshi; vol. 83; (1962); p. 228; Chem.Abstr.; vol. 59; nb. 522; (1963), View in Reaxys; Patent; Simikow et al.; SU449029; (1975); Ref. Zh., Khim.; vol. 7; nb. N354P; (1976), View in Reaxys; Cohen; Parsons; Journal of the American Chemical Society; vol. 92; (1970); p. 7603, View in Reaxys; Sellers; Suschitzky; Journal of the Chemical Society [Section] C: Organic; (1969); p. 2139,2140, 2142, View in Reaxys; Yonemura, Hiroshi; Nishino, Hiroshi; Kurosawa, Kazu; Bulletin of the Chemical Society of Japan; vol. 59; (1986); p. 3153 - 3160, View in Reaxys 67 of 96

Melting Point [°C]

85 - 86

Solvent (Melting Point)

light petroleum

Grant, Richard D.; Pinhey, John T.; Rizzardo, Ezio; Smith, Geoffrey C.; Australian Journal of Chemistry; vol. 38; nb. 10; (1985); p. 1505 - 1519, View in Reaxys 68 of 96

Melting Point [°C]

83 - 84

Solvent (Melting Point)

petroleum ether

Stone, Paul G.; Cohen, Saul G.; Journal of the American Chemical Society; vol. 104; nb. 12; (1982); p. 3435 - 3440, View in Reaxys 69 of 96

Melting Point [°C]

Schoenberg,A.; Praefcke,K.; Chemische Berichte; vol. 99; (1966); p. 205 - 212, View in Reaxys; Fetizon,M. et al.; Tetrahedron; vol. 31; (1975); p. 165 - 170, View in Reaxys; Staudinger; Kon; Justus Liebigs Annalen der Chemie; vol. 384; (1911); p. 88, View in Reaxys; Cohen; Recueil des Travaux Chimiques des Pays-Bas; vol. 38; (1919); p. 121, View in Reaxys; Saxena; Kulshreshtha; Journal of the Indian Chemical Society; vol. 48; (1971); p. 137, View in Reaxys; Pruefcke et al.; Chemische Berichte; vol. 107; (1974); p. 2931,2936, View in Reaxys; Kashin, A. N.; Bumagin, N. A.; Beletskaya, I. P.; Reutov, O. A.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 12; (1980); p. 2190 - 2195; Zhurnal Organicheskoi Khimii; vol. 16; nb. 12; (1980); p. 2561 - 2566, View in Reaxys; Kashin, A. N.; Bumagin, N. A.; Bessonova, M. P.; Beletskaya, I. P.; Reutov, O. A.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 7; (1980); p. 1153 - 1159; Zhurnal Organicheskoi Khimii; vol. 16; nb. 7; (1980); p. 1345 - 1352, View in Reaxys 70 of 96

Melting Point [°C]

80 - 82

Bonini,B.F. et al.; Gazzetta Chimica Italiana; vol. 107; (1977); p. 283 - 288, View in Reaxys; Scretlas; Cazianis; Tetrahedron; vol. 34; (1978); p. 933,935,939, View in Reaxys; Minabe; Suzuki; Journal of Organic Chemistry; vol. 40; (1975); p. 1298,1302, View in Reaxys; Nesmeyanov et al.; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 550,556,557-559, View in Reaxys; Trost; Kinson; Journal of Organic Chemistry; vol. 37; (1972); p. 1273, View in Reaxys; Patrick, Timothy B.; Cantrell, Gary L.; Inga, Sandra M.; Journal of Organic Chemistry; vol. 45; nb. 8; (1980); p. 1409 - 1413, View in Reaxys 71 of 96

Melting Point [°C]

Solvent (Melting Point)

ethanol

Miura, Masahiro; Nojima, Masamoto; Kusabayashi, Shigekazu; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1980); p. 1950 - 1954, View in Reaxys 72 of 96

Melting Point [°C]

82 - 85

Beelitz et al.; Chemiker-Zeitung; vol. 103; (1979); p. 179, View in Reaxys 73 of 96

Melting Point [°C]

81 - 82

Kuo,Y.-N.; Nye,M.J.; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995 - 2000, View in Reaxys; Lynch,E.R.; Journal of the Chemical Society; (1962); p. 3729 - 3733, View in Reaxys; Patent; Schering AG; DE2418503; (1975); Chem.Abstr.; vol. 84; nb. 30929, View in Reaxys; Akermark et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1365, View in Reaxys; Gait et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1974); p. 1248,1257, View in Reaxys; Wade et al.; Journal of Organic Chemistry; vol. 44; (1979); p. 3724, View in Reaxys 74 of 96

Melting Point [°C]

85 - 86

Sieglitz; Chemische Berichte; vol. 57; (1924); p. 317, View in Reaxys; Gukasyan; Shakhnazaryan; Armyanskii Khimicheskii Zhurnal; vol. 31; (1978); p. 711,712; Chem.Abstr.; vol. 90; nb. 87116x, View in Reaxys 75 of 96

Melting Point [°C]

80 - 80.5

Gorman et al.; Journal of Photochemistry; vol. 9; (1978); p. 11,14, View in Reaxys 76 of 96

Melting Point [°C]

82 - 84

Minabe,M. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 3373 - 3376, View in Reaxys; Goerner,R.N. et al.; Journal of Organic Chemistry; vol. 42; nb. 1; (1977); p. 19 - 28, View in Reaxys 77 of 96

Melting Point [°C]

78 - 80

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 571 - 577, View in Reaxys 78 of 96

Melting Point [°C]

72 - 73

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Huisgen et al.; Chemische Berichte; vol. 110; (1977); p. 514,518, View in Reaxys 79 of 96

Melting Point [°C]

75 - 78

Eckell,A.; Huisgen,R.; Chemische Berichte; vol. 110; (1977); p. 559 - 570, View in Reaxys 80 of 96

Melting Point [°C]

82 - 83

Horner,L.; Fernekess,H.; Chemische Berichte; vol. 94; (1961); p. 712 - 724, View in Reaxys; Pagano,A.H.; Shechter,H.; Journal of Organic Chemistry; vol. 35; (1970); p. 295 - 303, View in Reaxys; Wislicenus; Waldmueller; Chemische Berichte; vol. 41; (1908); p. 3338, View in Reaxys; Gokel; Durst; Synthesis; (1976); p. 168,180, View in Reaxys; Rosini et al.; Journal of Organic Chemistry; vol. 39; (1974); p. 3504, View in Reaxys; Huurdeman et al.; Tetrahedron Letters; (1971); p. 3449, View in Reaxys 81 of 96

Melting Point [°C]

Cirigottis,K.A. et al.; Australian Journal of Chemistry; vol. 27; (1974); p. 2209 - 2228, View in Reaxys 82 of 96

Melting Point [°C]

83.2

Tanaka et al.; Nippon Kagaku Kaishi; (1973); p. 126,127-130, View in Reaxys 83 of 96

Melting Point [°C]

82.5

Metz; Synthesis; (1972); p. 612, View in Reaxys 84 of 96

Melting Point [°C]

84 - 85

Rawson; Wynberg; Recueil des Travaux Chimiques des Pays-Bas; vol. 90; (1971); p. 39,43, 44, View in Reaxys 85 of 96

Melting Point [°C]

81.5 - 82.5

Solvent (Melting Point)

benzene; petroleum ether

Yamase et al.; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 162,163, 164; Chem.Abstr.; vol. 70; nb. 95983; (1969), View in Reaxys 86 of 96

Melting Point [°C]

Solvent (Melting Point)

acetic acid

Schoenberg,A.; Praefcke,K.; Chemische Berichte; vol. 99; (1966); p. 205 - 212, View in Reaxys 87 of 96

Melting Point [°C]

82 - 83.5

Chiba; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 1289,1292, View in Reaxys 88 of 96

Melting Point [°C]

84 - 85

Solvent (Melting Point)

hexane

Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys 89 of 96

Melting Point [°C]

83.5 - 84.5

Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys 90 of 96

Melting Point [°C]

81.5

Colonge,J.; Daunis,H.; Bulletin de la Societe Chimique de France; (1961); p. 2238 - 2241, View in Reaxys 91 of 96

Melting Point [°C]

Solvent (Melting Point)

aq. ethanol

Davies; Ennis; Journal of the Chemical Society; (1960); p. 1488,1490, View in Reaxys 92 of 96

Melting Point [°C]

Copeland et al.; Journal of the Chemical Society; (1960); p. 3230,3233, View in Reaxys 93 of 96

Melting Point [°C]

Solvent (Melting Point)

aq. methanol

Jeanes; Adams; Journal of the American Chemical Society; vol. 59; (1937); p. 2608,2619, View in Reaxys 94 of 96

Melting Point [°C]

84 - 86

Schmidt,J.; Wagner; Chemische Berichte; vol. 43; (1910); p. 1800; Justus Liebigs Annalen der Chemie; vol. 387; (1912); p. 159, View in Reaxys

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95 of 96

Solvent (Melting Point)

ethanol

P.Groth, Chemische Krystallographie 5.Teil <Leipzig 1919> S. 429, View in Reaxys; v. Reusch; Justus Liebigs Annalen der Chemie; vol. 193; (1878); p. 118, View in Reaxys; Friedlaender; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 1; (1877); p. 623; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1877); p. 742, View in Reaxys 96 of 96

Melting Point [°C]

83.5 - 84

Fittig; Ostermayer; Justus Liebigs Annalen der Chemie; vol. 166; (1873); p. 363, View in Reaxys Boiling Point (9) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

342

References Diehl, Fabrice; Barbier, Jacques; Duprez, Daniel; Guibard, Isabelle; Mabilon, Gil; Applied Catalysis A: General; vol. 504; (2015); p. 37 - 43, View in Reaxys

177

760

Hajipour; Mallakpour; Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals; vol. 356; (2001); p. 371 - 387, View in Reaxys

179

760

Hajipour; Mohammadpoor-Baltork; Kianfar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 38; nb. 2; (1999); p. 221 - 224, View in Reaxys

177

Hajipour, Abdol Reza; Mohammadpoor-Baltork, Iraj; Niknam, Kurosh; Organic Preparations and Procedures International; vol. 31; nb. 3; (1999); p. 335 - 341, View in Reaxys

120

Dutt, Sachchidananda; Banerjee, Santanu; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 64; (1987); p. 704 - 705, View in Reaxys

160 - 165

6-7

Dutta, Hasi; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Santanu; Journal of the Indian Chemical Society; vol. 64; (1987); p. 706 - 707, View in Reaxys

341.5

760

Goerner,R.N. et al.; Journal of Organic Chemistry; vol. 42; nb. 1; (1977); p. 19 - 28, View in Reaxys; Graebe; Rateanu; Justus Liebigs Annalen der Chemie; vol. 279; (1894); p. 266 Anm., View in Reaxys

341.5

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys

235 - 250

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys

Sublimation (1) Sublimation [°C] 100

Pressure (Sublimation) [Torr]

References

0.5

Badger; Journal of the Chemical Society; (1941); p. 535,537, View in Reaxys

Refractive Index (2) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

References

1.6272

656.3

99.4

v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys

1.6369

589

99.4

v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys

Density (4) 1 of 4

Measurement Temperature 21.24 [°C] Type (Density)

crystallographic

Location

supporting information

Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 2 of 4

Density [g·cm-3]

1.254

Krishnan; Banerjee; Philosophical Transactions of the Royal Society of London; vol. <A> 234; (1935); p. 265,280, View in Reaxys 3 of 4

Density [g·cm-3]

1.228

Mukherjee; Indian Journal of Physics (1926-1976); vol. 8; (1933); p. 147,149, View in Reaxys

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4 of 4

Density [g·cm-3]

1.13

Reference Temperature [°C]

Measurement Temperature 99.4 [°C] v. Auwers; Fruehling; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 224, View in Reaxys Adsorption (MCS) (2) 1 of 2

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

zeolite L

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 2 of 2

Description (Adsorption (MCS))

Desorption

Partner (Adsorption (MCS))

methylsilicone stationary phase

Krieger; Hites; Environmental Science and Technology; vol. 28; nb. 6; (1994); p. 1129 - 1133, View in Reaxys Association (MCS) (15) 1 of 15

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

methanol; water

Partner (Association (MCS))

cucurbit[7]uril

Ghosh, Indrajit; Mukhopadhyay, Arindam; Koner, Apurba Lal; Samanta, Subhas; Nau, Werner M.; Moorthy, Jarugu Narasimha; Physical Chemistry Chemical Physics; vol. 16; nb. 31; (2014); p. 16436 - 16445, View in Reaxys 2 of 15

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

octanol

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb. 1-3; (2007); p. 44 - 48, View in Reaxys 3 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

heptane

Partner (Association (MCS))

1,2,3,4-tetrahydroisoquinoline

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys 4 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

H2O

Comment (Association (MCS))

ambient temperature. Object(s) of Study: concentration dependence

Partner (Association (MCS))

alpha cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys

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5 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Comment (Association (MCS))

concentration dependence

Partner (Association (MCS))

alpha cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys 6 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

β-cyclodextrin

Murphy; Barros; Barnes; Mayer; Marconi; Bohne; Journal of Physical Chemistry A; vol. 103; nb. 1; (1999); p. 137 - 146, View in Reaxys 7 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 8 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

cyclohexane

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 9 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

ethanol

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 10 of 15

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

dimethylsulfoxide

Partner (Association (MCS))

hydroxylamine, sodium methoxide, methanol

Tachibana, Masaki; Furusawa, Motohisa; Bulletin of the Chemical Society of Japan; vol. 61; nb. 7; (1988); p. 2353 - 2358, View in Reaxys 11 of 15

Description (Association (MCS))

UV/VIS spectrum of the complex

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Solvent (Association (MCS))

propan-2-ol

Partner (Association (MCS))

1,4-diaza-bicyclo[2.2.2]octane

Peters, K. S.; Freilich, S. C.; Schaeffer, C. G.; Journal of the American Chemical Society; vol. 102; nb. 17; (1980); p. 5701 5702, View in Reaxys 12 of 15

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

tetrahydrofuran

Partner (Association (MCS))

Sr/Hg

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys 13 of 15

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

tetrahydrofuran

Partner (Association (MCS))

Ba/Hg

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys 14 of 15

Description (Association (MCS))

Stability constant of the complex with ...

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys 15 of 15

Description (Association (MCS))

Enthalpy of association

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys Chromatographic Data (6) Chromatographic Location data HPLC (High performance liquid chromatography)

References

supporting informa- Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Cattion alysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys

HPLC (High performance liquid chromatography)

Serra, Stefano; European Journal of Organic Chemistry; vol. 2015; nb. 29; (2015); p. 6472 6478, View in Reaxys; Hall, Emma A.; Sarkar, Md Raihan; Bell, Stephen G.; Catalysis Science and Technology; vol. 7; nb. 7; (2017); p. 1537 - 1548, View in Reaxys

TLC (Thin layer chromatography)

Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Mendkovich, Andrey S.; Syroeshkin, Mikhail A.; Nasybullina, Darya V.; Mikhailov, Mikhail N.; Gultyai, Vadim P.; Elinson, Mikhail N.; Rusakov, Alexander I.; Electrochimica Acta; vol. 191; (2016); p. 962 - 973, View in Reaxys

GC (Gas chromatography)

supporting informa- Nagaki, Aiichiro; Ichinari, Daisuke; Yoshida, Jun-Ichi; Journal of the American Chemical Sotion ciety; vol. 136; nb. 35; (2014); p. 12245 - 12248, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys

GC (Gas chromatography)

Sigrist, Rolf; Hansen, Hans-Juergen; Helvetica Chimica Acta; vol. 97; nb. 8; (2014); p. 1165 1175, View in Reaxys; Cao, Gang; Xu, Zhiwei; Wu, Xin; Li, Qingli; Chen, Xiaocheng; Natural Product Research; vol. 28; nb. 19; (2014); p. 1607 - 1612, View in Reaxys; Sharma, Anubhuti; Sood, Salej; Agrawal; Kant; Bhatt; Pattanayak; Asian Journal of Chemistry; vol. 28; nb. 7; (2016); p. 1633 - 1637, View in Reaxys

TLC (Thin layer chromatography)

supporting informa- Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yation suhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys

Circular Dichroism (1)

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Solvent (Circular Dichroism)

Comment (Circular Dichroism)

References

various solvent(s)

300 - 400 nm

Schipper, Pieter E.; O'Brien, Joanne M.; Ridley, Damon D.; Journal of Physical Chemistry; vol. 89; (1985); p. 5805 - 5810, View in Reaxys

Crystal Phase (4) Description (Crystal Phase)

Comment (Crystal Phase)

References

Rate of transition

Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 3845, View in Reaxys

Crystal structure determination

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys; Garten; Head; Nature (London, United Kingdom); vol. 205; (1965); p. 160, View in Reaxys; Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys; Luss; Smith; Acta Crystallographica, Section B: Structural Crystallography and Crystal Chemistry; vol. 28; (1972); p. 884, View in Reaxys

Polymorphism

Ueber die Existenz Kofler; Mikrochemie; vol. 34; (1948); p. 20,21; Chem.Abstr.; (1948); p. 8713, View in Reaxys instabiler Modifikationen vom F: 72grad, F: 54grad und F: 52grad.

Crystal structure determination

a=16 Angstroem, b=12.5 Angstroem, c=18.63 Angstroem, n=16.; aus dem Roentgendiagramm ermittelt.

Crystal Property Description (16) Colour & Other Location Properties yellow

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys

References

supporting informa- Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte tion Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys; Li, Hu; Zhu, Ru-Yi; Shi, Wen-Juan; He, Ke-Han; Shi, Zhang-Jie; Organic Letters; vol. 14; nb. 18; (2012); p. 4850 - 4853,4, View in Reaxys; Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 - 2745, View in Reaxys; Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p. 4888 - 4891, View in Reaxys; Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys; Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 - 3219, View in Reaxys; Guo, Wei; Lu, Liang-Qiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 - 2297,5, View in Reaxys; Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys; Wei, Baosheng; Li, Heng; Zhang, Wen-Xiong; Xi, Zhenfeng; Organometallics; vol. 34; nb. 7; (2015); p. 1339 - 1344, View in Reaxys; Song, Juan; Wei, Fuliang; Sun, Wei; Li, Ke; Tian, Yanan; Liu, Chao; Li, Yali; Xie, Linghai; Organic Letters; vol. 17; nb. 9; (2015); p. 2106 - 2109, View in Reaxys; Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys; Motiwala, Hashim F.; Vekariya, Rakesh H.; Aubé, Jeffrey; Organic Letters; vol. 17; nb. 21; (2015); p. 5484 - 5487, View in Reaxys; Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys; Papaianina; Amsharov; Chemical Communications; vol. 52; nb. 7; (2016); p. 1505 - 1508, View in Reaxys; Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys; Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p. 4952 - 4961, 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; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys; Guo, Shu; Zeng, Renyou; Li, Caiye; Synthetic Communications; vol. 46; nb. 17; (2016); p. 1446 - 1453, View in Reaxys; Alanthadka, Anitha; Devi, E. Sankari; Nagarajan, Subbiah; Sridharan, Vellaisamy; Suvitha, Ambigapathy; Maheswari, C. Uma; European Journal of Organic Chemistry; vol. 2016; nb. 28; (2016); p. 4872 - 4880,

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yellow

Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768,6, View in Reaxys; Parida, Keshaba Nanda; Jhulki, Samik; Mandal, Susovan; Moorthy, Jarugu Narasimha; Tetrahedron; vol. 68; nb. 47; (2012); p. 9763 - 9768, 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; Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7220 - 7225, View in Reaxys; Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys; Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys; Hossain, Md. Munkir; Shyu, ShinGuang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys; Laha, Joydev K.; Patel, Ketul V.; Dubey, Gurudutt; Jethava, Krupal P.; Organic and Biomolecular Chemistry; vol. 15; nb. 10; (2017); p. 2199 - 2210, View in Reaxys; Wu, Jianglong; Liu, Yan; Liu, Ping; Gu, Chengzhi; Letters in Organic Chemistry; vol. 14; nb. 4; (2017); p. 254 - 260, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys; Liu, Li; Qiang, Jian; Bai, Shuhua; Li, Yang; Miao, Chunbao; Li, Jian; Applied Organometallic Chemistry; vol. 31; nb. 12; (2017); Art.No: E3817, View in Reaxys; Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys Paragraph 0064; 0068; 0072

yellow-brown yellow

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys Laha, Joydev K.; Jethava, Krupal P.; Patel, Sagarkumar; Patel, Ketul V.; Journal of Organic Chemistry; vol. 82; nb. 1; (2017); p. 76 - 85, View in Reaxys

Paragraph 0056; 0058

green

Patent; Baoshun Technology Co., Ltd.; Dalian University of Technology; Yu Limei; Gao Zhanxian; Yan Jun; Hou Lin; Li Huifeng; He Yongchao; Shi Zhengmao; (8 pag.); CN103804162; (2017); (B) Chinese, View in Reaxys Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys

yellow

Page/Page column 2; 5

white

supporting informa- Wei, Peng; Zhang, Datong; Gao, Zhigang; Cai, Wenqing; Xu, Weiren; Tang, Lida; Zhao, tion Guilong; Synthetic Communications; vol. 45; nb. 12; (2015); p. 1457 - 1470, View in Reaxys; Dai, Wen; Lv, Ying; Wang, Lianyue; Shang, Sensen; Chen, Bo; Li, Guosong; Gao, Shuang; Chemical Communications; vol. 51; nb. 56; (2015); p. 11268 - 11271, View in Reaxys

32/144

2018-06-21 20:37:19

white

Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys

colourless

Lenze, Matthew; Martin, Erin T.; Rath, Nigam P.; Bauer, Eike B.; ChemPlusChem; vol. 78; nb. 1; (2013); p. 101 - 116, View in Reaxys

yellow

supporting informa- Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angetion wandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; 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; Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys; Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys; Cosner, Casey C.; Cabrera, Pablo J.; Byrd, Katherine M.; Adams Thomas, Asia M.; Helquist, Paul; Organic Letters; vol. 13; nb. 8; (2011); p. 2071 - 2073, View in Reaxys; Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Lockner, Jonathan W.; Dixon, Darryl D.; Risgaard, Rune; Baran, Phil S.; Organic Letters; vol. 13; nb. 20; (2011); p. 5628 - 5631, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Seo, Sangwon; Slater, Mark; Greaney, Michael F.; Organic Letters; vol. 14; nb. 10; (2012); p. 2650 - 2653, View in Reaxys; Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, ChienHong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys

yellow

Patent; Symyx Technologies, Inc.; US6350916; (2002); (B1) English, View in Reaxys; Campo; Larock; Organic letters; vol. 2; nb. 23; (2000); p. 3675 - 3677, View in Reaxys; Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Campo, Marino A.; Larock, Richard C.; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5616 - 5620, View in Reaxys; Guram, Anil S.; Bei, Xiaohong; Turner, Howard W.; Organic Letters; vol. 5; nb. 14; (2003); p. 2485 - 2487, View in Reaxys; Kawabata, Hirotoshi; Hayashi, Masahiko; Tetrahedron Letters; vol. 45; nb. 28; (2004); p. 5457 - 5459, View in Reaxys; Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys; Yang, Guanyu; Zhang, Qiaohong; Miao, Hong; Tong, Xinli; Xu, Jie; Organic Letters; vol. 7; nb. 2; (2005); p. 263 - 266, View in Reaxys; Bei, Xiaohong; Hagemeyer, Alfred; Volpe, Anthony; Saxton, Robert; Turner, Howard; Guram, Anil S.; Journal of Organic Chemistry; vol. 69; nb. 25; (2004); p. 8626 - 8633, View in Reaxys; Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys; Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys; Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb. 3; (2009); p. 312 - 315, View in Reaxys; Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Molecules; vol. 15; nb. 4; (2010); p. 2631 2650, View in Reaxys; Saikia, Gunin; Iyer, Parameswar K.; Journal of Organic Chemistry; vol. 75; nb. 8; (2010); p. 2714 - 2717, View in Reaxys; Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys; Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys; Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys; Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, Xiao-Feng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys; Wang, Lianyue; Li, Jun; Yang, Hua; Lv, Ying; Gao, Shuang; Journal of Organic Chemistry; vol. 77; nb. 1; (2012); p. 790 - 794, View in Reaxys; Li, Dan-Dan; Yuan, Ting-Ting; Wang, Guan-Wu; Journal of Organic Chemistry; vol. 77; nb. 7; (2012); p. 3341 3347, View in Reaxys

white

Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys

gelbe Nadeln

Jeanes; Adams; Journal of the American Chemical Society; vol. 59; (1937); p. 2608,2619, View in Reaxys

weisse Nadeln oder Platten

Carnelley; Dunn; Chemische Berichte; vol. 21; (1888); p. 2005, View in Reaxys

gelb

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p. 623; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1877); p. 742, View in Reaxys Crystal System (1) Crystal System Location Rhombic

