4-Methylbenzaldehyde (p-Tolualdehyde, 4-MeBA) by Asch

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2016-04-07 08h:45m:45s (EST)

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Reaxys ID 385772 View in Reaxys

1/1 CAS Registry Number: 104-87-0 Chemical Name: p-tolualdehyde; p-tolylaldehyde Linear Structure Formula: C6H4(COH)(CH3) Molecular Formula: C8H8O Molecular Weight: 120.151 Type of Substance: isocyclic InChI Key: FXLOVSHXALFLKQ-UHFFFAOYSA-N Note:

Substance Label (455) Label References 2d

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Tourani, Hesam; Naimi-Jamal, Mohammad Reza; Dekamin, Mohammad Ghorban; Amirnejad, Meysam; Comptes Rendus Chimie; vol. 15; nb. 11-12; (2012); p. 1072 - 1076, View in Reaxys; Malkov, Andrei V.; Stoncius, Sigitas; Bell, Mark; Castelluzzo, Fabiomassimo; Ramirez-Lopez, Pedro; Biedermannova, Lada; Langer, Vratislav; Rulisek, Lubomir; Kocovsky, Pavel; Chemistry - A European Journal; vol. 19; nb. 28; (2013); p. 9167 - 9185, View in Reaxys; Khoobi, Mehdi; Alipour, Masoumeh; Moradi, Alireza; Sakhteman, Amirhossein; Nadri, Hamid; Razavi, Seyyede Faeze; Ghandi, Mehdi; Foroumadi, Alireza; Shafiee, Abbas; European Journal of Medicinal Chemistry; vol. 68; (2013); p. 291 - 300, View in Reaxys; Satasia, Shailesh P.; Kalaria, Piyush N.; Raval, Dipak K.; Organic and Biomolecular Chemistry; vol. 12; nb. 11; (2014); p. 1751 - 1758, View in Reaxys; Xiang, Ziwei; Liang, Yiru; Chen, Xiang; Wu, Qi; Lin, Xianfu; Amino Acids; vol. 46; nb. 8; (2014); p. 1929 - 1937, View in Reaxys; Apotrosoaei, Maria; Vasincu, Ioana Mirela; Dragan, Maria; Buron, Frdric; Routier, Sylvain; Profire, Lenuta; Molecules; vol. 19; nb. 9; (2014); p. 13824 - 13847, View in Reaxys; Wang, Cong-Shuai; Zhu, Ren-Yi; Zhang, Yu-Chen; Shi, Feng; Chemical Communications; vol. 51; nb. 59; (2015); p. 11798 - 11801, View in Reaxys; Maleki, Behrooz; Zonoz, Farrokhzad Mohammadi; Akhlaghi, Hossien Ali; Organic Preparations and Procedures International; vol. 47; nb. 5; (2015); p. 361 - 367, View in Reaxys; Maleki, Behrooz; Baghayeri, Mehdi; RSC Advances; vol. 5; nb. 97; (2015); p. 79746 - 79758, View in Reaxys

Soule, Jean-Francois; Miyamura, Hiroyuki; Kobayashi, Shu; Chemical Communications; vol. 49; nb. 4; (2013); p. 355 - 357, View in Reaxys; Yu-Mei, Zhang; Hong-Li, Zhang; Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry; vol. 44; nb. 8; (2014); p. 1115 - 1118, View in Reaxys; Khoobi, Mehdi; Ghanoni, Farzaneh; Nadri, Hamid; Moradi, Alireza; Hamedani, Morteza Pirali; Moghadam, Farshad Homayouni; Emami, Saeed; Vosooghi, Mohsen; Zadmard, Reza; Foroumadi, Alireza; Shafiee, Abbas; European Journal of Medicinal Chemistry; vol. 89; (2015); p. 296 - 303, View in Reaxys; Xia, Jianhui; Shao, Ailong; Tang, Shan; Gao, Xinlong; Gao, Meng; Lei, Aiwen; Organic and Biomolecular Chemistry; vol. 13; nb. 22; (2015); p. 6154 - 6157, View in Reaxys; Wang, Xiaoyu; Du, Chuan; Shi, Hui; Pang, Yadong; Jin, Shengfei; Hou, Yuqian; Wang, Yanshi; Peng, Xiaoshi; Xiao, Jianyong; Liu, Yang; Liu, Yongxiang; Cheng, Maosheng; Tetrahedron; vol. 71; nb. 38; (2015); p. 6744 - 6748, View in Reaxys; Sivakumari, Thakkellapati; Chadha, Anju; RSC Advances; vol. 5; nb. 111; (2015); p. 91594 - 91600, View in Reaxys

Nishimura, Rodolfo H.V.; Toledo, Fabiano T.; Lopes, Joao L.C.; Clososki, Giuliano C.; Tetrahedron Letters; vol. 54; nb. 4; (2013); p. 287 - 290, View in Reaxys; Kumar, Raju Suresh; Ramar, Alagar; Perumal, Subbu; Almansour, Abdulrahman I.; Arumugam, Natarajan; Ali, Mohamed Ashraf; Synthetic Communications; vol. 43; nb. 20; (2013); p. 2763 - 2772, View in Reaxys; Jia, Fan; Liu, Kaisheng; Xi, Hui; Lu, Shenglin; Li, Zhiping; Tetrahedron Letters; vol. 54; nb. 47; (2013); p. 6337 - 6340, View in Reaxys; Liu, Peng; Lei, Min; Hu, Lihong; Tetrahedron; vol. 69; nb. 48; (2013); p. 10405 - 10413, View in Reaxys; Yu, Lian; Cao, Jian; Organic and Biomolecular Chemistry; vol. 12; nb. 23; (2014); p. 3986 - 3990, View in Reaxys; Bhunia, Anup; Kaicharla, Trinadh; Porwal, Digvijay; Gonnade, Rajesh G.; Biju, Akkattu T.; Chemical Communications; vol. 50; nb. 77; (2014); p. 11389 - 11392, View in Reaxys; Iqbal, Naeem; Cho, Eun Jin; Advanced Synthesis and Catalysis; vol. 357; nb. 10; (2015); p. 2187 - 2192, View in Reaxys; Yang, Jiefang; Chen, Xingyu; Wang, Zhiqian; Tetrahedron Letters; vol. 56; nb. 41; (2015); p. 5673 - 5675; Art.No: 46660, View in Reaxys

Khan, Pasha M.; El-Gendy, Bahaa El-Dien M.; Kumar, Naresh; Garcia-Ordonez, Ruben; Lin, Li; Ruiz, Claudia H.; Cameron, Michael D.; Griffin, Patrick R.; Kamenecka, Theodore M.; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 2; (2013); p. 532 - 536, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p. 1867 - 1871, View in Reaxys; Prati, Federica; De Simone, Angela; Bisignano, Paola; Armirotti, Andrea; Summa, Maria; Pizzirani, Daniela; Scarpelli, Rita; Perez, Daniel I.; Andrisano, Vincenza; Perez-Castillo, Ana; Monti, Barbara; Massenzio, Francesca; Polito, Letizia; Racchi, Marco; Favia, Angelo D.; Bottegoni, Giovanni; Martinez, Ana; Bolognesi, Maria Laura; Cavalli, Andrea; Angewandte Chemie - International Edition; vol. 54; nb. 5; (2015); p. 1578 - 1582; Angew. Chem.; (2015), View in Reaxys

Vereshchagin, Anatolii N.; Elinson, Michail N.; Dorofeeva, Evgeniya O.; Stepanov, Nikita O.; Zaimovskaya, Tatiana A.; Nikishin, Gennady I.; Tetrahedron; vol. 69; nb. 7; (2013); p. 1945 - 1952, View in Reaxys; Ramachandran, P. Veeraraghavan; Chanda, Prem B.; Otoo, Barnabas; Tetrahedron Letters; vol. 55; nb. 7; (2014); p. 1289 - 1291, View in Reaxys; Mukherjee, Munmun; Zhou, Yubai; Gupta, Anil K.; Guan, Yong; Wulff, William D.; European Journal of Organic Chemistry; vol. 2014; nb. 7; (2014); p. 1386 - 1390, View in Reaxys; Mukherjee, Munmun; Zhou, Yubai; Gupta, Anil K.; Guan, Yong; Wulff, William D.; European Journal of Organic Chemistry; vol. 2014; nb. 7; (2014); p. 1386 - 1390, View in Reaxys; Gomha, Sobhi M.; Abbas, Ikhlass M.; Elneairy, Mohamed A. A.; Elaasser, Mahmoud M.; Mabrouk, Bazada K. A.; Journal of the Serbian Chemical Society; vol. 80; nb. 10; (2015); p. 1251 - 1264, View in Reaxys

Wang, Jing; Liu, Chao; Yuan, Jiwen; Lei, Aiwen; Angewandte Chemie - International Edition; vol. 52; nb. 8; (2013); p. 2256 - 2259; Angew. Chem.; vol. 125; nb. 8; (2013); p. 2312 - 2315, View in Reaxys; Ding, Lei; Chen, Jing; Hu, Yifan; Xu, Juan; Gong, Xing; Xu, Dongfang; Zhao, Baoguo; Li, Hexing; Organic Letters; vol. 16; nb. 3; (2014); p. 720 - 723, View in Reaxys; Wang, Yang; Tu, Man-Su; Shi, Feng; Tu, Shu-Jiang; Advanced Synthesis and Catalysis; vol. 356; nb. 9; (2014); p. 2009 - 2019, View in Reaxys; Eskandari; Karami; Khodabakhshi; Chemistry of Heterocyclic Compounds; vol. 50; nb. 12; (2015); p. 1658 - 1664; Khim. Geterotsikl. Soedin.; vol. 50; nb. 12; (2014); p. 1807 - 1813,7, View in Reaxys; El Remaily, Mahmoud Abd El Aleem

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Ali Ali; Naidu, Veluru Ramesh; Ni, Shengjun; Franzn, Johan; European Journal of Organic Chemistry; vol. 2015; nb. 30; (2015); p. 6610 - 6614, View in Reaxys; Zhang, Jian; Lin, Shao-Xia; Cheng, Dao-Juan; Liu, Xin-Yuan; Tan, Bin; Journal of the American Chemical Society; vol. 137; nb. 44; (2015); p. 14039 - 14042, View in Reaxys 3h

Nguyen, Dinh Thanh; Le, The Hoai; Bui, Thi Thu Trang; European Journal of Medicinal Chemistry; vol. 60; (2013); p. 199 - 207, View in Reaxys; Rostamizadeh, Shahnaz; Nojavan, Masoomeh; Aryan, Reza; Isapoor, Elyass; Azad, Mohammad; Journal of Molecular Catalysis A: Chemical; vol. 374-375; (2013); p. 102 - 110, View in Reaxys; Fareghi-Alamdari, Reza; Golestanzadeh, Mohsen; Agend, Farima; Zekri, Negar; Canadian Journal of Chemistry; vol. 91; nb. 10; (2013); p. 982 - 991, View in Reaxys; Rahmani, Salman; Amoozadeh, Ali; Kolvari, Eskandar; Catalysis Communications; vol. 56; (2014); p. 184 - 188, View in Reaxys; Dekamin, Mohammad G.; Eslami, Mohammad; Green Chemistry; vol. 16; nb. 12; (2014); p. 4914 - 4921, View in Reaxys; Maleki, Ali; Kamalzare, Maryam; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6931 - 6934, View in Reaxys; Gladysz, John A.; Safaei, Hamid Reza; Nouri, Sara; Helvetica Chimica Acta; vol. 97; nb. 11; (2014); p. 1539 - 1545, View in Reaxys; Nikam, Mukesh D.; Mahajan, Pravin S.; Chate, Asha V.; Dabhade, Sanjay K.; Gill, Charansingh H.; Journal of the Chilean Chemical Society; vol. 60; nb. 1; (2015); p. 2847 2850, View in Reaxys; Amiri, Ali Alinasab; Javanshir, Shahrzad; Dolatkhah, Zahra; Dekamin, Mohammad G.; New Journal of Chemistry; vol. 39; nb. 12; (2015); p. 9665 - 9671, View in Reaxys

Shi, Feng; Xing, Gui-Juan; Tan, Wei; Zhu, Ren-Yi; Tu, Shujiang; Organic and Biomolecular Chemistry; vol. 11; nb. 9; (2013); p. 1482 - 1489, View in Reaxys; Chen, Wen-Bing; Han, Wen-Yong; Han, Yan-Yan; Zhang, Xiao-Mei; Yuan, Wei-Cheng; Tetrahedron; vol. 69; nb. 26; (2013); p. 5281 - 5286, View in Reaxys; Hossein Nia, Roghayeh; Mamaghani, Manouchehr; Shirini, Farhad; Tabatabaeian, Khalil; Journal of Heterocyclic Chemistry; vol. 51; nb. 2; (2014); p. 363 - 367, View in Reaxys; Zhu, Xiao-Tong; Liu, Jia-Yan; Jiang, Bo; Tu, Shu-Jiang; Journal of Heterocyclic Chemistry; vol. 52; nb. 1; (2015); p. 92 - 96, View in Reaxys; Montaghami, Alireza; Montazeri, Naser; Oriental Journal of Chemistry; vol. 30; nb. 3; (2014); p. 1361 - 1364, View in Reaxys; Patel, Amit B.; Kumari, Premlata; Chikhalia, Kishor H.; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 54B; nb. 2; (2015); p. 260 - 271, View in Reaxys; Gao, Jun; Ren, ZhiGang; Lang, Jian-Ping; Journal of Organometallic Chemistry; vol. 792; (2015); p. 88 - 92; Art.No: 18908, View in Reaxys; Abdolrazaghnezhad, Azam; Hassanabadi, Alireza; Journal of Chemical Research; vol. 39; nb. 7; (2015); p. 423 - 424, View in Reaxys

Radulovic, Niko S.; Miltojevic, Ana B.; Vukicevic, Rastko D.; Comptes Rendus Chimie; vol. 16; nb. 3; (2013); p. 257 - 270, View in Reaxys; Qi, Wenke; Wang, Peipei; Fan, Liyuan; Zhang, Songlin; Journal of Organic Chemistry; vol. 78; nb. 12; (2013); p. 5918 - 5924, View in Reaxys; Liberto, Natalia Aparecida; De Paiva Silva, Sarah; De Fatima, Angelo; Fernandes, Sergio Antonio; Tetrahedron; vol. 69; nb. 38; (2013); p. 8245 - 8249, View in Reaxys; Indrasena; Riyaz; Naidu; Dubey; Asian Journal of Chemistry; vol. 26; nb. 8; (2014); p. 2221 - 2225, View in Reaxys; Zhu, Kailong; Shaver, Michael P.; Thomas, Stephen P.; European Journal of Organic Chemistry; vol. 2015; nb. 10; (2015); p. 2119 - 2123, View in Reaxys; Billamboz, Muriel; Sotto, Nicolas; Chevrin-Villette, Carole; Len, Christophe; RSC Advances; vol. 5; nb. 57; (2015); p. 46026 - 46030, View in Reaxys; Li, Yu-Ling; Wang, Kai; Zhao, Bo; Jiang, Qiu-Shi; Du, Bai-Xiang; Chen, Cai-Fa; Research on Chemical Intermediates; vol. 41; nb. 8; (2015); p. 5149 - 5158, View in Reaxys

Maiti, Gourhari; Karmakar, Rajiv; Kayal, Utpal; Tetrahedron Letters; vol. 54; nb. 23; (2013); p. 2920 - 2923, View in Reaxys; Kunzler, Alice; Neuenfeldt, Patricia D.; Das Neves, Adriana M.; Pereira, Claudio M.P.; Marques, Gabriela H.; Nascente, Patricia S.; Fernandes, Maureen H.V.; Huebner, Silvia O.; Cunico, Wilson; European Journal of Medicinal Chemistry; vol. 64; (2013); p. 74 - 80, View in Reaxys; Noroozi Pesyan, Nader; Shokr, Alireza; Behroozi, Mohammad; Sahin, Ertan; Journal of the Iranian Chemical Society; vol. 10; nb. 3; (2013); p. 565 - 575, View in Reaxys; Hazeri, Nourallah; Masoumnia, Amin; Mghsoodlou, Malek Taher; Salahi, Sajjad; Kangani, Mehrnoosh; Kianpour, Samira; Kiaee, Shiva; Abonajmi, Jasem; Research on Chemical Intermediates; vol. 41; nb. 7; (2015); p. 4123 - 4131, View in Reaxys; Yamashita, Yasuhiro; Cui, Yi; Xie, Peizhong; Kobayashi, Shu; Organic Letters; vol. 17; nb. 24; (2015); p. 6042 - 6045, View in Reaxys

10h

Periasamy, Mariappan; Reddy, Polimera Obula; Sanjeevakumar, Nalluri; European Journal of Organic Chemistry; nb. 18; (2013); p. 3866 - 3875, View in Reaxys; Tang, Li-Wei; Dong, Xiao; Zhou, Zhi-Ming; Liu, Ying-Qiang; Dai, Li; Zhang, Man; RSC Advances; vol. 5; nb. 7; (2015); p. 4758 - 4765, View in Reaxys

Safari, Javad; Zarnegar, Zohre; Borujeni, Mahmoud Borjian; Chemical Papers; vol. 67; nb. 7; (2013); p. 688 - 695, View in Reaxys; Nikpassand; Zare Fekri; Sina; Abed; Marvi; Russian Journal of General Chemistry; vol. 85; nb. 8; (2015); p. 1959 - 1964; Zh. Obshch. Khim.; vol. 85; nb. 8; (2015), View in Reaxys

Wang, Zhong-Chang; Duan, Yong-Tao; Qin, Ya-Juan; Wang, Peng-Fei; Luo, Yin; Wen, Qing; Yang, YongAn; Sun, Juan; Hu, Yang; Sang, Ya-Li; Zhu, Hai-Liang; European Journal of Medicinal Chemistry; vol. 65; (2013); p. 456 - 563, View in Reaxys; Liu, Jun-Zheng; Zhang, Shu-En; Nie, Feilin; Yang, Ying; Tang, YanBo; Yin, Wenwen; Tian, Jin-Ying; Ye, Fei; Xiao, Zhiyan; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 23; (2013); p. 6217 - 6222, View in Reaxys; Masesane, Ishmael B.; Mihigo, Shetonde O.; Synthetic Communications; vol. 45; nb. 13; (2015); p. 1546 - 1551, View in Reaxys

Watanabe, Yudai; Shimada, Naoyuki; Anada, Masahiro; Hashimoto, Shunichi; Tetrahedron Asymmetry; vol. 25; nb. 1; (2014); p. 63 - 73, View in Reaxys; Chong, Chang Che; Hirao, Hajime; Kinjo, Rei; Angewandte Chemie, International Edition; vol. 54; nb. 1; (2015); p. 190 - 194; Angewandte Chemie; nb. 1; (2015); p. 5, View in Reaxys

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Saffar-Teluri, Ali; Research on Chemical Intermediates; vol. 40; nb. 3; (2014); p. 1061 - 1067, View in Reaxys; Gogoi, Pinky; Dutta, Arup Kumar; Sarma, Parishmita; Borah, Ruli; Applied Catalysis A: General; vol. 492; nb. 1; (2015); p. 133 - 139, View in Reaxys

4-MeC&6%H&4%CHO

Khaligh, Nader Ghaffari; Shirini, Farhad; Ultrasonics Sonochemistry; vol. 22; (2015); p. 397 - 403,7, View in Reaxys

Shah, Dhruvin R.; Modh, Rahul P.; Desai, Dhara D.; Chikhalia, Kishor H.; Indian Journal of Chemistry Section B Organic and Medicinal Chemistry; vol. 53B; nb. 9; (2014); p. 1169 - 1177, View in Reaxys; Beltr, Jorge; Gimeno, M. Concepcin; Herrera, Raquel P.; Beilstein Journal of Organic Chemistry; vol. 10; (2014); p. 2206 - 2214, View in Reaxys; Safaei, Hamid Reza; Safaei, Maryam; Shekouhy, Mohsen; RSC Advances; vol. 5; nb. 9; (2015); p. 6797 - 6806, View in Reaxys

1d; 2d

Fan, Li-Yan; Shang, Ying-Hui; Li, Xiang-Xiong; Hua, Wen-Jun; Chinese Chemical Letters; vol. 26; nb. 1; (2015); p. 77 - 80, View in Reaxys

Duarte, Tiago A. G.; Estrada, Ana C.; Simes, Mrio M. Q.; Santos, Isabel C. M. S.; Cavaleiro, Ana M. V.; Neves, M. Graca P. M. S.; Cavaleiro, Jos A. S.; Catalysis Science and Technology; vol. 5; nb. 1; (2015); p. 351 - 363, View in Reaxys; Liu, Chengkou; Fang, Zheng; Yang, Zhao; Li, Qingwen; Guo, Shiyu; Zhang, Kai; Ouyang, Pingkai; Guo, Kai; Tetrahedron Letters; vol. 56; nb. 44; (2015); p. 5973 - 5976, View in Reaxys

Rayati, Saeed; Bohloulbandi, Elaheh; Zakavi, Saeed; Inorganic Chemistry Communications; vol. 54; (2015); p. 38 - 40, View in Reaxys

18, R1=4-Me

Roman, Bart I.; De Ryck, Tine; Verhasselt, Sigrid; Bracke, Marc E.; Stevens, Christian V.; Bioorganic and Medicinal Chemistry Letters; vol. 25; nb. 5; (2015); p. 1027 - 1031, View in Reaxys

IId

Sangshetti; Khan; Kute; Zaheer; Ahmed; Russian Journal of Organic Chemistry; vol. 51; nb. 1; (2015); p. 69 - 73; Russ.J.Org.Chem.; vol. 51; nb. 1; (2015); p. 69 - 73,5, View in Reaxys

3a; 4a

Miyazaki, Takahiro; Nishino, Kota; Yoshimoto, Shunsuke; Ogiwara, Yohei; Sakai, Norio; European Journal of Organic Chemistry; vol. 2015; nb. 9; (2015); p. 1991 - 1994, View in Reaxys

T-1,E-2 P

Islam; Borah; Acharya; RSC Advances; vol. 5; nb. 17; (2015); p. 13239 - 13245, View in Reaxys

Faigl; Dek; Erdlyi; Holczbauer; Czugler; Nyerges; Mtravölgyi; Chirality; vol. 27; nb. 3; (2015); p. 216 - 222, View in Reaxys

Liu, Fang-Hui; Song, Yu-Bao; Zhai, Li-Juan; Li, Ming; Journal of Heterocyclic Chemistry; vol. 52; nb. 2; (2015); p. 322 - 329, View in Reaxys

aldehyde 2g

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

Lee, Jihoon; Panek, James S.; Journal of Organic Chemistry; vol. 80; nb. 6; (2015); p. 2959 - 2971, View in Reaxys

Atahan, Alparslan; Durmus, Sefa; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 144; (2015); p. 61 - 67, View in Reaxys

Xie, Chen; Wu, Lingmin; Han, Jianlin; Soloshonok, Vadim A.; Pan, Yi; Angewandte Chemie - International Edition; vol. 54; nb. 20; (2015); p. 6019 - 6023; Angew. Chem.; vol. 127; nb. 20; (2015); p. 6117 - 6121,5, View in Reaxys

Kamal, Ahmed; Sastry, K. N. Visweswara; Chandrasekhar; Mani, Geeta Sai; Adiyala, Praveen Reddy; Nanubolu, Jagadeesh Babu; Singarapu, Kiran Kumar; Maurya, Ram Awatar; Journal of Organic Chemistry; vol. 80; nb. 9; (2015); p. 4325 - 4335, View in Reaxys; Fan, Wenyou; Yang, Youqing; Lei, Jianhua; Jiang, Qijian; Zhou, Wang; Journal of Organic Chemistry; vol. 80; nb. 17; (2015); p. 8782 - 8789, View in Reaxys

IIa

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

2 for 4b

Yang, Xiaojuan; Zhang, Chong; Wu, Liqiang; RSC Advances; vol. 5; nb. 24; (2015); p. 18945 - 18951, View in Reaxys

Hua, Yuanda; Jung, Seongjeong; Roh, James; Jeon, Junha; Journal of Organic Chemistry; vol. 80; nb. 9; (2015); p. 4661 - 4671, View in Reaxys

Zhang, Huan-Huan; Luo, Yong-Chun; Wang, Hua-Peng; Chen, Wei; Xu, Peng-Fei; Organic Letters; vol. 16; nb. 18; (2014); p. 4896 - 4899, View in Reaxys; Gan, Zong-Jie; Wang, Yu-Hua; Xu, Yun-Gen; Guo, Ting; Wang, Jun; Song, Qiao; Xu, Xue-Jun; Hu, Shi-Yuan; Wang, Yu-Jun; Wang, De-Chuan; Sun, De-Zhu; Zhang, Di; Xi, Tao; Li, Hao-Dong; Zhang, Hai-Bo; Hang, Tai-Jun; Lu, Hong-Guo; Liu, Jing-Gen; Organic and Biomolecular Chemistry; vol. 13; nb. 20; (2015); p. 5656 - 5673, View in Reaxys

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S17

Shen, Mei-Hua; Pan, Ying-Peng; Jia, Zhi-Hong; Ren, Xin-Tao; Zhang, Ping; Xu, Hua-Dong; Organic and Biomolecular Chemistry; vol. 13; nb. 17; (2015); p. 4851 - 4854, View in Reaxys