References

supporting informa- Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biotion molecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys

Dielectric Constant (1) References Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie; vol. 63; (1959); p. 1110,1111-1120; Chem.Abstr.; nb. 5194; (1960), View in Reaxys Dissociation Exponent (5) 1 of 5

Comment (Dissociation Exponent)

(pk')Radikal: pK(a)

Rao; Hayon; Analytical Chemistry; vol. 48; (1976); p. 564,565, View in Reaxys 2 of 5

Comment (Dissociation Exponent)

(pk')e-(aq)-Addukt (Ketyl): pk (Tab.II)

Hayon et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 2072, View in Reaxys 3 of 5

Comment (Dissociation Exponent)

(k')S445

Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 33; (1971); p. 419,421, View in Reaxys 4 of 5

Comment (Dissociation Exponent)

(pk')pK(a)-Best. (UV-spektrometrisch) in wssr. H2SO4

Greig; Johnson; Journal of the American Chemical Society; vol. 90; (1968); p. 6453, View in Reaxys 5 of 5

Comment (Dissociation Exponent)

(pk')pK(BH+): -6.65

Stewart et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 1065,1066, View in Reaxys Electrical Data (4) 1 of 4

Description (Electrical Da- Dielectric relaxation time ta) Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie; vol. 63; (1959); p. 1110,1111-1120; Chem.Abstr.; nb. 5194; (1960), View in Reaxys

2 of 4

Description (Electrical Da- Electrical properties ta) Davies; Swain; Chemical Physics Letters; vol. 2; (1968); p. 42, View in Reaxys

3 of 4

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Loesungen in Benzol, CCl4 und Heptan bei 20-60grad/1000-9700 MHz bzw. 1.25-50 cm. Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 63; (1959); p. 1110,1116, View in Reaxys

4 of 4

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Benzol, CCl4 und Heptan geloestem Fluoren-9-on bei 20-60grad. Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys; Zeil et al.; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 63; (1959); p. 1110,1116, View in Reaxys

Electrical Moment (10) 1 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.7

Method (Electrical Moment)

Microwave absorption

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Solvent (Electrical Moment)

benzene

Fessenden, Richard W.; Carton, Paul M.; Shimamori, H.; Scalano, Juan C.; Journal of Physical Chemistry; vol. 86; (1982); p. 3803 - 3811, View in Reaxys 2 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in o-Terphenyl

Crossley et al.; Journal of Chemical Physics; vol. 69; (1978); p. 1980, View in Reaxys 3 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (tabelliert)

Nagai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1022, View in Reaxys 4 of 10

Description (Electrical Moment)

Dipole moment

Davies; Swain; Transactions of the Faraday Society; vol. 67; (1971); p. 1637,1647,1648, View in Reaxys 5 of 10

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys 6 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.34

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 7 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.38

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 8 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.38

Temperature (Electrical Moment) [°C]

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Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Pitt; Smyth; Journal of the American Chemical Society; vol. 80; (1958); p. 1061, View in Reaxys 9 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.35

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Hughes; Le Fevre; Le Fevre; Journal of the Chemical Society; (1937); p. 202,206, View in Reaxys 10 of 10

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.29

Method (Electrical Moment)

Dielectric constant (β)

Solvent (Electrical Moment)

benzene

Bergmann; Engel; Hoffmann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 17; (1932); p. 92,97, View in Reaxys; Bergmann; Engel; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 37; (1931); p. 563,566, View in Reaxys Electrochemical Behaviour (5) Description (Elec- Comment (Electrotrochemical Behav- chemical Behaviour) iour)

References

Polarography

House,H.O.; Umen,M.J.; Journal of the American Chemical Society; vol. 94; (1972); p. 5495 5497, View in Reaxys; Kalinowski et al.; Transactions of the Faraday Society; vol. 62; (1966); p. 918, View in Reaxys; Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys; Karpinets; Bezuglyi; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2116,1857,1859, View in Reaxys; Tsebrii et al.; Sov. Prog. Chem. (Engl. Transl.); vol. 41; nb. 7; (1975); p. 702,27, View in Reaxys; Kemula et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 6863, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p. 685, 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; Berg; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 229; (1965); p. 138,141, View in Reaxys

Electrochemical properties

Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 33; (1971); p. 419,421, View in Reaxys; Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 73; (1976); p. 163,168, View in Reaxys; Saveant; Binh; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 88; (1978); p. 27,30, View in Reaxys; Lunazzi et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 162,163, View in Reaxys; Vykhodtseva; Nekrasov; Doklady Physical Chemistry; vol. 220-225; (1975); p. 861, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p. 685, View in Reaxys

Basicity

Paspaleev; Kojucharova; Monatshefte fuer Chemie; vol. 100; (1969); p. 1213,1216, View in Reaxys

Thermodynamic parameters for autoprotolysis

mit Diphenylamin.

Pusin; Rikovski; Milutinovic; Glasnik Hemijskog Drustva Beograd; vol. 14; (1949); p. 173,177; Chem.Abstr.; (1952); p. 4344, View in Reaxys

Basicity

gegen starke Saeuren.

Stobbe; Seydel; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 141, View in Reaxys

Electrochemical Characteristics (39)

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1 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Location

supporting information

Comment (Electrochemical Characteristics)

Other electrode; potential diagram; 0.1 M tetrabutylammonium hexafluorophosphate

Li, Shuangjiang; Aljhdli, Merfat; Thakellapalli, Haresh; Farajidizaji, Behzad; Zhang, Yu; Akhmedov, Novruz G.; Milsmann, Carsten; Popp, Brian V.; Wang, Kung K.; Organic Letters; vol. 19; nb. 15; (2017); p. 4078 - 4081, View in Reaxys 2 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Comment (Electrochemical Characteristics)

transmitted electrons -1; Cathodic peak potential; -1.23 V; Saturated calomel electrode (SCE); potential diagram; 0.1 M tetrabutylammonium perchlorate

Product

radical anion of fluorene-9-one

Mendkovich, Andrey S.; Syroeshkin, Mikhail A.; Nasybullina, Darya V.; Mikhailov, Mikhail N.; Gultyai, Vadim P.; Elinson, Mikhail N.; Rusakov, Alexander I.; Electrochimica Acta; vol. 191; (2016); p. 962 - 973, View in Reaxys 3 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Temperature (Electrochemical Characteristics) [°C]

Location

supporting information

Comment (Electrochemical Characteristics)

Saturated calomel electrode (SCE); potential diagram; 0.03 M Bu4NClO4

Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko; Journal of Organic Chemistry; vol. 81; nb. 22; (2016); p. 11043 - 11056, View in Reaxys 4 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Comment (Electrochemical Characteristics)

Saturated calomel electrode (SCE); potential diagram; 0.1 M N-tetrabutylammonium tetrafluoroborate

Reche, Irene; Gallardo, Iluminada; Guirado, Gonzalo; New Journal of Chemistry; vol. 38; nb. 10; (2014); p. 5030 - 5036, View in Reaxys 5 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Comment (Electrochemical Characteristics)

Saturated silver chloride electrode; potential diagram; 0.1M tetrabutylammonium hexafluorophosphate

Guenes, Arzu; Cihaner, Atilla; Oenal, Ahmet M.; Electrochimica Acta; vol. 89; (2013); p. 339 - 345, View in Reaxys 6 of 39

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

dichloromethane

Location

supporting information

Comment (Electrochemical Characteristics)

Other electrode; potential diagram; 0.1 mol L−1 tetrabutylammonium hexafluorophosphate

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Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide; water

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

transmitted electrons -1; Cathodic peak potential; -1.79 V; Ferrocene/ferrocenium; potential diagram; 0.1 M Bu4NClO4

Product

C13H8O(1+)

Mendkovich; Syroeshkin; Mikhailov; Ranchina; Rusakov; Russian Chemical Bulletin; vol. 62; nb. 7; (2013); p. 1668 - 1670; Izv. Akad. Nauk, Ser. Khim.; nb. 7; (2013); p. 1668 - 1670,3, View in Reaxys 8 of 39

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Location

supporting information

Cocherel, Nicolas; Poriel, Cyril; Rault-Berthelot, Joelle; Barriere, Frederic; Audebrand, Nathalie; Slawin, Alexandra M. Z.; Vignau, Laurence; Chemistry - A European Journal; vol. 14; nb. 36; (2008); p. 11328 - 11342, View in Reaxys; Amaya, Toru; Hifumi, Maiko; Okada, Michiaki; Shimizu, Yasutomo; Moriuchi, Toshiyuki; Segawa, Kouji; Ando, Yoichi; Hirao, Toshikazu; Journal of Organic Chemistry; vol. 76; nb. 19; (2011); p. 8049 - 8052, View in Reaxys; Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Bryan E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys 9 of 39

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys; Carbas, Buket Bezgin; Kivrak, Arif; Oenal, Ahmet M.; Electrochimica Acta; vol. 58; nb. 1; (2011); p. 223 230, View in Reaxys 10 of 39

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys; Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys 11 of 39

Description (Electrochemical Characteristics)

cyclic voltammetry

Solvent (Electrochemical Characteristics)

dimethylformamide

Rejnak, Michal; Klima, Jiri; Svoboda, Jiri; Ludvik, Jiri; Collection of Czechoslovak Chemical Communications; vol. 69; nb. 1; (2004); p. 242 - 260, View in Reaxys; Wang, Changsheng; Batsanov, Andrei S.; Bryce, Martin R.; Sage, Ian; Organic Letters; vol. 6; nb. 13; (2004); p. 2181 - 2184, View in Reaxys 12 of 39

Description (Electrochemical Characteristics)

oxidation potential

Solvent (Electrochemical Characteristics)

acetonitrile; various solvent(s)

Jacques; Allonas; Sarbach; Haselbach; Vauthey; Chemical Physics Letters; vol. 378; nb. 1-2; (2003); p. 185 - 191, View in Reaxys 13 of 39

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Enemaerke, Rasmus J.; Christensen, Torben B.; Jensen, Henrik; Daasbjerg, Kim; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2001); p. 1620 - 1630, View in Reaxys

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14 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

tetrahydrofuran

Temperature (Electrochemical Characteristics) [°C]

Enemaerke, Rasmus J.; Hertz, Trille; Skrydstrup, Troels; Daasbjerg, Kim; Chemistry - A European Journal; vol. 6; nb. 20; (2000); p. 3747 - 3754, View in Reaxys 15 of 39

Description (Electrochemical Characteristics)

cyclic voltammetry

Solvent (Electrochemical Characteristics)

tetrahydrofuran

Temperature (Electrochemical Characteristics) [°C]

24.85

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

Svyatkina; Dmitrieva; Kurov; Russian Journal of General Chemistry; vol. 66; nb. 2; (1996); p. 303 - 305, View in Reaxys 17 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

Comment (Electrochemical Characteristics)

-1.25 V; Product: /BRN= 4046027/. No. of transm. electrons: 1. Method: potentiometry

Product

fluorenone radical anion potassium contact ion pair

Umemoto, Kisaburo; Nagase, Yutaka; Sasaki, Yukio; Bulletin of the Chemical Society of Japan; vol. 67; nb. 12; (1994); p. 3245 - 3248, View in Reaxys 18 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.21 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 19 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

39/144

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Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.25 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 20 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

N,N-dimethyl-acetamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.27 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 21 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 22 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

hexamethylphosphoric acid triamide

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.45 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 23 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

various solvent(s)

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Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.15 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 24 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

various solvent(s)

Temperature (Electrochemical Characteristics) [°C]

298

Comment (Electrochemical Characteristics)

-1.29 V; Type: Reversible half-wave potential. Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: polarography. Description: 0.1 M LiClO4, dropping mercury electrode, vs. sat. calomel electrode

Product

fluorenone ketyl radical anion

Karpinets, A. P.; Bezuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 8.2; (1991); p. 1820 - 1821,1681 - 1682, View in Reaxys 25 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

House,H.O. et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 8471 - 8475, View in Reaxys; Pragst et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 257; (1976); p. 465,471, View in Reaxys; Wilkinson; Garner; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p. 222,224, View in Reaxys; Rashkov et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 1797,1801, View in Reaxys; Loutfy; Loutfy; Canadian Journal of Chemistry; vol. 50; (1972); p. 4052,4054, View in Reaxys; Kalinowski; Chemical Physics Letters; vol. 7; (1970); p. 55, View in Reaxys; Karpinets; Bezuglyi; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 2116,1857,1859, View in Reaxys; Kalinowski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 18; (1970); p. 685, View in Reaxys; Fournier, Francoise; Berthelot, Jacques; Pascal, Yves-Louis; Canadian Journal of Chemistry; vol. 61; (1983); p. 2121 - 2125, View in Reaxys; Loutfy; Hsiao; Ong; Keoshkerian; Canadian Journal of Chemistry; vol. 62; nb. 10; (1984); p. 1877 - 1885, View in Reaxys; Nagaoka, Tsutomu; Fukunaga, Toshikazu; Yoshino, Takashi; Watanabe, Iwao; Nakayama, Toshiro; Okazaki, Satoshi; Analytical Chemistry; vol. 60; nb. 24; (1988); p. 2766 - 2769, View in Reaxys; Karpinets, A. P.; Benzuglyi, V. D.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 6; (1980); p. 1376 - 1379,1119 - 1122, View in Reaxys; Wagner, Elzbieta; Kalinowski, Marek K.; Monatshefte fuer Chemie; vol. 116; (1985); p. 1413 - 1418, View in Reaxys 26 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

1.28 V; Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: 0.1M tetrabutylammonium perchlorate, saturated calomel electrode

Product

fluorenone ketyl radical anion

Empis, Jose M. A.; Herold, Bernardo J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1986); p. 425 - 430, View in Reaxys 27 of 39

Description (Electrochemical Characteristics)

redox potential

Comment (Electrochemical Characteristics)

-1.28 V; Product: /BRN= 4139898/. No. of transm. electrons: 1. Method: not given. Description: mercury drop electrode, comparison electrode - saturated calomel electrode

Product

fluorenone ketyl radical anion

Pragst, Fritz; Stoesser, Reinhard; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 25; nb. 6; (1985); p. 222, View in Reaxys 28 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

24.9

Comment (Electrochemical Characteristics)

1.71 V; Product: /BRN= 3550463/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: glassy carbon, Pt or Au electrodes

Product

9,10-anthraquinone radical anion

Nagaoka, Tsutomu; Okazaki, Satoshi; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2340 - 2344, View in Reaxys 29 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide; H2O

Comment (Electrochemical Characteristics)

1.24 V; Product: /BRN= 3873884/. No. of transm. electrons: 1. Method: polarography. Description: calomel/sat. KCl; TBABr. Byprod.: alcohol (INO 380)

Product

difluorenyl-1,1'diol-1,1' * fluorenol

Fournier, F.; Berthelot, J.; Pascal, Y. L.; Tetrahedron; vol. 40; nb. 2; (1984); p. 339 - 347, View in Reaxys 30 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide; H2O

Comment (Electrochemical Characteristics)

1.91 V; Product: /BRN= 3873884/. Method: polarography. Description: calomel/sat. KCl; TBABr. Byprod.:INO 380

Product

difluorenyl-1,1'diol-1,1' * fluorenol

Fournier, F.; Berthelot, J.; Pascal, Y. L.; Tetrahedron; vol. 40; nb. 2; (1984); p. 339 - 347, View in Reaxys 31 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

Type: Reversible half-wave potential

Svaan, Morten; Parker, Vernon D.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 38; nb. 9; (1984); p. 759 - 766, View in Reaxys 32 of 39

Description (Electrochemical Characteristics)

redox potential

Gorman et al.; Journal of Photochemistry; vol. 9; (1978); p. 11,14, View in Reaxys; Pons, Jean-Marc; Santelli, Maurice; Tetrahedron Letters; vol. 23; nb. 47; (1982); p. 4937 - 4940, View in Reaxys; Cerfontain, Hans; Geenevasen, Jan A. J.; Noort, Paul C. M. van; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 1057 - 1062, View in Reaxys 33 of 39

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

0.1

Comment (Electrochemical Characteristics)

-1.53 V; Product: /BRN= 3546256/. No. of transm. electrons: 1. Method: voltammetry. Description: reversible potential, a mercury electrode vs. Ag/Ag+

Product

radical anion of fluorene-9-one

Svaan, Morten; Parker, Vernon D.; Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry; vol. 36; nb. 6; (1982); p. 365 - 370, View in Reaxys 34 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

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Solvent (Electrochemical Characteristics)

acetonitrile

Comment (Electrochemical Characteristics)

-1.26 V; Product: /BRN= 3546256/. No. of transm. electrons: 1. Method: not given. Description: vs. SCE, (n-Bu)4NClO4, supp. electrolite

Product

radical anion of fluorene-9-one

Miyashita, Tokuji; Matsuda, Minoru; Bulletin of the Chemical Society of Japan; vol. 54; nb. 6; (1981); p. 1740 - 1742, View in Reaxys 35 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in Formamid-Acetamid-Gemischen.

Hook et al.; Journal of Physical Chemistry; vol. 58; (1954); p. 81, View in Reaxys 36 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in Formamid.

Letaw; Gropp; Journal of Physical Chemistry; vol. 57; (1953); p. 964, View in Reaxys 37 of 39

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

in wss.-aethanol. Loesungen vom pH 1,2-12,2.

Day et al.; Journal of the American Chemical Society; vol. 74; (1952); p. 2741,2742, View in Reaxys; Day; Kirkland; Journal of the American Chemical Society; vol. 72; (1950); p. 2766, View in Reaxys 38 of 39

Description (Electrochemical Characteristics)

oxidation potential

Adkins et al.; Journal of the American Chemical Society; vol. 71; (1949); p. 3622,3623, View in Reaxys; Baker; Adkins; Journal of the American Chemical Society; vol. 62; (1940); p. 3305,3306, View in Reaxys 39 of 39

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Ashworth; Collection of Czechoslovak Chemical Communications; vol. 13; (1948); p. 229,237-243, View in Reaxys Electron Binding (2) Description (Elec- References tron Binding) Electronic states

Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys; Soep, Benoît; Mestdagh, Jean-Michel; Briant, Marc; Gaveau, Marc-André; Poisson, Lionel; Physical Chemistry Chemical Physics; vol. 18; nb. 33; (2016); p. 22914 - 22920, View in Reaxys

Electron affinity

Chen; Wentworth; Journal of Chemical Physics; vol. 63; (1975); p. 3183,3189, View in Reaxys

Energy Barriers (1) References Herkstroeter et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 4537,4539, View in Reaxys Energy Data (MCS) (1) 1 of 1

Description (Energy Data (MCS))

Entropy of mixtures

Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys Enthalpy of Combustion (1) Comment (Enthal- References py of Combustion) Enthalpy of combustion given

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva, Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys

Enthalpy of Formation (2)

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Comment (Enthalpy of Formation)

References

Enthalpy of formation given

Further Information (68) Description (FurReferences ther Information) Further information Beitz; Miller; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1979); p. 4579, View in Reaxys Further information Greene et al.; Journal of Chemical Physics; vol. 70; (1979); p. 1247, View in Reaxys Further information Borisevich; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 42; nb. 2; (1978); p. 1; ; p. 226, View in Reaxys Further information Barwise et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 1814,1817, View in Reaxys Further information Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys Further information Khel'mer et al.; Bulletin of the Academy of Sciences of the USSR, Physical Series (English Translation); vol. 40; nb. 2; (1976); p. 111; ; p. 348, View in Reaxys Further information Gaines et al.; Analytical Chemistry; vol. 47; (1975); p. 1373, View in Reaxys Further information Nakamura et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 1593, View in Reaxys Further information Parsons et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 6643,6645, View in Reaxys Further information Canters; de Boer; Molecular Physics; vol. 27; (1974); p. 665,675,677,678-683, View in Reaxys Further information Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys Further information Shears; Williams; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 69; (1973); p. 608, View in Reaxys Further information Potapov et al.; High Energy Chemistry; vol. 6; (1972); p. 347; ; p. 392, View in Reaxys Further information Davies; Swain; Transactions of the Faraday Society; vol. 67; (1971); p. 1637,1647,1648, View in Reaxys Further information Chapman et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 2918,2924, View in Reaxys Further information Potapov; Sorokin; High Energy Chemistry; vol. 5; (1971); p. 435; ; p. 487, View in Reaxys Further information Ioune; Tanizaki; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 73; (1970); p. 48,57, View in Reaxys Further information Axelrod et al.; Tetrahedron Letters; (1969); p. 5031, View in Reaxys Further information Gautier; Miocque; Moskowitz; Blanc-Guenee; Annales pharmaceutiques francaises; vol. 27; nb. 4; (1969); p. 303 308, View in Reaxys Further information Mullen Orloff; Journal of Molecular Spectroscopy; vol. 30; (1969); p. 140, View in Reaxys Further information Gocmen; Coudane; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 269; (1969); p. 467, View in Reaxys Further information Norris; Weissman; Journal of Physical Chemistry; vol. 73; (1969); p. 3119, View in Reaxys Further information Liu; Edman; Journal of the American Chemical Society; vol. 91; (1969); p. 1492, View in Reaxys Further information Caldwell; Journal of Organic Chemistry; vol. 34; (1969); p. 1886, View in Reaxys Further information Deboer; Journal of the American Chemical Society; vol. 91; (1969); p. 1855, View in Reaxys Further information Pacifici; Irick Jun.; Tetrahedron Letters; (1969); p. 2207, View in Reaxys Further information Wohl; Tetrahedron; vol. 24; (1968); p. 6889, View in Reaxys Further information Canters et al.; Chemical Physics Letters; vol. 1; (1968); p. 627, View in Reaxys Further information Sauers; Shurpik; Journal of Organic Chemistry; vol. 33; (1968); p. 799, View in Reaxys Further information Liu; Gale; Journal of the American Chemical Society; vol. 90; (1968); p. 1897, View in Reaxys Further information Saltiel; Journal of the American Chemical Society; vol. 90; (1968); p. 6394,6395, View in Reaxys

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Further information Rudzit et al.; Pharmaceutical Chemistry Journal; nb. 5; (1967); p. 245; Khimiko-Farmatsevticheskii Zhurnal; nb. 5; (1967); p. 14, View in Reaxys Further information Cantrell; Shechter; Journal of the American Chemical Society; vol. 89; (1967); p. 5877,5884, View in Reaxys Further information Hirota; Journal of the American Chemical Society; vol. 89; (1967); p. 32,37, View in Reaxys Further information Hirota; Journal of Physical Chemistry; vol. 71; (1967); p. 127,133, View in Reaxys Further information Ramirez,F. et al.; Journal of the American Chemical Society; vol. 89; (1967); p. 6283 - 6288, View in Reaxys Further information Normant; Bulletin de la Societe Chimique de France; (1966); p. 3601,3606, View in Reaxys Further information Kalinowski; Grabowski; Transactions of the Faraday Society; vol. 62; (1966); p. 926,931, View in Reaxys Further information Nelsen; Bartlett; Journal of the American Chemical Society; vol. 88; (1966); p. 143,148, View in Reaxys Further information Michl et al.; Journal of Physical Chemistry; vol. 70; (1966); p. 1732,1734,1735, View in Reaxys Further information Astakhova; Khidekel'; Doklady Chemistry; vol. 162; (1965); p. 558; Doklady Akademii Nauk SSSR; vol. 162; (1965); p. 1057, View in Reaxys Further information Shuman; Amstutz; Recueil des Travaux Chimiques des Pays-Bas; vol. 84; (1965); p. 441,445, View in Reaxys Further information Eland; Danby; Journal of the Chemical Society; (1965); p. 5935,5936, View in Reaxys Further information Faust et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 20; (1965); p. 1128,1133, View in Reaxys Further information Heller; Wasserman; Journal of Chemical Physics; vol. 42; (1965); p. 949,952, View in Reaxys Further information Shigorin; Potapov; Doklady Physical Chemistry; vol. 161; (1965); p. 237,238; ; p. 406, View in Reaxys Further information Doerr; Dehler; Tetrahedron Letters; (1965); p. 189,191, View in Reaxys Further information Fritzsche; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 459, View in Reaxys Further information Hirota et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2537, View in Reaxys Further information Demmering; Doerr; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 19; (1964); p. 365, View in Reaxys Further information Berg; Kramarczyk; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 296, View in Reaxys Further information Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys Further information Luckhurst; Orgel; Molecular Physics; vol. 8; (1964); p. 117,118, View in Reaxys Further information Cookson; Wallis; Proceedings of the Chemical Society, London; (1963); p. 58, View in Reaxys Further information Nelles; Streicher; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 3; (1963); p. 188, View in Reaxys Further information Haase; Zeil; Zeitschrift fuer Naturforschung; vol. 18a; (1963); p. 828, View in Reaxys Further information Dehl; Fraenkel; Journal of Chemical Physics; vol. 39; (1963); p. 1793, View in Reaxys Further information Russel et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4155,4156, View in Reaxys Further information Kasakowa; Syrkin; Journal of Structural Chemistry; vol. 3; (1962); p. 518; Zhurnal Strukturnoi Khimii; vol. 3; (1962); p. 536, View in Reaxys Further information Hirota; Weissman; Molecular Physics; vol. 5; (1962); p. 537, View in Reaxys Further information Mathias; Warhurst; Transactions of the Faraday Society; vol. 58; (1962); p. 948,949, View in Reaxys Further information Copeland et al.; Chemistry and Industry (London, United Kingdom); (1960); p. 98, View in Reaxys Further information Kemula; Naturwissenschaften; vol. 47; (1960); p. 514, View in Reaxys Further information Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 343,345, View in Reaxys Further information Beynon; Williams; Applied Spectroscopy; vol. 14; (1960); p. 156,158, View in Reaxys Further information Carter et al.; Transactions of the Faraday Society; vol. 56; (1960); p. 455,456, View in Reaxys Further information Mathias; Warhurst; Transactions of the Faraday Society; vol. 56; (1960); p. 348, View in Reaxys Further information Beynon; Advances in Mass Spectrometry; (1959); p. 328,348, View in Reaxys Interatomic Distances and Angles (1) Description References

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Electron distribution

Mc Clelland; Transactions of the Faraday Society; vol. 57; (1961); p. 2073, View in Reaxys

Ionization Potential (2) Ionization Potential Method (Ionization [eV] Potential) 8.37

Photoelectron Spectroscopy

References Soep, Benoît; Mestdagh, Jean-Michel; Briant, Marc; Gaveau, Marc-André; Poisson, Lionel; Physical Chemistry Chemical Physics; vol. 18; nb. 33; (2016); p. 22914 - 22920, View in Reaxys Potapov et al.; High Energy Chemistry; vol. 6; (1972); p. 347; ; p. 392, View in Reaxys; Aussems et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 487, View in Reaxys; Centineo et al.; Journal of Molecular Structure; vol. 44; (1978); p. 203,204, View in Reaxys; Potapov; Sorokin; High Energy Chemistry; vol. 5; (1971); p. 435; ; p. 487, View in Reaxys; Shigorin; Potapov; Doklady Physical Chemistry; vol. 161; (1965); p. 237,238; ; p. 406, View in Reaxys

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

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

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys Liquid/Solid Systems (MCS) (6) 1 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

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

29.99

Partner (Liquid/Solid Systems (MCS))

dibenzofuran; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 2 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

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

29.99

Partner (Liquid/Solid Systems (MCS))

9H-fluorene; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 3 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

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

29.99

Partner (Liquid/Solid Systems (MCS))

acenaphthene; ethanol

Wei, Yufeng; Dang, Leping; Zhang, Xiangyang; Cui, Weimin; Wei, Hongyuan; Journal of Chemical and Engineering Data; vol. 57; nb. 4; (2012); p. 1279 - 1287, View in Reaxys 4 of 6

Description (Liquid/Solid Systems (MCS))

Liquid/solid phase diagram

Partner (Liquid/Solid Systems (MCS))

o-terphenyl

Murthy, S. S. N.; Kumar, Deepak; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 14; (1993); p. 2423 2428, View in Reaxys 5 of 6

Description (Liquid/Solid Systems (MCS))

Eutectic

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

51.2

Comment (Liquid/Solid Systems (MCS))

thermische Analyse.

Partner (Liquid/Solid Systems (MCS))

acenaphthene

Pfeiffer; Justus Liebigs Annalen der Chemie; vol. 440; (1924); p. 247,248, 259, 261, 285, 286, 289, View in Reaxys 6 of 6

Description (Liquid/Solid Systems (MCS))

Eutectic

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

Comment (Liquid/Solid Systems (MCS))

thermische Analyse.

Partner (Liquid/Solid Systems (MCS))

naphthalen-2-ylamine

Pfeiffer; Justus Liebigs Annalen der Chemie; vol. 440; (1924); p. 247,248, 259, 261, 285, 286, 289, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

Anisotropy of mag- Bergmann et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 474,476, netic susceptibility View in Reaxys Magnetic Susceptibility (3) Magnetic Suscepti- Comment (Magnet- References bility ic Susceptibility) [10-6cm3mol-1] -99.4

Matsunaga; Bulletin of the Chemical Society of Japan; vol. 31; (1958); p. 774, View in Reaxys

-101.4

Bergmann et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 49; (1952); p. 474,476, View in Reaxys paramagnetic.

Krishnan; Banerjee; Philosophical Transactions of the Royal Society of London; vol. <A> 234; (1935); p. 265,280, View in Reaxys; Bose; Phil. Mag.; vol. <7> 21; (1936); p. 1119,1124, View in Reaxys; Mueller; Janke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 45; (1939); p. 380,392, View in Reaxys

Molecular Deformation (2) Description (MoReferences lecular Deformation) Force constants

Sahini; Ciurea; Revue Roumaine de Chimie; vol. 17; (1972); p. 273,276-279,282, View in Reaxys; Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Fundamental vibra- Kolev, Tsonko; Journal of Molecular Structure; vol. 349; (1995); p. 381 - 384, View in Reaxys tions Other Thermochemical Data (2) Description (Other References Thermochemical Data) Thermodynamic properties

Engel et al.; Journal of the American Chemical Society; vol. 100; (1978); p. 7009,7010, View in Reaxys; Liberman; Batra; Journal of Chemical Physics; vol. 59; (1973); p. 3723,3727, View in Reaxys; Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys

Enthalpy

Valentine; Hammond; Journal of the American Chemical Society; vol. 94; (1972); p. 3449,3452, View in Reaxys

Solubility (MCS) (5) 1 of 5

Saturation

in solution

Alsten, John G. Van; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 38; nb. 4; (1993); p. 605 - 610, View in Reaxys 2 of 5

Temperature (Solubility (MCS)) [°C]

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Solvent (Solubility (MCS))

ethanol

Comment (Solubility (MCS))

100 g solvent dissolves. 7.5 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 3 of 5

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

diethyl ether

Comment (Solubility (MCS))

100 g solvent dissolves. 31 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 4 of 5

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

CCl4

Comment (Solubility (MCS))

100 g solvent dissolves. 19 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys 5 of 5

Temperature (Solubility (MCS)) [°C]

Solvent (Solubility (MCS))

benzene

Comment (Solubility (MCS))

100 g solvent dissolves. 68 g Substance.

Huntress; Hershberg; Cliff; Journal of the American Chemical Society; vol. 53; (1931); p. 2720,2724, View in Reaxys Solution Behaviour (MCS) (1) 1 of 1

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 23 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

maleic anhydride-hexyl vinyl copolymer

Zdanowicz, Vincent S.; Strauss, Ulrich P.; Journal of Physical Chemistry B; vol. 102; nb. 1; (1998); p. 40 - 43, View in Reaxys Space Group (2) Space Group 61

Location

Comment (Space Group)

References

supporting informa- a = 16.0871 Å; b = Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Contion 12.5495 Å; c = gde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 18.6772 Å; Z = 16; 1592, View in Reaxys T = 294.4 K; Method = X-ray diffraction; atomic positions available

Iball; Zeitschrift fuer Kristallographie, Kristallgeometrie, Kristallphysik, Kristallchemie; vol. 94; (1936); p. 397,404, View in Reaxys

Transport Phenomena (MCS) (2) 1 of 2

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

dimethylformamide

Temperature (Transport Phenomena (MCS)) [°C]

24.9

48/144

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Partner (Transport Phenomena (MCS))

tetrabutylammonium perchlorate

Nagaoka, Tsutomu; Okazaki, Satoshi; Journal of Physical Chemistry; vol. 89; nb. 11; (1985); p. 2340 - 2344, View in Reaxys 2 of 2

Description (Transport Phenomena (MCS))

Diffusion

Guttenplan; Cohen; Tetrahedron Letters; (1972); p. 2163, View in Reaxys Vapour Pressure (89) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

Comment (Vapour Pressure)

References

0.000667567

39.03

Diagram; Solid

0.000862586

41.05

Diagram; Solid

0.00107261

42.95

Diagram; Solid

0.00135014

45.02

Diagram; Solid

0.00168767

47.04

Diagram; Solid

0.0020477

48.95

Diagram; Solid

0.00258026

51.03

Diagram; Solid

0.00322532

53.03

Diagram; Solid

0.00337534

53.72

Diagram; Solid

0.0039604

54.95

Diagram; Solid

0.0039754

55.16

Diagram; Solid

0.00457546

56.67

Diagram; Solid

0.00478548

57.02

Diagram; Solid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

49/144

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Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.00540054

58.14

Diagram; Solid

0.0059706

59.02

Diagram; Solid

0.0060006

54.69

Diagram; Liquid

0.00637564

59.65

Diagram; Solid

0.00712571

56.66

Diagram; Liquid

0.00732823

60.94

Diagram; Solid

0.00735074

61.13

Diagram; Solid

0.00840084

58.63

Diagram; Liquid

0.00847585

62.62

Diagram; Solid

0.009976

60.64

Diagram; Liquid

0.009976

64.09

Diagram; Solid

0.0114761

65.59

Diagram; Solid

0.0119262

62.62

Diagram; Liquid

0.0132763

67.05

Diagram; Solid

0.0138764

64.58

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

50/144

2018-06-21 20:37:19

Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.0153765

68.53

Diagram; Solid

0.0162766

66.56

Diagram; Liquid

0.0176268

70.03

Diagram; Solid

0.0193519

68.6

Diagram; Liquid

0.020402

71.52

Diagram; Solid

0.0224272

70.56

Diagram; Liquid

0.0233273

73.04

Diagram; Solid

0.0261026

72.5

Diagram; Liquid

0.0266277

74.52

Diagram; Solid

0.0306781

74.52

Diagram; Liquid

0.0306781

76.01

Diagram; Solid

0.0350285

77.49

Diagram; Solid

0.0351035

76.5

Diagram; Liquid

0.0408041

78.98

Diagram; Solid

0.0408791

78.47

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

51/144

2018-06-21 20:37:19

Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.0472547

80.47

Diagram; Liquid

0.0548305

82.42

Diagram; Liquid

0.0630063

84.43

Diagram; Liquid

0.0735824

86.66

Diagram; Liquid

0.0830333

88.43

Diagram; Liquid

0.0834083

88.41

Diagram; Liquid

0.0963846

90.63

Diagram; Liquid

0.108461

92.36

Diagram; Liquid

0.124587

94.58

Diagram; Liquid

0.141539

96.37

Diagram; Liquid

0.161941

98.56

Diagram; Liquid

0.182643

100.37

Diagram; Liquid

0.207621

102.51

Diagram; Liquid

0.234623

104.31

Diagram; Liquid

0.264701

106.49

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

52/144

2018-06-21 20:37:19

Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.296655

108.24

Diagram; Liquid

0.333858

110.44

Diagram; Liquid

0.376613

112.31

Diagram; Liquid

0.423417

114.4

Diagram; Liquid

0.531203

118.35

Diagram; Liquid

0.581683

120.25

Diagram; Liquid

0.657216

122.25

Diagram; Liquid

0.725698

124.2

Diagram; Liquid

0.816832

126.19

Diagram; Liquid

0.90159

128.16

Diagram; Liquid

1.0066

130.14

Diagram; Liquid

1.16862

133.09

Diagram; Liquid

1.23462

134.1

Diagram; Liquid

1.35614

136.02

Diagram; Liquid

1.51065

138.05

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

53/144

2018-06-21 20:37:19

Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 1.65467

140.01

Diagram; Liquid

1.83018

142.01

Diagram; Liquid

2.00945

143.95

Diagram; Liquid

2.21122

145.97

Diagram; Liquid

2.43174

147.9

Diagram; Liquid

2.66277

149.88

Diagram; Liquid

2.90504

151.84

Diagram; Liquid

3.21632

153.86

Diagram; Liquid

3.50285

155.79

Diagram; Liquid

3.83288

157.61

Diagram; Liquid

4.18092

159.76

Diagram; Liquid

4.53045

161.74

Diagram; Liquid

4.952

163.7

Diagram; Liquid

5.40354

165.71

Diagram; Liquid

5.88359

167.69

Diagram; Liquid

Monte, Manuel J. S.; Calvinho, Maria M. G.; Almeida, Ana R. R. P.; Amaral, Luisa M. P. F.; Lobo Ferreira, Ana I. M. C.; Ribeiro Da Silva,

54/144

2018-06-21 20:37:19

Maria D. M. C.; Notario, Rafael; Journal of Chemical and Engineering Data; vol. 57; nb. 9; (2012); p. 2486 - 2496,11, View in Reaxys 0.000124 - 0.018

298.2 - 343.2

Table exists

Hansen, Philip C.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 31; nb. 1; (1986); p. 1 - 3, View in Reaxys

NMR Spectroscopy (155) 1 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 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; Finney, Laura C.; Mitchell, Lorna J.; Moody, Christopher J.; Green Chemistry; vol. 20; nb. 10; (2018); p. 2242 - 2249, View in Reaxys 2 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Urgoitia, Garazi; Sanmartin, Raul; Herrero, Maria Teresa; Dominguez, Esther; Green Chemistry; vol. 13; nb. 8; (2011); p. 2161 - 2166, View in Reaxys; Finney, Laura C.; Mitchell, Lorna J.; Moody, Christopher J.; Green Chemistry; vol. 20; nb. 10; (2018); p. 2242 - 2249, View in Reaxys 3 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Seo, Sangwon; Slater, Mark; Greaney, Michael F.; Organic Letters; vol. 14; nb. 10; (2012); p. 2650 - 2653, View in Reaxys; Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys; Chebolu, Rajesh; Bahuguna, Ashish; Sharma, Reena; Mishra, Vivek Kumar; Ravikumar; Chemical Communications; vol. 51; nb. 84; (2015); p. 15438 - 15441, View in Reaxys; Komagawa, Hiromi; Maejima, Yukako; Nagano, Takashi; Synlett; vol. 27; nb. 5; (2016); p. 789 - 793, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys; Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Catalysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys 4 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

55/144

2018-06-21 20:37:19

Location

supporting information

Maji, Arun; Rana, Sujoy; Akanksha; Maiti, Debabrata; Angewandte Chemie - International Edition; vol. 53; nb. 9; (2014); p. 2428 - 2432; Angew. Chem.; vol. 126; nb. 9; (2014); p. 2460 - 2464,5, View in Reaxys; Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 - 3219, View in Reaxys; Wang, Guang-Zu; Li, Xing-Long; Dai, Jian-Jun; Xu, Hua-Jian; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7220 7225, View in Reaxys; Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys; Song, Juan; Wei, Fuliang; Sun, Wei; Li, Ke; Tian, Yanan; Liu, Chao; Li, Yali; Xie, Linghai; Organic Letters; vol. 17; nb. 9; (2015); p. 2106 2109, View in Reaxys; Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, View in Reaxys; Devari, Shekaraiah; Rizvi, Masood Ahmad; Shah, Bhahwal Ali; Tetrahedron Letters; vol. 57; nb. 30; (2016); p. 3294 - 3297, 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; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Synthetic Communications; vol. 46; nb. 21; (2016); p. 1747 - 1758, View in Reaxys; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Laha, Joydev K.; Patel, Ketul V.; Dubey, Gurudutt; Jethava, Krupal P.; Organic and Biomolecular Chemistry; vol. 15; nb. 10; (2017); p. 2199 - 2210, View in Reaxys; Wu, Jianglong; Liu, Yan; Liu, Ping; Gu, Chengzhi; Letters in Organic Chemistry; vol. 14; nb. 4; (2017); p. 254 - 260, View in Reaxys; Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Wu, Jianglong; Liu, Yan; Ma, Xiaowei; Liu, Ping; Gu, Chengzhi; Dai, Bin; Chinese Journal of Chemistry; vol. 35; nb. 9; (2017); p. 1391 - 139, View in Reaxys; Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, 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; Gao, Qian; Xu, Senmiao; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 208 - 212, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys; Laudadio, Gabriele; Govaerts, Sebastian; Wang, Ying; Ravelli, Davide; Koolman, Hannes F.; Fagnoni, Maurizio; Djuric, Stevan W.; Noël, Timothy; Angewandte Chemie - International Edition; vol. 57; nb. 15; (2018); p. 4078 - 4082; Angew. Chem.; vol. 130; nb. 15; (2018); p. 4142 - 4146,5, View in Reaxys 5 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Fukuyama, Takahide; Maetani, Shinji; Miyagawa, Kazusa; Ryu, Ilhyong; Organic Letters; vol. 16; nb. 12; (2014); p. 3216 3219, View in Reaxys; Baars, Hannah; Unoh, Yuto; Okada, Takeshi; Hirano, Koji; Satoh, Tetsuya; Tanaka, Ken; Bolm, Carsten; Miura, Masahiro; Chemistry Letters; vol. 43; nb. 11; (2014); p. 1782 - 1784, View in Reaxys; Guo, Wei; Lu, LiangQiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 - 2297,5, View in Reaxys; Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys; Sun, Denan; Li, Bijin; Lan,

56/144

2018-06-21 20:37:19

Jingbo; Huang, Quan; You, Jingsong; Chemical Communications; vol. 52; nb. 18; (2016); p. 3635 - 3638, 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; Yang, Yiwen; Ma, Hongxia; Tetrahedron Letters; vol. 57; nb. 47; (2016); p. 5278 - 5280, View in Reaxys; Laha, Joydev K.; Patel, Ketul V.; Dubey, Gurudutt; Jethava, Krupal P.; Organic and Biomolecular Chemistry; vol. 15; nb. 10; (2017); p. 2199 - 2210, View in Reaxys; Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys; Ramanathan, Mani; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung; Organic Letters; vol. 19; nb. 21; (2017); p. 5840 - 5843, View in Reaxys; Ruzi, Rehanguli; Zhang, Muliang; Ablajan, Keyume; Zhu, Chengjian; Journal of Organic Chemistry; vol. 82; nb. 23; (2017); p. 12834 - 12839, 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; Gao, Qian; Xu, Senmiao; Organic and Biomolecular Chemistry; vol. 16; nb. 2; (2018); p. 208 - 212, View in Reaxys; Huang, Tianzeng; Chen, Tieqiao; Han, Li-Biao; Journal of Organic Chemistry; vol. 83; nb. 5; (2018); p. 2959 - 2965, View in Reaxys 7 of 155

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

Konishi, Hideyuki; Futamata, Suguru; Wang, Xi; Manabe, Kei; Advanced Synthesis and Catalysis; vol. 360; nb. 9; (2018); p. 1805 - 1809, View in Reaxys 8 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 9 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

Paragraph 0064; 0068; 0072

Patent; Zhejiang University of Technology; Liu Yunkui; Zhang Wei; Zhang Wenxia; (9 pag.); CN105085205; (2018); (B) Chinese, View in Reaxys 10 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

57/144

2018-06-21 20:37:19

Location

supporting information

Yi, Chae S.; Kwon, Ki-Hyeok; Lee, Do W.; Organic Letters; vol. 11; nb. 7; (2009); p. 1567 - 1569, View in Reaxys; Zarei, Amin; Khazdooz, Leila; Aghaei, Hamidreza; Gheisari, Mohammad Mehdi; Alizadeh, Shahrzad; Golestanifar, Laleh; Tetrahedron; vol. 73; nb. 49; (2017); p. 6954 - 6961, View in Reaxys 11 of 155

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; Wei, Baosheng; Li, Heng; Zhang, Wen-Xiong; Xi, Zhenfeng; Organometallics; vol. 34; nb. 7; (2015); p. 1339 - 1344, View in Reaxys; Wang, Xiaolu; Liu, Mengjia; Wang, Yuqing; Fan, Hongyan; Wu, Jie; Huang, Chao; Hou, Hongwei; Inorganic Chemistry; vol. 56; nb. 21; (2017); p. 13329 - 13336, View in Reaxys 12 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Seo, Sangwon; Slater, Mark; Greaney, Michael F.; Organic Letters; vol. 14; nb. 10; (2012); p. 2650 - 2653, View in Reaxys; Seth, Saona; Jhulki, Samik; Moorthy, Jarugu Narasimha; European Journal of Organic Chemistry; nb. 12; (2013); p. 2445 2452, View in Reaxys; Ma, Jiaqi; Hu, Zhiming; Li, Meichao; Zhao, Weijuan; Hu, Xinquan; Mo, Weimin; Hu, Baoxiang; Sun, Nan; Shen, Zhenlu; Tetrahedron; vol. 71; nb. 38; (2015); p. 6733 - 6739, View in Reaxys; Chebolu, Rajesh; Bahuguna, Ashish; Sharma, Reena; Mishra, Vivek Kumar; Ravikumar; Chemical Communications; vol. 51; nb. 84; (2015); p. 15438 15441, View in Reaxys; Komagawa, Hiromi; Maejima, Yukako; Nagano, Takashi; Synlett; vol. 27; nb. 5; (2016); p. 789 793, View in Reaxys; Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi; Chemistry - An Asian Journal; vol. 11; nb. 16; (2016); p. 2312 - 2315, View in Reaxys; Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys 13 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys; Guo, Wei; Lu, Liang-Qiu; Wang, Yue; Wang, Ya-Ni; Chen, Jia-Rong; Xiao, Wen-Jing; Angewandte Chemie - International Edition; vol. 54; nb. 7; (2015); p. 2265 - 2269; Angew. Chem.; vol. 127; nb. 7; (2015); p. 2293 - 2297,5, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys; Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 14 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