Mahmoodi, Nosrat O.; Ramzanpour, Sahar; Ghanbari Pirbasti, Fateme; Archiv der Pharmazie; vol. 348; nb. 4; (2015); p. 275 - 282, View in Reaxys; Matake, Ryosuke; Niwa, Yuki; Matsubara, Hiroshi; Organic Letters; vol. 17; nb. 10; (2015); p. 2354 - 2357, View in Reaxys; Kumagai, Yuta; Naoe, Takashi; Nishikawa, Keisuke; Osaka, Kazuyuki; Morita, Toshio; Yoshimi, Yasuharu; Australian Journal of Chemistry; vol. 68; nb. 11; (2015); p. 1668 - 1671, View in Reaxys

Javorskis, Tomas; Sriubaite, Simona; Bagdiunas, Gintautas; Orentas, Edvinas; Chemistry - A European Journal; vol. 21; nb. 25; (2015); p. 9157 - 9164, View in Reaxys

10g

Kaur, Hardeep; Balzarini, Jan; De Kock, Carmen; Smith, Peter J.; Chibale, Kelly; Singh, Kamaljit; European Journal of Medicinal Chemistry; vol. 101; (2015); p. 52 - 62; Art.No: 7951, View in Reaxys

S-4a

Zhang, Jian; Wang, Heng; Ren, Shaobo; Zhang, Wei; Liu, Yunkui; Organic Letters; vol. 17; nb. 12; (2015); p. 2920 - 2923, View in Reaxys

Xu, Xuefeng; Zhang, Xu; Liu, Wenming; Zhao, Qiang; Wang, Zhiqiang; Yu, Lintao; Shi, Fu; Tetrahedron Letters; vol. 56; nb. 24; (2015); p. 3790 - 3792, View in Reaxys

Sashidhara, Koneni V.; Palnati, Gopala Reddy; Singh, L. Ravithej; Upadhyay, Amit; Avula, Srinivasa Rao; Kumar, Abdhesh; Kant, Ruchir; Green Chemistry; vol. 17; nb. 7; (2015); p. 3766 - 3770, View in Reaxys

T4E3S1

Movahed, Siyavash Kazemi; Shariatipour, Monire; Dabiri, Minoo; RSC Advances; vol. 5; nb. 42; (2015); p. 33423 - 33431, View in Reaxys

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

1{10}

Salami-Ranjbaran, Elmira; Khosropour, Ahmad R.; Mohammadpoor-Baltork, Iraj; Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; ACS Combinatorial Science; vol. 17; nb. 8; (2015); p. 452 - 458, View in Reaxys

2{17}

Yugandhar; Srivastava, Ajay Kumar; ACS Combinatorial Science; vol. 17; nb. 8; (2015); p. 474 - 481, View in Reaxys

3{10}

Park, Sujin; Kwon, Dah In; Lee, Jeeyeon; Kim, Ikyon; ACS Combinatorial Science; vol. 17; nb. 8; (2015); p. 459 - 469, View in Reaxys

Billamboz, Muriel; Len, Christophe; ChemSusChem; vol. 8; nb. 10; (2015); p. 1664 - 1675, View in Reaxys

Oshiro, Paula Beatriz; Da Silva Gomes Lima, Paula Souza; De Menezes, Manoel Lima; Da Silva-Filho, Luiz Carlos; Tetrahedron Letters; vol. 56; nb. 30; (2015); p. 4476 - 4479; Art.No: 46371, View in Reaxys

c31

Chen, Meihang; Hu, Deyu; Li, Xiangyang; Yang, Song; Zhang, Weiying; Li, Pei; Song, Baoan; Bioorganic and Medicinal Chemistry Letters; vol. 25; nb. 18; (2015); p. 3840 - 3844; Art.No: 22957, View in Reaxys

Cui, Xin; Xu, Mei-Chen; Zhang, Ling-Juan; Yao, Ru-Xin; Zhang, Xian-Ming; Dalton Transactions; vol. 44; nb. 28; (2015); p. 12711 - 12716, View in Reaxys

2, Ar = 4CH3C6H4

Palakshi Reddy; Sarveswari; Vijayakumar; Research on Chemical Intermediates; vol. 41; nb. 9; (2015); p. 6877 - 6883; Art.No: 1784, View in Reaxys

2, Ar = 4H3CC6H4

Farahi, Mahnaz; Karami, Bahador; Banaki, Zohreh; Chinese Chemical Letters; vol. 26; nb. 9; (2015); p. 1065 - 1067, View in Reaxys

20c

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

Asahara, Haruyasu; Arikiyo, Keita; Nishiwaki, Nagatoshi; Beilstein Journal of Organic Chemistry; vol. 11; (2015); p. 1241 - 1245, View in Reaxys

19a

Tanemura, Kiyoshi; Suzuki, Tsuneo; Chemistry Letters; vol. 44; nb. 6; (2015); p. 797 - 799, View in Reaxys

Liu, Chengkou; Fang, Zheng; Yang, Zhao; Li, Qingwen; Guo, Shiyu; Guo, Kai; RSC Advances; vol. 5; nb. 97; (2015); p. 79699 - 79702, View in Reaxys

65b

Bertrand, Sophie M.; Ancellin, Nicolas; Beaufils, Benjamin; Bingham, Ryan P.; Borthwick, Jennifer A.; Boullay, Anne-Bndicte; Boursier, Eric; Carter, Paul S.; Chung, Chun-Wa; Churcher, Ian; Dodic, Nerina; Fouchet, Marie-Hlne; Fournier, Charlne; Francis, Peter L.; Gummer, Laura A.; Herry, Kenny; Hobbs, Andrew; Hobbs, Clare I.; Homes, Paul; Jamieson, Craig; Nicodeme, Edwige; Pickett, Stephen D.; Reid, Iain H.; Simpson, Graham L.; Sloan, Lisa A.; Smith, Sarah E.; Somers, Donald O.N.; Spitzfaden, Claus; Suckling, Colin J.; Valko, Klara; Washio, Yoshiaki; Young, Robert J.; Journal of Medicinal Chemistry; vol. 58; nb. 18; (2015); p. 7140 - 7163, View in Reaxys

40/464

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2dd

Wan, Miao; Lou, Hongxiang; Liu, Lei; Chemical Communications; vol. 51; nb. 73; (2015); p. 13953 - 13956, View in Reaxys

1; 7; 13

Maghsoodlou, Malek Taher; Hazeri, Nourallah; Lashkari, Mojtaba; Shahrokhabadi, Fereshteh Nejad; Naghshbandi, Behzad; Kazemi-Doost, Mohammad Saeed; Rashidi, Mahnaz; Mir, Fatemeh; Kangani, Mehrnoosh; Salahi, Sajjad; Research on Chemical Intermediates; vol. 41; nb. 10; (2015); p. 6985 - 6997, View in Reaxys

Edjlali, Laden; Khanamiri, Rahim Hosseinzdeh; Abolhasani, Jafar; Monatshefte fuer Chemie; vol. 146; nb. 8; (2015); p. 1339 - 1342, View in Reaxys; Liu, Chulong; Bao, Hailin; Wang, Dingsheng; Wang, Xinyan; Li, Yadong; Hu, Yuefei; Tetrahedron Letters; vol. 56; nb. 46; (2015); p. 6460 - 6462, View in Reaxys

2g; 2e

Girish, Yarabhally R.; Sharath Kumar, Kothanahally S.; Thimmaiah, Kuntebommanahalli N.; Rangappa, Kanchugarakoppal S.; Shashikanth, Sheena; RSC Advances; vol. 5; nb. 92; (2015); p. 75533 - 75546, View in Reaxys

6-5

Lee, Chia-Hsin; Wu, Wen-Chun; Dangate, Prasad S.; Shen, Li-Ching; Chung, Wen-Sheng; Sun, ChungMing; ACS Combinatorial Science; vol. 17; nb. 10; (2015); p. 623 - 630, View in Reaxys

Yadav, Sneha; Khurana, Jitender M.; Chinese Journal of Catalysis; vol. 36; nb. 7; (2015); p. 1042 - 1046, View in Reaxys

Naveen, Kanagaraj; Nandakumar, Avanashiappan; Perumal, Paramasivan Thirumalai; RSC Advances; vol. 5; nb. 91; (2015); p. 74438 - 74446, View in Reaxys

1d; 1f

Abdollahi-Alibeik, Mohammad; Rezaeipoor-Anari, Ali; Letters in Organic Chemistry; vol. 12; nb. 9; (2015); p. 651 - 658, View in Reaxys

14e

Truong, Vuong Van; Nam, Tran Duy; Hung, Truong Ngoc; Nga, Nguyen Thi; Quan, Pham Minh; Chinh, Luu Van; Jung, Sang-Hun; Bioorganic and Medicinal Chemistry Letters; vol. 25; nb. 22; (2015); p. 5182 - 5185, View in Reaxys

1{5}

Kalla, Reddi Mohan Naidu; Park, Huiju; Lee, Hye Ri; Suh, Hongsuk; Kim, Il; ACS Combinatorial Science; vol. 17; nb. 11; (2015); p. 691 - 697, View in Reaxys

3a; 3k

Dommaraju, Yuvaraj; Bora, Shruti; Prajapati, Dipak; Organic and Biomolecular Chemistry; vol. 13; nb. 35; (2015); p. 9181 - 9185, View in Reaxys

2(3)

Dar, Ajaz A.; Enjamuri, Nagasuresh; Shadab; Ali, Nahid; Khan, Abu T.; ACS Combinatorial Science; vol. 17; nb. 11; (2015); p. 671 - 681, View in Reaxys

Wang, Shuo-En; Wang, Linfei; He, Qiuqin; Fan, Renhua; Angewandte Chemie - International Edition; vol. 54; nb. 46; (2015); p. 13655 - 13658; Angew. Chem.; vol. 127; nb. 46; (2015); p. 13859 - 13862,4, View in Reaxys

11d

Wang, Chao; Huang, Lingling; Lu, Min; Zhao, Bei; Wang, Yaorong; Zhang, Yong; Shen, Qi; Yao, Yingming; RSC Advances; vol. 5; nb. 115; (2015); p. 94768 - 94775, View in Reaxys

Venkatasatyanarayana; Lakshmana Rao; Thirumala Chary; Ram; Balram; Laxminarayana; Asian Journal of Chemistry; vol. 27; nb. 6; (2015); p. 2267 - 2272, View in Reaxys

14b

Fesenko, Anastasia A.; Shutalev, Anatoly D.; Tetrahedron; vol. 71; nb. 51; (2015); p. 9528 - 9543, View in Reaxys

Dang, Qin-Qin; Zhan, Yu-Fen; Duan, Li-Na; Zhang, Xian-Ming; Dalton Transactions; vol. 44; nb. 46; (2015); p. 20027 - 20031, View in Reaxys

122a

Patent; BIOCRYST PHARMACEUTICALS, INC.; KOTIAN, Pravin, L.; BABU, Yarlagadda, S.; WU, Minwan; CHINTAREDDY, Venkat, R.; KUMAR, V., Satish; ZHANG, Weihe; WO2015/134998; (2015); (A1) English, View in Reaxys

Yang, Xiaodong; Yang, Shenghua; Xiang, Likui; Pang, Xiaobo; Chen, Baohua; Huang, Guosheng; Yan, Rulong; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3732 - 3736, View in Reaxys

10d

Aziz-Ur-Rehman; Rasool, Shahid; Abbasi, M. Athar; Siddiqui, Sabahat Z.; Sattar, Almas; Khan, Khalid Mohammed; Ahmad, Irshad; Afzal, Saira; Journal of the Chemical Society of Pakistan; vol. 37; nb. 4; (2015); p. 776 - 786, View in Reaxys

IIb

Shirini; Zolfigol; Azadbar; Russian Journal of Organic Chemistry; vol. 37; nb. 11; (2001); p. 1600 - 1602, View in Reaxys; Kozlov; Tereshko; Russian Journal of Organic Chemistry; vol. 50; nb. 7; (2014); p. 1006 1011; Zh. Org. Khim.; vol. 50; nb. 7; (2014); p. 1024 - 1028,5, View in Reaxys

Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 6292, View in Reaxys; Maurya, Hardesh K.; Gupta, Atul; RSC Advances; vol. 4; nb. 42; (2014); p. 22106 22114, View in Reaxys

Hajipour, Abdol Reza; Mallakpour, Shadpour E.; Samimi, Heshmat A.; Synthetic Communications; vol. 32; nb. 24; (2002); p. 3831 - 3838, View in Reaxys; Li, Huanrong; Guan, Bingtao; Wang, Wenjin; Xing, Dong;

41/464

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Fang, Zhao; Wan, Xiaobing; Yang, Liping; Shi, Zhangjie; Tetrahedron; vol. 63; nb. 35; (2007); p. 8430 8434, View in Reaxys; Chaniyara, Ravi; Thakrar, Shailesh; Kakadiya, Rajesh; Marvania, Bhavin; Detroja, Dilip; Vekariya, Nikhil; Upadhyay, Kuldip; Manvar, Atul; Shah, Anamik; Journal of Heterocyclic Chemistry; vol. 51; nb. 2; (2014); p. 466 - 474, View in Reaxys; Marques, Gabriela H.; Kunzler, Alice; Bareno, Valeria D.O.; Drawanz, Bruna B.; Mastelloto, Hellen G; Leite, Fabio R.M.; Nascimento, Gustavo G.; Nascente, Patricia S.; Siqueira, Geonir M.; Cunico, Wilson; Medicinal Chemistry; vol. 10; nb. 4; (2014); p. 355 - 360, View in Reaxys 7d

North, Michael; Stewart, Emma L.; Young, Carl; Tetrahedron: Asymmetry; vol. 23; nb. 15-16; (2012); p. 1218 - 1225,8, View in Reaxys; Pindi, Suresh; Wu, Jianbin; Li, Guigen; Journal of Organic Chemistry; vol. 78; nb. 8; (2013); p. 4006 - 4012, View in Reaxys; Xiao, Bo; Easun, Timothy L.; Dhakshinamoorthy, Amarajothi; Cebula, Izabela; Beton, Peter H.; Titman, Jeremy J.; Garcia, Hermenegildo; Thomas, K. Mark; Schröder, Martin; Journal of Materials Chemistry A; vol. 2; nb. 46; (2014); p. 19889 - 19896, View in Reaxys

Gianino, Joseph B.; Ashfeld, Brandon L.; Journal of the American Chemical Society; vol. 134; nb. 44; (2012); p. 18217 - 18220,4, View in Reaxys; Gianino, Joseph B.; Ashfeld, Brandon L.; Journal of the American Chemical Society; vol. 134; nb. 44; (2012); p. 18217 - 18220, View in Reaxys; Kovaliov, Marina; Weitman, Michal; Major, Dan Thomas; Fischer, Bilha; Journal of Organic Chemistry; vol. 79; nb. 15; (2014); p. 7051 7062, View in Reaxys

Garcia-Alvarez, Rocio; Diaz-Alvarez, Alba E.; Crochet, Pascale; Cadierno, Victorio; RSC Advances; vol. 3; nb. 17; (2013); p. 5889 - 5894, View in Reaxys; Niknam, Khodabakhsh; Borazjani, Nassim; Rashidian, Reza; Jamali, Abbas; Chinese Journal of Catalysis; vol. 34; nb. 12; (2013); p. 2245 - 2254, View in Reaxys; Li, Pan; Zhao, Jingjing; Lang, Rui; Xia, Chungu; Li, Fuwei; Tetrahedron Letters; vol. 55; nb. 2; (2014); p. 390 - 393, View in Reaxys; Guan, Mingyu; Wang, Chao; Zhang, Jingyu; Zhao, Yingsheng; RSC Advances; vol. 4; nb. 90; (2014); p. 48777 - 48782, View in Reaxys

Dogan, Oezdemir; Isci, Muhammet; Aygun, Muhittin; Tetrahedron Asymmetry; vol. 24; nb. 9-10; (2013); p. 562 - 567, View in Reaxys; Fan, Ning-Juan; Bai, Yu-Bin; Zhang, Fei-Yu; Luo, Bo; Tang, Jiang-Jiang; Zhang, Qiang-Zhe; Gao, Jin-Ming; Steroids; vol. 78; nb. 9; (2013); p. 874 - 879, View in Reaxys; Liu, Kegang; Zhang, Guoqi; Tetrahedron Letters; vol. 56; nb. 1; (2014); p. 243 - 246, View in Reaxys; Periasamy, Mariappan; Reddy, Polimera Obula; Edukondalu, Athukuri; Dalai, Manasi; Alakonda, Laxman M.; Udaykumar, Bantu; European Journal of Organic Chemistry; vol. 2014; nb. 27; (2014); p. 6067 - 6076, View in Reaxys

Lukaszewicz, Ewa; Kupinska, Anna; Majewski, Piotr; Heteroatom Chemistry; vol. 24; nb. 4; (2013); p. 298 - 308, View in Reaxys; Gediz Erturk, Aliye; Bekdemir, Yunus; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 189; nb. 2; (2014); p. 285 - 292, View in Reaxys

Thanh, Nguyen Dinh; Quoc, Nguyen Van; Letters in Organic Chemistry; vol. 10; nb. 2; (2013); p. 85 - 90, View in Reaxys; Heravi, Majid. M.; Hashemi, Elaheh; Beheshtiha, Yahya Shirazi; Kamjou, Khadijeh; Toolabi, Maryam; Hosseintash, Nastaran; Journal of Molecular Catalysis A: Chemical; vol. 392; (2014); p. 173 180, View in Reaxys

Zhao, Li-Ming; Ma, Feng-Yan; Jin, Hai-Shan; Ma, Jiao; Wang, Huan; Fu, Chuan-Zhao; European Journal of Organic Chemistry; nb. 31; (2013); p. 7193 - 7199, View in Reaxys; Zhao, Li-Ming; Dou, Fei; Sun, Rui; Zhang, Ai-Li; Synlett; vol. 25; nb. 10; (2014); p. 1431 - 1434; Art.No: ST-2014-W0179-L, View in Reaxys

Boobalan, Ramalingam; Chen, Chinpiao; Advanced Synthesis and Catalysis; vol. 355; nb. 17; (2013); p. 3443 - 3450, View in Reaxys; Lill, Andreas P.; Rödl, Carmen B.; Steinhilber, Dieter; Stark, Holger; Hofmann, Bettina; European Journal of Medicinal Chemistry; vol. 89; (2014); p. 503 - 523, View in Reaxys

2f; 6n

Siddiqui; Srivastava, Arjita; Shamim, Shayna; Srivastava, Anjali; Waseem, Malik A.; Shireen; Rahila; Abumhdi, Afaf A.H.; Srivastava, Anushree; Rai, Pragati; Journal of Molecular Catalysis A: Chemical; vol. 382; (2014); p. 126 - 135, View in Reaxys

Rajesh, U. Chinna; Manohar, Sunny; Rawat, Diwan S.; Advanced Synthesis and Catalysis; vol. 355; nb. 16; (2013); p. 3170 - 3178, View in Reaxys; Soeta, Takahiro; Matsuzaki, Syunsuke; Ukaji, Yutaka; Chemistry A European Journal; vol. 20; nb. 17; (2014); p. 5007 - 5012, View in Reaxys

S-2b

Nandakumar, Avanashiappan; Kiruthika, Selvarangam E.; Naveen, Kanagaraj; Perumal, Paramasivan Thirumalai; Organic and Biomolecular Chemistry; vol. 12; nb. 6; (2014); p. 876 - 880, View in Reaxys; Kiruthika, Selvarangam E.; Perumal, Paramasivan Thirumalai; Organic Letters; vol. 16; nb. 2; (2014); p. 484 487, View in Reaxys; Kiruthika, Selvarangam E.; Nandakumar, Avanashiappan; Perumal, Paramasivan Thirumalai; Organic Letters; vol. 16; nb. 17; (2014); p. 4424 - 4427, View in Reaxys

Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p. 2330 - 2333, View in Reaxys

Rana, Aniruddhasinh M.; Desai, Kishor R.; Jauhari, Smita; Research on Chemical Intermediates; vol. 40; nb. 2; (2014); p. 761 - 777, View in Reaxys; Khatri, Taslimahemad T.; Shah, Viresh H.; Journal of the Korean Chemical Society; vol. 58; nb. 4; (2014); p. 366 - 376, View in Reaxys

13c

Loschonsky, Sabrina; Waltzer, Simon; Fraas, Sonja; Wacker, Tobias; Andrade, Susana L. A.; Kroneck, Peter M. H.; Mueller, Michael; ChemBioChem; vol. 15; nb. 3; (2014); p. 389 - 392, View in Reaxys

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2016-04-07 09:00:27

Zare Fekri; Nikpassand; Goldoost; Russian Journal of General Chemistry; vol. 83; nb. 12; (2013); p. 2352 2360, View in Reaxys; Saluja, Pooja; Khurana, Jitender M.; Nikhil, Kumar; Roy, Partha; RSC Advances; vol. 4; nb. 65; (2014); p. 34594 - 34603, View in Reaxys

Chunhong, Zhao; Liu, Fei; Gou, Shaohua; Tetrahedron Asymmetry; vol. 25; nb. 3; (2014); p. 278 - 283, View in Reaxys

11'

Zhang, Zheng-Lin; She, Yuan-Bin; Fu, Hai-Yan; Song, Xu-Feng; Sun, Zhi-Cheng; Heterocycles; vol. 89; nb. 2; (2014); p. 503 - 514, View in Reaxys

2, R&3% = 4-Me

Rajaguru, Kandasamy; Suresh, Rajendran; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai; Organic Letters; vol. 16; nb. 3; (2014); p. 744 - 747, View in Reaxys

Borah, Ruli; Dutta, Arup Kumar; Sarma, Parishmita; Dutta, Champak; Sarma, Bipul; RSC Advances; vol. 4; nb. 21; (2014); p. 10912 - 10917, View in Reaxys; Krzeszewski, Maciej; Thorsted, Bjarne; Brewer, Jonathan; Gryko, Daniel T.; Journal of Organic Chemistry; vol. 79; nb. 7; (2014); p. 3119 - 3128, View in Reaxys

Babu, B. Madhu; Thakur, Pramod B.; Nageswara Rao; Santosh Kumar; Meshram; Tetrahedron Letters; vol. 55; nb. 11; (2014); p. 1868 - 1872, View in Reaxys

Mita, Tsuyoshi; Higuchi, Yuki; Sato, Yoshihiro; Organic Letters; vol. 16; nb. 1; (2014); p. 14 - 17, View in Reaxys

11b

Song, Xixi; Liu, Ai-Xiang; Liu, Shan-Shan; Gao, Wen-Chao; Wang, Min-Can; Chang, Junbiao; Tetrahedron; vol. 70; nb. 7; (2014); p. 1464 - 1470, View in Reaxys

2{4}

Anvar, Salma; Mohammadpoor-Baltork, Iraj; Tangestaninejad, Shahram; Moghadam, Majid; Mirkhani, Valiollah; Khosropour, Ahmad Reza; Landarani Isfahani, Amir; Kia, Reza; ACS Combinatorial Science; vol. 16; nb. 3; (2014); p. 93 - 100, View in Reaxys

Shih, Yi-Shan; Boobalan, Ramalingam; Chen, Chinpiao; Lee, Gene-Hsian; Tetrahedron Asymmetry; vol. 25; nb. 4; (2014); p. 327 - 333, View in Reaxys

3(6)

Ryabukhin, Sergey V.; Panov, Dmitriy M.; Granat, Dmitry S.; Ostapchuk, Eugeniy N.; Kryvoruchko, Dmitriy V.; Grygorenko, Oleksandr O.; ACS Combinatorial Science; vol. 16; nb. 3; (2014); p. 146 - 153, View in Reaxys

TolC(O)H

Groom, Laura R.; Russell, Adam F.; Schwarz, Andrew D.; Mountford, Philip; Organometallics; vol. 33; nb. 4; (2014); p. 1002 - 1019, View in Reaxys; Groom, Laura R.; Schwarz, Andrew D.; Nova, Ainara; Clot, Eric; Mountford, Philip; Organometallics; vol. 32; nb. 24; (2013); p. 7520 - 7539, View in Reaxys

St. Denis, Jeffrey D.; Scully, Conor C. G.; Lee, C. Frank; Yudin, Andrei K.; Organic Letters; vol. 16; nb. 5; (2014); p. 1338 - 1341, View in Reaxys

SM-Tab-4-2

Kong, Xiangjin; Chen, Ligong; Applied Catalysis A: General; vol. 476; (2014); p. 34 - 38, View in Reaxys

Safaei-Ghomi, Javad; Ghasemzadeh, Mohammad Ali; South African Journal of Chemistry; vol. 67; (2014); p. 27 - 32, View in Reaxys; Vafajoo, Zahra; Veisi, Hojat; Maghsoodlou, Malek Taher; Ahmadian, Hossein; Comptes Rendus Chimie; vol. 17; nb. 4; (2014); p. 301 - 304, View in Reaxys

18o

Barbero, Margherita; Cadamuro, Silvano; Dughera, Stefano; Torregrossa, Roberta; Organic and Biomolecular Chemistry; vol. 12; nb. 23; (2014); p. 3902 - 3911, View in Reaxys

2c'

Ma, Xinyi; Li, Zhongfeng; Liu, Feijie; Cao, Shengli; Rao, Honghua; Advanced Synthesis and Catalysis; vol. 356; nb. 8; (2014); p. 1741 - 1746, View in Reaxys

2; 3

Rasouli, Mohammad Ali; Mahdavi, Mohammad; Firoozpour, Loghman; Shafiee, Abbas; Foroumadi, Alireza; Tetrahedron; vol. 70; nb. 25; (2014); p. 3931 - 3934, View in Reaxys

IIe

Kiyani, Hamzeh; Ghorbani, Fatemeh; Chemical Papers; vol. 68; nb. 8; (2014); p. 1104 - 1112, View in Reaxys