58/144

2018-06-21 20:37:19

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys; Liu, Yangyang; Wang, Boliang; Journal of Chemical Research; vol. 38; nb. 7; (2014); p. 427 - 431, View in Reaxys; Liu, Li; Qiang, Jian; Bai, Shuhua; Li, Yang; Miao, Chunbao; Li, Jian; Applied Organometallic Chemistry; vol. 31; nb. 12; (2017); Art.No: E3817, View in Reaxys 15 of 155

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, View in Reaxys; Lim, Minkyung; Oh, Seungchan; Rhee, Hakjune; Bulletin of the Korean Chemical Society; vol. 32; (2011); p. 3179 - 3182, View in Reaxys; Obst, Martin; König, Burkhard; Beilstein Journal of Organic Chemistry; vol. 12; (2016); p. 2358 - 2363, View in Reaxys; Liu, Li; Qiang, Jian; Bai, Shuhua; Li, Yang; Miao, Chunbao; Li, Jian; Applied Organometallic Chemistry; vol. 31; nb. 12; (2017); Art.No: E3817, View in Reaxys 16 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

22.84

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Tang, Jing; Zhao, Shijun; Wei, Yuanyuan; Quan, Zhengjun; Huo, Congde; Organic and Biomolecular Chemistry; vol. 15; nb. 7; (2017); p. 1589 - 1592, View in Reaxys 18 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

59/144

2018-06-21 20:37:19

Laha, Joydev K.; Jethava, Krupal P.; Patel, Sagarkumar; Patel, Ketul V.; Journal of Organic Chemistry; vol. 82; nb. 1; (2017); p. 76 - 85, View in Reaxys 19 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Hu, Guang; Ramakumar, Kinthada; Brenner-Moyer, Stacey E.; Journal of Organic Chemistry; vol. 82; nb. 13; (2017); p. 6972 - 6977, View in Reaxys 20 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

Paragraph 0088

Patent; Nanjing University of Posts and Telecommunications; Song Juan; Wei Fuliang; Sun Wei; Li Yali; Xie Linghai; (32 pag.); CN104844400; (2017); (B) Chinese, View in Reaxys 21 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Location

Paragraph 0088

Patent; Nanjing University of Posts and Telecommunications; Song Juan; Wei Fuliang; Sun Wei; Li Yali; Xie Linghai; (32 pag.); CN104844400; (2017); (B) Chinese, View in Reaxys 22 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

25.84

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

supporting information

Ramanathan, Mani; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung; Organic Letters; vol. 19; nb. 21; (2017); p. 5840 5843, View in Reaxys 23 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys 24 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

60/144

2018-06-21 20:37:19

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys; Wang, Xing; Chen, Rui-Xi; Wei, Zeng-Feng; Zhang, Chen-Yang; Tu, Hai-Yang; Zhang, Ai-Dong; Journal of Organic Chemistry; vol. 81; nb. 1; (2016); p. 238 - 249, View in Reaxys 25 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p. 4888 - 4891, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Tetrahedron; vol. 72; nb. 29; (2016); p. 4252 - 4257, View in Reaxys; Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys; Alanthadka, Anitha; Devi, E. Sankari; Nagarajan, Subbiah; Sridharan, Vellaisamy; Suvitha, Ambigapathy; Maheswari, C. Uma; European Journal of Organic Chemistry; vol. 2016; nb. 28; (2016); p. 4872 - 4880, View in Reaxys; Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 - 5683, View in Reaxys 26 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Fukuda, Naohiro; Izumi, Minoru; Ikemoto, Tomomi; Tetrahedron Letters; vol. 56; nb. 25; (2015); p. 3905 - 3908, View in Reaxys; Evoniuk, Christopher J.; Hill, Sean P.; Hanson, Kenneth; Alabugin, Igor V.; Chemical Communications; vol. 52; nb. 44; (2016); p. 7138 - 7141, View in Reaxys 27 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Cai, Zhiqiang; Hou, Xu; Hou, Ling; Hu, Zhiquan; Zhang, Bo; Jin, Zhengsheng; Synlett; vol. 27; nb. 3; (2016); p. 395 398; Art.No: ST-2015-W0682-L, View in Reaxys 28 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

61/144

2018-06-21 20:37:19

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Evoniuk, Christopher J.; Hill, Sean P.; Hanson, Kenneth; Alabugin, Igor V.; Chemical Communications; vol. 52; nb. 44; (2016); p. 7138 - 7141, View in Reaxys 29 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

20.34

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

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p. 4952 - 4961, View in Reaxys 30 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.14

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

supporting information

Bhardwaj, Madhvi; Sharma, Harsha; Paul, Satya; Clark, James H.; New Journal of Chemistry; vol. 40; nb. 6; (2016); p. 4952 - 4961, View in Reaxys 31 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Mishra, Kalpana; Pandey, Ashok Kumar; Singh, Jay Bahadur; Singh, Radhey M.; Organic and Biomolecular Chemistry; vol. 14; nb. 26; (2016); p. 6328 - 6336, View in Reaxys; Alanthadka, Anitha; Devi, E. Sankari; Nagarajan, Subbiah; Sridharan, Vellaisamy; Suvitha, Ambigapathy; Maheswari, C. Uma; European Journal of Organic Chemistry; vol. 2016; nb. 28; (2016); p. 4872 - 4880, View in Reaxys; Wang, Huiqiao; Wang, Zhong; Huang, Hongchun; Tan, Jiajing; Xu, Kun; Organic Letters; vol. 18; nb. 21; (2016); p. 5680 - 5683, View in Reaxys 32 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

62/144

2018-06-21 20:37:19

Temperature (NMR Spectroscopy) [°C]

21.8

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

supporting information

Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys 33 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

18.7

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

supporting information

Furusawa, Takuma; Morimoto, Tsumoru; Oka, Nagato; Tanimoto, Hiroki; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi; Chemistry Letters; vol. 45; nb. 4; (2016); p. 406 - 408, View in Reaxys 34 of 155

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 155

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 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

63/144

2018-06-21 20:37:19

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Location

supporting information

Li, Hu; Zhu, Ru-Yi; Shi, Wen-Juan; He, Ke-Han; Shi, Zhang-Jie; Organic Letters; vol. 14; nb. 18; (2012); p. 4850 - 4853,4, View in Reaxys; Motiwala, Hashim F.; Vekariya, Rakesh H.; Aubé, Jeffrey; Organic Letters; vol. 17; nb. 21; (2015); p. 5484 - 5487, View in Reaxys 38 of 155

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

Temperature (NMR Spectroscopy) [°C]

24.84

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

supporting information

Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys 40 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

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

supporting information

Ang, Wei Jie; Lam, Yulin; Organic and Biomolecular Chemistry; vol. 13; nb. 4; (2015); p. 1048 - 1052, View in Reaxys 41 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

64/144

2018-06-21 20:37:19

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 42 of 155

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 43 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 151 scopy) [MHz] Location

supporting information

Fukuda, Naohiro; Izumi, Minoru; Ikemoto, Tomomi; Tetrahedron Letters; vol. 56; nb. 25; (2015); p. 3905 - 3908, View in Reaxys 44 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Dai, Wen; Lv, Ying; Wang, Lianyue; Shang, Sensen; Chen, Bo; Li, Guosong; Gao, Shuang; Chemical Communications; vol. 51; nb. 56; (2015); p. 11268 - 11271, View in Reaxys 45 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

21.84

65/144

2018-06-21 20:37:19

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

supporting information

Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys 46 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Fang, Xin-Qiang; Xu, Hua-Jian; Jiang, Hong; Liu, You-Cheng; Fu, Yao; Wu, Yun-Dong; Tetrahedron Letters; vol. 50; nb. 3; (2009); p. 312 - 315, View in Reaxys; Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, Xiao-Feng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 47 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 303 scopy) [MHz] Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 48 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 76.2 scopy) [MHz] Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

66/144

2018-06-21 20:37:19

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 50 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

water-d2; d(4)-methanol

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys 52 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 62.5 scopy) [MHz] Bellardita; Loddo; Mele; Panzeri; Parrino; Pibiri; Palmisano; RSC Advances; vol. 4; nb. 77; (2014); p. 40859 - 40864, View in Reaxys 53 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

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

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys; Nguyen, Thanh Vinh; Hall, Michael; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6895 - 6898, View in Reaxys 54 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.84

67/144

2018-06-21 20:37:19

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

supporting information

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys 56 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 303 scopy) [MHz] Location

supporting information

Prebil, Rok; Stavber, Gaj; Stavber, Stojan; European Journal of Organic Chemistry; vol. 2014; nb. 2; (2014); p. 395 - 402, View in Reaxys 57 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wang, Jin-Quan; He, Liang-Nian; New Journal of Chemistry; vol. 33; nb. 8; (2009); p. 1637 - 1640, View in Reaxys; Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Puenner, Florian; Schieven, Justin; Hilt, Gerhard; Organic Letters; vol. 15; nb. 18; (2013); p. 4888 - 4891, View in Reaxys 58 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 2970, View in Reaxys

68/144

2018-06-21 20:37:19

59 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] An, Gwangil; Ahn, Hyunseok; De Castro, Kathlia A.; Rhee, Hakjune; Synthesis; nb. 3; (2010); p. 477 - 485; Art.No: F19009SS, View in Reaxys; Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys; Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys 60 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 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; Fukuda, Naohiro; Kajiwara, Takeshi; Katou, Tomoaki; Majima, Keisuke; Ikemoto, Tomomi; Synlett; vol. 24; nb. 11; (2013); p. 1438 - 1442; Art.No: ST-2013-U0273-L, View in Reaxys 61 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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; Fukuda, Naohiro; Kajiwara, Takeshi; Katou, Tomoaki; Majima, Keisuke; Ikemoto, Tomomi; Synlett; vol. 24; nb. 11; (2013); p. 1438 - 1442; Art.No: ST-2013-U0273-L, View in Reaxys 62 of 155

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 63 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

69/144

2018-06-21 20:37:19

Frequency (NMR Spectro- 300 scopy) [MHz] Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 64 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 75.5 scopy) [MHz] Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 65 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys; Cosner, Casey C.; Cabrera, Pablo J.; Byrd, Katherine M.; Adams Thomas, Asia M.; Helquist, Paul; Organic Letters; vol. 13; nb. 8; (2011); p. 2071 - 2073, View in Reaxys; Havare, Nizam; Plattner, Dietmar A.; Organic Letters; vol. 14; nb. 19; (2012); p. 5078 - 5081,4, View in Reaxys 66 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wang, Congyang; Piel, Isabel; Glorius, Frank; Journal of the American Chemical Society; vol. 131; (2009); p. 4194 - 4195, View in Reaxys; Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys; Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 67 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

70/144

2018-06-21 20:37:19

Wang, Congyang; Piel, Isabel; Glorius, Frank; Journal of the American Chemical Society; vol. 131; (2009); p. 4194 - 4195, View in Reaxys; Tilly, David; Fu, Jian-Min; Zhao, Bao-Ping; Alessi, Manlio; Castanet, Anne-Sophie; Snieckus, Victor; Mortier, Jacques; Organic Letters; vol. 12; nb. 1; (2010); p. 68 - 71, View in Reaxys; Jin, Can; Zhang, Li; Su, Weike; Synlett; nb. 10; (2011); p. 1435 - 1438; Art.No: W06511ST, View in Reaxys; Lockner, Jonathan W.; Dixon, Darryl D.; Risgaard, Rune; Baran, Phil S.; Organic Letters; vol. 13; nb. 20; (2011); p. 5628 - 5631, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 68 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys; Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 69 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys; Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Wang, Jin-Quan; He, Liang-Nian; New Journal of Chemistry; vol. 33; nb. 8; (2009); p. 1637 - 1640, View in Reaxys; Cui, Li-Qian; Liu, Kai; Zhang, Chi; Organic and Biomolecular Chemistry; vol. 9; nb. 7; (2011); p. 2258 - 2265, View in Reaxys; Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys; Wang, Lianyue; Li, Jun; Yang, Hua; Lv, Ying; Gao, Shuang; Journal of Organic Chemistry; vol. 77; nb. 1; (2012); p. 790 - 794, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 70 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Wang, Lianyue; Li, Jun; Yang, Hua; Lv, Ying; Gao, Shuang; Journal of Organic Chemistry; vol. 77; nb. 1; (2012); p. 790 794, View in Reaxys 71 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

71/144

2018-06-21 20:37:19

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.74

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

supporting information

Li, Dan-Dan; Yuan, Ting-Ting; Wang, Guan-Wu; Journal of Organic Chemistry; vol. 77; nb. 7; (2012); p. 3341 - 3347, View in Reaxys 72 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 73 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 74 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene-d6

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

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 75 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

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

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 76 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz]

72/144

2018-06-21 20:37:19

Original Text (NMR Spectroscopy)

Location

supporting information

Signals [ppm]

7.29; 7.47 - 7.54; 7.66

Kind of signal

t, J=7.3 Hz, 2H; m, 4H; d, J=7.3 Hz, 2H

NMR (CDCl3, 400 MHz) β 7.29 (t, J=7.3 Hz, 2H), 7.47-7.54 (m, 4H), 7.66 (d, J=7.3 Hz, 2H)

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys 78 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys 79 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

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

supporting information

Liu, Tao-Ping; Liao, Yuan-Xi; Xing, Chun-Hui; Hu, Qiao-Sheng; Organic Letters; vol. 13; nb. 9; (2011); p. 2452 - 2455, View in Reaxys 80 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Liu, Tao-Ping; Liao, Yuan-Xi; Xing, Chun-Hui; Hu, Qiao-Sheng; Organic Letters; vol. 13; nb. 9; (2011); p. 2452 - 2455, View in Reaxys

73/144

2018-06-21 20:37:19

81 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75.5 scopy) [MHz] Zhang, Xin; Ji, Xuan; Jiang, Shanshan; Liu, Lili; Weeks, Brandon L.; Zhang, Zhao; Green Chemistry; vol. 13; nb. 7; (2011); p. 1891 - 1896, View in Reaxys 82 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300.1 scopy) [MHz] Location

supporting information

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys 83 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys 84 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.74

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

supporting information

74/144

2018-06-21 20:37:19

Wang, Azhong; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 75; nb. 7; (2010); p. 2321 - 2326, View in Reaxys 86 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

24.94

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

supporting information

Wang, Azhong; Jiang, Huanfeng; Journal of Organic Chemistry; vol. 75; nb. 7; (2010); p. 2321 - 2326, View in Reaxys 87 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 88 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Catir, Mustafa; Kilic, Hamdullah; Synlett; nb. 9; (2010); p. 1319 - 1322, View in Reaxys 89 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 200 scopy) [MHz] Location

supporting information

Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 90 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 50 scopy) [MHz] Location

supporting information

75/144

2018-06-21 20:37:19

Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys 91 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

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

supporting information

Yi, Chae S.; Kwon, Ki-Hyeok; Lee, Do W.; Organic Letters; vol. 11; nb. 7; (2009); p. 1567 - 1569, View in Reaxys 92 of 155

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

23.7

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 93 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 94 of 155

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 95 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz]

76/144

2018-06-21 20:37:19

Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 96 of 155

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

tetradeuteriomethanol

Frequency (NMR Spectro- 500 scopy) [MHz] Nakamura, Hideyuki; Tomonaga, Yuzo; Miyata, Kana; Uchida, Mitsuo; Terao, Yoshiyasu; Environmental Science and Technology; vol. 41; nb. 7; (2007); p. 2190 - 2195, View in Reaxys 97 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

tetradeuteriomethanol

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys; Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys 99 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100.6 scopy) [MHz] Sano, Yuki; Tanaka, Takanori; Hayashi, Masahiko; Chemistry Letters; vol. 36; nb. 12; (2007); p. 1414 - 1415, View in Reaxys 100 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Chvatal, Ivan; Vymetal, Jan; Pecha, Jaroslav; Simanek, Vilim; Dolejs, Ladislav; et al.; Collection of Czechoslovak Chemical Communications; vol. 48; nb. 1; (1983); p. 112 - 122, View in Reaxys; Diesveld, J. W.; Borkent, J.H.; Laarhoven, W. H.; Tetrahedron; vol. 38; nb. 12; (1982); p. 1803 - 1808, View in Reaxys; Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p. 5425 - 5430, View in Reaxys; Yang, Guanyu; Zhang, Qiaohong; Miao, Hong; Tong, Xinli; Xu, Jie; Organic Letters; vol. 7; nb. 2; (2005); p. 263 - 266, View in Reaxys; Oota, Atsushi;

77/144

2018-06-21 20:37:19

Imai, Toshinobu; Yamazaki, Ayumi; Oba, Toru; Karikomi, Michinori; Minabe, Masahiro; Bulletin of the Chemical Society of Japan; vol. 79; nb. 2; (2006); p. 333 - 335, View in Reaxys; Singh, Krishna Nand; Kumar, Rajesh; Shukla, Ajay Kumar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 8; (2007); p. 1347 - 1351, View in Reaxys 101 of 155

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

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

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 102 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

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

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 103 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Comment (NMR Spectroscopy)

ambient temperature

Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys 104 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Tilly, David; Samanta, Subhendu S.; De, Asish; Castanet, Anne-Sophie; Mortier, Jacques; Organic Letters; vol. 7; nb. 5; (2005); p. 827 - 830, View in Reaxys 105 of 155

Nucleus (NMR Spectroscopy)

Coupling Nuclei

78/144

2018-06-21 20:37:19

Solvents (NMR Spectroscopy)

CDCl3

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CD3CN

Frequency (NMR Spectro- 50.3 scopy) [MHz] Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb. 17; (2005); p. 6609 - 6615, View in Reaxys 107 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Boberg, Friedrich; Schmidt, Wolfgang; Garming, Alfons; Phosphorus and Sulfur and the Related Elements; vol. 21; (1984); p. 315 - 320, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys 108 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

acetone-d6

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 270 scopy) [MHz] Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys 109 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectro- 67.5 scopy) [MHz] Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys 110 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

79/144

2018-06-21 20:37:19

Olah, Georgen A.; Nakajima, Tadashi; Prakash, G. K. Surya; Angewandte Chemie; vol. 92; nb. 10; (1980); p. 837 - 838, View in Reaxys; Majumder; Chakraborti; Journal of the Indian Chemical Society; vol. 66; nb. 11; (1989); p. 834 - 837, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p. 5425 5430, View in Reaxys 111 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Branch, Catherine S.; Bott, Simon G.; Barron, Andrew R.; Journal of Organometallic Chemistry; vol. 666; nb. 1-2; (2003); p. 23 - 34, View in Reaxys 112 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

26.85

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Mobli, Mehdi; Smith, Richard J.; Magnetic Resonance in Chemistry; vol. 41; nb. 1; (2003); p. 26 36, View in Reaxys 113 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

26.85

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Mobli, Mehdi; Smith, Richard J.; Magnetic Resonance in Chemistry; vol. 41; nb. 1; (2003); p. 26 36, View in Reaxys 114 of 155

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Chatani; Kamitani; Oshita; Fukumoto; Murai; Journal of the American Chemical Society; vol. 123; nb. 50; (2001); p. 12686 - 12687, View in Reaxys; Ibrahim, Yehia A.; Al-Awadi, Nouria A.; Kual, Kamini; Tetrahedron; vol. 59; nb. 29; (2003); p. 5425 - 5430, View in Reaxys 115 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 80 scopy) [MHz]

80/144

2018-06-21 20:37:19

Lukasiewicz, Marcin; Bogdal, Dariusz; Pielichowski, Jan; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1269 - 1272, View in Reaxys 116 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Sancassan, Fernando; Petrillo, Giovanni; Abraham, Raymond J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1965 - 1972, View in Reaxys; Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 117 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 119 of 155

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; Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys; Coletta, Flaviano; Gazzetta Chimica Italiana; vol. 127; nb. 4; (1997); p. 221 - 226, View in Reaxys 120 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Coletta, Flaviano; Gazzetta Chimica Italiana; vol. 127; nb. 4; (1997); p. 221 - 226, View in Reaxys 121 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

solid

81/144

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Temperature (NMR Spectroscopy) [°C]

Fung; Tong, Tat-Hung; Dollase, Thilo; Magnuson, Matthew L.; Journal of Magnetic Resonance - Series A; vol. 123; nb. 1; (1996); p. 56 - 63, View in Reaxys 122 of 155

Description (NMR Spectroscopy)

NMR with shift reagents

Wolkowski,Z.W.; Tetrahedron Letters; (1971); p. 821 - 824, View in Reaxys; Ammon,H.L.; Mazzocchi,P.H.; Colicelli,E.J.; Organic Magnetic Resonance; vol. 11; (1978); p. 1, View in Reaxys; Mazzocchi et al.; Tetrahedron Letters; (1973); p. 573,574, View in Reaxys; Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 - 28, View in Reaxys; Abraham, Raymond J.; Bergen, Helen A.; Chadwick, Derek J.; Sancassan, Fernando; Journal of the Chemical Society, Chemical Communications; nb. 17; (1982); p. 998 - 1000, View in Reaxys; Sancassan, Fernando; Petrillo, Giovanni; Abraham, Raymond J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1965 - 1972, View in Reaxys 123 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

acetonitrile

Temperature (NMR Spectroscopy) [°C]

Baumstark; Graham; Boykin; Tetrahedron Letters; vol. 31; nb. 7; (1990); p. 957 - 960, View in Reaxys; Boykin, D. W.; Nowak-Wydra, Barbara; Magnetic Resonance in Chemistry; vol. 29; nb. 2; (1991); p. 152 - 155, View in Reaxys; Boykin, David W.; Kumar, Arvind; Journal of Molecular Structure; vol. 298; (1993); p. 121 - 128, View in Reaxys 124 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys; Negrebetskii, Vad. V.; Russian Journal of General Chemistry; vol. 63; nb. 9.2; (1993); p. 1436 - 1440; Zhurnal Obshchei Khimii; vol. 63; nb. 9; (1993); p. 2059 - 2066, View in Reaxys 125 of 155

Description (NMR Spectroscopy)

Linewidth of NMR absorption

Negrebetskii, Vad. V.; Russian Journal of General Chemistry; vol. 63; nb. 9.2; (1993); p. 1436 - 1440; Zhurnal Obshchei Khimii; vol. 63; nb. 9; (1993); p. 2059 - 2066, View in Reaxys 126 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys 127 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

82/144

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Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys 128 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys 129 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys 130 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

dimethylsulfoxide

Temperature (NMR Spectroscopy) [°C]

Kurkovskaya L. N.; Negrebetskii, Vad. V.; Traven, V. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 9.2; (1991); p. 2097 - 2104,1945 - 1951, View in Reaxys 131 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

Krivdin, L. B.; Kalabin, G. A.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 11; (1988); p. 2045 2051; Zhurnal Organicheskoi Khimii; vol. 24; nb. 11; (1988); p. 2268 - 2275, View in Reaxys 132 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

acetone-d6

83/144

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133 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Hauser, A.; Thurner, J.-U.; Hinzmann, B.; Journal fuer Praktische Chemie (Leipzig); vol. 330; nb. 3; (1988); p. 367 - 378, View in Reaxys 134 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Hirayama, Masatoshi; Suzuki, Hideto; Ohhata, Hiroshi; Chemistry Letters; (1987); p. 413 - 416, View in Reaxys; Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 136 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

various solvent(s)

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 137 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

various solvent(s)

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 138 of 155

Description (NMR Spectroscopy)

2D-NMR

Hirayama, Masatoshi; Ohhata, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 60; nb. 8; (1987); p. 2751 - 2756, View in Reaxys 139 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

84/144

2018-06-21 20:37:19

Jaccard, Guy; Lauterwein, Juergen; Helvetica Chimica Acta; vol. 69; (1986); p. 1469 - 1485, View in Reaxys 140 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

28.7

Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys 141 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

Mieloszynski, J. L.; Andrieu, C. G.; Schneider, M.; Paquer, D.; Recueil des Travaux Chimiques des Pays-Bas; vol. 104; nb. 1; (1985); p. 9 - 15, View in Reaxys 142 of 155

Description (NMR Spectroscopy)

NOE

Wilson, Nancy K.; Magnetic Resonance in Chemistry; vol. 23; nb. 1; (1985); p. 12 - 15, View in Reaxys 143 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Honzl, Jan; Lovy, Jan; Tetrahedron; vol. 40; nb. 10; (1984); p. 1885 - 1892, View in Reaxys 144 of 155

Description (NMR Spectroscopy)

CIDNP

Honzl, Jan; Lovy, Jan; Tetrahedron; vol. 40; nb. 10; (1984); p. 1885 - 1892, View in Reaxys 145 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

benzene-d6

Diesveld, J. W.; Borkent, J.H.; Laarhoven, W. H.; Tetrahedron; vol. 38; nb. 12; (1982); p. 1803 - 1808, View in Reaxys 146 of 155

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CS2

Temperature (NMR Spectroscopy) [°C]

24.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 147 of 155

Description (NMR Spectroscopy)

Chemical shifts

85/144

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Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

fluorosulfonic acid; not given

Temperature (NMR Spectroscopy) [°C]

-70

Olah, Georgen A.; Nakajima, Tadashi; Prakash, G. K. Surya; Angewandte Chemie; vol. 92; nb. 10; (1980); p. 837 - 838, View in Reaxys 148 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

-48.2 - 51.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 149 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

24.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 150 of 155

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

36.9

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 151 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CS2

Temperature (NMR Spectroscopy) [°C]

24.9

Comment (NMR Spectroscopy)

1H-1H.

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 152 of 155

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

86/144

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Temperature (NMR Spectroscopy) [°C]

36.9

Comment (NMR Spectroscopy)

1H-13C.

Drake, J. A. G.; Jones, D. W.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 36; (1980); p. 23 28, View in Reaxys 153 of 155

Description (NMR Spectroscopy)

NMR

Bartlett,P.D.; Landis,M.E.; Journal of the American Chemical Society; vol. 99; (1977); p. 3033 - 3037, View in Reaxys; Dehmlow,E.V. et al.; Justus Liebigs Annalen der Chemie; (1977); p. 1617 - 1624, View in Reaxys; Stothers,J.B.; Tan,C.T.; Wilson,N.K.; Organic Magnetic Resonance; vol. 9; (1977); p. 408, View in Reaxys; Giraud,J.; Marzin,C.; Organic Magnetic Resonance; vol. 12; (1979); p. 647, View in Reaxys; Knothe,L.; Prinzbach,H.; Justus Liebigs Annalen der Chemie; (1977); p. 687, View in Reaxys; Jackman,L.M.; Trewella,J.C.; Journal of the American Chemical Society; vol. 98; (1976); p. 5712, View in Reaxys; Koster,P.B.; Runsink,J.; Janssen,M.J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 393, View in Reaxys; Takeshita; Hirota; Journal of Chemical Physics; vol. 58; (1973); p. 3745, View in Reaxys; Balkau; Heffernan; Australian Journal of Chemistry; vol. 24; (1971); p. 2305,2308, View in Reaxys; Kuo; Nye; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995,1999, View in Reaxys; Cardillo et al.; Synthesis; (1976); p. 394, View in Reaxys; Canters; de Boer; Molecular Physics; vol. 26; (1973); p. 1185,1194, View in Reaxys 154 of 155

Description (NMR Spectroscopy)

Spin-spin relaxation time (T2)

Liu; Edman; Journal of the American Chemical Society; vol. 90; (1968); p. 213, View in Reaxys 155 of 155

Description (NMR Spectroscopy)

Spectrum

Martin et al.; Tetrahedron; vol. 20; (1964); p. 1505,1513, 1514, View in Reaxys IR Spectroscopy (55) 1 of 55

Description (IR Spectroscopy)

Bands; Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Bryan E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys; Srivastava, Manish; Srivastava, Anamika; Goyal, Ashu; Mishra, Aakanksha; Tomer, Preeti; Dwivedi, Jaya; Kishore; Journal of Physical Organic Chemistry; vol. 30; nb. 2; (2017); Art.No: E3602, View in Reaxys 2 of 55

Description (IR Spectroscopy)

Spectrum

Location

supporting information

Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Phillips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys; Zarei, Amin; Khazdooz, Leila; Aghaei, Hamidreza; Gheisari, Mohammad Mehdi; Alizadeh, Shahrzad; Golestanifar, Laleh; Tetrahedron; vol. 73; nb. 49; (2017); p. 6954 - 6961, View in Reaxys 3 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Comment (IR Spectroscopy)

film

Hu, Yixin; Zhou, Lihong; Lu, Wenjun; Synthesis (Germany); vol. 49; nb. 17; (2017); p. 4007 - 4016, View in Reaxys 4 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Location

supporting information

Malekafzali; Malinovska; Patureau; New Journal of Chemistry; vol. 41; nb. 15; (2017); p. 6981 - 6985, View in Reaxys

87/144

2018-06-21 20:37:19

5 of 55

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Solvent (IR Spectroscopy)

potassium bromide

Albertin, Gabriele; Antoniutti, Stefano; Bortoluzzi, Marco; Botter, Alessandra; Castro, Jesús; Inorganic Chemistry; vol. 55; nb. 11; (2016); p. 5592 - 5602, View in Reaxys 6 of 55

Description (IR Spectroscopy)

Intensity of IR bands; Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Albertin, Gabriele; Antoniutti, Stefano; Botter, Alessandra; Castro, Jesús; Inorganic Chemistry; vol. 54; nb. 5; (2015); p. 2091 - 2093, View in Reaxys 7 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

sodium chloride; chloroform

Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 8 of 55

Description (IR Spectroscopy)

Bands

Sieglitz,A.; Troester,H.; Chemische Berichte; vol. 96; (1963); p. 2577 - 2594, View in Reaxys; Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys; Bergmann,E.D.; Solomonovici,A.; Synthesis; (1970); p. 183 - 189, View in Reaxys; Flett,M.S.C.; Spectrochimica Acta; vol. 18; (1962); p. 1537 - 1556, View in Reaxys; Dunken; Fritzsche; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 249, View in Reaxys; Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys; Brown; Spectrochimica Acta; vol. 18; (1962); p. 1065,1066, View in Reaxys; Branch, Catherine S.; Bott, Simon G.; Barron, Andrew R.; Journal of Organometallic Chemistry; vol. 666; nb. 1-2; (2003); p. 23 - 34, View in Reaxys; Mohammadpoor-Baltork, Iraj; Sadeghi, Majid M. M.; Esmayilpour, Karim; Journal of Chemical Research - Part S; nb. 6; (2003); p. 348 - 350, View in Reaxys; Mohammadpoor-Baltork, Iraj; Memarian, Hamid Reza; Bahrami, Kiumars; Monatshefte fur Chemie; vol. 135; nb. 4; (2004); p. 411 - 418, View in Reaxys; Shaabani, Ahmad; Mirzaei, Peiman; Naderi, Soheila; Lee, Donald G.; Tetrahedron; vol. 60; nb. 50; (2004); p. 11415 - 11420, View in Reaxys; Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys; Saikia, Gunin; Iyer, Parameswar K.; Journal of Organic Chemistry; vol. 75; nb. 8; (2010); p. 2714 - 2717, View in Reaxys; Kidwai, Mazaahir; Bhardwaj, Saurav; Applied Catalysis A: General; vol. 387; nb. 1-2; (2010); p. 1 - 4, View in Reaxys; Geraghty, Niall W.A.; McArdle, Patrick; Mullen, Laverne M.A.; Tetrahedron; vol. 67; nb. 19; (2011); p. 3546 - 3552, View in Reaxys; Lv, Xiao-Ming; Kong, Ling-Jie; Lin, Qi; Liu, XiaoFeng; Zhou, Ya-Ming; Jia, Yu; Synthetic Communications; vol. 41; nb. 21; (2011); p. 3215 - 3222, View in Reaxys; Tandon, Praveen K.; Singh, Santosh B.; Singh, Satpal; Kesarwani, Bhawana; Journal of the Indian Chemical Society; vol. 89; nb. 10; (2012); p. 1363 - 1367, View in Reaxys; Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 9 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys 10 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Wan, Jung-Chih; Huang, Jun-Min; Jhan, Yu-Huei; Hsieh, Jen-Chieh; Organic Letters; vol. 15; nb. 11; (2013); p. 2742 2745, View in Reaxys 11 of 55

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Haggam, Reda A.; Tetrahedron; vol. 69; nb. 31; (2013); p. 6488 - 6494, View in Reaxys 12 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

88/144

2018-06-21 20:37:19

Zhang, Xin; Ji, Xuan; Su, Ruifei; Weeks, Brandon L.; Zhang, Zhao; Deng, Songlu; ChemPlusChem; vol. 78; nb. 7; (2013); p. 703 - 711, View in Reaxys 13 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys; Paul, Sunanda; Samanta, Shubhankar; Ray, Jayanta K.; Tetrahedron Letters; vol. 51; nb. 42; (2010); p. 5604 - 5608, View in Reaxys; Kumar, R. Arun; Maheswari, C. Uma; Ghantasala, Satheesh; Jyothi; Reddy, K. Rajender; Advanced Synthesis and Catalysis; vol. 353; nb. 2-3; (2011); p. 401 - 410, View in Reaxys; Nishida, Shunsuke; Hayashi, Masahiko; Synlett; vol. 23; nb. 11; (2012); p. 1683 - 1685, View in Reaxys 14 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent, solid phase)

Su, Yijin; Zhang, Liangren; Jiao, Ning; Organic Letters; vol. 13; nb. 9; (2011); p. 2168 - 2171, View in Reaxys; Gandeepan, Parthasarathy; Hung, Chen-Hsun; Cheng, Chien-Hong; Chemical Communications; vol. 48; nb. 75; (2012); p. 9379 - 9381, View in Reaxys 15 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 16 of 55

Description (IR Spectroscopy)

Intensity of IR bands; ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat (no solvent, solid phase)

Location

supporting information

Bluemke, Tobias D.; Klatt, Thomas; Koszinowski, Konrad; Knochel, Paul; Angewandte Chemie - International Edition; vol. 51; nb. 39; (2012); p. 9926 - 9930, View in Reaxys 17 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent)

Shejwalkar, Pushkar; Rath, Nigam P.; Bauer, Eike B.; Dalton Transactions; vol. 40; nb. 29; (2011); p. 7617 - 7631, View in Reaxys; Thirunavukkarasu, Vedhagiri S.; Cheng, Chien-Hong; Chemistry - A European Journal; vol. 17; nb. 52; (2011); p. 14723 - 14726, View in Reaxys 18 of 55

Description (IR Spectroscopy)

Bands

Location

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys 19 of 55

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

89/144

2018-06-21 20:37:19

20 of 55

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Location

supporting information

Comment (IR Spectroscopy)

neat (no solvent, solid phase)

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys 21 of 55

Description (IR Spectroscopy)

Reflection spectrum

Silvestre, Samuel M.; Salvador, Jorge A.R.; Tetrahedron; vol. 63; nb. 11; (2007); p. 2439 - 2445, View in Reaxys 22 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Lukasiewicz, Marcin; Bogdal, Dariusz; Pielichowski, Jan; Advanced Synthesis and Catalysis; vol. 345; nb. 12; (2003); p. 1269 - 1272, View in Reaxys; Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys; Qian, Weixing; Jin, Erlei; Bao, Weiliang; Zhang, Yongmin; Angewandte Chemie - International Edition; vol. 44; nb. 6; (2005); p. 952 - 955, View in Reaxys; Barluenga, Jose; Trincado, Monica; Rubio, Eduardo; Gonzalez, Jose M.; Angewandte Chemie - International Edition; vol. 45; nb. 19; (2006); p. 3140 - 3143, View in Reaxys; Singh, Krishna Nand; Kumar, Rajesh; Shukla, Ajay Kumar; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 46; nb. 8; (2007); p. 1347 - 1351, View in Reaxys 23 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

cyclohexane

Temperature (IR Spectroscopy) [°C]

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb. 1-3; (2007); p. 44 - 48, View in Reaxys 24 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

cyclohexane

Temperature (IR Spectroscopy) [°C]

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb. 1-3; (2007); p. 44 - 48, View in Reaxys 25 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

octan-1-ol

Temperature (IR Spectroscopy) [°C]

19.84 - 49.84

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb. 1-3; (2007); p. 44 - 48, View in Reaxys 26 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

octan-1-ol

Temperature (IR Spectroscopy) [°C]

Hirai, Satori; Banno, Motohiro; Ohta, Kaoru; Palit, Dipak K.; Tominaga, Keisuke; Chemical Physics Letters; vol. 450; nb. 1-3; (2007); p. 44 - 48, View in Reaxys 27 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

KBr

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Comment (IR Spectroscopy)

ambient temperature

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 28 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

ambient temperature

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 29 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CD3CN

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited singlet state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 30 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CD3CN

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited singlet state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 31 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

heptane

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 32 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

heptane

Comment (IR Spectroscopy)

ground state. Object(s) of Study: excited triplet state

Tanaka, Satomi; Kato, Chihiro; Horie, Kazuyuki; Hamaguchi, Hiro-O; Chemical Physics Letters; vol. 381; nb. 3-4; (2003); p. 385 - 391, View in Reaxys 33 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

vapour

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys 34 of 55

Description (IR Spectroscopy)

Vibrational energy transfer

Zalesskaya, G. A.; Yakovlev, D. L.; Sambor, E. G.; Prikhodchenko, D. V.; Journal of Applied Spectroscopy; vol. 68; nb. 1; (2001); p. 150 - 158; Zhurnal Prikladnoi Spektroskopii; vol. 68; nb. 1; (2001); p. 110 - 115, View in Reaxys 35 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

91/144

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Kalinovskii; Pogorelov; Gelbshtein; Akhmetov; Russian Journal of General Chemistry; vol. 71; nb. 9; (2001); p. 1457 - 1462, View in Reaxys 36 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

3056 - 747 cm**(-1)

Mirafzal, Gholam A.; Lozeva, Albena M.; Tetrahedron Letters; vol. 39; nb. 40; (1998); p. 7263 - 7266, View in Reaxys 37 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

1715 1/cm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys 38 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

nujol

Comment (IR Spectroscopy)

1950 - 645 cm**(-1)

Dutt, Sachchidananda; Banerjee, Santanu; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 64; (1987); p. 704 - 705, View in Reaxys; Dutta, Hasi; Hazra, Banasri; Banerjee, Amalendu; Banerjee, Santanu; Journal of the Indian Chemical Society; vol. 64; (1987); p. 706 - 707, View in Reaxys; Banerjee, Amalendu; Mandal, Dinabandhu; Ray, Arindam; Banerjee, Pulak; Banerjee, Gopal Chandra; Journal of the Indian Chemical Society; vol. 72; nb. 3; (1995); p. 205 - 208, View in Reaxys 39 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

polyethylene; potassium bromide

Kolev, Tsonko; Journal of Molecular Structure; vol. 349; (1995); p. 381 - 384, View in Reaxys 40 of 55

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1728 - 204 cm**(-1)

Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys 41 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1720 cm**(-1)

Zaitsev, B. E.; Zhdamarov, O. S.; Sheban, G. V.; Pleshakov, V. G.; Grigor'ev, G. V.; Prostakov, N. S.; Chemistry of Heterocyclic Compounds (New York, NY, United States); (1988); p. 294 - 299; Khimiya Geterotsiklicheskikh Soedinenii; vol. 24; nb. 3; (1988); p. 361 - 366, View in Reaxys 42 of 55

Description (IR Spectroscopy)

Intensity of IR bands

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1730 - 651 cm**(-1)

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Dunkin, Ian R.; Bell, Gordon A.; Tetrahedron; vol. 41; (1985); p. 339 - 348, View in Reaxys 44 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3500 - 700 cm**(-1)

Chiu; Biemann; Krishnan; Hill; Analytical Chemistry; vol. 56; nb. 9; (1984); p. 1610 - 1615, View in Reaxys 45 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

1736 cm**(-1)

Chiu; Biemann; Krishnan; Hill; Analytical Chemistry; vol. 56; nb. 9; (1984); p. 1610 - 1615, View in Reaxys 46 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

1720 cm**(-1)

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

1835 - 432 cm**(-1)

Banerjee, Amalendu; Dutt, Sachchidananda; Sengupta, Dipanjan; Adak, Mohini Mohan; Samaddar, Haraprasad; Journal of the Indian Chemical Society; vol. 60; (1983); p. 275 - 277, View in Reaxys 48 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

solid

Comment (IR Spectroscopy)

1800 - 1500 cm**(-1)

Zaitsev B. E.; Grekhova, N. G.; Sheban, G. V.; Dyumaev, K. M.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 18; nb. 10; (1982); p. 1079 - 1083; Khimiya Geterotsiklicheskikh Soedinenii; vol. 18; nb. 10; (1982); p. 1388 - 1392, View in Reaxys 49 of 55

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

solid

Comment (IR Spectroscopy)

1720 - 1610 cm**(-1)

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1720 cm**(-1)

Saito, Takao; Oikawa, Isao; Motoki, Shinichi; Bulletin of the Chemical Society of Japan; vol. 53; nb. 4; (1980); p. 1023 1027, View in Reaxys 51 of 55

Description (IR Spectroscopy)

93/144

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Juchnovski,I. et al.; Monatshefte fuer Chemie; vol. 101; (1970); p. 1712 - 1719, View in Reaxys; Tochtermann,W. et al.; Chemische Berichte; vol. 105; (1972); p. 1431 - 1438, View in Reaxys; Whitesides,G.M.; Ehmann,W.J.; Journal of the American Chemical Society; vol. 92; nb. 19; (1970); p. 5625 - 5640, View in Reaxys; Trost,B.M.; Kinson,P.L.; Journal of the American Chemical Society; vol. 97; nb. 9; (1975); p. 2438 - 2449, View in Reaxys; Bartlett,P.D.; Landis,M.E.; Journal of the American Chemical Society; vol. 99; (1977); p. 3033 - 3037, View in Reaxys; Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Battaglia et al.; Synthesis; (1971); p. 378, View in Reaxys; Olah; Welch; Journal of the American Chemical Society; vol. 100; (1978); p. 5396,5397, View in Reaxys; Kuo; Nye; Canadian Journal of Chemistry; vol. 51; (1973); p. 1995,1999, View in Reaxys; Minato; Bulletin of the Chemical Society of Japan; vol. 36; (1963); p. 1020, View in Reaxys; Schroeder; Mazur; Journal of the American Chemical Society; vol. 100; (1978); p. 7339,7345, View in Reaxys; Cardillo et al.; Synthesis; (1976); p. 394, View in Reaxys; Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys; Bostwick et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 1505,1506, 1508, View in Reaxys; Beelitz et al.; Chemiker-Zeitung; vol. 103; (1979); p. 179, View in Reaxys; Sahini; Ciurea; Revue Roumaine de Chimie; vol. 17; (1972); p. 273,276-279,282, View in Reaxys; Davies; Waring; Journal of the Chemical Society [Section] C: Organic; (1968); p. 2332, View in Reaxys 52 of 55

Description (IR Spectroscopy)

Polarization of IR bands

Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys 53 of 55

Description (IR Spectroscopy)

Spectrum

Demmering; Doerr; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 19; (1964); p. 365, View in Reaxys; Latham et al.; Analytical Chemistry; vol. 34; (1962); p. 311,312, View in Reaxys 54 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

tetrachloroethene

Comment (IR Spectroscopy)

2000 - 1250 cm**(-1)

Bruice; Sayigh; Journal of the American Chemical Society; vol. 81; (1959); p. 3416,3419, View in Reaxys 55 of 55

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

benzene

Comment (IR Spectroscopy)

10000 - 667 cm**(-1)

Ueberreiter; Rabel; Zeitschrift fuer Physikalische Chemie (Leipzig); <N.F.> 13 <1957> 95, 96, View in Reaxys Mass Spectrometry (39) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

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GCMS (Gas chromatography mass spectrometry); Spectrum

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Spectrum

supporting information

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mol peak

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HRMS (High resolution mass spectrometry); Spectrum

supporting information

Zhang, Jintang; Wang, Zhentao; Wang, Ye; Wan, Changfeng; Zheng, Xiaoqi; Wang, Zhiyong; Green Chemistry; vol. 11; nb. 12; (2009); p. 1973 - 1978, View in Reaxys

FAB (Fast atom bombardment); HRMS (High resolution mass spectrometry)

supporting informa- mol peak tion

Thirunavukkarasu, Vedhagiri S.; Parthasarathy, Kanniyappan; Cheng, Chien-Hong; Angewandte Chemie - International Edition; vol. 47; nb. 49; (2008); p. 9462 - 9465, View in Reaxys

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

supporting information

Nagano, Takashi; Kobayashi, Shu; Chemistry Letters; vol. 37; nb. 10; (2008); p. 1042 - 1043, View in Reaxys

spectrum; electron impact (EI)

Koenig, Johann; Balfanz, Eckhard; Funcke, Werner; Romanowski, Thomas; Analytical Chemistry; vol. 55; nb. 4; (1983); p. 599 - 603, View in Reaxys; Shevtsov, V. K.; Zvolinskii, V. P.; Zakharov, P. I.; Pleshakov, V. G.; Alekseeva, L. A.; Prostakov, N. S.; Journal of Organic Chemistry USSR (English Translation); vol. 18; (1982); p. 2140 - 2145; Zhurnal Organicheskoi Khimii; vol. 18; nb. 11; (1982); p. 2415 - 2421, View in Reaxys; Kamata, Keigo; Kasai, Jun; Yamaguchi, Kazuya; Mizuno, Noritaka; Organic Letters; vol. 6; nb. 20; (2004); p. 3577 - 3580, View in Reaxys

spectrum

collisional activation

Madhusudanan, K. P.; Durani, S.; Reddy, D. M.; Kapil, R. S.; Itagaki, Y.; Nojima, K.; Organic Mass Spectrometry; vol. 26; nb. 4; (1991); p. 298 304, View in Reaxys

fragmentation pattern; spectrum

metastable ions

Guidugli, F. H.; Ardanaz, C. E.; Kavka, J.; Garibay, M. E.; Joseph-Nathan, P.; Organic Mass Spectrometry; vol. 21; (1986); p. 117 - 124, View in Reaxys

spectrum

positive secondary ions

Ross, Mark M.; Colton, Richard J.; Analytical Chemistry; vol. 55; nb. 1; (1983); p. 150 - 153, View in Reaxys

ion current profiles; Proctor, C. J.; Kralj, B.; Larka, E. A.; Porter, C. J.; Maquestiau, A.; Bemetastable ions ynon, J. H.; Organic Mass Spectrometry; vol. 16; nb. 7; (1981); p. 312 322, View in Reaxys chemical ionization (CI)

IKE(S) (ion kinetic energy (spectrum))

Maquestiau, Andre; Flammang, Robert; Nielsen, Lawrence; Organic Mass Spectrometry; vol. 15; nb. 7; (1980); p. 376 - 379, View in Reaxys Beynon et al.; Journal of Physical Chemistry; vol. 63; (1959); p. 1861,1862, View in Reaxys; Eland; Danby; Journal of the Chemical Society; (1965); p. 5935,5936, View in Reaxys; Faust et al.; Zeitschrift fuer Naturforschung,