Scharnagel, Dagmar; Prause, Felix; Kaldun, Johannes; Haase, Robert G.; Breuning, Matthias; Chemical Communications; vol. 50; nb. 50; (2014); p. 6623 - 6625, View in Reaxys

4MeC&6%H&4%C HO

Huo, Cong-De; Bao, Xia-Zhen; Hu, Dong-Cheng; Jia, Xiao-Dong; Sun, Chou-Gu; Wang, Cheng; Chinese Chemical Letters; vol. 25; nb. 5; (2014); p. 699 - 701, View in Reaxys; Zhang, Weijie; Tang, Ruiren; Yu, Huirong; Gao, Shu; Applied Organometallic Chemistry; vol. 28; nb. 7; (2014); p. 545 - 551, View in Reaxys

A1b

Chandrasekhar, Sosale; Shrinidhi, Annadka; Synthetic Communications; vol. 44; nb. 14; (2014); p. 2051 2056, View in Reaxys

1'b

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

43/464

2016-04-07 09:00:27

pMeC&6%H&4%C HO

Huang, Chang-Yao; Kuan, Kai-Yuan; Liu, Yi-Hong; Peng, Shie-Ming; Liu, Shiuh-Tzung; Organometallics; vol. 33; nb. 11; (2014); p. 2831 - 2836, View in Reaxys

1b-c

Hosseini-Sarvari, Mona; Moeini, Fatemeh; Combinatorial Chemistry and High Throughput Screening; vol. 17; nb. 5; (2014); p. 439 - 449, View in Reaxys

Xia, Xuanshu; Toy, Patrick H.; Beilstein Journal of Organic Chemistry; vol. 10; (2014); p. 1397 - 1405, View in Reaxys

sm 2 of 3c,3i

Mahernia, Shabnam; Mahdavi, Mohammad; Adib, Mehdi; Synlett; vol. 25; nb. 9; (2014); Art.No: ST-2014D0129-L, View in Reaxys

2b; 5b

Barge, Madhuri; Salunkhe, Rajashri; RSC Advances; vol. 4; nb. 59; (2014); p. 31177 - 31183, View in Reaxys

IIg

Aly; Ibrahim; Okael; Gherbawy; Russian Journal of Bioorganic Chemistry; vol. 40; nb. 2; (2014); p. 214 - 227; Bioorg. Khim.; vol. 40; nb. 2; (2014); p. 214 - 227,14, View in Reaxys

Atar, Amol B.; Kim, Jong Tae; Lim, Kwon Taek; Jeong, Yeon Tae; Synthetic Communications; vol. 44; nb. 18; (2014); p. 2679 - 2691, View in Reaxys

10k

Wolinska, Ewa; Tetrahedron Asymmetry; vol. 25; nb. 15; (2014); p. 1122 - 1128, View in Reaxys

Kulkarni, Pramod; Journal of the Chilean Chemical Society; vol. 59; nb. 1; (2014); p. 2319 - 2321, View in Reaxys; Veeranarayana Reddy, Mudumala; Kim, Jong Su; Lim, Kwon Taek; Tae Jeong, Yeon; Tetrahedron Letters; vol. 55; nb. 47; (2014); p. 6459 - 6462, View in Reaxys

XIb

Babak; Gella; Semenenko; Shishkina; Shishkin; Musatov; Lipson; Russian Journal of Organic Chemistry; vol. 50; nb. 7; (2014); p. 1048 - 1055; Zh. Org. Khim.; vol. 50; nb. 7; (2014); p. 1048 - 1055,7, View in Reaxys

Tan, Da-Wei; Xie, Jing-Bo; Li, Qi; Li, Hong-Xi; Li, Jun-Chi; Li, Hai-Yan; Lang, Jian-Ping; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14061 - 14071, View in Reaxys

Cai, Hao; Zhou, Yu; Zhang, Dong; Xu, Jinyi; Liu, Hong; Chemical Communications; vol. 50; nb. 94; (2014); p. 14771 - 14774, View in Reaxys

15i

Kannan, Masanam; Punniyamurthy, Tharmalingam; Tetrahedron Asymmetry; vol. 25; nb. 18-19; (2014); p. 1331 - 1339, View in Reaxys

Sm for 1f

Wahl, Benoit; Cabr, Albert; Woodward, Simon; Lewis, William; Tetrahedron Letters; vol. 55; nb. 42; (2014); p. 5829 - 5831, View in Reaxys

IIs

Du, Liyong; Gao, Jing; Yang, Shuyang; Wang, Dawei; Han, Xinxin; Xu, Yongjian; Ding, Yuqiang; Russian Journal of General Chemistry; vol. 84; nb. 11; (2014); p. 2200 - 2204, View in Reaxys

Chinh, L. V.; Hung, T. N.; Nga, N. T.; Mai, T. T. N.; Hang, T. T. N.; Tarasevich, V. A.; Russian Journal of Organic Chemistry; vol. 50; nb. 12; (2014); p. 1767 - 1774; Zhurnal Organicheskoi Khimii; vol. 50; nb. 12; (2014); p. 1786 - 1793,8, View in Reaxys

4-MB

Feng, Dawei; Gu, Zhi-Yuan; Chen, Ying-Pin; Park, Jihye; Wei, Zhangwen; Sun, Yujia; Bosch, Mathieu; Yuan, Shuai; Zhou, Hong-Cai; Journal of the American Chemical Society; vol. 136; nb. 51; (2014); p. 17714 - 17717, View in Reaxys

Li, Jin-Liang; Liu, Li; Pei, Yu-Ning; Zhu, Hua-Jie; Tetrahedron; vol. 70; nb. 47; (2014); p. 9077 - 9083, View in Reaxys

De Andrade Bartolomeu, Aloisio; De Menezes, Manoel Lima; Da Silva Filho, Luiz Carlos; Chemical Papers; vol. 68; nb. 11; (2014); p. 1593 - 1600, View in Reaxys; De Andrade Bartolomeu, Aloisio; De Menezes, Manoel Lima; De Silva Filho, Luiz Carlos; Chemical Papers; vol. 68; nb. 11; (2014); p. 1593 - 1600, View in Reaxys

Yoon, Yeong Keng; Ali, Mohamed Ashraf; Wei, Ang Chee; Choon, Tan Soo; Leng, Lim Wan; Wei, Oo Chuan; Letters in Organic Chemistry; vol. 11; nb. 10; (2014); p. 785 - 789, View in Reaxys

Rana, Aniruddhasinh M.; Trivedi, Pooja; Desai, Kishor R.; Jauhari, Smita; Medicinal Chemistry Research; vol. 23; nb. 10; (2014); p. 4320 - 4336, View in Reaxys

Capitta, Francesca; De Luca, Lidia; Porcheddu, Andrea; RSC Advances; vol. 4; nb. 103; (2014); p. 59297 - 59301, View in Reaxys

Rafiski, Zbigniew; Kozakiewicz, Anna; Rafiska, Katarzyna; Tetrahedron; vol. 70; nb. 35; (2014); p. 5739 5745, View in Reaxys

Mohammadi, Marzieh; Bardajee, Ghasem Rezanejade; Pesyan, Nader Noroozi; RSC Advances; vol. 4; nb. 108; (2014); p. 62888 - 62894, View in Reaxys

44/464

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S1b

Leow, Dasheng; Chen, Ying-Ho; Hung, Tzu-Hang; Su, Ying; Lin, Yi-Zhen; European Journal of Organic Chemistry; vol. 2014; nb. 33; (2014); p. 7347 - 7352, View in Reaxys

Tan, Jianwen; Bednarek, Pawel; Liu, Jikai; Schneider, Bernd; Svatos, Ales; Hahlbrock, Klaus; Phytochemistry; vol. 65; nb. 6; (2004); p. 691 - 699, View in Reaxys; Ge, Wenlei; Zhu, Xun; Wei, Yunyang; RSC Advances; vol. 3; nb. 27; (2013); p. 10817 - 10822, View in Reaxys

13a

Tzirakis, Manolis D.; Lykakis, Ioannis N.; Panagiotou, George D.; Bourikas, Kyriakos; Lycourghiotis, Alexis; Kordulis, Christos; Orfanopoulos, Michael; Journal of Catalysis; vol. 252; nb. 2; (2007); p. 178 - 189, View in Reaxys; Sharma, Upendra K.; Sharma, Nandini; Kumar, Rajesh; Sinha, Arun K.; Amino Acids; vol. 44; nb. 3; (2013); p. 1031 - 1037, View in Reaxys

Patent; FIRMENICH SA; SANTORO, Francesco; SAUDAN, Lionel; SAUDAN, Michel, Alfred, Joseph; SAUDAN, Sylvia, Joyeuse, Adelaide; WO2012/84810; (2012); (A1) English, View in Reaxys; Patent; FIRMENICH SA; Santoro, Francesco; Saudan, Lionel; Saudan, Christophe; US2013/274487; (2013); (A1) English, View in Reaxys

VIIIh

Galeta, Juraj; Man, Stanislav; Potacek, Milan; Chemical Papers; vol. 67; nb. 1; (2013); p. 29 - 39, View in Reaxys

1r,3r

Azarifar, Davood; Najminejad, Zohreh; Khosravi, Kaveh; Synthetic Communications; vol. 43; nb. 6; (2013); p. 826 - 836, View in Reaxys

Rajak, Harish; Singh Thakur, Bhupendra; Singh, Avineesh; Raghuvanshi, Kamlesh; Sah, Anil Kumar; Veerasamy, Ravichandran; Sharma, Prabodh Chander; Singh Pawar, Rajesh; Kharya, Murli Dhar; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 3; (2013); p. 864 - 868, View in Reaxys

aldehyde-j

Nandagokula, Chidananda; Poojary, Boja; Vittal, Sumangala; Shenoy, Shalini; Shetty, Prashanth; Tangavelu, Arulmoli; Medicinal Chemistry Research; vol. 22; nb. 1; (2013); p. 253 - 266, View in Reaxys

4-MeC6H4

Khurana, Jitender M.; Lumb, Anshika; Chaudhary, Ankita; Nand, Bhaskara; RSC Advances; vol. 3; nb. 6; (2013); p. 1844 - 1854, View in Reaxys

Soni, Ajay; Rehman, Abdul; Naik, Keshav; Dastidar, Sunanda; Alam; Ray, Abhijit; Chaira, Tridib; Shah, Vanya; Palle, Venkata P.; Cliffe, Ian A.; Sattigeri, Viswajanani J.; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 5; (2013); p. 1482 - 1485, View in Reaxys

4d; pMeC6H4CHO

Ternel, Jeremy; Roussel, Pascal; Agbossou-Niedercorn, Francine; Gauvin, Regis M.; Catalysis Science and Technology; vol. 3; nb. 3; (2013); p. 580 - 583, View in Reaxys

Shanmugam, Muniyappapillai Jeganathan; Mohan Das, Thangamuthu; Carbohydrate Research; vol. 368; (2013); p. 40 - 46, View in Reaxys; Zheng, Jing; Deng, Lijuan; Chen, Minfeng; Xiao, Xuzhi; Xiao, Shengwei; Guo, Cuiping; Xiao, Gaokeng; Bai, Liangliang; Ye, Wencai; Zhang, Dongmei; Chen, Heru; European Journal of Medicinal Chemistry; vol. 65; (2013); p. 158 - 167, View in Reaxys

Bezier, David; Park, Sehoon; Brookhart, Maurice; Organic Letters; vol. 15; nb. 3; (2013); p. 496 - 499, View in Reaxys

Fretz, Samuel J.; Hadad, Christopher M.; Hart, David J.; Vyas, Shubham; Yang, Dexi; Journal of Organic Chemistry; vol. 78; nb. 1; (2013); p. 83 - 92, View in Reaxys

3{4}

Safaei, Shirin; Mohammadpoor-Baltork, Iraj; Khosropour, Ahmad Reza; Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Khavasi, Hamid Reza; ACS Combinatorial Science; vol. 15; nb. 3; (2013); p. 141 - 146, View in Reaxys

Wu, Shaoxiang; Guo, Jiyi; Sohail, Muhammad; Cao, Chengyao; Chen, Fu-Xue; Journal of Fluorine Chemistry; vol. 148; (2013); p. 19 - 29, View in Reaxys

Patel, Divyesh; Kumari, Premlata; Patel, Navin B.; Medicinal Chemistry Research; vol. 22; nb. 2; (2013); p. 726 - 744, View in Reaxys

2a;2f

Singh, Sushma; Sharma, Laxmi Kant; Saraswat, Apoorv; Siddiqui, Ibadur R.; Kehri, Harbans K.; Singh, Rana K. Pal; RSC Advances; vol. 3; nb. 13; (2013); p. 4237 - 4245, View in Reaxys

46b

Wang, Zhi-Gang; Chen, Liqun; Chen, Jiebo; Zheng, Jian-Feng; Gao, Weiwei; Zeng, Zhiping; Zhou, Hu; Zhang, Xiao-Kun; Huang, Pei-Qiang; Su, Ying; European Journal of Medicinal Chemistry; vol. 62; (2013); p. 632 - 648, View in Reaxys

9{5}

Kiim, Sumin; Lim, Chaemin; Lee, Sukjin; Lee, Seokwoo; Cho, Hyunkyung; Lee, Joo-Youn; Shim, Dong Sup; Park, Hee Dong; Kim, Sanghee; ACS Combinatorial Science; vol. 15; nb. 4; (2013); p. 208 - 215, View in Reaxys

p-Me-benzaldehyde

Veisi, Hojat; Sedrpoushan, Alireza; Zolfigol, Mohammad Ali; Mohanazadeh, Farajollah; Hemmati, Saba; Journal of Heterocyclic Chemistry; vol. 50; nb. SUPPL.1; (2013); p. E204-E206, View in Reaxys

3ab

Luo, Hai-Qing; Dong, Wen; Loh, Teck-Peng; Tetrahedron Letters; vol. 54; nb. 22; (2013); p. 2833 - 2836, View in Reaxys

45/464

2016-04-07 09:00:27

1{3}

Zonouzi, Afsaneh; Hosseinzadeh, Fatemeh; Karimi, Nastaran; Mirzazadeh, Roghieh; Ng, Seik Weng; ACS Combinatorial Science; vol. 15; nb. 5; (2013); p. 240 - 246, View in Reaxys

1{6}

Biswas, Kallolmay; Kumar, Arvind; Das Sarma, Koushik; ACS Combinatorial Science; vol. 15; nb. 5; (2013); p. 255 - 260, View in Reaxys

Shairgojray, Bashir Ahmad; Dar, Aijaz Ahmad; Bhat, Bilal Ahmad; Tetrahedron Letters; vol. 54; nb. 19; (2013); p. 2391 - 2394, View in Reaxys; Escorihuela, Jorge; Altava, Belen; Burguete, M. Isabel; Luis, Santiago V.; Tetrahedron; vol. 69; nb. 2; (2013); p. 551 - 558, View in Reaxys

13j

Myles, Lauren; Gathergood, Nicholas; Connon, Stephen J.; Chemical Communications; vol. 49; nb. 46; (2013); p. 5316 - 5318, View in Reaxys

8{6}

Maiti, Barnali; Chanda, Kaushik; Selvaraju, Manikandan; Tseng, Chih-Chung; Sun, Chung-Ming; ACS Combinatorial Science; vol. 15; nb. 6; (2013); p. 291 - 297, View in Reaxys

Kamimura, Akio; Komatsu, Hiroyuki; Moriyama, Takaaki; Nozaki, Yuichiro; Tetrahedron; vol. 69; nb. 29; (2013); p. 5968 - 5972, View in Reaxys

32b

Tyagi, Vikas; Khan, Shahnawaz; Chauhan, Prem M. S.; Synlett; vol. 24; nb. 10; (2013); p. 1291 - 1297; Art.No: ST-2013-D0247-L, View in Reaxys

Khurana, Jitender M.; Vij, Kanika; Synthetic Communications; vol. 43; nb. 17; (2013); p. 2294 - 2304, View in Reaxys

33c

Kumar, Vemula Praveen; Chandrasekhar, Srivari; Organic Letters; vol. 15; nb. 14; (2013); p. 3610 - 3613, View in Reaxys

Delany, Eoghan G.; Fagan, Claire-Louise; Gundala, Sivaji; Mari, Alessandra; Broja, Thomas; Zeitler, Kirsten; Connon, Stephen J.; Chemical Communications; vol. 49; nb. 58; (2013); p. 6510 - 6512, View in Reaxys

14k

Wolinska, Ewa; Tetrahedron; vol. 69; nb. 35; (2013); p. 7269 - 7278, View in Reaxys

entry 17

Li, Haoquan; Misal Castro, Luis C.; Zheng, Jianxia; Roisnel, Thierry; Dorcet, Vincent; Sortais, JeanBaptiste; Darcel, Christophe; Angewandte Chemie - International Edition; vol. 52; nb. 31; (2013); p. 8045 8049; Angew. Chem.; vol. 125; nb. 31; (2013); p. 8203 - 8207, View in Reaxys

13{2}

Cornier, Patricia G.; Delpiccolo, Carina M.L.; Boggian, Dora B.; Mata, Ernesto G.; Tetrahedron Letters; vol. 54; nb. 35; (2013); p. 4742 - 4745, View in Reaxys

5{2}

Val, Cristina; Crespo, Abel; Yaziji, Vicente; Coelho, Alberto; Azuaje, Jhonny; El Maatougui, Abdelaziz; Carbajales, Carlos; Sotelo, Eddy; ACS Combinatorial Science; vol. 15; nb. 7; (2013); p. 370 - 378, View in Reaxys

1e sm

Kulkarni, Pramod S.; Kondhare, Dasharath D.; Varala, Ravi; Zubaidha, Pudukulathan K.; Journal of the Serbian Chemical Society; vol. 78; nb. 7; (2013); p. 909 - 916, View in Reaxys

Ulus, Ramazan; Yesildag, Ibrahim; Tanc, Muhammet; Buelbuel, Metin; Kaya, Muharrem; Supuran, Claudiu T.; Bioorganic and Medicinal Chemistry; vol. 21; nb. 18; (2013); p. 5799 - 5805, View in Reaxys

13ae

Garcia-Alvarez, Rocio; Zablocka, Maria; Crochet, Pascale; Duhayon, Carine; Majoral, Jean-Pierre; Cadierno, Victorio; Green Chemistry; vol. 15; nb. 9; (2013); p. 2447 - 2456, View in Reaxys

4-TolCHO

Matcha, Kiran; Narayan, Rishikesh; Antonchick, Andrey P.; Angewandte Chemie - International Edition; vol. 52; nb. 31; (2013); p. 7985 - 7989; Angew. Chem.; vol. 125; nb. 31; (2013); p. 8143 - 8147,5, View in Reaxys

8b,k,i

Harikrishnan, Palani Sokkan; Rajesh, Stephen Michael; Almansour, Abdulrahman I.; Perumal, Subbu; Arkivoc; vol. 2013; nb. 4; (2013); p. 1 - 14, View in Reaxys

1{12}

Zhou, Yu-Jing; Chen, Dong-Sheng; Li, Yu-Ling; Liu, Yun; Wang, Xiang-Shan; ACS Combinatorial Science; vol. 15; nb. 9; (2013); p. 498 - 502, View in Reaxys

22h

Mori, Mattia; Tintori, Cristina; Christopher, Robert Selwyne Arul; Radi, Marco; Schenone, Silvia; Musumeci, Francesca; Brullo, Chiara; Sanita, Patrizia; DelleMonache, Simona; Angelucci, Adriano; Kissova, Miroslava; Crespan, Emmanuele; Maga, Giovanni; Botta, Maurizio; ChemMedChem; vol. 8; nb. 3; (2013); p. 484 - 496, View in Reaxys

19f

Zhao, Hongwu; Yue, Yuanyuan; Li, Hailong; Sheng, Zhihui; Yang, Zhao; Meng, Wei; Chinese Journal of Chemistry; vol. 31; nb. 4; (2013); p. 485 - 493, View in Reaxys

Rapolu, Sreevani; Alla, Manjula; Bommena, Vittal Rao; Murthy, Ramalinga; Jain, Nishant; Bommareddy, Venkata Ramya; Bommineni, Madhava Reddy; European Journal of Medicinal Chemistry; vol. 66; (2013); p. 91 - 100, View in Reaxys

46/464

2016-04-07 09:00:27

11a

Kamal, Ahmed; Faazil, Shaikh; Ramaiah, M. Janaki; Ashraf, Md.; Balakrishna; Pushpavalli; Patel, Nibedita; Pal-Bhadra, Manika; Bioorganic and Medicinal Chemistry Letters; vol. 23; nb. 20; (2013); p. 5733 - 5739, View in Reaxys

pMeOC&6%H&4% CHO

Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz; ACS Catalysis; vol. 3; nb. 10; (2013); p. 2208 - 2217, View in Reaxys

PhCHO

Guo, Rui-Yun; An, Zhi-Min; Mo, Li-Ping; Yang, Shu-Tao; Liu, Hong-Xia; Wang, Shu-Xia; Zhang, ZhanHui; Tetrahedron; vol. 69; nb. 47; (2013); p. 9931 - 9938, View in Reaxys

10a

Singh, Rana Sanjay Kumar; Kashyap, Bishwapran; Phukan, Prodeep; Tetrahedron Letters; vol. 54; nb. 49; (2013); p. 6687 - 6690, View in Reaxys

IIIb

Kozlov; Tereshko; Russian Journal of Organic Chemistry; vol. 49; nb. 9; (2013); p. 1335 - 1343; Zh. Org. Khim.; vol. 49; nb. 9; (2013); p. 1350 - 1358,9, View in Reaxys

12b

Sathesh, Venkatesan; Sathishkumar, Munusamy; Ramachandran, Gunasekar; Rathore, Ravindranath S.; Sathiyanarayanan, Kulathu Iyer; RSC Advances; vol. 3; nb. 45; (2013); p. 23035 - 23045, View in Reaxys

1'd

Bhanuchandra; Kuram, Malleswara Rao; Sahoo, Akhila K.; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 11824 - 11834, View in Reaxys

3{5}

Kanchithalaivan, Selvaraj; Sivakumar, Sathiyamoorthi; Ranjith Kumar, Raju; Elumalai, Palani; Ahmed, Qazi Naveed; Padala, Anil K.; ACS Combinatorial Science; vol. 15; nb. 12; (2013); p. 631 - 638, View in Reaxys

1{9}

Guo, Rui-Yun; An, Zhi-Min; Mo, Li-Ping; Wang, Rui-Zhi; Liu, Hong-Xia; Wang, Shu-Xia; Zhang, ZhanHui; ACS Combinatorial Science; vol. 15; nb. 11; (2013); p. 557 - 563, View in Reaxys

Wang, Xiang; Li, Pei; Li, Zhining; Yin, Juan; He, Ming; Xue, Wei; Chen, Zhiwei; Song, Baoan; Journal of Agricultural and Food Chemistry; vol. 61; nb. 40; (2013); p. 9575 - 9582, View in Reaxys

Nishikawa, Keisuke; Fukuda, Hiroshi; Abe, Masato; Nakanishi, Kazunari; Taniguchi, Tomoya; Nomura, Takashi; Yamaguchi, Chihiro; Hiradate, Syuntaro; Fujii, Yoshiharu; Okuda, Katsuhiro; Shindo, Mitsuru; Phytochemistry; vol. 96; (2013); p. 132 - 147, View in Reaxys

Zheng, Bing; Li, Zhiyuan; Liu, Feipeng; Wu, Yanhua; Shen, Junjian; Bian, Qinghua; Hou, Shicong; Wang, Ming; Molecules; vol. 18; nb. 12; (2013); p. 15422 - 15433, View in Reaxys

Heravi, Majid M.; Ajami, Dariush; Tabar-Heydar, Kourosh; Monatshefte fur Chemie; vol. 130; nb. 2; (1999); p. 337 - 339, View in Reaxys; Kurzwernhart, Andrea; Kandioller, Wolfgang; Baechler, Simone; Bartel, Caroline; Martic, Sanela; Buczkowska, Magdalena; Muehlgassner, Gerhard; Jakupec, Michael A.; Kraatz, Heinz-Bernhard; Bednarski, Patrick J.; Arion, Vladimir B.; Marko, Doris; Keppler, Bernhard K.; Hartinger, Christian G.; Journal of Medicinal Chemistry; vol. 55; nb. 23; (2012); p. 10512 - 10522, View in Reaxys

4-MePhCHO

Aspinall, Helen C.; Greeves, Nicholas; Smith, Peter M.; Tetrahedron Letters; vol. 40; nb. 9; (1999); p. 1763 - 1766, View in Reaxys; Giacco, Tiziana Del; Lipparoni, Luca; Ranchella, Michele; Rol, Cesare; Sebastiani, Giovanni Vittorio; Journal of the Chemical Society, Perkin Transactions 2; nb. 9; (2001); p. 1802 - 1807, View in Reaxys; Albadi, Jalal; Iravani, Nasir; Dehghan, Farzaneh; Shirinic, Farhad; ; vol. 36; nb. 10; (2012); p. 610 - 611,2, View in Reaxys

Xing, Ping; Zang, Wei; Huang, Zuo-Gang; Zhan, Yue-Xiong; Zhu, Chuan-Jun; Jiang, Biao; Synlett; vol. 23; nb. 15; (2012); p. 2269 - 2273, View in Reaxys

2-sm2,10sm2

Ansari, Farzana Latif; Kalsoom, Saima; Zaheer-Ul-Haq; Ali, Zahra; Jabeen, Farukh; Medicinal Chemistry Research; vol. 21; nb. 9; (2012); p. 2329 - 2339, View in Reaxys

13b

Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S.; Green Chemistry; vol. 14; nb. 10; (2012); p. 2912 - 2921, View in Reaxys