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Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 20; (1965); p. 1128,1133, View in Reaxys; Schwarz et al.; Journal of Heterocyclic Chemistry; vol. 13; (1976); p. 877, View in Reaxys; Beynon; Advances in Mass Spectrometry; (1959); p. 328,348, View in Reaxys; Koch; Markgraf; Journal of Heterocyclic Chemistry; vol. 8; (1971); p. 225,230, View in Reaxys; Krylowa et al.; Neftekhimiya; vol. 16; (1976); p. 581,582; Chem.Abstr.; vol. 85; nb. 159734; (1976), View in Reaxys; Gaines et al.; Analytical Chemistry; vol. 47; (1975); p. 1373, View in Reaxys; Patel; Politzer; Griffin; Laseter; Biomedical Mass Spectrometry; vol. 5; nb. 12; (1978); p. 664 670, View in Reaxys; Szabo et al.; Justus Liebigs Annalen der Chemie; (1977); p. 747,758, View in Reaxys; BELL JH; IRELAND S; SPEARS AW; Analytical Chemistry; vol. 41; nb. 2; (1969); p. 310 - 313, View in Reaxys; Beynon; Williams; Applied Spectroscopy; vol. 14; (1960); p. 156,158, View in Reaxys; Cheshire et al.; Tetrahedron; vol. 23; (1967); p. 1669, View in Reaxys UV/VIS Spectroscopy (115) 1 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Location

supporting information

Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Journal of the American Chemical Society; vol. 135; nb. 46; (2013); p. 17494 - 17500, View in Reaxys; Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Chemical Communications; vol. 50; nb. 79; (2014); p. 11701 - 11704, View in Reaxys; Bume, Desta Doro; Harry, Stefan Andrew; Pitts, Cody Ross; Lectka, Thomas; Journal of Organic Chemistry; vol. 83; nb. 3; (2018); p. 1565 - 1575, View in Reaxys 2 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Location

supporting information

Paul, Subhasis; Guin, Joyram; Green Chemistry; vol. 19; nb. 11; (2017); p. 2530 - 2534, View in Reaxys 3 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

258; 295; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

22000; 950; 71

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

258

Tan, Ke Xin; Lintang, Hendrik O.; Maniam, Subashani; Langford, Steven J.; Bakar, Mohd Bakri; Tetrahedron; vol. 72; nb. 35; (2016); p. 5402 - 5413, View in Reaxys 5 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

377

98/144

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Ext./Abs. Coefficient [l·mol-1cm-1]

260

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

379

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

382

Ext./Abs. Coefficient [l·mol-1cm-1]

280

Description (UV/VIS Spectroscopy)

in the presence of additive(s); Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Location

supporting information

Xia, Ji-Bao; Zhu, Chen; Chen, Chuo; Chemical Communications; vol. 50; nb. 79; (2014); p. 11701 - 11704, View in Reaxys 9 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Zhu, Xiao-Qing; Chen, Xi; Mei, Lian-Rui; Organic Letters; vol. 13; nb. 9; (2011); p. 2456 - 2459, View in Reaxys; Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys 10 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

393

Ext./Abs. Coefficient [l·mol-1cm-1]

300

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

N,N-dimethyl acetamide

Absorption Maxima (UV/ VIS) [nm]

420; 520; 640; 510

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys

99/144

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12 of 115

Description (UV/VIS Spectroscopy)

in the presence of additive(s); Spectrum

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol. 264; (2013); p. 1 - 11, View in Reaxys 13 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

309

Ext./Abs. Coefficient [l·mol-1cm-1]

1600

Robert, Patricia; Bolduc, Andreanne; Skene, W. G.; Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment, and General Theory; vol. 116; nb. 37; (2012); p. 9305 - 9314,10, View in Reaxys 14 of 115

Solvent (UV/VIS Spectroscopy)

dichloromethane

Absorption Maxima (UV/ VIS) [nm]

258

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys 15 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Location

supporting information

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys 16 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrachloromethane

Absorption Maxima (UV/ VIS) [nm]

425

Okamoto, Hideki; Yamaji, Minoru; Gohda, Shin; Kubozono, Yoshihiro; Komura, Noriko; Sato, Kaori; Sugino, Hisako; Satake, Kyosuke; Organic Letters; vol. 13; nb. 10; (2011); p. 2758 - 2761, View in Reaxys 17 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

chloroform

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

dichloromethane

Location

supporting information

Absorption Maxima (UV/ VIS) [nm]

393

Ext./Abs. Coefficient [l·mol-1cm-1]

262

Description (UV/VIS Spectroscopy)

Spectrum

100/144

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Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

286

Li, Zhuomin; Deng, Wenli; Journal of Chemical Crystallography; vol. 41; nb. 10; (2011); p. 1534 - 1538, View in Reaxys 20 of 115

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

290

Reddy, Sabbasani Rajasekhara; Titu, Devamani; Chadha, Anju; JAOCS, Journal of the American Oil Chemists' Society; vol. 87; nb. 7; (2010); p. 747 - 754, View in Reaxys 21 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys 22 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Ramart-Lucas; Hoch; Bulletin de la Societe Chimique de France; vol. <5> 2; (1935); p. 1376,1378, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 23 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 24 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Weininger; Ren; Wang; Chen; McGimpsey; Journal of Physical Chemistry A; vol. 103; nb. 28; (1999); p. 5477 - 5484, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 25 of 115

Solvent (UV/VIS Spectroscopy)

pentane

Absorption Maxima (UV/ VIS) [nm]

413.993

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 26 of 115

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

413.993

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 27 of 115

Solvent (UV/VIS Spectroscopy)

heptane

Absorption Maxima (UV/ VIS) [nm]

415.007

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Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 28 of 115

Solvent (UV/VIS Spectroscopy)

toluene

Absorption Maxima (UV/ VIS) [nm]

425.007

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 29 of 115

Solvent (UV/VIS Spectroscopy)

butyl acetate

Absorption Maxima (UV/ VIS) [nm]

423.998

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 30 of 115

Solvent (UV/VIS Spectroscopy)

ethyl acetate

Absorption Maxima (UV/ VIS) [nm]

426.003

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 31 of 115

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

424.628

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 32 of 115

Solvent (UV/VIS Spectroscopy)

1,2-dichloro-benzene

Absorption Maxima (UV/ VIS) [nm]

428.009

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 33 of 115

Solvent (UV/VIS Spectroscopy)

acetone

Absorption Maxima (UV/ VIS) [nm]

426.003

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 34 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

428.009

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys 35 of 115

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: 23 deg C

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys 36 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

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Comment (UV/VIS Spectroscopy)

Remark: 23 deg C

Absorption Maxima (UV/ VIS) [nm]

421

Lathioor, Edward C.; Leigh, William J.; Photochemistry and Photobiology; vol. 82; nb. 1; (2006); p. 291 - 300, View in Reaxys 37 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

toluene

Biczok, Laszlo; Berces, Tibor; Inoue, Haruo; Journal of Physical Chemistry A; vol. 103; nb. 20; (1999); p. 3837 - 3842, View in Reaxys; Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys 38 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

250; 294; 308; 324

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb. 17; (2005); p. 6609 - 6615, View in Reaxys 39 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

380

Kolano, Christoph; Bucher, Goetz; Schade, Olaf; Grote, Dirk; Sander, Wolfram; Journal of Organic Chemistry; vol. 70; nb. 17; (2005); p. 6609 - 6615, View in Reaxys 40 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CHCl3

Comment (UV/VIS Spectroscopy)

ambient temperature

Chi, Chunyan; Im, Chan; Enkelmann, Volker; Ziegler, Andreas; Lieser, Guenter; Wegner, Gerhard; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6833 - 6845, View in Reaxys 41 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys 42 of 115

Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ VIS) [nm]

250; 295; 385

Ext./Abs. Coefficient [l·mol-1cm-1]

40738; 8317; 741

Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol. 75; nb. 2; (2005); p. 272 - 277, View in Reaxys 43 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

ambient temperature

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Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 2408, View in Reaxys 44 of 115

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: absorption spectrum at 20 grad C; gas

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 45 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

Remark: 20 grad C

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 46 of 115

Description (UV/VIS Spectroscopy)

Singlet-triplet band

Comment (UV/VIS Spectroscopy)

Remark: Electron energy loss spectrum at 40 grad C; gas

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 47 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

Remark: Electron energy loss spectrum at 40 grad C

Borisevich; Kazakov; Kukhto; Murtazaliev; Khristoforov; Artyukhov; Ivanov; Journal of Applied Spectroscopy; vol. 71; nb. 5; (2004); p. 681 - 685, View in Reaxys 48 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Friedel,R.A.; Orchin,M.; Ultraviolet Spectra of Aromatic Compounds <New York 1951> Nr. 329, View in Reaxys; Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 49 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol; cyclohexane

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1:4

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 50 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol; cyclohexane

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1:3

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

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51 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

butan-1-ol

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys 52 of 115

Solvent (UV/VIS Spectroscopy)

H2O

Comment (UV/VIS Spectroscopy)

in the presence of additives

Absorption Maxima (UV/ VIS) [nm]

256

Courtney, Michael C.; MacCormack, Aoife C.; More O'Ferrall, Rory A.; Journal of Physical Organic Chemistry; vol. 15; nb. 8; (2002); p. 529 - 539, View in Reaxys 53 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

vapour

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys 54 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

heptane

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 - 150, View in Reaxys 55 of 115

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Comment (UV/VIS Spectroscopy)

Remark: at 298 K

Absorption Maxima (UV/ VIS) [nm]

248.4; 256.9; 293.5; 307.2

Ext./Abs. Coefficient [l·mol-1cm-1]

57777; 84760; 3809; 1769

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Comment (UV/VIS Spectroscopy)

Remark: at 298 K

Absorption Maxima (UV/ VIS) [nm]

322.7; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

847; 275

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

382

Ext./Abs. Coefficient [l·mol-1cm-1]

280

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Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys 58 of 115

Solvent (UV/VIS Spectroscopy)

benzene

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

380

Ext./Abs. Coefficient [l·mol-1cm-1]

300

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys 59 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

377

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys 60 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

300 - 500 nm; Remark: 296 K

Absorption Maxima (UV/ VIS) [nm]

379

Ext./Abs. Coefficient [l·mol-1cm-1]

260

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys 61 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Comment (UV/VIS Spectroscopy)

300 - 450 nm

Biczok, Laszlo; Berces, Tibor; Linschitz, Henry; Journal of the American Chemical Society; vol. 119; nb. 45; (1997); p. 11071 - 11077, View in Reaxys 62 of 115

Solvent (UV/VIS Spectroscopy)

acetonitrile; aq. methanol

Absorption Maxima (UV/ VIS) [nm]

250; 258

Wischmann, Hartmut; Steinhart, Hans; Chemosphere; vol. 35; nb. 8; (1997); p. 1681 - 1698, View in Reaxys 63 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

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Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 64 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 65 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 66 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile; ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 67 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane; ethanol

Comment (UV/VIS Spectroscopy)

270 - 480 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys 68 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

200 - 500 nm

Lafleur, Arthur L.; Howard, Jack B.; Taghizadeh, Koli; Plummer, Elaine F.; Scott, Lawrence T.; Necula, Atena; Swallow, Kathleen C.; Journal of Physical Chemistry; vol. 100; nb. 43; (1996); p. 17421 - 17428, View in Reaxys 69 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

benzene

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 70 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

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Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 71 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CHCl3

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 72 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Comment (UV/VIS Spectroscopy)

280 - 333 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 73 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

propan-1-ol

Absorption Maxima (UV/ VIS) [nm]

291.4

Ext./Abs. Coefficient [l·mol-1cm-1]

17989

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 74 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane

Absorption Maxima (UV/ VIS) [nm]

289.9; 310.1

Ext./Abs. Coefficient [l·mol-1cm-1]

2931; 474

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 75 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

290.5; 310.9

Ext./Abs. Coefficient [l·mol-1cm-1]

3243; 458

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 76 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

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Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ VIS) [nm]

291.7; 306.5

Ext./Abs. Coefficient [l·mol-1cm-1]

2904.01; 180

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 77 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

benzene

Absorption Maxima (UV/ VIS) [nm]

291.9; 307.6

Ext./Abs. Coefficient [l·mol-1cm-1]

5458; 1963

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 78 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

tetrahydrofuran

Absorption Maxima (UV/ VIS) [nm]

292.1; 306.1

Ext./Abs. Coefficient [l·mol-1cm-1]

2449; 1262

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 79 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

292.4; 306.5

Ext./Abs. Coefficient [l·mol-1cm-1]

1968; 1007

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 80 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

292.5; 306.3

Ext./Abs. Coefficient [l·mol-1cm-1]

3013; 1439

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 81 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dimethylformamide

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Absorption Maxima (UV/ VIS) [nm]

292.7; 308.5

Ext./Abs. Coefficient [l·mol-1cm-1]

5458; 2104

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 82 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Absorption Maxima (UV/ VIS) [nm]

293.2; 307.6

Ext./Abs. Coefficient [l·mol-1cm-1]

2449; 1156.1

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 83 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

toluene

Absorption Maxima (UV/ VIS) [nm]

293.5; 307

Ext./Abs. Coefficient [l·mol-1cm-1]

7031; 1986.1

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 84 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

butan-1-ol

Absorption Maxima (UV/ VIS) [nm]

293.9; 312.8

Ext./Abs. Coefficient [l·mol-1cm-1]

597; 525

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 85 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

CHCl3

Absorption Maxima (UV/ VIS) [nm]

294.9; 307.8

Ext./Abs. Coefficient [l·mol-1cm-1]

1327; 679

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys 86 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

propan-2-ol; H2O

Comment (UV/VIS Spectroscopy)

200 - 500 nm; Ratio of solvents: 4:1

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Bauer, Rupert; Heisler, Guenter; Koenigstein, Christian; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 50; nb. 1; (1994); p. 57 - 68, View in Reaxys 87 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

propan-2-ol; H2O

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 4:1

Absorption Maxima (UV/ VIS) [nm]

205; 255; 298; 330

Ext./Abs. Coefficient [l·mol-1cm-1]

11000; 25000; 2000; 1800

Bauer; Heisler; Konigstein; Tetrahedron; vol. 49; nb. 30; (1993); p. 6591 - 6604, View in Reaxys; Bauer, Rupert; Heisler, Guenter; Koenigstein, Christian; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 50; nb. 1; (1994); p. 57 - 68, View in Reaxys 88 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Absorption Maxima (UV/ VIS) [nm]

374.95

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methylcyclohexane

Absorption Maxima (UV/ VIS) [nm]

374.95

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetone

Absorption Maxima (UV/ VIS) [nm]

380.08

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

acetonitrile

Absorption Maxima (UV/ VIS) [nm]

380.08

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ VIS) [nm]

450

McGimpsey, W. G.; Scaiano, J. C.; Tetrahedron Letters; vol. 27; nb. 5; (1986); p. 547 - 550, View in Reaxys

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93 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

53703; 72443; 2951; 245

Talapatra, Sunil K.; Bose, Srabani; Mallik, Asok K.; Talapatra, Bani; Tetrahedron; vol. 41; nb. 13; (1985); p. 2765 - 2770, View in Reaxys 94 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol; NaOH

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

53703; 72443; 2951; 245

Talapatra, Sunil K.; Bose, Srabani; Mallik, Asok K.; Talapatra, Bani; Tetrahedron; vol. 41; nb. 13; (1985); p. 2765 - 2770, View in Reaxys 95 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane; H2O

Comment (UV/VIS Spectroscopy)

Ratio of solvents: 1percent

Absorption Maxima (UV/ VIS) [nm]

258

Hoz, Shmaryahu; Gross, Zeev; Speizman, Dov; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 1143 - 1146, View in Reaxys 96 of 115

Description (UV/VIS Spectroscopy)

Triplet-triplet band

Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Kobayashi; Nagakura; Chemical Physics Letters; vol. 43; (1976); p. 429, View in Reaxys; Engel, Paul S.; Woods, Treacy L.; Page, Matthew A.; Journal of Physical Chemistry; vol. 87; nb. 1; (1983); p. 10 - 13, View in Reaxys 97 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

249; 257; 296; 380

Ext./Abs. Coefficient [l·mol-1cm-1]

56234; 87096; 3311; 263

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

235 - 426 nm

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Frolova, E. P.; Akhvlediani, R. N.; Suvorov, N. N.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 18; nb. 10; (1982); p. 1049 - 1054; Khimiya Geterotsiklicheskikh Soedinenii; vol. 18; nb. 10; (1982); p. 1358 - 1362, View in Reaxys 99 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ VIS) [nm]

256

Carey, Edwin; O'Ferrall, Rory A. More; Vernon, Nicholas M.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1581 - 1586, View in Reaxys 100 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

benzene

Absorption Maxima (UV/ VIS) [nm]

420

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys 101 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

propan-2-ol

Comment (UV/VIS Spectroscopy)

450 - 700 nm

Peters, K. S.; Freilich, S. C.; Schaeffer, C. G.; Journal of the American Chemical Society; vol. 102; nb. 17; (1980); p. 5701 5702, View in Reaxys 102 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Stobbe; Seydel; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 141, View in Reaxys; Stobbe; Justus Liebigs Annalen der Chemie; vol. 370; (1909); p. 97, View in Reaxys; Koster,P.B.; Runsink,J.; Janssen,M.J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 393, View in Reaxys; Lin; Topp; Chemical Physics; vol. 36; (1979); p. 365, View in Reaxys; Marchetti; Molecular Crystals and Liquid Crystals (1969-1991); vol. 16; (1972); p. 127, View in Reaxys; Filipescu et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 2276, View in Reaxys; Chen; Lin; Biochimica et Biophysica Acta; vol. 184; (1969); p. 634, View in Reaxys; Hayon et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 2072, View in Reaxys; Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Dehler; Doerr; Tetrahedron Letters; (1965); p. 2155,2157, View in Reaxys; Amand; Bensasson; Chemical Physics Letters; vol. 34; (1975); p. 44,46, 47, View in Reaxys; Mullen Orloff; Journal of Molecular Spectroscopy; vol. 30; (1969); p. 140, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p. 250,251, 253, 255, View in Reaxys; Treinin; Hayon; Journal of the American Chemical Society; vol. 98; (1976); p. 3884,3885, 3887, View in Reaxys; Moritani; Nagai; Nippon Kagaku Zasshi; vol. 86; (1965); p. 157; Chem.Abstr.; vol. 63; nb. 7789b, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys; McClelland; Transactions of the Faraday Society; vol. 57; (1961); p. 1458, View in Reaxys; Latham et al.; Analytical Chemistry; vol. 34; (1962); p. 311,312, View in Reaxys; Kadhim; Offen; Journal of Chemical Physics; vol. 47; (1967); p. 1289,1290, View in Reaxys; Kuboyama; Bulletin of the Chemical Society of Japan; vol. 37; (1964); p. 1540, View in Reaxys; Dehler; Fritz; Tetrahedron Letters; (1969); p. 2157, View in Reaxys 103 of 115

Description (UV/VIS Spectroscopy)

UV/VIS

Tochtermann,W. et al.; Chemische Berichte; vol. 105; (1972); p. 1431 - 1438, View in Reaxys; Akiba,K.-Y. et al.; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 2674 - 2683, View in Reaxys; Godfroid,J.-J.; Bulletin de la Societe Chimique de France; (1964); p. 2929 - 2943, View in Reaxys; Borowitz,I.J. et al.; Journal of Organic Chemistry; vol. 36; (1971); p. 553 560, View in Reaxys; Akiba et al.; Synthesis; (1977); p. 862, View in Reaxys; Rehak et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 697,702, View in Reaxys; Laemmle et al.; Journal of the American Chemical Society; vol. 93; (1971); p. 5120,5122, View in Reaxys; Shida et al.; Journal of Physical Chemistry; vol. 78; (1974); p. 741,742, View in Reaxys; Hoshino et al.; Journal of Physical Chemistry; vol. 78; (1974); p. 1473,1474, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Warren; Yandle; Journal of the Chemical Society; (1965); p. 5518, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Kuboyama; Chemical Physics Letters; vol. 41; (1976); p. 544, View in Reaxys; Mukherjee; Journal of Physical Chemistry; vol. 73; (1969); p. 4381, View in Reaxys; Rosencwaig; Hall; Analytical Chemistry; vol. 47; (1975); p. 548, View in Reaxys; BELL JH; IRELAND S; SPEARS AW;

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Analytical Chemistry; vol. 41; nb. 2; (1969); p. 310 - 313, View in Reaxys; Edward; Wong; Journal of the American Chemical Society; vol. 99; (1977); p. 4229,4231, View in Reaxys; Cheshire et al.; Tetrahedron; vol. 23; (1967); p. 1669, View in Reaxys; Harget et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 214, View in Reaxys 104 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Smith,G.G.; Bayer,R.P.; Tetrahedron; vol. 18; (1962); p. 323 - 331, View in Reaxys; Dahn; Nickel; Justus Liebigs Annalen der Chemie; vol. 667; (1963); p. 101,110, View in Reaxys; Osugi; Okishima; Nippon Kagaku Zasshi; vol. 92; (1971); p. 598,599, 600; Chem.Abstr.; vol. 75; nb. 156597; (1971), View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Wiemann; Godefroid; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 2608, View in Reaxys; Parry; Warren; Journal of the Chemical Society; (1965); p. 4049, View in Reaxys; Stewart et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 1065,1066, View in Reaxys 105 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

220 - 420 nm

Anderson et al.; Journal of the Chemical Society; (1959); p. 3992,3996, View in Reaxys 106 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

230 - 450 nm; bei 100 K.