28a

Boobalan, Ramalingam; Lee, Gene-Hsian; Chen, Chinpiao; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2511 - 2520, View in Reaxys

IIIi

Penta, S.; Rao Vedula, R.; Russian Journal of General Chemistry; vol. 82; nb. 8; (2012); p. 1464 - 1467,4; Zhurnal Obshchei Khimii; vol. 82; nb. 8; (2012); p. 1403 - 1406,4, View in Reaxys

20; 18

Manzini, Simone; Blanco, Cesar A. Urbina; Nolan, Steven P.; Advanced Synthesis and Catalysis; vol. 354; nb. 16; (2012); p. 3036 - 3044, View in Reaxys

10e

Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei; Angewandte Chemie - International Edition; vol. 51; nb. 51; (2012); p. 12790 - 12794; Angew. Chem.; (2012); p. 12962 - 12966, View in Reaxys

4, Ar=4-Me −C&6%H&4%

Hasaninejed, Alireza; Kazerooni, Maryam Rasekhi; Zare, Abdolkarim; Catalysis Today; vol. 196; nb. 1; (2012); p. 148 - 155, View in Reaxys

47/464

2016-04-07 09:00:27

1, R = 4-MeC6H4

Teffahi, Djamila; Hocine, Smain; Li, Chao-Jun; Letters in Organic Chemistry; vol. 9; nb. 8; (2012); p. 585 593, View in Reaxys

Na, Risong; Wang, Bo; Liu, Honglei; Bian, Qinghua; Zhong, Jiangchun; Wang, Min; Guo, Hongchao; Letters in Organic Chemistry; vol. 9; nb. 9; (2012); p. 622 - 627, View in Reaxys

Maity, Tanmoy; Saha, Debraj; Das, Soma; Koner, Subratanath; European Journal of Inorganic Chemistry; nb. 30; (2012); p. 4914 - 4920, View in Reaxys

Zhang, Boyu; Jiang, Zongxuan; Zhou, Xin; Lu, Shengmei; Li, Jun; Liu, Yan; Li, Can; Angewandte Chemie - International Edition; vol. 51; nb. 52; (2012); p. 13159 - 13162; Angew. Chem.; vol. 124; nb. 52; (2012); p. 13336 - 13339,4, View in Reaxys

SM to 2d

Ashok; Vijaya Lakshmi; Indian Journal of Heterocyclic Chemistry; vol. 21; nb. 4; (2012); p. 337 - 340, View in Reaxys

Li, Chia-Yi; Kuo, Yi-Yin; Tsai, Jie-Hong; Yap, Glenn P. A.; Ong, Tiow-Gan; Chemistry - An Asian Journal; vol. 6; nb. 6; (2011); p. 1520 - 1524, View in Reaxys

p-Tolu-A

Kim, Ki-Hyun; Hong, Yoon-Jung; Pal, Raktim; Jeon, Eui-Chan; Koo, Yoon-Seo; Sunwoo, Young; Chemosphere; vol. 70; nb. 5; (2008); p. 807 - 820, View in Reaxys

tab.,entry 5, prod- Bailey, Aaron D.; Baru, Ashvin R.; Tasche, Kendall K.; Mohan, Ram S.; Tetrahedron Letters; vol. 49; nb. uct 4; (2008); p. 691 - 694, View in Reaxys Tab.1.run14

Wang, Feng; Ueda, Wataru; Chemistry Letters; vol. 37; nb. 2; (2008); p. 184 - 185, View in Reaxys

Table 1, entry 6

Su, Fang-Zheng; Liu, Yong-Mei; Wang, Lu-Cun; Cao, Yong; He, He-Yong; Fan, Kang-Nian; Angewandte Chemie - International Edition; vol. 47; nb. 2; (2008); p. 334 - 337, View in Reaxys

Aldehyde C; C

Patent; Terada, Masahiro; Ube, Hitoshi; Yokoyama, Shigeko; Shimizu, Hideo; US2008/154036; (2008); (A1) English, View in Reaxys

Table 1, entry 2

Liu, Da-Xue; Zhang, Li-Cheng; Wang, Quan; Da, Chao-Shan; Xin, Zhuo-Qun; Wang, Rui; Choi, Michael C. K.; Chan, Albert S. C.; Organic Letters; vol. 3; nb. 17; (2001); p. 2733 - 2735, View in Reaxys; Fan, Xuesen; Zhang, Xinying; Zhang, Yongmin; Journal of Chemical Research; nb. 4; (2004); p. 290 - 291, View in Reaxys; Rostami, Amin; Mahboubifar, Marjan; Khazaei, Ardeshir; South African Journal of Chemistry; vol. 61; (2008); p. 9 - 12, View in Reaxys

T.1., Prod. from Subs.4

Venkatesan; Kumar, A. Senthil; Zen; Tetrahedron Letters; vol. 49; nb. 28; (2008); p. 4339 - 4341, View in Reaxys

11, R=4-Me

Gallou, Fabrice; Haenggi, Ruedi; Hirt, Hans; Marterer, Wolfgang; Schaefer, Frank; Seeger-Weibel, Manuela; Tetrahedron Letters; vol. 49; nb. 34; (2008); p. 5024 - 5027, View in Reaxys

product, tab 1/4

Tang, Jingting; Zhu, Jinlong; Shen, Zongxuan; Zhang, Yawen; Tetrahedron Letters; vol. 48; nb. 11; (2007); p. 1919 - 1921, View in Reaxys

Tab. 1, entry 2

Hashemi, Mohammed M.; Ghazanfari, Dadkhoda; Akhbari, Maryam; Monatshefte fur Chemie; vol. 135; nb. 7; (2004); p. 793 - 797, View in Reaxys; Oezguen, Beytiye; Yaylaoglu, Ayse; Sendil, Kivilcim; Monatshefte fur Chemie; vol. 138; nb. 2; (2007); p. 161 - 163, View in Reaxys

table 1, entry 4. prod.

Bortolini, Olga; De Nino, Antonio; Fogagnolo, Marco; Fantin, Giancarlo; Mariuolo, Loredana; Tocci, Amedeo; Chemistry Letters; vol. 36; nb. 3; (2007); p. 472 - 473, View in Reaxys

T. 2., E.2., product Jia, Xueshun; Liu, Xiaotao; Li, Jian; Zhao, Peichao; Zhang, Yongmin; Tetrahedron Letters; vol. 48; nb. 6; (2007); p. 971 - 974, View in Reaxys Product, Tab.1, run 4

Liu, Zhong-Quan; Zhao, Yankai; Luo, Haiqing; Chai, Lingzhi; Sheng, Qiuju; Tetrahedron Letters; vol. 48; nb. 17; (2007); p. 3017 - 3019, View in Reaxys

Tab. 2, entry 2

Matsumoto, Tsutomu; Ueno, Masaharu; Kobayashi, Juta; Miyamura, Hiroyuki; Mori, Yuichiro; Kobayashi, Shue; Advanced Synthesis and Catalysis; vol. 349; nb. 4-5; (2007); p. 531 - 534, View in Reaxys

Gregg, Brian T.; Golden, Kathryn C.; Quinn, John F.; Journal of Organic Chemistry; vol. 72; nb. 15; (2007); p. 5890 - 5893, View in Reaxys

table 1, entry 2

Heravi, Majid M.; Sabaghiani, Ali J.; Bakavoli, Mehdi; Ghassemzadeh, Mitra; Bakhtiari, Khadijeh; Journal of the Chinese Chemical Society; vol. 54; nb. 1; (2007); p. 123 - 126, View in Reaxys

table 2 entry 2

Xie, Yi; Mo, Weimin; Xu, Dong; Shen, Zhenlu; Sun, Nan; Hu, Baoxiang; Hu, Xinquan; Journal of Organic Chemistry; vol. 72; nb. 11; (2007); p. 4288 - 4291, View in Reaxys

Tab 1/6 Byproduct Liu, Ye; Zhang, Hong-Jiao; Cai, Yue-Qin; Wu, Hai-Hong; Liu, Xiu-Li; Lu, Yong; Chemistry Letters; vol. 36; 2 nb. 7; (2007); p. 848 - 849, View in Reaxys Table 1, entry 5

Brennfuhrer, Anne; Neumann, Helfried; Beller, Matthias; Synlett; nb. 16; (2007); p. 2537 - 2540, View in Reaxys

48/464

2016-04-07 09:00:27

Table 1, entry 16

Shaabani, Ahmad; Rahmati, Abbas; Naderi, Soheila; Synthetic Communications; vol. 37; nb. 22; (2007); p. 4035 - 4042, View in Reaxys

Table 2. product 2 Luan, Yi; Wang, Ge; Luck, Rudy L.; Yang, Mu; Han, Xiao; Chemistry Letters; vol. 36; nb. 10; (2007); p. 1236 - 1237, View in Reaxys Tab.1, entry 13, prod.

Moorthy, Jarugu Narasimha; Singhal, Nidhi; Senapati, Kalyan; Organic and Biomolecular Chemistry; vol. 5; nb. 5; (2007); p. 767 - 771, View in Reaxys

Table 3, entry 5

Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7087 - 7090, View in Reaxys; Shi, Feng; Tse, Man Kin; Pohl, Marga-Matina; Brueckner, Angelika; Zhang, Shengmao; Beller, Matthias; Angewandte Chemie - International Edition; vol. 46; nb. 46; (2007); p. 8866 - 8868, View in Reaxys

(p)-5

Kantlehner, Willi; Leonhardt, Sylvia; Ziegler, Georg; Scherr, Oliver; Kress, Ralf; Goeppert, Alain; Sommer, Jean; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 62; nb. 8; (2007); p. 995 - 1014, View in Reaxys

4-CH3C6H4CHO

Shen, Yanchang; Ni, Jiahong; Li, Ping; Sun, Jie; Journal of the Chemical Society - Perkin Transactions 1; nb. 4; (1999); p. 509 - 512, View in Reaxys; Matsushita, Tsuyoshi; Ebitani, Kohki; Kaneda, Kiyotomi; Chemical Communications; nb. 3; (1999); p. 265 - 266, View in Reaxys; Khosropour, Ahmad R.; Khodaei, Mohammad M.; Ghaderi, Sattar; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 61; nb. 3; (2006); p. 326 - 330, View in Reaxys

product 2

Yamaguchi, Kazuya; Mizuno, Noritaka; Angewandte Chemie - International Edition; vol. 41; nb. 23; (2002); p. 4538 - 4542, View in Reaxys; Farhadi, Saeid; Zaringhadam, Parisa; Sahamieh, Reza Zarei; Tetrahedron Letters; vol. 47; nb. 12; (2006); p. 1965 - 1968, View in Reaxys

product, entry 20

Joseph, Jomy K.; Jain, Suman L.; Sain, Bir; European Journal of Organic Chemistry; nb. 3; (2006); p. 590 594, View in Reaxys

substrate, tab 1

Sun, Wei; Yu, Bingsheng; Kuehn, Fritz E.; Tetrahedron Letters; vol. 47; nb. 12; (2006); p. 1993 - 1996, View in Reaxys

Tab. 2, entry 3

Partenheimer, Walt; Advanced Synthesis and Catalysis; vol. 348; nb. 4-5; (2006); p. 559 - 568, View in Reaxys

Tab. 2, entry 28

Cooper, Thea; Novak, Andrew; Humphreys, Luke D.; Walker, Matthew D.; Woodward, Simon; Advanced Synthesis and Catalysis; vol. 348; nb. 6; (2006); p. 686 - 690, View in Reaxys

T.I, Entry 10, Product

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

entry 2

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

Product T1, E1b

Desai; Pore; Tamhankar; Jadhav; Wadgaonkar; Tetrahedron Letters; vol. 47; nb. 48; (2006); p. 8559 - 8561, View in Reaxys

prod., Tab. 1, entry 2

Wang, Naiwei; Liu, Renhua; Chen, Jiping; Liang, Xinmiao; Chemical Communications; nb. 42; (2005); p. 5322 - 5324, View in Reaxys; Bailey, Aaron D.; Cherney, Steven M.; Anzalone, Peter W.; Anderson, Erin D.; Ernat, Justin J.; Mohan, Ram S.; Synlett; nb. 2; (2006); p. 215 - 218, View in Reaxys

product, tab 3/2

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

Tab. 1, entry 6

Sendil, Kivilcim; Oezguen, Beytiye; Monatshefte fur Chemie; vol. 137; nb. 12; (2006); p. 1529 - 1533, View in Reaxys

Table 1, entry 9

Jain, Suman L.; Sharma, Vishal B.; Sain, Bir; Bulletin of the Chemical Society of Japan; vol. 79; nb. 10; (2006); p. 1601 - 1603, View in Reaxys

prod., Tab. 2, entry 9

Hajipour, Abdol R.; Zarei, Amin; Khazdooz, Leila; Ruoho, Arnold E.; Synthesis; nb. 9; (2006); p. 1480 1484, View in Reaxys

Tab. 1, entry 5, prod.

Zolfigol, Mohammad Ali; Shirini, Farhad; Choghamarani, Arash Ghorbani; Synthesis; nb. 12; (2006); p. 2043 - 2046, View in Reaxys

Table 3. product 22

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

p-MeC6H4CHO

Bandgar; Kulkarni, Sameer A.; Nigal; Organic Preparations and Procedures International; vol. 30; nb. 6; (1998); p. 706 - 709, View in Reaxys; Iwama, Tetsuo; Kinoshita, Hironori; Kataoka, Tadashi; Tetrahedron Letters; vol. 40; nb. 19; (1999); p. 3741 - 3744, View in Reaxys; Cherng, Yie-Jia; Fang, Jim-Min; Lu, TaJung; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 3207 - 3212, View in Reaxys; Minisci, Francesco; Punta, Carlo; Recupero, Francesco; Fontana, Francesca; Pedulli, Gian Franco; Chemical Communications; nb. 7; (2002); p. 688 - 689, View in Reaxys; Harada, Toshiro; Kanda, Kousou; Organic Letters; vol. 8;

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nb. 17; (2006); p. 3817 - 3819, View in Reaxys; Willemse, J. Alexander; Bezuidenhoudt, Barend C. B.; Holzapfel, Cedric W.; Synthesis; nb. 15; (2006); p. 2543 - 2550, View in Reaxys aldehyde from 1b

Moya-Barrios, Reinaldo; Cozens, Frances L.; Journal of the American Chemical Society; vol. 128; nb. 46; (2006); p. 14836 - 14844, View in Reaxys

4-CH3-C6H4CHO

Firouzabadi; Fakoorpour; Hazarkhani; Synthetic Communications; vol. 31; nb. 24; (2001); p. 3859 - 3862, View in Reaxys; Khodaei, Mohammad Mehdi; Khosropour, Ahmad Reza; Jowkar, Mahbubeh; Synthesis; nb. 8; (2005); p. 1301 - 1304; Art.No: Z21704SS, View in Reaxys

tab1, col2, entry9

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

2, tab. 2. entry 3

Zhang, Zhan-Hui; Yin, Liang; Li, Yi; Wang, Yong-Mei; Tetrahedron Letters; vol. 46; nb. 5; (2005); p. 889 893, View in Reaxys

10c

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

Table 3, entry 2

Liu, Renhua; Dong, Chunyan; Liang, Xinmiao; Wang, Xiujuan; Hu, Xinquan; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 729 - 731, View in Reaxys

Tab.2.run4

Jiang, Nan; Ragauskas, Arthur J.; Tetrahedron Letters; vol. 46; nb. 19; (2005); p. 3323 - 3326, View in Reaxys

Tab. 1, Ent. 4, prod.

Narender; Reddy, M. Somi; Kumar, V. Pavan; Nageswar; Rao, K. Rama; Tetrahedron Letters; vol. 46; nb. 12; (2005); p. 1971 - 1973, View in Reaxys

Tab. 2

Partenheimer, Walt; Advanced Synthesis and Catalysis; vol. 347; nb. 4; (2005); p. 580 - 590, View in Reaxys

Product, T. 1, Entry 11

Tajbakhsh, Mahmoud; Alimohammadi, Kamal; Behmadi, Hossein; Barghamadi, Mohammad; Journal of Chemical Research; nb. 1; (2005); p. 35 - 37, View in Reaxys

prod., Tab. 1, entry 5

Wu, Xue-E.; Ma, Li; Ding, Meng-Xian; Gao, Lian-Xun; Synlett; nb. 4; (2005); p. 607 - 610; Art.No: U34204ST, View in Reaxys

pr. of table 1 entry Heravi, Majid M.; Derikvand, Fatemeh; Ghassemzadeh, Mitra; Neumueller, Bernhard; Tetrahedron Letters; 7 vol. 46; nb. 37; (2005); p. 6243 - 6245, View in Reaxys Table 1, product 2 Pearson, Anthony J.; Kwak, Yoonhyun; Tetrahedron Letters; vol. 46; nb. 32; (2005); p. 5417 - 5419, View in Reaxys Tab. 2, entry 18

Campestrini, Sandro; Carraro, Massimo; Ciriminna, Rosaria; Pagliaro, Mario; Tonellato, Umberto; Advanced Synthesis and Catalysis; vol. 347; nb. 6; (2005); p. 825 - 832, View in Reaxys

Tab. 1, entry 9

Geisslmeir, David; Jary, Walther G.; Falk, Heinz; Monatshefte fur Chemie; vol. 136; nb. 9; (2005); p. 1591 1599, View in Reaxys

Gogoi, Pranjal; Hazarika, Parasa; Konwar, Dilip; Journal of Organic Chemistry; vol. 70; nb. 5; (2005); p. 1934 - 1936, View in Reaxys

Table 3, entry 6

Jiang, Nan; Ragauskas, Arthur J.; Organic Letters; vol. 7; nb. 17; (2005); p. 3689 - 3692, View in Reaxys

Tab.1.Ent. 7-8.substrate

Chen, Yinghua; Zhu, Zhenyu; Zhang, Jie; Shen, Jianzhong; Zhou, Xigeng; Journal of Organometallic Chemistry; vol. 690; nb. 16; (2005); p. 3783 - 3789, View in Reaxys

aldehyde, T. 1, en- Ansari; Joyasawal, Sipak; Gupta, Manoj K.; Yadav; Gree; Tetrahedron Letters; vol. 46; nb. 44; (2005); p. try d 7507 - 7510, View in Reaxys Tab. II, entry 8

Hosseinzadeh, Rahman; Tajbakhsh, Mahmood; Ramzanian-Lehmali, Farhad; Sadatshahabi, Marzieh; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 180; nb. 10; (2005); p. 2279 - 2283, View in Reaxys

9a, X = Me

Kim, Yun Bong; Kim, Min Kyoun; Kang, Sung Ho; Kim, Yong Hae; Synlett; nb. 13; (2005); p. 1995 - 1998; Art.No: U12705ST, View in Reaxys

2e/4c

Zhang, Suhong; Xu, Liang; Trudell, Mark L.; Synthesis; nb. 11; (2005); p. 1757 - 1760; Art.No: M08704SS, View in Reaxys

Tab. 2, entry 6

Paraskevopoulou, Patrina; Petalidou, Eleftheria; Psaroudakis, Nikos; Stavropoulos, Pericles; Mertis, Konstantinos; Monatshefte fur Chemie; vol. 136; nb. 12; (2005); p. 2035 - 2039, View in Reaxys

1, R=p-MeC6H4

Nishigaichi, Yutaka; Ueda, Narifumi; Tamura, Ken-Ichi; Takuwa, Akio; Synlett; nb. 16; (2005); p. 2519 2521; Art.No: U25505ST, View in Reaxys

prod., Tab.1, entry Hosseinzadeh, Rahman; Tajbakhsh, Mahmood; Vahedi, Hossein; Synlett; nb. 18; (2005); p. 2769 - 2770; 1 Art.No: D19905ST, View in Reaxys

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Tab.1, entry 5

Lakouraj, Moslem M.; Tajbakhsh, Mahmood; Shirini, Farhad; Asady Tamami, Mohammad V.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 180; nb. 11; (2005); p. 2423 - 2429, View in Reaxys

p-CH3C6H4CHO

Fodili, Moktar; Amari, Mohamed; Kolli, Bellara; Robert, Albert; Baudy-Floc'h, Michele; Le Grel, Philippe; Synthesis; nb. 5; (1999); p. 811 - 814, View in Reaxys; Tajbakhsh; Lakouraj; Fadavi; Synthetic Communications; vol. 34; nb. 7; (2004); p. 1173 - 1181, View in Reaxys

Tab. 1, entry 4

Degirmenbasi, Nebahat; Oezguen, Beytiye; Monatshefte fur Chemie; vol. 135; nb. 4; (2004); p. 407 - 410, View in Reaxys

table 1, entry 4

Liu, Renhua; Liang, Xinmiao; Dong, Chunyan; Hu, Xinquan; Journal of the American Chemical Society; vol. 126; nb. 13; (2004); p. 4112 - 4113, View in Reaxys

Tab. 5-6, No. 2

Oezguen, Beytiye; Degirmenbasi, Nebahat; Monatshefte fuer Chemie; vol. 135; nb. 5; (2004); p. 483 - 492, View in Reaxys

6f, R'=4-CH3C6H4 R''=H

Rajkumar, G. Abraham; Sivamurugan; Arabindoo, Banumathi; Murugesan; Indian Journal of Chemistry Section B Organic and Medicinal Chemistry; vol. 43; nb. 5; (2004); p. 936 - 946, View in Reaxys

2, R1=4-MeC6H4, Firouzabadi, Habib; Iranpoor, Nasser; Hassani, Hassan; Sobhani, Sara; Synthetic Communications; vol. R2=H 34; nb. 11; (2004); p. 1967 - 1972, View in Reaxys Table 1, entry 3

Habibi, Mohammad H.; Farhadi, Saeid; Journal of Chemical Research; nb. 4; (2004); p. 296 - 297, View in Reaxys; Niu, Hongying; Zhang, Xinying; Guo, Haiming; Wang, Jianji; Journal of Chemical Research; nb. 11; (2004); p. 764 - 765, View in Reaxys

Tab. 2, entry 2b

Hosseinzadeh, Rahman; Tajbakhsh, Mahmood; Shakoori, Alireza; Niaki, Mohammad Yazdani; Monatshefte fur Chemie; vol. 135; nb. 10; (2004); p. 1243 - 1249, View in Reaxys

Table I, entry 2

Ghorbani-Vaghei, Ramin; Khazaei, Ardeshir; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 179; nb. 9; (2004); p. 1787 - 1791, View in Reaxys

Entry 1, Tab. I

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

Tab. 1, entry 4, prod.

Narender; Somi Reddy; Rama Rao; Synthesis; nb. 11; (2004); p. 1741 - 1743, View in Reaxys

3, R = p-MeC6H4, Reddy, M. Somi; Narender; Rao, K. Rama; Synthetic Communications; vol. 34; nb. 21; (2004); p. 3875 - 3881, R1 = H View in Reaxys Run 5, product

Kumar, Anil; Jain, Nidhi; Chauhan; Synthetic Communications; vol. 34; nb. 15; (2004); p. 2835 - 2842, View in Reaxys

product T. 1, e. 9

Xie, Haibo; Zhang, Suobo; Duan, Haifeng; Tetrahedron Letters; vol. 45; nb. 9; (2004); p. 2013 - 2015, View in Reaxys

tab. 1, entry 2, ald. Suresh Babu; Lokanatha Rai; Tetrahedron Letters; vol. 45; nb. 42; (2004); p. 7969 - 7970, View in Reaxys 4-MeC6H4CHO

Heravi, Majid M.; Ajami, Dariush; Aghapoor, Kuoumars; Ghassemzadeh, Mitra; Chemical Communications; nb. 9; (1999); p. 833 - 834, View in Reaxys; Dijksman, Arne; Arends, Isabel W.C.E.; Sheldon, Roger A.; Chemical Communications; nb. 16; (1999); p. 1591 - 1592, View in Reaxys; Blum, Jochanan; Berlin, Olga; Milstein, David; Ben-David, Yehoshua; Wassermann, Birgit C.; Schutte, Stefan; Schumann, Herbert; Synthesis; nb. 4; (2000); p. 571 - 575, View in Reaxys; Firouzabadi, Habib; Iranpoor, Nasser; Amani, Kamal; Synthesis; nb. 3; (2003); p. 408 - 412, View in Reaxys

4(CH3)C6H4CHO

Hashemi, Mohammed M.; Ahmadibeni, Yusef; Monatshefte fur Chemie; vol. 134; nb. 3; (2003); p. 411 - 418, View in Reaxys

T.2, e.2, product

Iranpoor, Nasser; Firouzabadi, Habib; Shaterian, Hamid Reza; Tetrahedron Letters; vol. 44; nb. 25; (2003); p. 4769 - 4773, View in Reaxys

T. 1., prod. 15

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

entry 18, 28

Mohammadpoor-Baltork, Iraj; Khodaei, Mohammad Mehdi; Hajipour, Abdol R.; Aslani, Esmaeil; Monatshefte fur Chemie; vol. 134; nb. 4; (2003); p. 539 - 543, View in Reaxys

Tab.2., run 3, aldeh.

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

Velcheva, Evelina A.; Juchnovski, Ivan N.; Binev, Ivan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 59; nb. 8; (2003); p. 1745 - 1749, View in Reaxys

T., product, run 2

Xu, Liang; Trudell, Mark L.; Tetrahedron Letters; vol. 44; nb. 12; (2003); p. 2553 - 2555, View in Reaxys

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Tab.1, subst., entry 2

Palaniappan, Srinivasan; Narender, Puli; Saravanan, Chandrasekaran; Rao, Vaidya Jayathirtha; Synlett; nb. 12; (2003); p. 1793 - 1796, View in Reaxys

Tab.1, entry 3, prod.

Krishnaveni, N. Srilakshmi; Surendra; Nageswar; Rao, K. Rama; Synthesis; nb. 13; (2003); p. 1968 - 1970, View in Reaxys

Product, Tab.1, run 18

Shirini; Zolfigol; Safari; Mohammadpoor-Baltork; Mirjalili; Tetrahedron Letters; vol. 44; nb. 40; (2003); p. 7463 - 7465, View in Reaxys

Table 2, Entry 9, prod

Bagherzadeh, Mojtaba; Tetrahedron Letters; vol. 44; nb. 50; (2003); p. 8943 - 8945, View in Reaxys

Tab. 3, entry 4

Degirmenbasi, Nebahat; Oezguen, Beytiye; Monatshefte fur Chemie; vol. 134; nb. 12; (2003); p. 1565 - 1569, View in Reaxys

Tab.II, entry 9

Tajbakhsh, Mahmood; Mohammadpoor-Baltork, Iraj; Ramzanian-Lehmali, Farhad; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 178; nb. 12; (2003); p. 2617 - 2620, View in Reaxys

Tab.II, entry 9, 15, Tajbakhsh, Mahmood; Mohammadpoor-Baltork, Iraj; Ramzanian-Lehmali, Farhad; Phosphorus, Sulfur 31 and Silicon and the Related Elements; vol. 178; nb. 12; (2003); p. 2621 - 2625, View in Reaxys Tab. I, entry 21, 22 Zolfigol, Mohammad Ali; Poor-Baltork, Iraj Mohammad; Mirjalili, Bibi Fatemeh; Shirini, Farhad; Salehzadeh, Sadegh; Keypour, Hassan; Ghorbani-Choghamarani, Arash; Zebarjadian, Mohammad Hassan; Mohammadi, Kamal; Hazar, Azizeh; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 178; nb. 12; (2003); p. 2735 - 2743, View in Reaxys Tab. 1, Entry 3, Prod.

Krishnaveni, N. Srilakshmi; Surendra, K.; Nageswar, Y. V. D.; Rao, K. Rama; Synthesis; nb. 15; (2003); p. 2295 - 2297, View in Reaxys

t.1, product, entry 6

Salehi; Khodaei; Yazdanipoor; Polish Journal of Chemistry; vol. 77; nb. 10; (2003); p. 1281 - 1286, View in Reaxys

14a

Smitha; Reddy, Ch. Sanjeeva; Tetrahedron; vol. 59; nb. 48; (2003); p. 9571 - 9576, View in Reaxys

4MBA

Ghanadzadeh Gilani; Mamaghani; Anbir; Journal of Solution Chemistry; vol. 32; nb. 7; (2003); p. 625 - 636, View in Reaxys

ArCHO (entry 4)

Deady, Leslie W.; Devine, Shane M.; Rogers, Michael L.; Organic Preparations and Procedures International; vol. 35; nb. 6; (2003); p. 627 - 630, View in Reaxys

p-CH3C6H4-CHO Medien, Hesham A. A.; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 58; nb. 12; (2003); p. 1201 - 1205, View in Reaxys prod., Tab. 2, entry 4

Yamaguchi, Kazuya; Mizuno, Noritaka; Chemistry - A European Journal; vol. 9; nb. 18; (2003); p. 4353 4361, View in Reaxys

2, entry 2

Liu, Huawei; Peng, Lizeng; Zhang, Tao; Li, Yulin; New Journal of Chemistry; vol. 27; nb. 8; (2003); p. 1159 - 1160, View in Reaxys

p-Me-C6H4CHO

Carelli, Italo; Chiarotto, Isabella; Cacchi, Sandro; Pace, Paola; Amatore, Christian; Jutand, Anny; Meyer, Gilbert; European Journal of Organic Chemistry; nb. 6; (1999); p. 1471 - 1473, View in Reaxys; Kumar, Ashok; Sharma, Pradeep K.; Banerji, Kalyan K.; Journal of Physical Organic Chemistry; vol. 15; nb. 10; (2002); p. 721 - 727, View in Reaxys

tab.1.col.4.run 4.

Russ, Rainer; Zelinski, Thomas; Anke, Timm; Tetrahedron Letters; vol. 43; nb. 5; (2002); p. 791 - 793, View in Reaxys

Product, Tab. 2, run 2

Fujita, Ken-Ichi; Furukawa, Shigetoyo; Yamaguchi, Ryohei; Journal of Organometalic Chemistry; vol. 649; nb. 2; (2002); p. 289 - 292, View in Reaxys

TALD

Burri, Raju; Jun, Ki-Won; Kim, Young-Ho; Kim, Ji Man; Park, Sang-Eon; Yoo, Jin S.; Chemistry Letters; nb. 2; (2002); p. 212 - 213, View in Reaxys

Tab.1, entry 4

Degirmenbasi, Nebahat; Oezguen, Beytiye; Monatshefte fur Chemie; vol. 133; nb. 11; (2002); p. 1417 - 1421, View in Reaxys

product Ib

Mirjalili; Zolfigol; Bamoniri; Russian Journal of Organic Chemistry; vol. 38; nb. 5; (2002); p. 761 - 762, View in Reaxys

tab1, col4, run2

Hosseinzadeh, Rahman; Tajbakhsh, Mahmood; Niaki, Mohammad Yazdani; Tetrahedron Letters; vol. 43; nb. 51; (2002); p. 9413 - 9416, View in Reaxys

product, T1, E6

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

4, R1=H, R2=pMeC6H4

Khazaei, Ardeshir; Vaghei, Ramin Ghorbani; Molecules; vol. 7; nb. 5; (2002); p. 465 - 468, View in Reaxys

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2016-04-07 09:00:27

2c (2d)

Firouzabadi, Habib; Iranpoor, Nasser; Hazarkhani, Hassan; Karimi, Babak; Journal of Organic Chemistry; vol. 67; nb. 8; (2002); p. 2572 - 2576, View in Reaxys

table 2, entry 4

Minisci, Francesco; Punta, Carlo; Recupero, Francesco; Fontana, Francesca; Franco Pedulli, Gian; Journal of Organic Chemistry; vol. 67; nb. 8; (2002); p. 2671 - 2676, View in Reaxys

Nishiwaki, Yoshiki; Sakaguchi, Satoshi; Ishii, Yasutaka; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5663 - 5668, View in Reaxys

Tab.4, entry 4.1-4.7

Ten Brink, Gerd-Jan; Arends, Isabel W. C. E.; Sheldon, Roger A.; Advanced Synthesis and Catalysis; vol. 344; nb. 3-4; (2002); p. 355 - 369, View in Reaxys

p-Me-C6H4-CHO

De Araujo, Aline D.; Bacher, Edmond; Joachim Demnitz; Santos, Douglas A.; Heterocycles; vol. 51; nb. 1; (1999); p. 29 - 36, View in Reaxys; Heravi; Ajami; Ghassemzadeh; Tabar-Hydar; Synthetic Communications; vol. 31; nb. 14; (2001); p. 2097 - 2100, View in Reaxys

1, R1=R2=H, R3=CH3

Nair, Vijay; Bindu; Balagopal, Lakshmi; Tetrahedron Letters; vol. 42; nb. 10; (2001); p. 2043 - 2044, View in Reaxys

Tab. 1, entry 10

Khazaei, Ardeshir; Ghorbani Vaghei, Ramin; Tajbakhsh, Mahmoud; Tetrahedron Letters; vol. 42; nb. 30; (2001); p. 5099 - 5100, View in Reaxys

table 1/2

Mohajerani; Heravi; Ajami; Monatshefte fur Chemie; vol. 132; nb. 7; (2001); p. 871 - 873, View in Reaxys

Table 1, entry 4

Shirini; Tajik; Jalili; Synthetic Communications; vol. 31; nb. 19; (2001); p. 2885 - 2889, View in Reaxys

table I, entry 2

Heravi; Kiakojoori; Mojtahedi; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 40; nb. 4; (2001); p. 329 - 330, View in Reaxys

Table 2, entry 4

Bensari, Ahlem; Renaud, Jean-Luc; Riant, Olivier; Organic Letters; vol. 3; nb. 24; (2001); p. 3863 - 3865, View in Reaxys

Table 1, line 1, prod.

Bagno, Alessandro; Kantlehner, Willi; Scherr, Oliver; Vetter, Jens; Ziegler, Georg; European Journal of Organic Chemistry; nb. 15; (2001); p. 2947 - 2954, View in Reaxys

table 1 lin3 5

Lin, Zhong-Ping; Aue, Walter A.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 56; nb. 1; (2000); p. 111 - 117, View in Reaxys

aldehyde 1

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

Alekar; Gopinathan; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 39; nb. 4; (2000); p. 439 - 441, View in Reaxys

Dayan; Ben-David; Rozen; Journal of Organic Chemistry; vol. 65; nb. 25; (2000); p. 8816 - 8818, View in Reaxys

2, R = 4CH3C6H4

Ito, Akihiro; Kishida, Masayuki; Kurusu, Yasuhiko; Masuyama, Yoshiro; Journal of Organic Chemistry; vol. 65; nb. 2; (2000); p. 494 - 498, View in Reaxys

Table 4 Entry 4 Ald.

Keller, Felix; Rippert, Andreas Johannes; Helvetica Chimica Acta; vol. 82; nb. 1; (1999); p. 125 - 137, View in Reaxys

R3COR4, R3=pMePh, R4=H

Katritzky; Bao; Fang; Qi; Prakash; Tetrahedron Letters; vol. 40; nb. 2; (1999); p. 253 - 256, View in Reaxys

substrate (table, en 3)

Sharifi; Mojtahedi; Saidi; Tetrahedron Letters; vol. 40; nb. 6; (1999); p. 1179 - 1180, View in Reaxys

4-Me-PhCHO

Graham, Andrew E.; Synthetic Communications; vol. 29; nb. 4; (1999); p. 697 - 703, View in Reaxys

4-Me-C6H4-CHO

Nagamatsu, Tomohisa; Yamasaki, Hiroo; Akiyama, Toshihiko; Hara, Sachiko; Mori, Kenya; Kusakabe, Hitoshi; Synthesis; nb. 4; (1999); p. 655 - 663, View in Reaxys

p-MePhCHO

Julienne, Karinc; Metzner, Patrick; Henryon, Vivien; Journal of the Chemical Society - Perkin Transactions 1; nb. 6; (1999); p. 731 - 735, View in Reaxys

Tab. entry 8, substrate

Anand, R. Vijaya; Saravanan; Singh, Vinod K.; Synlett; nb. 4; (1999); p. 415 - 416, View in Reaxys

2. educt to 4

Davoust; Granet; Krausz; Carre; Guilloton; Tetrahedron Letters; vol. 40; nb. 13; (1999); p. 2513 - 2516, View in Reaxys

R'CHO, R' = pMeC6H4

Ogura, Katsuyuki; Arai, Takayuki; Kayano, Akio; Akazome, Motohiro; Tetrahedron Letters; vol. 40; nb. 13; (1999); p. 2537 - 2540, View in Reaxys

4-MeC6H4HCO

Oba, Makoto; Yoshihara, Masahiro; Roppongi, Chiharu; Nishiyama, Kozaburo; Heterocycles; vol. 50; nb. 1; (1999); p. 195 - 201, View in Reaxys

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2 (run 2)

Heravi, Majid M.; Ajami, Dariush; Mojtahedi, Mohammad M.; Ghassemzadeh, Mitra; Tetrahedron Letters; vol. 40; nb. 3; (1999); p. 561 - 562, View in Reaxys

Ar=l

Kamal, Marwan R.; El-Abadelah, Mustafa M.; Mohammad, Amer A.; Meier, Herbert; Heterocycles; vol. 50; nb. 2; (1999); p. 819 - 832, View in Reaxys

10m

Meester, Wim J. N.; Rutjes, Floris P. J. T.; Hermkens, Pedro H. H.; Hiemstra, Henk; Tetrahedron Letters; vol. 40; nb. 8; (1999); p. 1601 - 1604, View in Reaxys

R1=R2=p-Me-Ph

Palacios, Francisco; Gil, Marie J.; Martinez De Marigorta, Eduardo; Rodriguez, Marta; Tetrahedron Letters; vol. 40; nb. 12; (1999); p. 2411 - 2414, View in Reaxys

t.1,pr.,entry 8

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

Zhang, Wen-Chun; Li, Chao-Jun; Journal of Organic Chemistry; vol. 64; nb. 9; (1999); p. 3230 - 3236, View in Reaxys

Deshpande, Anil M.; Argade, Narshinha P.; Natu, Arvind A.; Eckman, Joseph; Bioorganic and Medicinal Chemistry; vol. 7; nb. 6; (1999); p. 1237 - 1240, View in Reaxys

4-MeC6H4-CHO

Yang, Jun; Li, Chao-Jun; Synlett; nb. 6; (1999); p. 717 - 718, View in Reaxys

4-CH3-C6H4COH Alajarin, Mateo; Vidal, Angel; Tovar, Fulgencio; Arrieta, Ana; Lecea, Begona; Cossio, Fernando P.; Chemistry - A European Journal; vol. 5; nb. 3; (1999); p. 1106 - 1117, View in Reaxys p-CH3-C6H4CHO Akiyama, Takahiko; Takaya, Jun; Kagoshima, Hirotaka; Synlett; nb. 7; (1999); p. 1045 - 1048, View in Reaxys T.1, e.1, product

Coleman, Karl S.; Coppe, Maurice; Thomas, Christophe; Osborn, John A.; Tetrahedron Letters; vol. 40; nb. 19; (1999); p. 3723 - 3726, View in Reaxys

R1-PhCHO, R1=Me

Yu, Zhanru; Velasco, Dolores; Tetrahedron Letters; vol. 40; nb. 16; (1999); p. 3229 - 3232, View in Reaxys

2, R=4-Me-C6H4

Venkov, Atanas P.; Boyadjieva, Atanaska K.; Synthetic Communications; vol. 29; nb. 3; (1999); p. 487 - 494, View in Reaxys

entry 6

Mohammadpoor-Baltork; Aliyan; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2741 - 2746, View in Reaxys

entry 10

Wang, Guo-Ping; Chen, Zhen-Chu; Synthetic Communications; vol. 29; nb. 16; (1999); p. 2859 - 2866, View in Reaxys

Tab.1 entry 2

Heravi, Majid M.; Ajami, Dariush; Tabar-Hydar, Kourosh; Ghassemzadeh, Mitra; Journal of Chemical Research - Part S; nb. 5; (1999); p. 334 - 335, View in Reaxys

ArCHO, Ar=4(Me)Ph

Isobe, Toshio; Ishikawa, Tsutomu; Journal of Organic Chemistry; vol. 64; nb. 16; (1999); p. 5832 - 5835, View in Reaxys

2, R1=pCH3C6H4 R2=H

Park, Soo Jung; Keum, Gyochang; Kang, Soon Bang; Koh, Hun Yeong; Kim, Youseung; Duck Hyung, Lee; Tetrahedron Letters; vol. 39; nb. 39; (1998); p. 7109 - 7112, View in Reaxys

pMe-C6H4CHO

Aggarwal, Varinder K.; Blackburn, Paul; Fieldhouse, Robin; Jones, Ray V. H.; Tetrahedron Letters; vol. 39; nb. 46; (1998); p. 8517 - 8520, View in Reaxys

R1CHO R1=pMePh

Kobayashi, Shu; Aoki, Yoji; Tetrahedron Letters; vol. 39; nb. 40; (1998); p. 7345 - 7348, View in Reaxys

2, R1=p-MeC6H4, Firouzabadi, Habib; Iranpoor, Nasser; Karimi, Babak; Journal of Chemical Research - Part S; nb. 10; (1998); R2=H p. 664 - 665, View in Reaxys Tab 2, Ent f, alde- Groaning, Michael D.; Rowe, Bradley J.; Spilling, Christopher D.; Tetrahedron Letters; vol. 39; nb. 31; hyde (1998); p. 5485 - 5488, View in Reaxys 4-CH3-benzaldehyde

Nyquist, R. A.; Hasha, D. L.; Applied Spectroscopy; vol. 45; nb. 5; (1991); p. 849 - 859, View in Reaxys

Patent-Specific Data (21) Prophetic ComLocation in Patent References pound Page/Page column

Patent; VIFOR (INTERNATIONAL) AG; Dürrenberger, Franz; Burckhardt, Susanna; Geisser, Peter O.; Buhr, Wilm; Funk, Felix; Corden, Vincent A.; Davenport, Tara; Jaeger, Stefan; Slack, Mark; Yarnold, Christopher J.; Yau, Wei Tsung; Courtney, Stephen M.; US2012/196853; (2012); (A1) English, View in Reaxys; Patent; Shionogi and Co., Ltd.; KAI, Hiroyuki; ENDOH, Takeshi; JIKIHARA, Sae; ASAHI, Kentaro; HORIGUCHI, Tohru; EP2604260; (2013); (A1) English, View in Reaxys; Patent; BECCARI, Andrea Rosario; BIANCHINI, Gianluca; LIBERATI, Chiara; FANI', Michela; ZIPPOLI,

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Mara; US2014/371274; (2014); (A1) English, View in Reaxys; Patent; Neuron Biopharma S.A.; RAMOS MARTÍN, María del Carmen; CAMPOY GARCÍA, Sonia; BURGOS MUÑOZ, Javier Santos; ADRIO FONDEVILA, José Luis; VELASCO ALVAREZ, Javier; EP2813222; (2014); (A2) English, View in Reaxys; Patent; Ramos Martin, Maria del Carmen; Campoy García, Sonia; Burgos Muñoz, Javier Santos; Adrio Fondevila, José Luis; Velasco Alvarez, Javier; US2015/11621; (2015); (A1) English, View in Reaxys; Patent; Janssen Pharmaceutica NV; Leonard, Kristi A.; Barbay, Kent; Edwards, James P.; Kreutter, Kevin D.; Kummer, David A.; Maharoof, Umar; Nishimura, Rachel; Urbanski, Maud; Venkatesan, Hariharan; Wang, Aihua; Wolin, Ronald L.; Woods, Craig R.; Fourie, Anne; Xue, Xiaohua; Cummings, Maxwell D.; Jones, William Moore; Goldberg, Steven; US2015/105366; (2015); (A1) English, View in Reaxys; Patent; HOFFMANN-LA ROCHE INC.; Hu, Hui; Jiang, Min; Jin, Taiguang; Niu, Rui; Wang, Jianhua; Wang, Min; Yang, Song; Yuan, Taichang; Zhou, Chengang; Zhou, Zheng; US2015/158815; (2015); (A1) English, View in Reaxys Patent; FIRMENICH SA; Santoro, Francesco; Saudan, Lionel; Saudan, Christophe; US2013/274487; (2013); (A1) English, View in Reaxys Patent; FIRMENICH SA; SANTORO, Francesco; SAUDAN, Lionel; SAUDAN, Michel, Alfred, Joseph; SAUDAN, Sylvia, Joyeuse, Adelaide; WO2012/84810; (2012); (A1) English, View in Reaxys Patent; UANG, Biing-Jiun; Wu, Ping-Yu; Wu, Hsyueh-Liang; US2011/295042; (2011); (A1) English, View in Reaxys Patent; ABRAXIS BIOSCIENCE, LLC; TAO, Chunlin; WANG, Qinwei; DESAI, Neil; WO2010/144423; (2010); (A1) English, View in Reaxys Patent; Japan Science and Technology Agency; EP2067761; (2009); (A1) English, View in Reaxys Patent; GIVAUDAN SA; WO2008/71027; (2008); (A1) English, View in Reaxys Patent; MASSACHUSETTS INSTITUTE OF TECHNOLOGY; WO2007/27752; (2007); (A1) English, View in Reaxys prophetic product

Claim

Patent; L'Oreal S.A.; US7204857; (2007); (B1) English, View in Reaxys Patent; GIVAUDAN SA; WO2007/71089; (2007); (A1) English, View in Reaxys Patent; SCHERING AKTINGESELLSCHAFT; WO2006/63805; (2006); (A1) German, View in Reaxys Patent; SANOFI-AVENTIS DEUTSCHLAND GMBH; WO2006/66694; (2006); (A1) German, View in Reaxys Patent; Sato, Kazuhiko; Usui, Yoko; US2006/167311; (2006); (A1) English, View in Reaxys

prophetic product

Patent; Sandoz, Inc.; US3932430; (1976); (A1) English, View in Reaxys; Patent; E. R. Squibb and Sons, Inc.; US3954744; (1976); (A1) English, View in Reaxys; Patent; Sandoz, Inc.; US4103013; (1978); (A1) English, View in Reaxys; Patent; SmithKline Corporation; US4175127; (1979); (A1) English, View in Reaxys; Patent; Petrolite Corporation; US4311841; (1982); (A1) English, View in Reaxys; Patent; Schering Corporation; US4376769; (1983); (A1) English, View in Reaxys; Patent; Syntex U.S.A. Inc.; US5716954; (1998); (A1) English, View in Reaxys; Patent; Basu; Amaresh; Gahman; Timothy C.; Girten; Beverly E.; Griffith; Michael C.; Hecht; Curtis C.; Kiely; John S.; Slivka; Sandra R.; US6127381; (2000); (A1) English, View in Reaxys; Patent; Brophy, John H.; Pesa, Frederick A.; Tonkovich, Anna Lee; McDaniel, Jeffrey S.; Jarosch, Kai Tod Paul; US2004/220434; (2004); (A1) English, View in Reaxys; Patent; SmithKline Beecham Corporation; US7074770; (2006); (B1) English, View in Reaxys; Patent; Sterling Drug Inc.; US4257954; (1981); (A1) English, View in Reaxys; Patent; Sandoz, Inc.; US4024262; (1977); (A1) English, View in Reaxys; Patent; Nippon Shokubai Co., Ltd.; EP1205462; (2002); (A1) English, View in Reaxys Patent; OTSUKA PHARMACEUTICAL FACTORY, INC.; US2005/256087; (2005); (A1) English, View in Reaxys Patent; Mizuno, Noritaka; Yamaguchi, Kazuya; Ishida, Hajime; US2004/204597; (2004); (A1) English, View in Reaxys Patent; MOCHIDA PHARMACEUTICAL CO., LTD.; EP1182192; (2002); (A1) English, View in Reaxys Patent; Laboratorios del Dr. Esteve, S.A.; US6353117; (2002); (B1) English, View in Reaxys

55/464

2016-04-07 09:00:27

Patent; The University of Tennessee Research Corporation; US6353112; (2002); (B1) English, View in Reaxys Patent; Ajinomoto Co., Inc.; US6350766; (2002); (B1) English, View in Reaxys Patent; G.D. Searle and Co.; EP1223167; (2002); (A2) English, View in Reaxys Related Structure (1) Related Structure References Die beim Erhitzen Comrie,A.M.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry mit KCN und (1972-1999); (1972); p. 1193, View in Reaxys; Comrie; Journal of the Chemical Society [Section] C: Organic; N2H4+2 HCl in (1968); p. 446; Journal of the Chemical Society [Section] C: Organic; (1971); p. 2807, View in Reaxys Aethanol erhaltene Verbindung (s. E III 1017) ist nicht als 1,3,4,6Tetra-#p!-tolyl-2,5,7-triazanorborn-2-en, sondern als 3,4,5Tri-#p!-tolyl-1#H!pyrazol zu formulieren; vgl. diesbezueglich. Derivative (40) Comment (Deriva- Derivative tive)

References

4-methylbenzaldehyde 2,4-dinitrophenylhydrazone

Lai, Tapan K.; Banerji, Julie; Chatterjee, Asima; Basak, Bidyut; Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry; vol. 44; nb. 6; (2005); p. 1309 - 1311, View in Reaxys

N1-(2,4-dinitrophenyl)-N2-(4methylbenzylidene)hydrazine

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

4-methylbenzaldehyde 2,4-dinitrophenylhydrazone

Smith, Richard F.; Soelch, Richard R.; Feltz, Timothy P.; Martinelli, Michael J.; Geer, Susan M.; Journal of Heterocyclic Chemistry; vol. 18; (1981); p. 319 - 325, View in Reaxys; Shankaran, K.; Rao, A.S.; Synthetic Communications; vol. 10; nb. 7; (1980); p. 573 - 580, View in Reaxys

By formation of compound with 2,4-dinitrophenylhydrazine. Melting point at: 238 C 240 C

Entwistle, Ian D.; Boehm, Peter; Johnstone, Robert A. W.; Telford, Robert P.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1980); p. 27 - 30, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 235.5grad

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

als 2,4-Dinitrophenylhydrazon

Johnstone; Telford; Journal of the Chemical Society, Chemical Communications; (1978); p. 354, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 209-210grad

Garwood et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and BioOrganic Chemistry (1972-1999); (1975); p. 2471, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 234-235grad

Garwood et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and BioOrganic Chemistry (1972-1999); (1975); p. 2471, View in Reaxys

Tosylhydrazon C15H16N2O2S: F:149-151.5grad

Jones,W.M. et al.; Journal of the American Chemical Society; vol. 95; (1973); p. 826 - 835, View in Reaxys

Komplex mit BF3: ΔH(Add.); NMR

Gal et al.; Bulletin de la Societe Chimique de France; (1973); p. 1150,1151, View in Reaxys

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Dinitrophenylhydrazon: F: 228-230grad

Kremlev et al.; Voprosy Khimii i Khimicheskoi Tekhnologii; vol. 25; (1972); p. 32,33-36; Chem.Abstr.; vol. 78; nb. 110775z; Chem. Zentralbl.; Ref.Zh.Khim. No 16 <1972> Zh 217, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 238-240grad

Morris et al.; Journal of Organic Chemistry; vol. 37; (1972); p. 1244,1245,1246, View in Reaxys