Doerr; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 61; (1957); p. 950,951, View in Reaxys 107 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

378

Bergmann et al.; Bulletin de la Societe Chimique de France; (1951); p. 669,680, View in Reaxys 108 of 115

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

dioxane

Absorption Maxima (UV/ VIS) [nm]

258; 294; 308; 328

Bergmann et al.; Bulletin de la Societe Chimique de France; (1951); p. 669,680, View in Reaxys 109 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Chaix; Bulletin de la Societe Chimique de France; vol. <4> 53; (1933); p. 700,708, View in Reaxys; Ramart-Lucas; Hoch; Bulletin de la Societe Chimique de France; vol. <5> 2; (1935); p. 1376,1378, View in Reaxys; Jones; Journal of the American Chemical Society; vol. 67; (1945); p. 2127,2130, 2144; Chemical Reviews (Washington, DC, United States); vol. 41; (1947); p. 353,361, 364, View in Reaxys; Stobbe; Chemische Berichte; vol. 44; (1911); p. 1486; Chemische Berichte; vol. 48; (1915); p. 442, View in Reaxys; Boeeseken; Cohen; Langedijk; Recueil des Travaux Chimiques des Pays-Bas; vol. 44; (1925); p. 184,188, View in Reaxys; Friedel,R.A.; Orchin,M.; Ultraviolet Spectra of Aromatic Compounds <New York 1951> Nr. 329, View in Reaxys; Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 536; (1938); p. 266,269, 272, 278, 282, View in Reaxys 110 of 115

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

benzene

Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 111 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CCl4

Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 112 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

light petroleum

Boeeseken; Cohen; Langedijk; Recueil des Travaux Chimiques des Pays-Bas; vol. 44; (1925); p. 184,188, View in Reaxys; Wittig; Lange; Justus Liebigs Annalen der Chemie; vol. 436; (1938); p. 266,271, View in Reaxys 113 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

H2SO4

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys 114 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

HCl; 1,2-dichloro-ethane

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys 115 of 115

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

SnCl4 / 1,2-dichloro-ethane; HCl / 1,2-dichloro-ethane

Anderson; Gooding; Journal of the American Chemical Society; vol. 57; (1935); p. 999,1006, View in Reaxys ESR Spectroscopy (6) 1 of 6

Description (ESR Spectro- CIDEP (chemically induced dynamic electron polarization) scopy) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 2 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- cyclohexane py) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 3 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- cyclohexane; ethanol py) Comment (ESR Spectroscopy)

Ratio of solvents: 5:1 v/v; in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys

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4 of 6

Description (ESR Spectro- Spectrum scopy) Solvents (ESR Spectrosco- ethanol; KOH py) Comment (ESR Spectroscopy)

in the presence of additives

Kawai, Akio; Yamamoto, Tetsuya; Okutsu, Tetsuo; Kinichi, Obi; Bulletin of the Chemical Society of Japan; vol. 72; nb. 12; (1999); p. 2625 - 2632, View in Reaxys 5 of 6

Description (ESR Spectro- ESR scopy) Takeshita; Hirota; Journal of Chemical Physics; vol. 58; (1973); p. 3745, View in Reaxys; YAMANASHI BS; MAZZA C; BOWERS KW; Applied Spectroscopy; vol. 25; nb. 4; (1971); p. 460 - 465, View in Reaxys; Sahini; Ciurea; Revue Roumaine de Chimie; vol. 14; (1969); p. 689,692, View in Reaxys; Nadjo; Saveant; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 30; (1971); p. 41,46, View in Reaxys

6 of 6

Description (ESR Spectro- ESR-hyperfine coupling constants scopy) Broze; Luz; Journal of Chemical Physics; vol. 51; (1969); p. 738,742, View in Reaxys

NQR Spectroscopy (1) Description (NQR References Spectroscopy) Nuclear quadrupole Butler, Leslie G.; Cheng, C. P.; Brown, Theodore L.; Journal of Physical Chemistry; vol. 85; nb. 19; (1981); p. 2738 resonance 2740, View in Reaxys Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Microwave spectrum

Konishi, S.; Morioka, Y.; Nakagawa, I.; Journal of Molecular Structure; vol. 64; (1980); p. 157 - 162, View in Reaxys

Raman Spectroscopy (7) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy)

Location

Bands; Spectrum

References Inada, Yuhi; Amaya, Toru; Hirao, Toshikazu; RSC Advances; vol. 5; nb. 24; (2015); p. 18523 - 18530, View in Reaxys

Spectrum

supporting informa- Eakins, Galen L.; Cooper, Matthew W.; Gerasimchuk, Nikolay N.; Philtion lips, Terry J.; Breyfogle, Bryan E.; Stearman, Chad J.; Canadian Journal of Chemistry; vol. 91; nb. 11; (2013); p. 1059 - 1071, View in Reaxys

Raman

supporting informa- Eakins, Galen L.; Alford, Joshua S.; Tiegs, Brandon J.; Breyfogle, Brytion an E.; Stearman, Chad J.; Journal of Physical Organic Chemistry; vol. 24; nb. 11; (2011); p. 1119 - 1128, View in Reaxys

Spectrum

solid

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Bands

solid

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Bands

Raman

Zwarich et al.; Journal of Molecular Spectroscopy; vol. 51; (1974); p. 38,42-47, View in Reaxys

Luminescence Spectroscopy (21) Description (Lumi- Comment (Luminescence Spectronescence Spectroscopy) scopy)

References

Luminescence maximum(a)

Kirichenko; Meshkova; Topilova; Kiriyak; Lyapunov; Kulygina; Luk'yanenko; Russian Journal of General Chemistry; vol. 75; nb. 2; (2005); p. 272 - 277, View in Reaxys

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Luminescence spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Luminescence lifetime

ambient temperature. Object(s) of Study: solvent dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Luminescence spectrum

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys

Luminescence quantum yield

Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Mitchell et al.; Journal of Chemical Physics; vol. 67; (1977); p. 4832, View in Reaxys; Korol'kova, N. V.; Val'kova, G. A.; Shigorin, D. N.; Grekhova, N. G.; Andrievskii, A. M.; Russian Journal of Physical Chemistry; vol. 63; nb. 12; (1989); p. 1792 - 1795; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 3272 - 3277, View in Reaxys; Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys; Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 - 3845, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Tachibana, Hiroshi; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 45; (1998); p. 8657 - 8663, View in Reaxys

Luminescence lifetime

Hunter; Transactions of the Faraday Society; vol. 66; (1970); p. 300,302, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Kobayashi; Nagakura; Chemical Physics Letters; vol. 43; (1976); p. 429, 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; Gastilovich, E. A.; Korol'kova, N. V.; Val'kova, G. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 11; (1991); p. 1527 - 1532; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 2881 - 2890, View in Reaxys; Biczok, Laszlo; Berces, Tibor; Journal of Physical Chemistry; vol. 92; nb. 13; (1988); p. 3842 - 3845, View in Reaxys; Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys; Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Luminescence quenching

Quenching with alcohols

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 - 1839, View in Reaxys

Electroluminescence

Gruzinskii, V. V.; Kukhto, A. V.; Journal of Applied Spectroscopy; vol. 50; nb. 2; (1989); p. 165 168; Zhurnal Prikladnoi Spektroskopii; vol. 50; nb. 2; (1989); p. 232 - 236, View in Reaxys

Luminescence quenching

Herkstroeter; Hammond; Journal of the American Chemical Society; vol. 88; (1966); p. 4769, View in Reaxys; Guttenplan; Cohen; Tetrahedron Letters; (1972); p. 2163, View in Reaxys; Loutfy; Loutfy; Canadian Journal of Chemistry; vol. 50; (1972); p. 4052,4054, View in Reaxys; Parsons; Cohen; Journal of the American Chemical Society; vol. 96; (1974); p. 2948,2950,2951, View in Reaxys; Fry et al.; Journal of the American Chemical Society; vol. 88; (1966); p. 4781, View in Reaxys; Goerner; Schulte-Fronhlinde; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 88; nb. 12; (1984); p. 1208 - 1216, View in Reaxys

Luminescence quenching

Quenching with Ph-1N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p. 2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with Ph-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p. 2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 1N-1N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p. 2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 1N-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p. 2803 - 2808, View in Reaxys

Luminescence quenching

Quenching with 2N-2N

Wismontski-Knittel, T.; Das, P. K.; Journal of Physical Chemistry; vol. 88; nb. 13; (1984); p. 2803 - 2808, 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

Luminescence quenching

Quenching with βpyran

Cerfontain, Hans; Geenevasen, Jan A. J.; Noort, Paul C. M. van; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 1057 - 1062, View in Reaxys

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Luminescence

Pragst et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 257; (1976); p. 465,471, View in Reaxys; Andrews; Journal of Physical Chemistry; vol. 82; (1978); p. 2304, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys

Emission spectrum in the infrared region

Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys

Degree of depolarization of luminescence

Krauss; Huber; Chemische Berichte; vol. 94; (1961); p. 2864,2869,2874, View in Reaxys

Luminescence quenching

Loeschung der Fluoreszenz in Ascorbinsaeure.

Luminescence quenching

Loeschung der Flu- Weber; Savic; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B>24; (1934); p. 68,71,73, oreszenz von Fluo- View in Reaxys renon-(9) in Benzol durch Phenol, oKresol und anderen organischen Verbindungen.

Fluorescence Spectroscopy (80) Description (Fluo- Solvent (Fluoresrescence Spectrocence Spectroscoscopy) py)

Weber; Radiologica; vol. 2; (1938); p. 57,61, View in Reaxys

Temperature (Fluorescence Spectroscopy) [°C]

Spectrum; Maxima

Location

supporting information

Comment (Fluores- References cence Spectroscopy) Li, Shuangjiang; Aljhdli, Merfat; Thakellapalli, Haresh; Farajidizaji, Behzad; Zhang, Yu; Akhmedov, Novruz G.; Milsmann, Carsten; Popp, Brian V.; Wang, Kung K.; Organic Letters; vol. 19; nb. 15; (2017); p. 4078 - 4081, View in Reaxys

Fluorescence quantum yield

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys; Andronico, Luca A.; Quintavalla, Arianna; Lombardo, Marco; Mirasoli, Mara; Guardigli, Massimo; Trombini, Claudio; Roda, Aldo; Chemistry - A European Journal; vol. 22; nb. 50; (2016); p. 18156 - 18168, View in Reaxys

Spectrum; Maxima; Fluorescence quantum yield

Tan, Ke Xin; Lintang, Hendrik O.; Maniam, Subashani; Langford, Steven J.; Bakar, Mohd Bakri; Tetrahedron; vol. 72; nb. 35; (2016); p. 5402 5413, View in Reaxys

Maxima; Fluorescence quantum yield; Fluorescence lifetime; Spectrum

Spectrum; Maxima

Samant, Vaishali; Varne, Mahendra; Palit, Dipak K.; Journal of Photochemistry and Photobiology A: Chemistry; vol.

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2018-06-21 20:37:19

264; (2013); p. 1 - 11, View in Reaxys Fluorescence quantum yield; Maxima; Spectrum; Fluorescence lifetime

Fluorescence

Dufresne, Stephane; Skalski, Thomas; Skene; Canadian Journal of Chemistry; vol. 89; nb. 2; (2011); p. 173 - 180, View in Reaxys Dahn; Nickel; Justus Liebigs Annalen der Chemie; vol. 667; (1963); p. 101,110, View in Reaxys; Monroe; Groff; Tetrahedron Letters; (1973); p. 3955, View in Reaxys; Snyder; Testa; Journal of Physical Chemistry; vol. 83; (1979); p. 3041, View in Reaxys; Davidson; Lambeth; Journal of the Chemical Society [Section] D: Chemical Communications; (1969); p. 1098, View in Reaxys; Mitchell et al.; Journal of Chemical Physics; vol. 67; (1977); p. 4832, View in Reaxys; Liptay et al.; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 23; (1968); p. 377,393, View in Reaxys; Zwarich; Bree; Journal of Molecular Spectroscopy; vol. 52; (1974); p. 329,331,333,339, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p. 250,251, 253, 255, View in Reaxys; Moritani; Nagai; Nippon Kagaku Zasshi; vol. 86; (1965); p. 157; Chem.Abstr.; vol. 63; nb. 7789b, View in Reaxys; Davies; Ennis; Journal of the Chemical Society; (1960); p. 1488,1490, View in Reaxys; Davis et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 2264, View in Reaxys; Caldwell; Tetrahedron Letters; (1969); p. 2121, View in Reaxys; Singer; Tetrahedron Letters; (1969); p. 923, View in Reaxys; Guttenplan; Cohen; Tetrahedron Letters; (1969); p. 2125, View in Reaxys; Singer et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 897, View in Reaxys; Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and

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2018-06-21 20:37:19

Biomolecular Spectroscopy; vol. 71; nb. 2; (2008); p. 537 542, View in Reaxys; Schneck, Crystal M.; Poncheri, Adam J.; Jennings, John T.; Snyder, Deanna L.; Worlinsky, Jill L.; Basu, Swarna; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 75; nb. 2; (2010); p. 624 628, View in Reaxys Spectrum

CH2Cl2

Zhang, Kai; Chen, Zhao; Yang, Chuluo; Tao, Youtian; Zou, Yang; Qin, Jingui; Cao, Yong; Journal of Materials Chemistry; vol. 18; nb. 3; (2008); p. 291 - 298, View in Reaxys

Spectrum

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

acetonitrile

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

hexane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

pentane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

hexane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

heptane

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

toluene

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

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Maxima

butyl acetate

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

ethyl acetate

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

tetrahydrofuran

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

1,2-dichloro-benzene

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

acetone

Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Maxima

acetonitrile

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys; Jozefowicz, Marek; Heldt, Janina R.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 316 - 320, View in Reaxys

Spectrum

cyclohexane; tetrahydrofuran

-0.16 - 99.84

temperature dependence

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

Spectrum

cyclohexane; ethanol

-0.16 - 99.84

temperature dependence

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

Maxima

cyclohexane; tetrahydrofuran

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

Maxima

cyclohexane; ethanol

Jozefowicz, Marek; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 2; (2007); p. 444 - 449, View in Reaxys

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Spectrum

toluene

Spectrum

CHCl3

Maxima

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys

Spectrum

film

Li, Jing; Li, Ming; Bo, Zhishan; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6930 - 6936, View in Reaxys

Chi, Chunyan; Im, Chan; Enkelmann, Volker; Ziegler, Andreas; Lieser, Guenter; Wegner, Gerhard; Chemistry - A European Journal; vol. 11; nb. 23; (2005); p. 6833 - 6845, View in Reaxys

Spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Fluorescence excitation spectrum

temperature dependence

Devaux, Andre; Minkowski, Claudia; Calzaferri, Gion; Chemistry - A European Journal; vol. 10; nb. 10; (2004); p. 2391 - 2408, View in Reaxys

Maxima

cyclohexane

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Maxima

butan-1-ol

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Maxima

dioxane

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

Fluorescence quantum yield

solvent dependence

122/144

Martinez, Claudia G.; Neuner, Annette; Marti, Cristina; Nonell, Santi; Braun, Andre M.; Oliveros, Esther; Helvetica Chimica Acta; vol. 86; nb. 2; (2003); p. 384 - 397, View in Reaxys

2018-06-21 20:37:19

Energy transfer from singlet state

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys

Fluorescence excitation spectrum

96.85

in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Fluorescence excitation spectrum

96.85

in the presence of organic compounds. Object(s) of Study: in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Spectrum

96.85

in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Spectrum

96.85

in the presence of organic compounds. Object(s) of Study: in the presence of rare gases

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

Fluorescence lifetime

96.85

Matsushita; Ichimura; Hikida; Chemical Physics Letters; vol. 360; nb. 1-2; (2002); p. 65 71, View in Reaxys

26.85

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 150, View in Reaxys

Spectrum

acetonitrile

Fluorescence decay acetonitrile kinetics; Spectrum

De, Avijit K.; Ganguly, Tapan; Canadian Journal of Chemistry; vol. 78; nb. 1; (2000); p. 139 150, View in Reaxys

Maxima

cyclohexane

472 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

benzene

485 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

acetonitrile

514 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Maxima

ethanol

562 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

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Maxima

ethanol

Fluorescence quenching

490 nm, 512 nm

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 18; (1998); p. 3018 - 3024, View in Reaxys

Quenching with ethanol

Yatsuhashi, Tomoyuki; Nakajima, Yuka; Shimada, Tetsuya; Tachibana, Hiroshi; Inoue, Haruo; Journal of Physical Chemistry A; vol. 102; nb. 45; (1998); p. 8657 - 8663, View in Reaxys

Spectrum

acetonitrile

666.67 - 322.58 nm Demeter, Attila; Timari, Geza; Kotschy, Andras; Berces, Tibor; Tetrahedron Letters; vol. 38; nb. 29; (1997); p. 5219 5222, View in Reaxys

Spectrum

ethanol

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

cyclohexane

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile; ethanol

400 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

acetonitrile; ethanol

440 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

cyclohexane; ethanol

440 - 700 nm

Fujii, Tsuneo; Sano, Masayuki; Mishima, Shozi; Hiratsuka, Hiroshi; Bulletin of the Chemical Society of Japan; vol. 69; nb. 7; (1996); p. 1833 1839, View in Reaxys

Spectrum

benzene

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Spectrum

hexane

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molec-

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ular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys Spectrum

CHCl3

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Spectrum

methanol

320 - 600 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

hexane

341 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

propan-1-ol

346 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

cyclohexane

347 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

dioxane

347.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

butan-1-ol

350 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

methanol

353 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

acetonitrile

346.75 nm; 504.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

benzene

351 nm; 486 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

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Maxima

toluene

Maxima

354 nm; 488.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

355.5 nm; 501 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

tetrahydrofuran

356.5 nm; 493.75 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

dimethylformamide

359.25 nm; 507.5 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

CH2Cl2

359.25 nm; 508.25 nm

Rani, S. Arathi; Sobhanadri, J.; Rao, T. A. Prasada; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 51; nb. 14; (1995); p. 2473 - 2480, View in Reaxys

Maxima

cyclohexane

505.08 nm

Maxima

methylcyclohexane

505.08 nm

Maxima

acetone

546.45 nm

Maxima

acetonitrile

546.45 nm

Spectrum

toluene

460 - 620 nm

Gruzinskii, V. V.; Kukhto, A. V.; Journal of Applied Spectroscopy; vol. 50; nb. 2; (1989); p. 165 - 168; Zhurnal Prikladnoi Spektroskopii; vol. 50; nb. 2;

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(1989); p. 232 - 236, View in Reaxys Maxima

benzene

Phosphorescence Spectroscopy (6) Description (Phos- Comment (Phosphorescence Spec- phorescence Spectroscopy) troscopy)

480 nm

Scaiano, J. C.; Wubbels, Gene G.; Journal of the American Chemical Society; vol. 103; nb. 3; (1981); p. 640 - 645, View in Reaxys

References

Triplet state energy

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Triplet state quenching

Yamaji, Minoru; Wakabayashi, Sayaka; Ueda, Shin-Ichi; Shizuka, Haruo; Tobita, Seiji; Chemical Physics Letters; vol. 368; nb. 1-2; (2003); p. 41 - 48, View in Reaxys

Energy transfer from triplet state

Zalesskaya, G. A.; Journal of Applied Spectroscopy; vol. 69; nb. 3; (2002); p. 328 - 336; Zhurnal Prikladnoi Spektroskopii; vol. 69; nb. 3; (2002); p. 287 - 294, View in Reaxys

Triplet state decay kinetics

Phosphorescence

Heller; Wasserman; Journal of Chemical Physics; vol. 42; (1965); p. 949,952, View in Reaxys; Huggenberger; Labhart; Helvetica Chimica Acta; vol. 61; (1978); p. 250,251, 253, 255, View in Reaxys; Yoshihara; Kearns; Journal of Chemical Physics; vol. 45; (1966); p. 1991,1999, View in Reaxys; Kadhim; Offen; Journal of Chemical Physics; vol. 47; (1967); p. 1289,1290, View in Reaxys

Spectrum

470 - 620 nm; bei 120 K.

Pesteil et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 239; (1954); p. 255, View in Reaxys

Other Spectroscopic Methods (2) Description (Other References Spectroscopic Methods) ESCA

Khel'mer, B. Yu.; Shelepin, O. E.; Shuvaev, A. T.; Mazalov, L. N.; Journal of Structural Chemistry; vol. 25; (1984); p. 325 - 327; Zhurnal Strukturnoi Khimii; vol. 25; nb. 2; (1984); p. 170 - 172, View in Reaxys

Photoelectron spec- Centineo et al.; Journal of Molecular Structure; vol. 44; (1978); p. 203,204, View in Reaxys trum Exposure Assessment (5) Exposure Sources

References

presence in carbonaceous aerosol particles

diesel soot and par- Matuschek, Georg; Karg, Erwin; Schroeppel, Andreas; Schulz, Holger; Schmid, Otmar; Enticles from tire and vironmental Science and Technology; vol. 41; nb. 24; (2007); p. 8406 - 8411, View in Reaxys break wear, diesel exhaust particles generated by a car at idle motor condition and laboratory generated aerosols (spark discharge C particles and diffusion flame soot)

presence in water in Lippe River (NorthRhine Westphalia, Germany)

samples taken on Dsikowitzky, Larissa; Schwarzbauer, Jan; Kronimus, Alexander; Littke, Ralf; Chemosphere; August 16-17, vol. 57; nb. 10; (2004); p. 1275 - 1288, View in Reaxys 1999; title comp. detected in 11 sites; GC-MS and GCFID analyses; biogenic or geogenic contribution; industrial influence

emission rates of 138.9 and 2.4 μg/L of gasoline-equivalent fuel burned for

motor vehicle traffic; Van Nuys Tunnel, Los Angeles, USA; 0600-1000

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 32; nb. 14; (1998); p. 2051 - 2060, View in Reaxys

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vapor and particle PDT, September phases, respectively 21, 1993; inside and outside tunnel; 7060 vehicles counted; average vehicle age: more than 7 years; catalyst and non-catalyst vehicles; average vehicle speed: ca. 64 km/h incineration of iodine bearing waste; presence in clean offgas; waste incineration plant; Germany depositions of aerosols and particulate matter as black crust; samples from the Sevilla cathedral (eastern side, major nave, and southern side); in limestone black weathering crust; percent intensity referenced to the highest peak of methyl n-docosanoate: <25

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys

air pollution in urFobe, Bart O.; Vleugels, Greta J.; Roekens, Eddy J.; Grieken, Rene E. Van; Hermosin, Berban environment of nardo; et al.; Environmental Science & Technology; vol. 29; nb. 6; (1995); p. 1691 - 1701, Sevilla, in Andalu- View in Reaxys cia (southwestern Spain); average temperatures: 10.7 deg C in January and 26.8 deg C in July; rain: 620 mm/ year; average relative humidity: 59 percent; effect of engine exhaust; GC/MS method

Concentration in the Environment (27) 1 of 27

Media (Concentration in the Environment)

wood

Contamination Concentration

27.5 μg/g CTW

Method, Remarks (Concentration in the Environment)

non-sterilized chipped creosote-contaminated wood samples collected; extracted with methanol in ultrasonic bath; GC-MS; conc. expressed as μg/g creosote treated wood (CTW); table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys 2 of 27

Media (Concentration in the Environment)

light-duty gasoline emission, gas-phase

Location

El Monte, California

Contamination Concentration

2.9 - 29 μg/l

Method, Remarks (Concentration in the Environment)

gas-phase emissions collec. from low-emission and three catalyst-equipped vehicles at HaagenSmit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v) and methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Jakober, Chris A.; Robert, Michael A.; Riddle, Sarah G.; Destaillats, Hugo; Charles, M. Judith; Green, Peter G.; Kleeman, Michael J.; Environmental Science and Technology; vol. 42; nb. 13; (2008); p. 4697 - 4703, View in Reaxys 3 of 27

Media (Concentration in the Environment)

light-duty gasoline emission, particle-phase

Location

El Monte, California

Contamination Concentration

0 - 0.3 μg/l

Method, Remarks (Concentration in the Environment)

particle phase emissions collec. from low-emission, three catalyst-equipped vehicles at HaagenSmit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; table

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Media (Concentration in the Environment)

heavy-duty diesel emission, gas-phase

Location

California

Contamination Concentration

190 - 1000 μg/l

Method, Remarks (Concentration in the Environment)

emissions from 1999 Freightliner Tractor operated under idle-creep, heavy heavy-duty diesel truck driving cycle condition; June 2003; ultrasonic extrac. in 1:1 hexane/DCM (v/v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; tab.