Komplex mit 1 Mol BF3, UV, IR, NMR

Rabinowitz; Grinvald; Journal of the American Chemical Society; vol. 94; (1972); p. 2724,2725, View in Reaxys

2,4-Dinitrophenylhydrazon. F: 234-236grad

Ichikawa et al.; Nippon Kagaku Zasshi; vol. 90; (1969); p. 212,213,215,217,218, View in Reaxys

BF3-Komplex: NMR, T(c)

Greenwald; Rabinovitz; Journal of the Chemical Society [Section] D: Chemical Communications; (1969); p. 642, View in Reaxys

2,4-Dinitrophenylhydrazon : F: 234grad (AcOH), rot

Yano et al.; Kogyo Kagaku Zasshi; vol. 71; (1968); p. 217,218, 219, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 231-233grad

Rawalay; Shechter; Journal of Organic Chemistry; vol. 32; (1967); p. 3129, View in Reaxys

2,4-Dinitrophenylhydrazon: F: 231-235grad

Komachiya et al.; Nippon Kagaku Zasshi; vol. 86; (1965); p. 856,860, View in Reaxys

Phenylhydrazon: F: 116grad

Gross,H.; Matthey,G.; Chemische Berichte; vol. 97; (1964); p. 2606 - 2613, View in Reaxys

2-Chlor-<5>thienylsulfonylhydrazon: F: 90-91grad

Munshi; Trivedi; Journal of the Indian Chemical Society; vol. 40; (1963); p. 1039, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 236-239grad

Backeberg; Staskun; Journal of the Chemical Society; (1962); p. 3961, View in Reaxys

2,4-Dinitrophenylhydrazon

Strickland; Bell; Industrial and Engineering Chemistry; vol. 53; (1961); p. 7,9, View in Reaxys

Semicarbazon: F: 216.5grad

Klouwen; Boelens; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 1022,1031, View in Reaxys

2,4-Dinitro-phenylhydrazon: F: 233-235grad

Crandall et al.; Journal of Organic Chemistry; vol. 25; (1960); p. 329,330, View in Reaxys

as 2-diphenylacetyl-3-<4-methylbenzylidenehydrazono>-indan-1-one (mp: 255-255.5 degree )

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

as 2,4-dinitro-phenylhydrazone (mp: 236 degree )

Hesse; Schroedel; Justus Liebigs Annalen der Chemie; vol. 607; (1957); p. 24,30, View in Reaxys

as 1,3-bis-<4chloro-benzyl>-2p-tolyl-imidazolidine (mp: 67-68 degree )

Billman et al.; Journal of Organic Chemistry; vol. 22; (1957); p. 538, View in Reaxys

as 4-nitro-phenylhydrazone (mp: 202 degree )

Wasoserman et al.; Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation); vol. 23; (1950); p. 869,873; Chem.Abstr.; (1952); p. 7537, View in Reaxys

57/464

2016-04-07 09:00:27

4-phenyl semicarbazone (mp: 190 degree )

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

as 2,4-dinitro-phenylhydrazone (mp: 243 degree )

Brovet; Arhiv za Kemiju; vol. 20; (1948); p. 70; Chem.Abstr.; (1950); p. 6829, View in Reaxys

bis-<2.6-dioxo-cyclohexyl>-p-tolylmethane (mp: 187 degree )

King; Felton; Journal of the Chemical Society; (1948); p. 1371, View in Reaxys

3-nitro-benzoylhydrazone (mp: 189-190,5 degree )

Vis; Recueil des Travaux Chimiques des Pays-Bas; vol. 58; (1939); p. 387,393, View in Reaxys; Robert; Recueil des Travaux Chimiques des Pays-Bas; vol. 56; (1937); p. 413,431, 433, View in Reaxys; Veibel; Acta Chemica Scandinavica (1947-1973); vol. 1; (1947); p. 54,63, View in Reaxys; Strain; Journal of the American Chemical Society; vol. 57; (1935); p. 758,760; Journal of Biological Chemistry; vol. 102; (1933); p. 137,142, View in Reaxys

4-p-tolyl-imidazolidinedione-(2.5) (mp: 182,5 degree )

Henze; Speer; Journal of the American Chemical Society; vol. 64; (1942); p. 522, View in Reaxys

phenylhydrazone (mp: 121 degree )

Grammaticakis; Bulletin de la Societe Chimique de France; vol. <5> 7; (1940); p. 527,669, View in Reaxys

4-thiocyanatophenylhydrazone (mp: 118-119 degree )

Horii; Yakugaku Zasshi; vol. 55; (1935); p. 880,884; dtsch. Ref. S. 165, 166; Chem. Zentralbl.; 1036 I 993, View in Reaxys

2.4-dinitro-phenylhydrazone (mp: 232,5-234,5 degree )

Strain; Journal of the American Chemical Society; vol. 57; (1935); p. 758,760; Journal of Biological Chemistry; vol. 102; (1933); p. 137,142, View in Reaxys

1.3-dimethyl-5<4-methyl-benzylidene>-barbituric acid (mp: 142-142,5 degree )

Akabori; Chemische Berichte; vol. 66; (1933); p. 151,158; Nippon Kagaku Kaishi; vol. 52; (1931); p. 844,850, View in Reaxys

p-nitro-phenylhydrazone (mp: 198 degree )

Kalb; Gross; Chemische Berichte; vol. 59; (1926); p. 733, View in Reaxys

p-nitro-phenylhydrazone (mp: 200.5 degree )

Stephen; Journal of the Chemical Society; vol. 127; (1925); p. 1877, View in Reaxys

p-bromo-phenylhydrazone (mp: 162 degree )

Graziani; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <5> 19 II; (1910); p. 192; Gazzetta Chimica Italiana; vol. 43 II; (1913); p. 539, View in Reaxys

Melting Point (5) 1 of 5

Melting Point [°C]

82 - 85

Firouzabadi, Habib; Sardarian, Alireza; Badparva, Hasan; Bulletin of the Chemical Society of Japan; vol. 69; nb. 3; (1996); p. 685 - 691, View in Reaxys; Iranpoor, Nasser; Firouzabadi, Habib; Zolfigol, Mohammad Ali; Bulletin of the Chemical Society of Japan; vol. 71; nb. 4; (1998); p. 905 - 908, View in Reaxys 2 of 5

Melting Point [°C]

205 - 207

Firouzabadi, Habib; Afsharifar, Gholam Reza; Bulletin of the Chemical Society of Japan; vol. 68; nb. 9; (1995); p. 2595 - 2602, View in Reaxys 3 of 5

Melting Point [°C]

112

El-Din, Ahmed Moukhtar Nour; Mourad, Aboul-Fetouh El-Said; Mekamer, Ramadan; Heterocycles; vol. 23; nb. 5; (1985); p. 1155 - 1160, View in Reaxys 4 of 5

Melting Point [°C]

105 - 106

58/464

2016-04-07 09:00:27

Bayer,E.; Breitmaier,E.; Chemische Berichte; vol. 102; nb. 3; (1969); p. 728 - 735, View in Reaxys 5 of 5

Melting Point [°C]

204

Denton; Suschitzky; Journal of the Chemical Society; (1963); p. 4741,4742, View in Reaxys Boiling Point (73) Boiling Point [°C] Pressure (Boiling Point) [Torr] 205

Location

Comment (Boiling References Point)

supporting information

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

207

Safaei-Ghomi, Javad; Hajipour, Abdol Reza; Journal of the Chinese Chemical Society; vol. 56; nb. 2; (2009); p. 416 - 418, View in Reaxys; SafaeiGhomi, Javad; Hajipour, Abdol R.; Organic Preparations and Procedures International; vol. 43; nb. 4; (2011); p. 372 - 376, View in Reaxys

204

760.051

supporting information

Liu, Lianghui; Yu, Mengmeng; Wayland, Bradford B.; Fu, Xuefeng; Chemical Communications; vol. 46; nb. 34; (2010); p. 6353 - 6355, View in Reaxys Nia, Shabnam; Gong, Xianchang; Drain, Charles Michael; Jurow, Matthew; Rizvi, Waqar; Qureshy, Meroz; Journal of Porphyrins and Phthalocyanines; vol. 14; nb. 7; (2010); p. 621 629, View in Reaxys

204

Heravi; Bakhtiari; Oskooie; Hekmatshoar; Russian Journal of Organic Chemistry; vol. 45; nb. 6; (2009); p. 863 - 864, View in Reaxys

Kantlehner, Willi; Anders, Ernst; Mezger, Jochen; Stoyanov, Edmont V.; Kress, Ralf; Wermann, Kurt; Frey, Wolfgang; Goerls, Helmar; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 63; nb. 4; (2008); p. 395 - 406, View in Reaxys

58 - 61

Liu, Qifa; Lu, Ming; Sun, Feng; Li, Jiang; Zhao, Yuebing; Synthetic Communications; vol. 38; nb. 23; (2008); p. 4188 - 4197, View in Reaxys

205 - 206

Bratulescu, George; Synthetic Communications; vol. 38; nb. 16; (2008); p. 2748 - 2752, View in Reaxys

202 - 203

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

Ghosh, Kumaresh; Adhikari, Suman; Journal of the Indian Chemical Society; vol. 85; nb. 9; (2008); p. 959 - 961, View in Reaxys

106 - 108

Hajipour, Abdol R.; Rafiee; Ruoho; Synlett; nb. 7; (2007); p. 1118 - 1120, View in Reaxys

204

Kremlev et al.; Voprosy Khimii i Khimicheskoi Tekhnologii; vol. 25; (1972); p. 32,33-36; Chem.Abstr.; vol. 78; nb. 110775z; Chem. Zentralbl.; Ref.Zh.Khim. No 16 <1972> Zh 217, View in Reaxys; Patent; Deutsche Advance Prod.; BE615018; (1962); DE; Chem.Abstr.; vol. 57; nb. 14941; (1962), View in Reaxys; Chaudhuri; Dehury; Hussain; Duarah; Gogoi; Organic Preparations and Procedures International; vol. 38; nb. 3; (2006); p. 331 - 336, View in Reaxys

59/464

2016-04-07 09:00:27

106 - 108

Hajipour, Abdol Reza; Rafiee, Fatemeh; Ruoho, Arnold E.; Synthetic Communications; vol. 36; nb. 17; (2006); p. 2563 - 2568, View in Reaxys

200 - 203

110 - 112

Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys 15

Jin, Tong-Shou; Zhao, Ying; Liu, Li-Bin; Li, Tong-Shuang; Journal of Chemical Research; nb. 7; (2005); p. 438 - 439, View in Reaxys

202

Hashemi, Mohammed M.; Ghazanfari, Dadkhoda; Akhbari, Maryam; Monatshefte fur Chemie; vol. 135; nb. 7; (2004); p. 793 - 797, View in Reaxys

109

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

110 - 111

Fan, Xuesen; Zhang, Xinying; Zhang, Yongmin; Journal of Chemical Research; nb. 4; (2004); p. 290 - 291, View in Reaxys

84 - 85

Zhang, Zhan-Hui; Journal of Chemical Research; nb. 11; (2004); p. 753 - 755, View in Reaxys

112 - 114

Jin, Tong-Shou; Sun, Guang; Li, Yan-Wei; Li, Tong-Shuang; Journal of Chemical Research Part S; nb. 1; (2003); p. 30 - 32, View in Reaxys

95 - 97

Jin, Tong-Shou; Li, Yan-Wei; Sun, Guang; Song, Xin-Ru; Li, Tong-Shuang; Journal of Chemical Research - Part S; nb. 6; (2003); p. 322 - 323, View in Reaxys

203

Barman, Dhiren C.; Saikia, Pramod; Prajapati, Dipak; Sandhu, Jagir S.; Synthetic Communications; vol. 32; nb. 22; (2002); p. 3407 - 3412, View in Reaxys

Bagno, Alessandro; Kantlehner, Willi; Scherr, Oliver; Vetter, Jens; Ziegler, Georg; European Journal of Organic Chemistry; nb. 15; (2001); p. 2947 - 2954, View in Reaxys; Kantlehner, Willi; Haug, Erwin; Scherr, Oliver; Ziegler, Georg; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 57; nb. 11; (2002); p. 1295 - 1304, View in Reaxys

104 - 106

Sato, Kazuhiko; Aoki, Masao; Takagi, Junko; Zimmermann, Klaus; Noyori, Ryoji; Bulletin of the Chemical Society of Japan; vol. 72; nb. 10; (1999); p. 2287 - 2306, View in Reaxys

80 - 82

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

104 - 106

Jin; Ma; Zhang; Li; Organic Preparations and Procedures International; vol. 30; nb. 4; (1998); p. 463 - 466, View in Reaxys

200

113 - 115

Bandgar; Kulkarni, Sameer A.; Nigal; Organic Preparations and Procedures International; vol. 30; nb. 6; (1998); p. 706 - 709, View in Reaxys 12

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

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Procedures International; vol. 29; nb. 4; (1997); p. 480 - 484, View in Reaxys 85

Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys

90 - 92

Brouard, Corinne; Pornet, Jacques; Miginiac, Leone; Tetrahedron; vol. 48; nb. 12; (1992); p. 2385 - 2400, View in Reaxys

112

Olah; Wu; Synthesis; nb. 5; (1991); p. 407 - 408, View in Reaxys

Kamitori, Yasuhiro; Hojo, Masaru; Masuda, Ryoichi; Ohara, Seiji; Kawasaki, Kazuyoshi; et al.; Journal of Heterocyclic Chemistry; vol. 27; nb. 3; (1990); p. 487 - 495, View in Reaxys

82 - 85

Svoboda, Jiri; Kocfeldova, Zuzana; Palecek, Jaroslav; Collection of Czechoslovak Chemical Communications; vol. 53; nb. 4; (1988); p. 822 832, View in Reaxys

207

Yaozeng Huang; Yanchang Shen; Chen Chen; Synthesis; nb. 6/7; (1985); p. 651 - 652, View in Reaxys

61 - 62

Nishiguchi, Ikuzo; Hirashima, Tsuneaki; Journal of Organic Chemistry; vol. 50; nb. 4; (1985); p. 539 - 541, View in Reaxys

Olah, George A.; Narang, Subhash C.; GarciaLuna, Armando; Salem, George F.; Synthesis; nb. 2; (1981); p. 146, View in Reaxys

110

Fresneda, P. M.; Lidon, M. J.; Molina, P.; Vilaplana, M. J.; Synthesis; nb. 9; (1981); p. 711 - 714, View in Reaxys

80 - 82

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

Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys

46 - 47

0.6

Olah, George A.; Arvanaghi, Massoud; Prakash, G.K. Surya; Synthesis; nb. 3; (1980); p. 220, View in Reaxys

72 - 73

Bansal, Raj Kumar; Sethi, Kanta; Bulletin of the Chemical Society of Japan; vol. 53; nb. 4; (1980); p. 1197 - 1198, View in Reaxys

202 - 204

HO; Synthesis; (1978); p. 936, View in Reaxys; Silver; Wood; Transactions of the Faraday Society; vol. 60; (1964); p. 5, View in Reaxys

204 - 205

760

Degani; Fochi; Synthesis; (1976); p. 757, View in Reaxys

Davis et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1478,1480,1481, View in Reaxys

204 - 205

Bornemann; Chemische Berichte; vol. 17; (1884); p. 1468, View in Reaxys; Bover; Zumann; Journal of the American Chemical Society; vol. 95; (1973); p. 2531,2533-2536, View in Reaxys

206

Ramegowda et al.; Tetrahedron; vol. 29; (1973); p. 3985,3986, View in Reaxys

61/464

2016-04-07 09:00:27

109 - 110

Ogata; Sawaki; Journal of the American Chemical Society; vol. 94; (1972); p. 4189,4190,4196, View in Reaxys

80 - 81.5

Horiie; Masomura; Kogyo Kagaku Zasshi; vol. 72; (1969); p. 686,687; Chem.Abstr.; vol. 72; nb. 66154; (1970), View in Reaxys

107 - 109

Okada et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1395,1396,1400, View in Reaxys

Ross,S.D. et al.; Journal of Organic Chemistry; vol. 33; nb. 2; (1968); p. 585 - 587, View in Reaxys

Ol'dekop et al.; Zhurnal Organicheskoi Khimii; vol. 4; (1968); p. 585,573, View in Reaxys

100 - 101

Ogata et al.; Tetrahedron; vol. 23; (1967); p. 1007, View in Reaxys

Bell,J.M. et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 4284 - 4292, View in Reaxys

106

Stephen; Journal of the Chemical Society; vol. 127; (1925); p. 1877, View in Reaxys; Ol'dekop; Kalinina; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 3473,3515, View in Reaxys

Patent; Ajinomoto; NL6405282; (1964); Chem.Abstr.; vol. 62; nb. 14574e; (1965), View in Reaxys

87 - 90

Gross,H.; Matthey,G.; Chemische Berichte; vol. 97; (1964); p. 2606 - 2613, View in Reaxys

130 - 132

Sisti,A. et al.; Journal of Organic Chemistry; vol. 27; (1962); p. 279 - 281, View in Reaxys

Bogdanov; Antonova; Trudy Vsesoyuznogo Nauchno-Issledovatel'skogo Instituta Sinteticheskikh i Natural'nykh Dushistykh Veshchestv; vol. 5; (1961); p. 16; Chem.Abstr.; vol. 58; nb. 467, View in Reaxys

201 - 203

Ol'dekop,Yu.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2904 - 2910,2706 2711, View in Reaxys

6.5

Klouwen; Boelens; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 1022,1031, View in Reaxys

80.5 - 81.5

12.5

Patent; Rieche et al.; DE22907; (1959); Chem.Abstr.; vol. 58; nb. 1407a; (1963), View in Reaxys

Levi; Nicholls; Industrial and Engineering Chemistry; vol. 50; (1958); p. 1005, View in Reaxys

118 - 120

Markees; Journal of Organic Chemistry; vol. 23; (1958); p. 1490, View in Reaxys

Forbes; Mueller; Canadian Journal of Chemistry; vol. 35; (1957); p. 488,498, View in Reaxys

85 - 86

Baker et al.; Journal of the Chemical Society; (1956); p. 404,410, View in Reaxys

Baker; Davies; Hemming; Journal of the Chemical Society; (1940); p. 692,702, View in Reaxys

Grammaticakis; Bulletin de la Societe Chimique de France; vol. <5> 7; (1940); p. 527,669, View in Reaxys

62/464

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203.5 - 204

760

Kahovec; Kohlrausch; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 38; (1938); p. 119,138, View in Reaxys

78.4 - 79.6

Kahovec; Kohlrausch; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 38; (1938); p. 119,138, View in Reaxys

102 - 105

Stephen; Short; Gladding; Journal of the Chemical Society; vol. 117; (1920); p. 525, View in Reaxys

102 - 104

Hebert; Bulletin de la Societe Chimique de France; vol. <4> 27; (1920); p. 50, View in Reaxys

204 98 - 100

fluessig. 20

Cannizzaro; Justus Liebigs Annalen der Chemie; vol. 124; (1862); p. 254, View in Reaxys Patent; Fabr. de Laire; DE268786; Fortschr. Teerfarbenfabr. Verw. Industriezweige; vol. 11; p. 197, View in Reaxys

Refractive Index (20) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Re- References fractive Index) [°C]

1.5454

589

Levi; Nicholls; Industrial and Engineering Chemistry; vol. 50; (1958); p. 1005, View in Reaxys; Gohar, G. A.; Egyptian Journal of Chemistry; vol. 41; nb. 1-6; (1998); p. 43 - 58, View in Reaxys

1.5458

589

Petrow; Sopow; Zhurnal Obshchei Khimii; vol. 25; (1955); p. 517,520, 522; engl. Ausg. S. 485, 487, 488, View in Reaxys; Gohar, Gamal A.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 79; nb. 1,4; (1993); p. 171 - 178, View in Reaxys

1.5479

589

Katritzky; Brown; Synthesis; (1978); p. 619, View in Reaxys

1.543

589

Davis et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1478,1480,1481, View in Reaxys

1.552

589

Kremlev et al.; Voprosy Khimii i Khimicheskoi Tekhnologii; vol. 25; (1972); p. 32,33-36; Chem.Abstr.; vol. 78; nb. 110775z; Chem. Zentralbl.; Ref.Zh.Khim. No 16 <1972> Zh 217, View in Reaxys

1.5368

589

Ross,S.D. et al.; Journal of Organic Chemistry; vol. 33; nb. 2; (1968); p. 585 - 587, View in Reaxys

1.547

589

Ol'dekop et al.; Zhurnal Organicheskoi Khimii; vol. 4; (1968); p. 585,573, View in Reaxys

1.5466

589

16.5

Ol'dekop; Kalinina; J. Gen. Chem. USSR (Engl. Transl.); vol. 34; (1964); p. 3473,3515, View in Reaxys

1.547

589

Ol'dekop,Yu.A. et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2904 - 2910,2706 - 2711, View in Reaxys

1.5463

589

Klouwen; Boelens; Recueil des Travaux Chimiques des Pays-Bas; vol. 79; (1960); p. 1022,1031, View in Reaxys

1.546

589

Forbes; Mueller; Canadian Journal of Chemistry; vol. 35; (1957); p. 488,498, View in Reaxys

1.5402

656.3

16.6

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

1.5437

656.3

11.9

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

1.547

589

16.6

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

1.5503

589

11.9

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

1.5641

486.1

16.6

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

63/464

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1.5676

486.1

11.9

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

1.58

434

16.6

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

1.5837

434

11.9

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

1.5484

589

Hanzlik; Bianchi; Chemische Berichte; vol. 32; (1899); p. 1287, View in Reaxys

Density (5) 1 of 5

Density [g·cm-3]

1.02

Reference Temperature [°C]

Measurement Tempera- 20 ture [°C] Levi; Nicholls; Industrial and Engineering Chemistry; vol. 50; (1958); p. 1005, View in Reaxys 2 of 5

Density [g·cm-3]

1.019

Reference Temperature [°C]

Measurement Tempera- 20 ture [°C] Petrow; Sopow; Zhurnal Obshchei Khimii; vol. 25; (1955); p. 517,520, 522; engl. Ausg. S. 485, 487, 488, View in Reaxys 3 of 5

Density [g·cm-3]

1.0194

Reference Temperature [°C]

Measurement Tempera- 16.7 ture [°C] v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys 4 of 5

Density [g·cm-3]

1.0261

Reference Temperature [°C]

Measurement Tempera- 12.8 ture [°C] v. Auwers; Chemische Berichte; vol. 45; (1912); p. 2779; Justus Liebigs Annalen der Chemie; vol. 408; (1915); p. 237, View in Reaxys 5 of 5

Density [g·cm-3]

1.072

Measurement Tempera- 12 ture [°C] Hanzlik; Bianchi; Chemische Berichte; vol. 32; (1899); p. 1287, View in Reaxys Association (MCS) (9) 1 of 9

Description (Association Stability constant of the complex with ... (MCS)) Solvent (Association (MCS))

acetic acid; H2O

Temperature (Association (MCS)) [°C]

14.85 - 44.85

Partner (Association (MCS))

hexamethylenetetramine-bromine

Gangwani; Sharma; Banerji; International Journal of Chemical Kinetics; vol. 32; nb. 10; (2000); p. 615 - 622, View in Reaxys

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2 of 9

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

BF3

Azzaro, Marcel; Gal, Jean Francois; Geribaldi, Serge; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 4; (1984); p. 771 - 774, View in Reaxys; Berthelot, Michel; Gal, JeanFrancois; Helbert, Maryvonne; Laurence, Christian; Maria, Pierre-Charles; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 82; nb. 4; (1985); p. 427 - 432, View in Reaxys 3 of 9

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

cyclohexane

Grosse, Constantino; Mechetti, Magdalena; Brito, Pedro; Canadian Journal of Chemistry; vol. 63; (1985); p. 1031 - 1034, View in Reaxys 4 of 9

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

decalin

Grosse, Constantino; Mechetti, Magdalena; Brito, Pedro; Canadian Journal of Chemistry; vol. 63; (1985); p. 1031 - 1034, View in Reaxys 5 of 9

Description (Association Dipole moment of the complex (MCS)) Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

heptane

Grosse, Constantino; Mechetti, Magdalena; Brito, Pedro; Canadian Journal of Chemistry; vol. 63; (1985); p. 1031 - 1034, View in Reaxys 6 of 9

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

CH2Cl2

Partner (Association (MCS))

boron trifluoride

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

methanol

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

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8 of 9

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

Partner (Association (MCS))

phenol

Shkumat, A. P.; Polyakov, V. K.; Tsukerman, S. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 51; nb. 6; (1981); p. 1395 - 1402,1183 - 1188, View in Reaxys 9 of 9

Description (Association Association with compound (MCS)) Seguin,J.-P. et al.; Bulletin de la Societe Chimique de France; (1974); p. 167 - 172, View in Reaxys

Chromatographic Data (5) Chromatographic Location data TLC (Thin layer chromatography)

References

supporting information

Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys; Xing, Qi; Lv, Hui; Xia, Chungu; Li, Fuwei; Chemical Communications; vol. 52; nb. 3; (2015); p. 489 - 492, View in Reaxys

GC (Gas chroma- supporting infortography) mation

Lee, Jia Ying; Fan, Wai Yip; Mak, Kar Hang Garvin; Leong, Weng Kee; Journal of Organometallic Chemistry; vol. 724; (2013); p. 275 - 280, View in Reaxys; Zhang, Hua; Fu, Luoling; Synthetic Communications; vol. 44; nb. 5; (2014); p. 610 - 619, View in Reaxys; Herbst, Annika; Khutia, Anupam; Janiak, Christoph; Inorganic Chemistry; vol. 53; nb. 14; (2014); p. 7319 - 7333, View in Reaxys; Nagaki, Aiichiro; Tsuchihashi, Yuta; Haraki, Suguru; Yoshida, Jun-ichi; Organic and Biomolecular Chemistry; vol. 13; nb. 26; (2015); p. 7140 - 7145, View in Reaxys; Hajnal, Ivan; Faber, Kurt; Schwab, Helmut; Hall, Mlanie; Steiner, Kerstin; Advanced Synthesis and Catalysis; vol. 357; nb. 14-15; (2015); p. 3309 - 3316, View in Reaxys

HPLC (High performance liquid chromatography)

Bechi, Beatrice; Herter, Susanne; McKenna, Shane; Riley, Christopher; Leimkühler, Silke; Turner, Nicholas J.; Carnell, Andrew J.; Green Chemistry; vol. 16; nb. 10; (2014); p. 4524 - 4529, View in Reaxys; Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys; Angulo, Beatriz; Garca, Jos I.; Herreras, Clara I.; Mayoral, Jos A.; Miana, Ana C.; Organic and Biomolecular Chemistry; vol. 13; nb. 35; (2015); p. 9314 - 9322, View in Reaxys; Paria, Sayantan; Ohta, Takehiro; Morimoto, Yuma; Ogura, Takashi; Sugimoto, Hideki; Fujieda, Nobutaka; Goto, Kei; Asano, Kaori; Suzuki, Takeyuki; Itoh, Shinobu; Journal of the American Chemical Society; vol. 137; nb. 34; (2015); p. 10870 - 10873, View in Reaxys

supporting information

LC (Liquid chromatography)

Mahmood, Shahid; Khalid, Azeem; Mahmood, Tariq; Arshad, Muhammad; LoyolaLicea, Juan Carlos; Crowley, David E.; RSC Advances; vol. 5; nb. 128; (2015); p. 106272 - 106279, View in Reaxys

GC (Gas chromatography)

Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz; ACS Catalysis; vol. 3; nb. 10; (2013); p. 2208 - 2217, View in Reaxys

Crystal Property Description (8) Colour & Other Location Properties

References

colourless

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 162, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys; Kamimura, Akio; Komatsu, Hiroyuki; Moriyama, Takaaki; Nozaki, Yuichiro; Tetrahedron; vol. 69; nb. 29; (2013); p. 5968 - 5972, View in Reaxys; Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol. 78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol. 45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Xie, Aming; Zhou, Xiangxiang; Feng, Liandong; Hu, Xinyu; Dong, Wei; Tetrahedron; vol. 70; nb. 21; (2014); p. 3514 - 3519, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys; Moriyama, Katsuhiko; Takemura, Misato; Togo,

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supporting information

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white

colourless

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supporting information

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yellow

supporting information

Uyanik, Muhammet; Fukatsu, Ryota; Ishihara, Kazuaki; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 456 - 460, View in Reaxys; Tucker-Schwartz, Alexander K.; Garrell, Robin L.; Chemistry - A European Journal; vol. 16; nb. 42; (2010); p. 12718 - 12726, View in Reaxys

yellow

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Dielectric Constant (1) References Misra; Saxena; Acta Physica et Chemica; vol. 24; (1978); p. 357,361, View in Reaxys Dissociation Exponent (3) 1 of 3

Comment (Dissociation Exponent)

(pk')pK(A)

Ostrovskii et al.; Zhurnal Organicheskoi Khimii; vol. 11; (1975); p. 1027,1015, View in Reaxys 2 of 3

Comment (Dissociation Exponent)

(pk')pK der Rk. mit OH-

Bover; Zuman; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 786,788, View in Reaxys 3 of 3

Comment (Dissociation Exponent)

(pk')-pK(BH+): 6.56

Yates; Scott; Canadian Journal of Chemistry; vol. 41; (1963); p. 2320,2323, 2326, View in Reaxys Electrical Data (1) 1 of 1

Description (Electrical Data)

Dielectric loss

Misra; Saxena; Acta Physica et Chemica; vol. 24; (1978); p. 357,361, View in Reaxys Electrical Data (MCS) (1) 1 of 1

Description (Electrical Data (MCS))

Dielectric constant

Temperature (Electrical Data (MCS)) [°C]

Comment (Electrical Da- concentration dependence ta (MCS)) Partner (Electrical Data (MCS))

cyclohexane

Ghanadzadeh Gilani; Mamaghani; Anbir; Journal of Solution Chemistry; vol. 32; nb. 7; (2003); p. 625 - 636, View in Reaxys Electrical Moment (8) 1 of 8

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.38466

Temperature (Electrical Moment) [°C]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

cyclohexane

Ghanadzadeh Gilani; Mamaghani; Anbir; Journal of Solution Chemistry; vol. 32; nb. 7; (2003); p. 625 - 636, View in Reaxys

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2 of 8

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

neat (no solvent)

Cheng, Lap-Tak; Tam, Wilson; Stevenson, Sylvia H.; Meredith, Gerald R.; Rikken, Geert; Marder, Seth R.; Journal of Physical Chemistry; vol. 95; nb. 26; (1991); p. 10631 - 10643, View in Reaxys 3 of 8

Description (Electrical Moment)

Dipole moment

Comment (Electrical Mo- μ (Tab.1) ment) Hossain; Hanson; Chemical Physics; vol. 30; (1978); p. 155, View in Reaxys 4 of 8

Description (Electrical Moment)

Dipole moment

Comment (Electrical Mo- μ ment) Gore et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 120, View in Reaxys 5 of 8

Description (Electrical Moment)

Dipole moment

Hammel; Smith; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 1852, View in Reaxys; Deshpande; Suryanarayana Rao; Current Science; vol. 36; (1967); p. 429, View in Reaxys; Lutskii et al.; Theoretical and Experimental Chemistry; vol. 2; (1966); p. 201; ; p. 264, View in Reaxys 6 of 8

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.24

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Estok; Dehn; Journal of the American Chemical Society; vol. 77; (1955); p. 4769, View in Reaxys 7 of 8

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.3

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Pearce; Berhenke; Journal of Physical Chemistry; vol. 39; (1935); p. 1008, View in Reaxys 8 of 8

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.3

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

dioxane

Pearce; Berhenke; Journal of Physical Chemistry; vol. 39; (1935); p. 1008, View in Reaxys

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Electrochemical Behaviour (4) Description (Elec- Comment (Electrochemical Betrochemical Behaviour) haviour) Basicity

gas

References

Mustanir; Shimada; Ohta; Mishima; Bulletin of the Chemical Society of Japan; vol. 73; nb. 8; (2000); p. 1845 - 1856, View in Reaxys

Proton affinity

Kukol, A.; Strehle, F.; Thielking, G.; Gruetzmacher, H.-Fr.; Organic Mass Spectrometry; vol. 28; nb. 10; (1993); p. 1107 - 1110, View in Reaxys; Anderson, Peter D. J.; Fernandez, M. Tereza; Pocsfalvi, Gabriella; Mason, Rod S.; Journal of the Chemical Society. Perkin Transactions 2; nb. 5; (1997); p. 873 - 879, View in Reaxys

Polarography

Galpern et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 26; (1971); p. 1206,1080, View in Reaxys; Laviron; Collection of Czechoslovak Chemical Communications; vol. 30; (1965); p. 4219,4233, View in Reaxys; Meyer; Annales de Chimie (Cachan, France); vol. 8; nb. 14; (1973); p. 315,325, View in Reaxys

Electrolytic dissociation / protonation equilibrium

in wss. H2SO4 bei Yates; Stewart; Canadian Journal of Chemistry; vol. 37; (1959); p. 664,665, 25grad. View in Reaxys

Electrochemical Characteristics (16) 1 of 16

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Location

supporting information

Finney, Eric E.; Ogawa, Kelli A.; Boydston, Andrew J.; Journal of the American Chemical Society; vol. 134; nb. 30; (2012); p. 12374 - 12377, View in Reaxys 2 of 16

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Amemiya, Fumihiro; Matsumoto, Hideyuki; Fuse, Keishi; Kashiwagi, Tsuneo; Kuroda, Chiaki; Fuchigami, Toshio; Atobe, Mahito; Organic and Biomolecular Chemistry; vol. 9; nb. 11; (2011); p. 4256 - 4265, View in Reaxys 3 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical methanol; H2O Characteristics) pH-Value (Electrochemi- 3 cal Characteristics) Comment (Electrochem- -1.3 V; Product: /BRN= 1856550/. No. of transm. electrons: 2 Method: voltammetry. Deical Characteristics) scription: membrane flow cell with rotating Pb disc electrode vs. SCE Product

4-Methylbenzyl alcohol

Guena, Thierry; Pletcher, Derek; Acta Chemica Scandinavica; vol. 52; nb. 1; (1998); p. 32 - 36, View in Reaxys 4 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical methanol; H2O Characteristics) pH-Value (Electrochemi- 3 cal Characteristics) Comment (Electrochem- -1.1 V; Product: /BRN= 2216394/. No. of transm. electrons: 1 Method: voltammetry. Deical Characteristics) scription: membrane flow cell with rotating Pb disc electrode vs. SCE Product

1,2-bis(4-methylphenyl)ethane-1,2-diol

Guena, Thierry; Pletcher, Derek; Acta Chemica Scandinavica; vol. 52; nb. 1; (1998); p. 32 - 36, View in Reaxys 5 of 16

Description (Electrochemical Characteristics)

polarographic current/voltage curve

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Cheng, Po-Chung; Nonaka, Tsutomu; Chou, Tse-Chuan; Bulletin of the Chemical Society of Japan; vol. 64; nb. 6; (1991); p. 1911 - 1915, View in Reaxys 6 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical tetrahydrofuran Characteristics) Comment (Electrochem- -2.44 V; Product: /BRN= 4177672/. No. of transm. electrons: 1. Method: cyclovoltammetry. ical Characteristics) Description: 0.5 M tetrabutylammonium perchlorate (TBAP)/Pt Product

4-Methyl-benzaldehyde

Arnett, Edward M.; Palmer, Carrie A.; Journal of the American Chemical Society; vol. 112; nb. 20; (1990); p. 7354 7360, View in Reaxys 7 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical tetrahydrofuran Characteristics) Comment (Electrochem- -2.05 V; Product: /BRN= 4177672/. No. of transm. electrons: 1. Method: voltammetry. Deical Characteristics) scription: second harmonic alternating current voltammetry (SHACV); 0.5 M LiClO4/Pt Product

4-Methyl-benzaldehyde

Arnett, Edward M.; Palmer, Carrie A.; Journal of the American Chemical Society; vol. 112; nb. 20; (1990); p. 7354 7360, View in Reaxys 8 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical acetonitrile Characteristics) Comment (Electrochem- -2.33 V; Product: /BRN= 4177672/. No. of transm. electrons: 1. Method: voltammetry. Deical Characteristics) scription: second harmonic alternating current voltammetry (SHACV); 0.1 M tetrabutylammonium tetrafluoroborate (TBAT)/Pt Product

4-Methyl-benzaldehyde

Arnett, Edward M.; Palmer, Carrie A.; Journal of the American Chemical Society; vol. 112; nb. 20; (1990); p. 7354 7360, View in Reaxys 9 of 16

Description (Electrochemical Characteristics)

oxidation potential

Chiba, Toshiro; Okimoto, Mitsuhiro; Nagai, Hiroshi; Takata, Yoshiyuki; Bulletin of the Chemical Society of Japan; vol. 55; nb. 1; (1982); p. 335 - 336, View in Reaxys 10 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Beno; Kada; Chemicke Zvesti; vol. 32; (1978); p. 155, View in Reaxys; Seguin et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 129, View in Reaxys; Jehlicka; Lakomy; Chemicky Prumysl; vol. 15; (1965); p. 163, View in Reaxys; Galpern et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 26; (1971); p. 1206,1080, View in Reaxys 11 of 16

Description (Electrochemical Characteristics)

redox potential

Seguin,J.-P. et al.; Bulletin de la Societe Chimique de France; (1974); p. 167 - 172, View in Reaxys 12 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in wss. Dioxan vom pH 0. ical Characteristics)

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Coulson et al.; Journal of the American Chemical Society; vol. 79; (1957); p. 1354,1355, View in Reaxys 13 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in Methansulfonsaeure. ical Characteristics) Wawzonek et al.; J. electroch. Soc.; vol. 103; (1956); p. 513,516, View in Reaxys 14 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in Loesungen vom pH 0-13. ical Characteristics) Holleck; Marsen; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 57; (1953); p. 944,954, View in Reaxys 15 of 16

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochem- in wss.-aethanol. Loesungen vom pH 1.7-3.2. ical Characteristics) Portillo; Varela; An. Bromatol.; vol. 2; (1950); p. 147,151, View in Reaxys; Gergely; Iredale; Journal of the Chemical Society; (1953); p. 3226,3229, View in Reaxys 16 of 16

Description (Electrochemical Characteristics)

redox potential

Comment (Electrochem- Reduktionspotential. ical Characteristics) Semerano; Chisini; Gazzetta Chimica Italiana; vol. 63; (1933); p. 802,810, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

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

Energy Barriers (1) References Sommer et al.; Journal of Magnetic Resonance (1969-1992); vol. 21; (1976); p. 93,96, View in Reaxys; Drakenberg; Journal of the Chemical Society, Chemical Communications; (1974); p. 1011, View in Reaxys; Grindley et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1975); p. 443, View in Reaxys; Silver; Wood; Transactions of the Faraday Society; vol. 60; (1964); p. 5, View in Reaxys Energy Data (MCS) (1) 1 of 1

Description (Energy Data (MCS))

Enthalpy of solution

Fuchs et al.; Canadian Journal of Chemistry; vol. 51; (1973); p. 4122, View in Reaxys; Korol' et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 860, View in Reaxys Enthalpy of Vaporization (1) Comment (Enthal- References py of Vaporization) Enthalpy of vapor- Ji, Chang; Day, Shannon E.; Ortega, Stephanie A.; Beall, Gary W.; Journal of Chemical and Engineering ization given Data; vol. 53; nb. 5; (2008); p. 1093 - 1097, View in Reaxys Further Information (25) Description (Fur- References ther Information) Further information

Lakshmi et al.; Journal of Chemical Physics; vol. 68; (1978); p. 4662, View in Reaxys

Further information

Migahed; Allam; Organic Mass Spectrometry; vol. 12; (1977); p. 695,696, View in Reaxys

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Further information

Harrigan; Hirota; Molecular Physics; vol. 31; (1976); p. 663,670, View in Reaxys

Further information

Seguin et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 278; (1974); p. 129, View in Reaxys

Further information

Gal et al.; Bulletin de la Societe Chimique de France; (1973); p. 1150,1151, View in Reaxys

Further information

Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys

Further information

Cheng; Hirota; Chemical Physics Letters; vol. 14; (1972); p. 415, View in Reaxys

Further information

Greenwald; Rabinovitz; Journal of the Chemical Society [Section] D: Chemical Communications; (1969); p. 642, View in Reaxys

Further information

Danyluk et al.; Canadian Journal of Chemistry; vol. 47; (1969); p. 4005, View in Reaxys

Further information

Yoder et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 539, View in Reaxys

Further information

Zaitsev; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 145,146, View in Reaxys

Further information

Gupta; Mital; Bulletin des Societes Chimiques Belges; vol. 76; (1967); p. 631,634, 636, View in Reaxys

Further information

Berlin,K.D.; Burpo,D.H.; Journal of Organic Chemistry; vol. 31; (1966); p. 1304 - 1306, View in Reaxys

Further information

German et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 2; (1966); p. 719,721; Khimiya Geterotsiklicheskikh Soedinenii; vol. 2; (1966); p. 938, View in Reaxys

Further information

Rasschaert,A. et al.; Bulletin des Societes Chimiques Belges; vol. 75; (1966); p. 449 - 455, View in Reaxys

Further information

Walsh; Kuivila; Journal of the American Chemical Society; vol. 88; (1966); p. 576,578, View in Reaxys

Further information

Blomquist; Acta Chemica Scandinavica (1947-1973); vol. 20; (1966); p. 1747,1753, View in Reaxys

Further information

Lutskii et al.; Theoretical and Experimental Chemistry; vol. 2; (1966); p. 201; ; p. 264, View in Reaxys

Further information

Cogrossi; Annali di Chimica (Rome, Italy); vol. 56; (1966); p. 270,278, 279, 282, View in Reaxys

Further information

Rae; Spectrochimica Acta; vol. 21; (1965); p. 1857, View in Reaxys

Further information

Sato et al.; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 1225, View in Reaxys

Further information

Deverse; King; Journal of Chemical Physics; vol. 41; (1964); p. 3833,3835, View in Reaxys

Further information

Scott; Tetrahedron Letters; (1962); p. 373,375, View in Reaxys

Further information

Aczel; Lumpkin; Analytical Chemistry; vol. 33; (1961); p. 386,387-389, View in Reaxys

Further information

Boyer; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 57; (1960); p. 381,382, View in Reaxys

Henry Constant (MCS) (1) 1 of 1

Comment (Henry Constant (MCS))

Henry constant given

Ji, Chang; Day, Shannon E.; Ortega, Stephanie A.; Beall, Gary W.; Journal of Chemical and Engineering Data; vol. 53; nb. 5; (2008); p. 1093 - 1097, View in Reaxys Ionization Potential (2) Ionization Poten- Method (Ionizatial [eV] tion Potential)

Comment (Ioniza- References tion Potential)

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9.34

Photoionization

Type: vertical. Higher potentials: 9.78

Gal, Jean-Francois; Geribaldi, Serge; Pfister-Guillouzo, Genevieve; Morris, David G.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 103 - 106, View in Reaxys Gibson; Canadian Journal of Chemistry; vol. 51; (1973); p. 3065,3066, View in Reaxys; Foffani et al.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 42; (1964); p. 221,228, View in Reaxys

Liquid Phase (1) Description (Liquid Phase)

Comment (Liquid Phase)

Self-association in solvent dependsolution ence

References Ghanadzadeh Gilani; Mamaghani; Anbir; Journal of Solution Chemistry; vol. 32; nb. 7; (2003); p. 625 - 636, View in Reaxys

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

Description (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/Liq- 27 uid Systems (MCS)) [°C] Partner (Liquid/Liquid Systems (MCS))

sodium lauryl sulfate

Bonar-Law, Richard P.; Journal of Organic Chemistry; vol. 61; nb. 11; (1996); p. 3623 - 3634, View in Reaxys Molecular Deformation (1) Description (MoReferences lecular Deformation) Fundamental vibrations Optics (1) Description (Optics) Natural birefringence

Silver; Wood; Transactions of the Faraday Society; vol. 60; (1964); p. 5, View in Reaxys

Comment (Optics) References Stroemungsdoppelbrechung bei 20grad.

Vorlaender; Kirchner; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 152; (1931); p. 47,54, View in Reaxys

Other Thermochemical Data (3) Description (Other References Thermochemical Data) Entropy

Misra; Saxena; Acta Physica et Chemica; vol. 24; (1978); p. 357,361, View in Reaxys

Enthalpy

Misra; Saxena; Acta Physica et Chemica; vol. 24; (1978); p. 357,361, View in Reaxys

Thermodynamic properties

Jost et al.; Journal of the Chemical Society [Section] D: Chemical Communications; (1971); p. 879, View in Reaxys; Misra; Saxena; Acta Physica et Chemica; vol. 24; (1978); p. 357,361, View in Reaxys

Solubility (MCS) (3) 1 of 3

Comment (Solubility (MCS))

loesl. in wss. Lsg. von Cetomacrogol

Wan; Hwang; Journal of pharmaceutical sciences; vol. 58; nb. 2; (1969); p. 262 - 264, View in Reaxys 2 of 3

Comment (Solubility (MCS))

b. 25grad in O-Hexadecylpolyethylenglykol (16, 24, 30, 60)

Mitchell; Wan; Journal of Pharmaceutical Sciences; vol. 53; (1964); p. 1467, View in Reaxys 3 of 3

Comment (Solubility (MCS))

in O-Dodecyl-polyethylenglykol (23) b. 25grad

Mitchell; Wan; Journal of Pharmaceutical Sciences; vol. 53; (1964); p. 1467, View in Reaxys Solution Behaviour (MCS) (3) 1 of 3

Description (Solution Be- Solubilizing haviour (MCS))

74/464

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Solvent (Solution Behav- H2O iour (MCS)) Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behav- 1,4-butanediol iour (MCS)) Breslow, Ronald; Connors, Richard V.; Journal of the American Chemical Society; vol. 117; nb. 24; (1995); p. 6601 - 6602, View in Reaxys 2 of 3

Description (Solution Be- Mutual solubility haviour (MCS)) Temperature (Solution Behaviour (MCS)) [°C]

0 - 90

Pressure (Solution Behaviour (MCS)) [Torr]

760

Partner (Solution Behav- water iour (MCS)) Stephenson, Richard M.; Journal of Chemical & Engineering Data; vol. 38; nb. 4; (1993); p. 630 - 633, View in Reaxys 3 of 3

Description (Solution Be- Solubilizing haviour (MCS)) Solvent (Solution Behav- H2O iour (MCS)) Temperature (Solution Behaviour (MCS)) [°C]

Partner (Solution Behav- 1-hexadecylpyridinium chloride iour (MCS)) Lee, Byung-Hwan; Christian, Sherril D.; Tucker, Edwin E.; Scamehorn, John F.; Journal of Physical Chemistry; vol. 95; nb. 1; (1991); p. 360 - 365, View in Reaxys NMR Spectroscopy (163) 1 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Li, Haoquan; Misal Castro, Luis C.; Zheng, Jianxia; Roisnel, Thierry; Dorcet, Vincent; Sortais, Jean-Baptiste; Darcel, Christophe; Angewandte Chemie - International Edition; vol. 52; nb. 31; (2013); p. 8045 - 8049; Angew. Chem.; vol. 125; nb. 31; (2013); p. 8203 - 8207, View in Reaxys; Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol. 78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Fujihara, Tetsuaki; Cong, Cong; Terao, Jun; Tsuji, Yasushi; Advanced Synthesis and Catalysis; vol. 355; nb. 17; (2013); p. 3420 - 3424, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol. 45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Zhang, Hua; Fu, Luoling; Synthetic Communications; vol. 44; nb. 5; (2014); p. 610 - 619, View in Reaxys; Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p. 2330 - 2333, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p. 1867 - 1871, View in Reaxys; Jiang, Jian-An; Du, Jia-Lei; Wang, Zhan-Guo; Zhang, Zhong-Nan; Xu, Xi; Zheng, Gan-Lin; Ji, Ya-Fei; Tetrahedron Letters; vol. 55; nb. 10; (2014); p. 1677 - 1681, View in Reaxys; Nicklaus, Celine M.; Phua, Pim Huat; Buntara, Teddy; Noel, Sebastien; Heeres, Hero J.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 355; nb. 14-15; (2013); p. 2839 - 2844, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 - 6104, View in Reaxys; Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, YongMing; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys; Walsh, Katie; Sneddon,

75/464

2016-04-07 09:00:27

Helen F.; Moody, Christopher J.; Organic Letters; vol. 16; nb. 19; (2014); p. 5224 - 5227, View in Reaxys; Gong, Jin-Long; Qi, Xinxin; Wei, Duo; Feng, Jian-Bo; Wu, Xiao-Feng; Organic and Biomolecular Chemistry; vol. 12; nb. 38; (2014); p. 7486 - 7488, View in Reaxys; Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 - 6575, View in Reaxys; Galletti, Paola; Funiciello, Federica; Soldati, Roberto; Giacomini, Daria; Advanced Synthesis and Catalysis; vol. 357; nb. 8; (2015); p. 1840 - 1848, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Wang, Shuo-En; Wang, Linfei; He, Qiuqin; Fan, Renhua; Angewandte Chemie - International Edition; vol. 54; nb. 46; (2015); p. 13655 - 13658; Angew. Chem.; vol. 127; nb. 46; (2015); p. 13859 - 13862,4, View in Reaxys; Liu, Chengkou; Fang, Zheng; Yang, Zhao; Li, Qingwen; Guo, Shiyu; Guo, Kai; Organic and Biomolecular Chemistry; vol. 14; nb. 2; (2015); p. 577 - 581, View in Reaxys; Xing, Qi; Lv, Hui; Xia, Chungu; Li, Fuwei; Chemical Communications; vol. 52; nb. 3; (2015); p. 489 - 492, View in Reaxys; Yu, Bo; Yang, Zhenzhen; Zhao, Yanfei; Hao, Leiduan; Zhang, Hongye; Gao, Xiang; Han, Buxing; Liu, Zhimin; Chemistry - A European Journal; vol. 22; nb. 3; (2016); p. 1097 - 1102, View in Reaxys; Bai, Cuihua; Li, Aiqin; Yao, Xianfang; Liu, Hongli; Li, Yingwei; Green Chemistry; vol. 18; nb. 4; (2016); p. 1061 - 1069, View in Reaxys 2 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Liu, Xiaolong; Xia, Qinqin; Zhang, Yuejiao; Chen, Congyan; Chen, Wanzhi; Journal of Organic Chemistry; vol. 78; nb. 17; (2013); p. 8531 - 8536, View in Reaxys; Chen, Congyan; Liu, Bo; Chen, Wanzhi; Synthesis (Germany); vol. 45; nb. 24; (2013); p. 3387 - 3391; Art.No: SS-2013-H0531-OP, View in Reaxys; Yu, Bo; Zhao, Yanfei; Zhang, Hongye; Xu, Jilei; Hao, Leiduan; Gao, Xiang; Liu, Zhimin; Chemical Communications; vol. 50; nb. 18; (2014); p. 2330 - 2333, View in Reaxys; Feng, Qiang; Song, Qiuling; Journal of Organic Chemistry; vol. 79; nb. 4; (2014); p. 1867 - 1871, View in Reaxys; Jiang, Jian-An; Du, Jia-Lei; Wang, Zhan-Guo; Zhang, Zhong-Nan; Xu, Xi; Zheng, Gan-Lin; Ji, Ya-Fei; Tetrahedron Letters; vol. 55; nb. 10; (2014); p. 1677 - 1681, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys; Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 - 6104, View in Reaxys; Walsh, Katie; Sneddon, Helen F.; Moody, Christopher J.; Organic Letters; vol. 16; nb. 19; (2014); p. 5224 - 5227, View in Reaxys; Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 - 6575, View in Reaxys; Galletti, Paola; Funiciello, Federica; Soldati, Roberto; Giacomini, Daria; Advanced Synthesis and Catalysis; vol. 357; nb. 8; (2015); p. 1840 1848, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Xing, Qi; Lv, Hui; Xia, Chungu; Li, Fuwei; Chemical Communications; vol. 52; nb. 3; (2015); p. 489 - 492, View in Reaxys; Yu, Bo; Yang, Zhenzhen; Zhao, Yanfei; Hao, Leiduan; Zhang, Hongye; Gao, Xiang; Han, Buxing; Liu, Zhimin; Chemistry - A European Journal; vol. 22; nb. 3; (2016); p. 1097 - 1102, View in Reaxys; Bai, Cuihua; Li, Aiqin; Yao, Xianfang; Liu, Hongli; Li, Yingwei; Green Chemistry; vol. 18; nb. 4; (2016); p. 1061 - 1069, View in Reaxys 3 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Frequency (NMR Spectroscopy) [MHz]