Media (Concentration in the Environment)

heavy-duty diesel emission, particle-phase

Location

California

Contamination Concentration

0 - 24 μg/l

Method, Remarks (Concentration in the Environment)

Media (Concentration in the Environment)

surface sediment

Location

river Elbe, Prelouc, Czech Republic

Contamination Concentration

20 ng/g dry wt

Method, Remarks (Concentration in the Environment)

samples (top 5 cm) collected using Van Veen grab; GCxGC-ToF-MS analyzed

Skoczynska, Ewa; Korytar, Peter; De Boer, Jacob; Environmental Science and Technology; vol. 42; nb. 17; (2008); p. 6611 6618, View in Reaxys 7 of 27

Media (Concentration in the Environment)

surface seawater

Location

Suruga Bay, Japan

Contamination Concentration

1.2 - 53.7 ng/l

Method, Remarks (Concentration in the Environment)

mean conc.; samples (2.7-11.5 m depth) collected from various sites on December 14-15, 2003; GC-MS

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb. 2; (2007); p. 279 - 286, View in Reaxys 8 of 27

Media (Concentration in the Environment)

ambient air

Location

Finokalia, Island of Crete, eastern Mediterranean

Contamination Concentration

46.3 fg/l

Method, Remarks (Concentration in the Environment)

average conc.; particulate phase conc.; samples collected using a modified high-volume sampler with 4 h sampling interval during 3-d intensive campaign on August 17-21, 2001; GC-MS analyzed; diagram

Tsapakis, Manolis; Stephanou, Euripides G.; Environmental Science and Technology; vol. 41; nb. 23; (2007); p. 8011 - 8017, View in Reaxys

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9 of 27

Media (Concentration in the Environment)

atmospheric particulate matter

Location

Lanzhou city, Gansu Province, Northwest of China

Contamination Concentration

0.64 pg/l air

Method, Remarks (Concentration in the Environment)

average conc.; total suspended particulate matter acquired from the Lanyuan hotel; 6 air samples collected in March 2003 during 24 h periods; flow rate: 0.8 m3/min; GC-MS and GC-FID analyses; triplicate measurements

Gao; Zhou; Ma; Chen; Hu; Bulletin of Environmental Contamination and Toxicology; vol. 72; nb. 5; (2004); p. 923 - 930, View in Reaxys 10 of 27

Media (Concentration in the Environment)

sediment

Location

Morava river basin, Czech Republic

Contamination Concentration

2.8 - 85.3 ng/g dry wt

Method, Remarks (Concentration in the Environment)

9 samples of surface sediment analyzed using GC/MS(EI)

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 11 of 27

Media (Concentration in the Environment)

soil

Location

Northern Germany (military existing material)

Contamination Concentration

4.1 mg/kg

Method, Remarks (Concentration in the Environment)

extraction by CH2Cl2/n-hexane; separation by acidity using solid-phase extraction (Chromaton SB/ silica gel column); elution by n-hexane/CH2Cl2, CH2Cl2/MeOH, MeOH/0.05 N HCl; cation-exchange solid-phase separation; GC, HPLC; matrix calibration

Steinhart; Meyer; Cartellieri; Analytical Chemistry; vol. 71; nb. 18; (1999); p. 4023 - 4029, View in Reaxys 12 of 27

Media (Concentration in the Environment)

sandy soil

Location

Northern Germany (wood-processing plant)

Contamination Concentration

1.6 mg/kg

Method, Remarks (Concentration in the Environment)

Steinhart; Meyer; Cartellieri; Analytical Chemistry; vol. 71; nb. 18; (1999); p. 4023 - 4029, View in Reaxys 13 of 27

Media (Concentration in the Environment)

airborne particulate

Location

Los Angeles; Southern California; USA

Contamination Concentration

10.5 - 49.2 mg/kg

Method, Remarks (Concentration in the Environment)

fine particulate matter; collected in 1993 at four urban sites with a different air pollution level: central Los-Angeles, Long Beach, Azuza and Roubidoux; extraction; fractionation; GC-SIMS analysis

Hannigan, Michael P.; Cass, Glen R.; Penman, Bruce W.; Crespi, Charles L.; Lafleur, Arthur L.; Busby Jr., William F.; Thilly, William G.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 32; nb. 22; (1998); p. 3502 - 3514, View in Reaxys 14 of 27

Media (Concentration in the Environment)

air, vapor phase

Location

Southern California, USA

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Contamination Concentration

0.1 - 14.11 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993; volatile, semivolative and particle-phase organics collected over Long Beach, Central Los Angeles, Azusa and Claremont

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 15 of 27

Media (Concentration in the Environment)

air, fine particulate matter

Location

Southern California, USA

Contamination Concentration

0 - 1.04 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993; volatile, semivolative and particle-phase organics collected over Long Beach, Central Los Angeles, Azusa and Claremont

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 16 of 27

Media (Concentration in the Environment)

air

Location

San Nicolas Island, Los Angeles area, USA

Contamination Concentration

0.07 pg/l

Method, Remarks (Concentration in the Environment)

September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 17 of 27

Media (Concentration in the Environment)

air

Location

Long Beach, Southern California, USA

Contamination Concentration

0.46 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 18 of 27

Media (Concentration in the Environment)

air

Location

Claremont, Southern California, USA

Contamination Concentration

8.31 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 19 of 27

Media (Concentration in the Environment)

air

Location

Azusa, Southern California, USA

Contamination Concentration

8.08 pg/l

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Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 20 of 27

Media (Concentration in the Environment)

air

Location

Central Los Angeles, Southern California, USA

Contamination Concentration

0.73 pg/l

Method, Remarks (Concentration in the Environment)

smog episode of September 8-9, 1993

Fraser, Matthew P.; Cass, Glen R.; Simoneit, Bernd R. T.; Rasmussen; Environmental Science and Technology; vol. 32; nb. 12; (1998); p. 1760 - 1770, View in Reaxys 21 of 27

Media (Concentration in the Environment)

airborne particles

Location

Washington, DC, USA

Contamination Concentration

1.6 mg/kg

Method, Remarks (Concentration in the Environment)

in SRM 1649 from NIST (Gaithersburg, MD); collected over ca.12-months period in the late 1970s; baghouse sampler with canvas bags; Soxhlet extraction (CH2Cl2); GC-MS analysis; standards: authentic for identification, structural isomer for quantification

Durant, John L.; Lafleur, Arthur L.; Plummer, Elaine F.; Taghizadeh, Koli; Busby Jr., William F.; Thilly, William G.; Environmental Science and Technology; vol. 32; nb. 13; (1998); p. 1894 - 1906, View in Reaxys 22 of 27

Media (Concentration in the Environment)

air

Location

Kenmore Square, Boston, MA, U.S.A.

Contamination Concentration

2.072 pg/l

Method, Remarks (Concentration in the Environment)

average conc.; from the roof of a National Ambient Air Quality Standards monitoring station; five 24-h air samples; June 1994; 4 m above ground level; micro-orifice impactor; GC/MS; distribution with particle size in an urban aerosol

Allen, Jonathan O.; Dookeran, Nameeta M.; Taghizadeh, Koli; Lafleur, Arthur L.; Smith, Kenneth A.; Sarofim, Adel F.; Environmental Science and Technology; vol. 31; nb. 7; (1997); p. 2064 - 2070, View in Reaxys 23 of 27

Media (Concentration in the Environment)

distillate fuel oil

Contamination Concentration

25.0 - 32.3 pg kJ-1

Method, Remarks (Concentration in the Environment)

fine particulate matter collected from an industrial boiler burning no. 2; emission rates measured; 5 experiments; samples collected during tests 2 and 5 subjected to GC/MS analysis; time: 185-375 min; boiler operated at 54-58 percent of its rated capacity

Rogge, Wolfgang F.; Hildemann, Lynn M.; Mazurek, Monica A.; Cass, Glen R.; Simoneit, Bernd R. T.; Environmental Science and Technology; vol. 31; nb. 10; (1997); p. 2731 - 2737, View in Reaxys 24 of 27

Media (Concentration in the Environment)

wastewater

Location

Sweden

Contamination Concentration

0 - 0.5 μg/l

Method, Remarks (Concentration in the Environment)

daily composite samples; in the effluent wastewater from Henriksdal Sewage Treatment Plant, Stockholm (0.5 μg/l; Jan. 1994), Goeteborg Regional Sewage Works (not detected; Dec. 1993), and Sjoelunda Sewage Works, Malmoe (not detected; Dec. 1993); GC/MS

Paxeus, Nicklas; Water Research; vol. 30; nb. 5; (1996); p. 1115 - 1122, View in Reaxys

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25 of 27

Media (Concentration in the Environment)

clean offgas

Location

Germany

Contamination Concentration

1.69 ng/l

Method, Remarks (Concentration in the Environment)

municipal waste incineration plant; water vapor condensation; XAD-resin filters; adsorption/thermodesorption; adsorption/elution; GC-FID analysis

Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys 26 of 27

Media (Concentration in the Environment)

smoke

Location

70 km north of Manaus, Amazonia

Contamination Concentration

4.0 ng/l

Method, Remarks (Concentration in the Environment)

smoke from burning forest litter; in northern forest reserve of Instituto Nacional de Pesquisas da Amazonia; November 1992; high volume filtration; extraction with CH2Cl2; methylation; separation by TLC; GC and GC-MS analysis

Radzi bin Abas, M.; Simoneit, B. R. T.; Elias, V.; Cabral, J. A.; Cardoso, J. N.; Chemosphere; vol. 30; nb. 5; (1995); p. 995 1016, View in Reaxys 27 of 27

Media (Concentration in the Environment)

urban atmosphere

Location

Barcelona, Spain

Contamination Concentration

2 - 7 pg*m-3

Method, Remarks (Concentration in the Environment)

two heavily trafficked sites; sampling in spring, fall, winter 1989-1990; Hi-Vol sampling system (MCV, Collbato, Spain); extraction with dichloromethane; GPC and NP-LC fractionation; cGC-MS analysis

Bayona, J. M.; Casellas, M.; Fernandez, P.; Solanas, A. M.; Albaiges, J.; Chemosphere; vol. 29; nb. 3; (1994); p. 441 - 450, View in Reaxys Biodegradation (3) 1 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Degradation Rate (Biodegradation) [%]

Ca. 100 percent

Exposure Period (Biodegradation)

44 d

Method, Remarks (Biodegradation)

33percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 44 d: 4.8 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys 2 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Method, Remarks (Biodegradation)

50percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 60 d: 18.8 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys

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3 of 3

Type (Biodegradation)

aerobic

Inoculum

Pleurotus ostreatus (SMR 684)

Concentration (Biodegradation)

27.5 μg/g CTW

Method, Remarks (Biodegradation)

60percent of creosote treated wood (CTW) chips added to dry wheat straw inoculated with mycelium of Pleurotus ostreatus; pressed to eliminate water; extracted with methanol in ultrasonic bath; GC-MS; title comp. conc. after 60 d: 8.4 μg/g CTW; table

Polcaro; Brancaleoni; Donati; Frattoni; Galli; Migliore; Rapana; Bulletin of Environmental Contamination and Toxicology; vol. 81; nb. 2; (2008); p. 180 - 184, View in Reaxys Abiotic Degradation, Photolysis (1) 1 of 1

Type (Abiotic Degradation, Photolysis)

photolysis

Concentration (Abiotic Degradation, Photolysis)

5 mg/l

Temperature (Abiotic Deg- 20 - 25 radation, Photolysis) [°C] Rate Constant

2.0E-2 1/min

Half-life Time (Abiotic Degradation, Photolysis) [h]

0.48

Method, Remarks (Abiotic photoreactor equipped with quartz immersion well; 125 W medium pressure mercury lamp; aqueDegradation, Photolysis) ous ethanolic solution of title comp.; photoreactor covered with aluminium foil; GC/MS; HPLC/UV; title comp. was practically stable during first 10 min Sabate; Bayona; Solanas; Chemosphere; vol. 44; nb. 2; (2001); p. 119 - 124, View in Reaxys Use (12) Laboratory Use and Use Pattern Handling

References

Pharmaceuticals

treating antiandrogen-resistant prostate cancer

Spectral sensitizer

Patent; CIBA HOLDING INC.; WO2009/47151; (2009); (A1) English, View in Reaxys

Sensitizer

Patent; FujiFilm Corporation; US2008/21223; (2008); (A1) English, View in Reaxys

Light stabilizer

Patent; FujiFilm Corporation; US2008/21223; (2008); (A1) English, View in Reaxys

aromatic ketone for generation enolates from 4,5-epoxymorphinan compounds in the presence of potassium tert-alkylate

Patent; Likhotvorik, Igor R.; Lisowski, Joseph J.; US2006/167258; (2006); (A1) English, View in Reaxys

Photoinitiator

Patent; KING PHARMACEUTICALS; WO2006/71844; (2006); (A2) English, View in Reaxys

determination of LiAlH4 in ether or THF solutions

Brown, Eric; Leze, Antoine; Touet, Joel; Tetrahedron Letters; vol. 32; nb. 34; (1991); p. 4309 4310, View in Reaxys

as sensitizer in the rearrangement of onitrobenzaldehyde to o-nitrosobenzoic acid

Filby, W. G.; Guenther, K.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 125; (1981); p. 21 - 26, View in Reaxys

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β, β* Sensibilisatorwirkung

Rehak et al.; Collection of Czechoslovak Chemical Communications; vol. 38; (1973); p. 697,702, View in Reaxys

Photosens. Decarboxylierung v. Phenoxyessigsaeure

Davidson et al.; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3480, View in Reaxys

Photosens. Decarboxylierung v. N(o-Chlorphenyl)glycin

Davidson et al.; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3480, View in Reaxys

Quantum Chemical Calculations (2) Calculated Proper- Method (Quantum ties Chemical Calculations) Molecular orbitals; Electronic energy levels; Transition energies

Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Electronic energy levels; Molecular orbitals

Ab initio calcns. (LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Location

References

supporting informa- Xie, Lili; Zhen, Xiaomeng; Huang, Shuping; Su, Xiaolong; Lin, Mai; Li, tion Yi; Green Chemistry; vol. 19; nb. 15; (2017); p. 3530 - 3534, View in Reaxys Spenst, Peter; Würthner, Frank; Angewandte Chemie - International Edition; vol. 54; nb. 35; (2015); p. 10165 - 10168; Angew. Chem.; vol. 127; nb. 35; (2015); p. 10303 - 10306,4, View in Reaxys

Medchem (29) 1 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

radioprotectant properties

Measurement Parameter

qualitative

Vatulina; Tuzhilkova; Bokova; Pharmaceutical Chemistry Journal; vol. 23; nb. 4; (1990); p. 325 - 329, View in Reaxys 2 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

LD 50: 2000 mg/kg, radioprotective activity, intraperitoneally (mouse)

Measurement Parameter

qualitative

Vatulina, G. G.; Bol'shakova, S. A.; Tuzhilkova, T. I.; Bokova, A. I.; Makhsudova, B.; et al.; Pharmaceutical Chemistry Journal; vol. 19; nb. 5; (1985); p. 326 - 330; Khimiko-Farmatsevticheskii Zhurnal; vol. 19; nb. 5; (1985); p. 552 - 557, View in Reaxys 3 of 29

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

Cmax

Unit

ng/g

Quantitative value

255

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Dunn, Derek; Hostetler, Greg; Iqbal, Mohamed; Marcy, Val R.; Lin, Yin Guo; Jones, Bruce; Aimone, Lisa D.; Gruner, John; Ator, Mark A.; Bacon, Edward R.; Chatterjee, Sankar; Bioorganic and Medicinal Chemistry Letters; vol. 22; nb. 11; (2012); p. 3751 - 3753, View in Reaxys 4 of 29

Bioassay Category

Pharmacokinetic

Bioassay Name

Pharmacokinetic

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

tmax

Unit

hour

Quantitative value

0.8

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Name

Substance Dose

116 mg/kg

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

AUC

Unit

ng.h/g

Quantitative value

2349

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |growth inhibition Target : Lactuca sativa L. c. v. sacramento, lettuceBioassay : activity evaluation by measuring the length of hypocotyl and radicle of the lettuce lettuce petri dish test; placing 10 lettuce seeds onto moistened filter paper treated with the chemical; incubation at 25 deg C, rel. humidity 60 percent with 12-h light/dark photoperiod (PPFD of light 80 μE/m2/sec) or in the dark

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

5 ppm

Qualitative Results

growth inhibition in hypocotyls, 15 percent higher when light is present; growth enhancement effect in radicles at 5-20 ppm both in the light and in the dark

Measurement Parameter

qualitative

Tsao, Rong; Eto, Morifusa; Chemosphere; vol. 32; nb. 7; (1996); p. 1307 - 1317, View in Reaxys 7 of 29

Substance Effect

Estrogen

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Bioassay : rat liver S9: rat hepatic 9000-g supernatant; positive control: trans-stilbene in vitro; twohybrid system with or without rat liver S9

Biological Species/NCBI ID

Saccharomyces cerevisiae

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

100 µM

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Hashimoto, Shinya; Ueda, Yasuhiro; Kurihara, Ryo; Shiraishi, Fujio; Environmental Toxicology and Chemistry; vol. 26; nb. 2; (2007); p. 279 - 286, View in Reaxys 8 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : aryl hydrocarbon receptor-mediated activity; effect onTarget : rat hepatoma H4IIEGud.Luc1.1 cell lineBioassay : cells stably transfected with a luciferase reporter gene in the alpha modification of minimal essential medium supplemented with 10 percent heat-inactivated FBS; title comp. in DMSO (final conc. <= 0.4 percent v/v); incubated for 6 and 24 h chemical-activated luciferase expression (CALUX) assay; induction equivalency factor (IEF) calculated as the ratio between EC25 of benzo<a>pyrene (BaP) or TCDD and concentration of the title comp. induced the equal level

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 9 of 29

Substance Effect

Estrogen

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : MVLN cellsBioassay : stably transfected with the p-Vit-tk-Luc plasmid cells in a 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F-12 nutrient mixture supplemented with 5 percent heat-inactivated FBS, insulin and sodium pyruvate title comp. in DMSO (final conc. <= 0.1 percent v/v); incubated for 24 h; induction equivalency factor (IEF) calculated as the ratio between EC25 of 17β-estradiol and concentration of the title comp. induced the equal level of luciferase activity

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 10 of 29

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : MVLN cellsBioassay : cells in a 1:1 mixture of Dulbecco's modified Eagle's medium and Ham's F-12 nutrient mixture supplemented with 5 percent heat-inactivated FBS, insulin and sodium pyruvate; title comp. in DMSO (final conc. <= 0.1 percent v/v); incubated for 24 h

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

10 µM

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 11 of 29

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : rat hepatoma H4IIEGud.Luc1.1 cell lineBioassay : cells in the alpha modification of minimal essential medium supplemented with 10 percent heat-inactivated FBS; title comp. in DMSO (final conc. <= 0.4 percent v/v); incubated for 24 h

Substance RN

1636531View in Reaxys

Substance Name

1448204

Substance Dose

10 µM

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Machala; Ciganek; Blaha; Minksova; Vondrac; Environmental Toxicology and Chemistry; vol. 20; nb. 12; (2001); p. 2736 2743, View in Reaxys 12 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 1-nitropyrene (1-NP, 2.0 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 13 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 2-nitrofluorene (2-NF, 6.0 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

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Substance Name

1448204

Qualitative Results

percent inhibition at the highest conc.: 4.8

Measurement Parameter

qualitative

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 14 of 29

Substance Effect

Antimutagenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : 6 different doses; means from 2 independent series in DMSO; mutagenicity induced by 3-nitrofluoranthene (3-NFA, 0.12 μg)

Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

percent inhibition at the highest conc.: 17.4

Measurement Parameter

qualitative

Edenharder; Tang; Food and Chemical Toxicology; vol. 35; nb. 3-4; (1997); p. 357 - 372, View in Reaxys 15 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : immobilityBioassay : 24 h old daphnids; 4 chambers with test solution and 4 chambers with control in aqueus medium; 5 daphnids in chamber filled with test solution for 24 h; temp. 20 deg C

Biological Species/NCBI ID

Daphnia magna

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

E(L)C50 15 mg/l

Measurement Parameter

qualitative

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 16 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Scenedesmus subspicatusBioassay : 12 h day/night photoperiod with blue and red wavelengths; for each concentration four replicate samples and one blank sample prepared in mineral medium; algal culture incubated with geometric dilution of 10 concentrations of title comp. for 7 days; at day 0 and after 7 days algal cells counted, biomass integral with interpolation used

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

31.4

Measurement pX

3.76

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 17 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

29.7

Measurement pX

3.78

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 18 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

21.8

Measurement pX

3.92

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 19 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

7.1

Measurement pX

4.4

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 20 of 29

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : immobilityBioassay : in standard water; 30 organisms exposured with dilution of title comp. for 24 h

Biological Species/NCBI ID

Thamnocephalus platyurus

Substance RN

1636531View in Reaxys

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Substance Name

1448204

Qualitative Results

E(L)C50 33 mg/l

Measurement Parameter

qualitative

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 21 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |growth inhibition Bioassay : logarithmic dilutions of metabolite in mineral medium; bacterial cultures incubated with title comp. in 26 deg C for cs. 16 h; turbidity of samples measured with spectrophotometer at 436 nm

Biological Species/NCBI ID

Pseudomonas putida

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

Measurement pX

3.49

Sepic, Ester; Bricelj, Mihael; Leskovsek, Hermina; Chemosphere; vol. 52; nb. 7; (2003); p. 1125 - 1133, View in Reaxys 22 of 29

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : receptor; activation ofTarget : mouse hepatoma H1L1.1c2 cellsBioassay : CALUX (chemical-activated luciferase expression) assay; cells incubated with title comp. in medium for 24 h at 37 deg C; luciferin added; aryl hydrocarbon receptor activity determined by luciferase activity

Substance RN

1636531View in Reaxys

Substance Name

1448204

Measurement Parameter

qualitative

Qualitative value

Measurement pX

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Transactivation assay

Bioassay Details

Effect : receptor; activation ofTarget : Saccharomyces cerevisiae YCM3Bioassay : ECTCDD25: conc. producing galactosidase activity equal to 25% of maximum response to TCDD yeast assay; yeast incubated with title comp. in medium for 18 h at 30 deg C; aryl hydrocarbon receptor activity determined by β-galactosidase activity; ECTCDD25 calculated

Substance RN

1636531View in Reaxys

Substance Name

1448204

Qualitative Results

ECTCDD25 2.9E3 nmol/l

Measurement Parameter

qualitative

Target Name

Indoleamine 2,3-dioxygenase [human]

Target Synonyms

indoleamine 2,3-dioxygenase

Target, Subunit, Species

Indoleamine 2,3-dioxygenase [human]

Target Mutant/Chimera Details

Indoleamine 2,3-dioxygenase [human]:Wild

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25 of 29

Target Species (Bioactivity)

human

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Inhibitory concentration of the compound against purified recombinant human INDOLEAMINE 2,3-DIOXYGENASE (2 ng/ul) expressed in Escherichia coli BL21 AI upon incubation for 60 min at 37 degree C in 100 mM phosphate buffer (pH 6.5) in presence of L-Trp (200 uM)

Biological Species/NCBI ID

human

Substance RN

1636531View in Reaxys

Measurement Parameter

IC50

Unit

µM

Measurement Object

IC50

Qualitative value

Quantitative value

200

Measurement pX

Concomitants: Compound name

L-Trp

Concomitants: Compound role

COM

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published toxic dose upon subcutaneous administration;Subcutaneous

Biological Species/NCBI ID

rat

Substance RN

1636531View in Reaxys

Substance Route of Adm.

subcutaneous administration

Measurement Parameter

TDLo

Unit

mg/kg

Qualitative value

Quantitative value

300

Material Safety Data Sheet, View in Reaxys 26 of 29

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose, 50% kill;Intraperitoneal;Acute toxicity

Biological Species/NCBI ID

mouse

Substance RN

1636531View in Reaxys

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

LD50

Unit

g/kg

Qualitative value

Quantitative value

Material Safety Data Sheet, View in Reaxys 27 of 29

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Mutagenic dose in Salmonella typhimurium;AMES test

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Biological Species/NCBI ID

Salmonella enterica serovar Typhimurium

Substance RN

1636531View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Vasilieva; Tanirbergenov; Abilev; Migatchev; Huttunen; Mutation Research; vol. 244; nb. 4; (1990); p. 321 - 329, View in Reaxys 28 of 29

Target Name

Androgen receptor (T877A) [human]

Target Synonyms

androgen receptor (t877a)

Target, Subunit, Species

Androgen receptor (T877A) [human]

Target Mutant/Chimera Details

Androgen receptor (T877A) [human]:Wild

Target Species (Bioactivity)

human

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Transactivation assay

Cells/Cell Lines

LNCaP cell line

Substance RN

1636531View in Reaxys

Substance Name

VPC-3002-table 1, VPC-ID 3002

Substance Dose

50 µM

Measurement Parameter

% Inhibition

Unit

Quantitative value

86.3

Measurement pX

5.1

Target Name

androgen receptor

Target Synonyms

androgen receptor; androgen receptor activity; ar; bfar; dhtr; dihydrotestosterone receptor; nr3c4; nuclear receptor subfamily 3 group c member 4

Target, Subunit, Species

androgen receptor

Target Mutant/Chimera Details

androgen receptor:Wild

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

Binding

Substance RN

1636531View in Reaxys

Substance Name

VPC-3002-table 1, VPC-ID 3002

Measurement Parameter

IC50

Unit

µM

Quantitative value

5.9

Measurement pX

5.23

Concomitants: Compound name

Fluormone AL Green

Concomitants: Compound role

RAD

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