400

Kalla, Reddi Mohan Naidu; Kim, Mi Ri; Kim, Yu Na; Kim, Il; New Journal of Chemistry; vol. 40; nb. 1; (2016); p. 687 - 693, View in Reaxys 4 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectroscopy) [MHz]

100

Kalla, Reddi Mohan Naidu; Kim, Mi Ri; Kim, Yu Na; Kim, Il; New Journal of Chemistry; vol. 40; nb. 1; (2016); p. 687 - 693, View in Reaxys

76/464

2016-04-07 09:00:27

5 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Location

supporting information

Pratihar, Sanjay; Organic and Biomolecular Chemistry; vol. 14; nb. 10; (2016); p. 2854 - 2865, View in Reaxys 6 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Location

supporting information

Primo, Ana; Puche, Marta; Pavel, Octavian D.; Cojocaru, Bogdan; Tirsoaga, Alina; Parvulescu, Vasile; Garca, Hermenegildo; Chemical Communications; vol. 52; nb. 9; (2016); p. 1839 - 1842, View in Reaxys 7 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100.6

Wang, Lian-Yue; Li, Jun; Lv, Ying; Zhang, Heng-Yun; Gao, Shuang; Journal of Organometallic Chemistry; vol. 696; nb. 20; (2011); p. 3257 - 3263, View in Reaxys; Chen, Bo; Li, Jun; Yang, Gang; Gao, Shuang; Research on Chemical Intermediates; vol. 41; nb. 6; (2015); p. 3929 - 3936, View in Reaxys 9 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Zhang, Guofu; Wang, Yong; Wen, Xin; Ding, Chengrong; Li, Ying; Chemical Communications; vol. 48; nb. 24; (2012); p. 2979 - 2981, View in Reaxys; Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei; Journal of the American Chemical Society; vol. 134; nb. 8; (2012); p. 3643 - 3646, View in Reaxys; Zheng, Jie; Lin, Shengyue; Zhu, Xianhao; Jiang, Biwang; Yang, Zhen; Pan, Zhengying; Chemical Communications; vol. 48; nb. 50; (2012); p. 6235 - 6237, View in Reaxys; Leduc, Andrew B.; Jamison, Timothy F.; Organic Process Research and Development; vol. 16; nb. 5; (2012); p. 1082 - 1089, View in Reaxys; Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei; Angewandte Chemie - International Edition; vol. 51; nb. 51; (2012); p. 12790 - 12794; Angew. Chem.; (2012); p. 12962 - 12966, View in Reaxys; Kamimura, Akio; Komatsu, Hiroyuki; Moriyama, Takaaki; Nozaki, Yuichiro; Tetrahedron; vol. 69; nb. 29; (2013); p. 5968 - 5972, View in Reaxys; Zhang, Guofu; Han, Xingwang; Luan, Yuxin; Wang, Yong; Wen, Xin; Ding, Chengrong; Chemical Communications; vol. 49; nb. 72; (2013); p. 7908 - 7910, View in Reaxys;

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2016-04-07 09:00:27

Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys 10 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Zhang, Guofu; Wang, Yong; Wen, Xin; Ding, Chengrong; Li, Ying; Chemical Communications; vol. 48; nb. 24; (2012); p. 2979 - 2981, View in Reaxys; Zheng, Jie; Lin, Shengyue; Zhu, Xianhao; Jiang, Biwang; Yang, Zhen; Pan, Zhengying; Chemical Communications; vol. 48; nb. 50; (2012); p. 6235 - 6237, View in Reaxys; Song, Xixi; Zhang, Xinshuai; Zhang, Shilei; Li, Hao; Wang, Wei; Chemistry - A European Journal; vol. 18; nb. 32; (2012); p. 9770 - 9774, View in Reaxys; Zhang, Guofu; Han, Xingwang; Luan, Yuxin; Wang, Yong; Wen, Xin; Ding, Chengrong; Chemical Communications; vol. 49; nb. 72; (2013); p. 7908 - 7910, View in Reaxys; Zhang, Guofu; Lei, Jie; Han, Xingwang; Luan, Yuxin; Ding, Chengrong; Shan, Shang; Synlett; vol. 26; nb. 6; (2015); p. 779 - 784, View in Reaxys 11 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 1256, View in Reaxys; Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys 12 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

78/464

2016-04-07 09:00:27

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys; Chen, Bo; Li, Jun; Yang, Gang; Gao, Shuang; Research on Chemical Intermediates; vol. 41; nb. 6; (2015); p. 3929 - 3936, View in Reaxys 14 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

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; Rohitha; Kulkarni; Narender; Synthetic Communications; vol. 43; nb. 21; (2013); p. 2853 - 2866, View in Reaxys; Han, Mi-Kyung; Kim, Sohwa; Kim, Sung Tae; Lee, Jong Chan; Synlett; vol. 26; nb. 17; (2015); p. 2434 - 2436; Art.No: ST-2015-U0545-L, View in Reaxys 15 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Original Text (NMR Spectroscopy)

Location

supporting information

Signals [ppm]

9.96; 7.77; 7.33; 2.44

Kind of signal

s, 1H; d, J = 8.0 Hz, 2H; d, J = 8.0 Hz, 2H; s, 3H

NMR (400 MHz, CDCl3, ppm): δ 9.96 (s, 1H), 7.77 (d, J = 8.0 Hz, 2H), 7.33 (d, J = 8.0 Hz, 2H), 2.44 (s, 3H)

Gao, Jun; Ren, Zhi-Gang; Lang, Jian-Ping; Journal of Organometallic Chemistry; vol. 792; (2015); p. 88 - 92; Art.No: 18908, View in Reaxys 16 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

137.41; 135.45; 129.2; 128.04; 71.8; 21.32

NMR (100 MHz, CDCl3, ppm): δ 137.41, 135.45, 129.20, 128.04, 71.8, 21.32

Gao, Jun; Ren, Zhi-Gang; Lang, Jian-Ping; Journal of Organometallic Chemistry; vol. 792; (2015); p. 88 - 92; Art.No: 18908, View in Reaxys 17 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

79/464

2016-04-07 09:00:27

Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys 18 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Location

supporting information

Zeng, Ling-Zhen; Wang, Chuan-Jun; Li, Ting-Ting; Gan, Xin; Li, Cong; Fu, Wen-Fu; Catalysis Communications; vol. 68; (2015); p. 84 - 87, View in Reaxys; Kim, Bo Ram; Oh, Jung Suk; Kim, Jinho; Lee, Chang Yeon; Bulletin of the Korean Chemical Society; vol. 36; nb. 12; (2015); p. 2799 - 2800, View in Reaxys 19 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Original Text (NMR Spectroscopy)

Location

supporting information

NMR (400 MHz, CDCl3): δ=9.96 (s, 1H), 7.78 (d, J=8.0 Hz, 2H), 7.33 (d, J=7.6 Hz, 2H), 2.44 (s, 3H)

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p. 8725 - 8731; Art.No: 27151, View in Reaxys 20 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

191.8; 145.4; 134.3; 129.8; 129.7; 21.8

NMR (100 MHz, CDCl3): δ=191.8, 145.4, 134.3, 129.8, 129.7, 21.8

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p. 8725 - 8731; Art.No: 27151, View in Reaxys 21 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Paria, Sayantan; Ohta, Takehiro; Morimoto, Yuma; Ogura, Takashi; Sugimoto, Hideki; Fujieda, Nobutaka; Goto, Kei; Asano, Kaori; Suzuki, Takeyuki; Itoh, Shinobu; Journal of the American Chemical Society; vol. 137; nb. 34; (2015); p. 10870 - 10873, View in Reaxys

80/464

2016-04-07 09:00:27

22 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

600

Location

supporting information

Shil, Arun K.; Kumar, Sandeep; Reddy, C. Bal; Dadhwal, Sumit; Thakur, Vandna; Das, Pralay; Organic Letters; vol. 17; nb. 21; (2015); p. 5352 - 5355, View in Reaxys 23 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

150

Location

supporting information

Shil, Arun K.; Kumar, Sandeep; Reddy, C. Bal; Dadhwal, Sumit; Thakur, Vandna; Das, Pralay; Organic Letters; vol. 17; nb. 21; (2015); p. 5352 - 5355, View in Reaxys 24 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Chaudhuri, Sangeeta Roy; Hartwig, Jan; Kupracz, Lukas; Kodanek, Torben; Wegner, Jens; Kirschning, Andreas; Advanced Synthesis and Catalysis; vol. 356; nb. 17; (2014); p. 3530 - 3538, View in Reaxys 25 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 - 2685, View in Reaxys; Hossain, Md. Munkir; Shyu, Shin-Guang; Advanced Synthesis and Catalysis; vol. 352; nb. 17; (2010); p. 3061 - 3068, View in Reaxys; Di, Lei; Hua, Zhang; Advanced Synthesis and Catalysis; vol. 353; nb. 8; (2011); p. 1253 - 1259, View in Reaxys; Zhang, Hua; Fu, Luoling; Synthetic Communications; vol. 44; nb. 5; (2014); p. 610 - 619, View in Reaxys 26 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy)

81/464

2016-04-07 09:00:27

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Song, Xixi; Zhang, Xinshuai; Zhang, Shilei; Li, Hao; Wang, Wei; Chemistry - A European Journal; vol. 18; nb. 32; (2012); p. 9770 - 9774, View in Reaxys; Perez, Juana M.; Cano, Rafael; Yus, Miguel; Ramon, Diego J.; European Journal of Organic Chemistry; nb. 24; (2012); p. 4548 - 4554, View in Reaxys; St. Denis, Jeffrey D.; Scully, Conor C. G.; Lee, C. Frank; Yudin, Andrei K.; Organic Letters; vol. 16; nb. 5; (2014); p. 1338 - 1341, View in Reaxys; Gowrisankar, Saravanan; Neumann, Helfried; Goerdes, Dirk; Thurow, Kerstin; Jiao, Haijun; Beller, Matthias; Chemistry - A European Journal; vol. 19; nb. 47; (2013); p. 15979 - 15984, View in Reaxys; Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys 27 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Perez, Juana M.; Cano, Rafael; Yus, Miguel; Ramon, Diego J.; European Journal of Organic Chemistry; nb. 24; (2012); p. 4548 - 4554, View in Reaxys; St. Denis, Jeffrey D.; Scully, Conor C. G.; Lee, C. Frank; Yudin, Andrei K.; Organic Letters; vol. 16; nb. 5; (2014); p. 1338 - 1341, View in Reaxys; Gowrisankar, Saravanan; Neumann, Helfried; Goerdes, Dirk; Thurow, Kerstin; Jiao, Haijun; Beller, Matthias; Chemistry - A European Journal; vol. 19; nb. 47; (2013); p. 15979 - 15984, View in Reaxys; Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys 28 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

101

Location

supporting information

Bezier, David; Park, Sehoon; Brookhart, Maurice; Organic Letters; vol. 15; nb. 3; (2013); p. 496 - 499, View in Reaxys; Li, Haoquan; Misal Castro, Luis C.; Zheng, Jianxia; Roisnel, Thierry; Dorcet, Vincent; Sortais, Jean-Baptiste; Darcel, Christophe; Angewandte Chemie - International Edition; vol. 52; nb. 31; (2013); p. 8045 8049; Angew. Chem.; vol. 125; nb. 31; (2013); p. 8203 - 8207, View in Reaxys; Nicklaus, Celine M.; Phua, Pim Huat; Buntara, Teddy; Noel, Sebastien; Heeres, Hero J.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 355; nb. 14-15; (2013); p. 2839 - 2844, View in Reaxys; Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, Shun-Jun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys 29 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Hamasaki, Akiyuki; Yasutake, Yutaro; Norio, Takafumi; Ishida, Tamao; Akita, Tomoki; Ohashi, Hironori; Yokoyama, Takushi; Honma, Tetsuo; Tokunaga, Makoto; Applied Catalysis A: General; vol. 469; (2014); p. 146 - 152, View in Reaxys; Zhang, Houcai; Liu, Ruiting; Zhou, Xigeng; Science China Chemistry; vol. 57; nb. 2; (2014); p. 282 - 288, View in Reaxys; Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 - 222, View in Reaxys; Du, Liyong; Gao, Jing; Yang, Shuyang; Wang, Dawei; Han, Xinxin; Xu, Yongjian; Ding, Yuqiang; Russian Journal of General Chemistry; vol. 84; nb. 11; (2014); p. 2200 - 2204, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568,

82/464

2016-04-07 09:00:27

View in Reaxys; Xu, Wenhao; Su, Weike; ; vol. 38; nb. 12; (2014); p. 710 - 714; Art.No: A3, View in Reaxys; Zhu, Xiao; Yang, Daoshan; Wei, Wei; Jiang, Min; Li, Lulu; Zhu, Xiangbing; You, Jinmao; Wang, Hua; RSC Advances; vol. 4; nb. 110; (2014); p. 64930 - 64935, View in Reaxys 30 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Hamasaki, Akiyuki; Yasutake, Yutaro; Norio, Takafumi; Ishida, Tamao; Akita, Tomoki; Ohashi, Hironori; Yokoyama, Takushi; Honma, Tetsuo; Tokunaga, Makoto; Applied Catalysis A: General; vol. 469; (2014); p. 146 - 152, View in Reaxys; Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 - 222, View in Reaxys; Fernandes, Rodney A.; Bethi, Venkati; RSC Advances; vol. 4; nb. 76; (2014); p. 40561 - 40568, View in Reaxys; Xu, Wenhao; Su, Weike; ; vol. 38; nb. 12; (2014); p. 710 - 714; Art.No: A3, View in Reaxys 31 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Chao, Duobin; Fu, Wen-Fu; Dalton Transactions; vol. 43; nb. 1; (2014); p. 306 - 310, View in Reaxys 32 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

303

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 33 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

76.2

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 34 of 163

Description (NMR Spec- Chemical shifts troscopy)

83/464

2016-04-07 09:00:27

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Dharmalingam, Sivanesan; Koo, Eunhae; Yoon, Sungho; Park, Gyoosoon; Bulletin of the Korean Chemical Society; vol. 35; nb. 3; (2014); p. 715 - 720, View in Reaxys; Li, Zhongzhou; Zhu, Wei; Bao, Jinlong; Zou, Xinzhuo; Synthetic Communications; vol. 44; nb. 8; (2014); p. 1155 - 1164, View in Reaxys 35 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Location

supporting information

Li, Zhongzhou; Zhu, Wei; Bao, Jinlong; Zou, Xinzhuo; Synthetic Communications; vol. 44; nb. 8; (2014); p. 1155 1164, View in Reaxys 36 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Original Text (NMR Spectroscopy)

Location

supporting information

Signals [ppm]

9.97; 7.78; 7.33; 2.44

Kind of signal

s, 1H; d, J=8.0, 2H; d, J=7.9, 2H; s, 3H

NMR (300 MHz, CDCl3) δ 9.97 (s, 1H), 7.78 (d, J=8.0, 2H), 7.33 (d, J=7.9, 2H), 2.44 (s, 3H)

Xie, Aming; Zhou, Xiangxiang; Feng, Liandong; Hu, Xinyu; Dong, Wei; Tetrahedron; vol. 70; nb. 21; (2014); p. 3514 - 3519, View in Reaxys 37 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Original Text (NMR Spectroscopy)

13C

Location

supporting information

Signals [ppm]

191.89; 145.44; 134.09; 129.75; 129.61; 21.78

NMR (75 MHz, CDCl3) δ 191.89, 145.44, 134.09, 129.75, 129.61, 21.78

Xie, Aming; Zhou, Xiangxiang; Feng, Liandong; Hu, Xinyu; Dong, Wei; Tetrahedron; vol. 70; nb. 21; (2014); p. 3514 - 3519, View in Reaxys

84/464

2016-04-07 09:00:27

38 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

600

Location

supporting information

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 39 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

150

Location

supporting information

Ma, Xinyi; Li, Zhongfeng; Liu, Feijie; Cao, Shengli; Rao, Honghua; Advanced Synthesis and Catalysis; vol. 356; nb. 8; (2014); p. 1741 - 1746, View in Reaxys 40 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 41 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Luo, Qun-Li; Nan, Wen-Hui; Li, Yu; Chen, Xiang; Arkivoc; vol. 2014; nb. 4; (2014); p. 350 - 361, View in Reaxys 42 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

85/464

2016-04-07 09:00:27

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Liu, Bing; Ben, Teng; Xu, Jun; Deng, Feng; Qiu, Shilun; New Journal of Chemistry; vol. 38; nb. 6; (2014); p. 2292 - 2299, View in Reaxys 43 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

22.84

Location

supporting information

Farsani, Mostafa Riahi; Jalilian, Fariba; Yadollahi, Bahram; Rudbari, Hadi Amiri; Polyhedron; vol. 76; (2014); p. 102 - 107, View in Reaxys 44 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

151

Location

supporting information

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 45 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Location

supporting information

Wang, Zhao-Gang; Jin, Yong; Cao, Xiao-Hua; Lu, Ming; New Journal of Chemistry; vol. 38; nb. 9; (2014); p. 4149 - 4154, View in Reaxys 46 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

86/464

2016-04-07 09:00:27

Tan, Da-Wei; Xie, Jing-Bo; Li, Qi; Li, Hong-Xi; Li, Jun-Chi; Li, Hai-Yan; Lang, Jian-Ping; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14061 - 14071, View in Reaxys 47 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Tan, Da-Wei; Xie, Jing-Bo; Li, Qi; Li, Hong-Xi; Li, Jun-Chi; Li, Hai-Yan; Lang, Jian-Ping; Dalton Transactions; vol. 43; nb. 37; (2014); p. 14061 - 14071, View in Reaxys 48 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 49 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Mitchell, Lorna J.; Moody, Christopher J.; Journal of Organic Chemistry; vol. 79; nb. 22; (2014); p. 11091 - 11100, View in Reaxys 50 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Description (NMR Spec- Chemical shifts; Spectrum troscopy)

87/464

2016-04-07 09:00:27

Nucleus (NMR Spectroscopy)

Temperature (NMR Spectroscopy) [°C]

-80.16

Location

supporting information

Pardo, Pilar; Carmona, Daniel; Lamata, Pilar; Rodrguez, Ricardo; Lahoz, Fernando J.; Garca-Ordua, Pilar; Oro, Luis A.; Organometallics; vol. 33; nb. 23; (2014); p. 6927 - 6936, View in Reaxys 52 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Zhu, Xiao; Yang, Daoshan; Wei, Wei; Jiang, Min; Li, Lulu; Zhu, Xiangbing; You, Jinmao; Wang, Hua; RSC Advances; vol. 4; nb. 110; (2014); p. 64930 - 64935, View in Reaxys 53 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

303

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 54 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Al-Etaibi, Alya M.; Al-Awadi, Nouria A.; Ibrahim, Maher R.; Ibrahim, Yehia A.; Arkivoc; vol. 2010; nb. 10; (2010); p. 149 - 162, View in Reaxys; Lin, Cheng-Kun; Lu, Ta-Jung; Tetrahedron; vol. 66; nb. 51; (2010); p. 9688 - 9693, View in Reaxys; Wang, Lian-Yue; Li, Jun; Lv, Ying; Zhang, Heng-Yun; Gao, Shuang; Journal of Organometallic Chemistry; vol. 696; nb. 20; (2011); p. 3257 - 3263, View in Reaxys; Shi, Xiang-Jun; Qian, Jie; Tan, Fan-Fan; Yu, Chuan-Ming; Journal of Chemical Research; vol. 37; nb. 7; (2013); p. 398 - 401, View in Reaxys 55 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

88/464

2016-04-07 09:00:27

Lin, Cheng-Kun; Lu, Ta-Jung; Tetrahedron; vol. 66; nb. 51; (2010); p. 9688 - 9693, View in Reaxys; Beldar; Sharma, Mamta; E-Journal of Chemistry; vol. 8; nb. 1; (2011); p. 288 - 292, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys 56 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Location

supporting information

Rajabi, Fatemeh; Karimi, Nafiseh; Saidi, Mohammad Reza; Primo, Ana; Varma, Rajender S.; Luque, Rafael; Advanced Synthesis and Catalysis; vol. 354; nb. 9; (2012); p. 1707 - 1711, View in Reaxys; Rajabi, Fatemeh; Pineda, Antonio; Naserian, Sareh; Balu, Alina Mariana; Luque, Rafael; Romero, Antonio A.; Green Chemistry; vol. 15; nb. 5; (2013); p. 1232 - 1237, View in Reaxys 57 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Temperature (NMR Spectroscopy) [°C]

Location

supporting information

Ohzu, Shingo; Ishizuka, Tomoya; Hirai, Yuichirou; Fukuzumi, Shunichi; Kojima, Takahiko; Chemistry - A European Journal; vol. 19; nb. 5; (2013); p. 1563 - 1567, View in Reaxys 58 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- [D3]acetonitrile scopy) Location

supporting information

Lee, Jia Ying; Fan, Wai Yip; Mak, Kar Hang Garvin; Leong, Weng Kee; Journal of Organometallic Chemistry; vol. 724; (2013); p. 275 - 280, View in Reaxys 59 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

27.04

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Fretz, Samuel J.; Hadad, Christopher M.; Hart, David J.; Vyas, Shubham; Yang, Dexi; Journal of Organic Chemistry; vol. 78; nb. 1; (2013); p. 83 - 92, View in Reaxys 60 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

27.04

Frequency (NMR Spectroscopy) [MHz]

100.6

89/464

2016-04-07 09:00:27

Location

supporting information

Fretz, Samuel J.; Hadad, Christopher M.; Hart, David J.; Vyas, Shubham; Yang, Dexi; Journal of Organic Chemistry; vol. 78; nb. 1; (2013); p. 83 - 92, View in Reaxys 61 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Kamimura, Akio; Nozaki, Yuichiro; Nishiyama, Mai; Nakayama, Masaharu; RSC Advances; vol. 3; nb. 2; (2013); p. 468 - 472, View in Reaxys 62 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

126

Kamimura, Akio; Nozaki, Yuichiro; Nishiyama, Mai; Nakayama, Masaharu; RSC Advances; vol. 3; nb. 2; (2013); p. 468 - 472, View in Reaxys 63 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys 64 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

300

Das, Pralay; Aggarwal, Nidhi; Guha, Nitul Ranjan; Tetrahedron Letters; vol. 54; nb. 23; (2013); p. 2924 - 2928, View in Reaxys 65 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

90/464

2016-04-07 09:00:27

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

Das, Pralay; Aggarwal, Nidhi; Guha, Nitul Ranjan; Tetrahedron Letters; vol. 54; nb. 23; (2013); p. 2924 - 2928, View in Reaxys 66 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

126

Location

supporting information

Kamimura, Akio; Komatsu, Hiroyuki; Moriyama, Takaaki; Nozaki, Yuichiro; Tetrahedron; vol. 69; nb. 29; (2013); p. 5968 - 5972, View in Reaxys 67 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013-U0386-L, View in Reaxys 68 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013-U0386-L, View in Reaxys 69 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

21.1

Location

supporting information

Description (NMR Spec- Chemical shifts; Spectrum troscopy)

91/464

2016-04-07 09:00:27

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

21.5

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Rohitha; Kulkarni; Narender; Synthetic Communications; vol. 43; nb. 21; (2013); p. 2853 - 2866, View in Reaxys 72 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

An, Gwangil; Ahn, Hyunseok; De Castro, Kathlia A.; Rhee, Hakjune; Synthesis; nb. 3; (2010); p. 477 - 485; Art.No: F19009SS, View in Reaxys; Han, Mikyoung; Jeong, Ku Sun; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 7; (2012); p. 2405 - 2406, View in Reaxys 73 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 - 2685, View in Reaxys; Srogl, Jiri; Voltrova, Svatava; Organic Letters; vol. 11; nb. 4; (2009); p. 843 - 845, View in Reaxys; Yin, Weili; Chu, Changhu; Lu, Qiongqiong; Tao, Jianwei; Liang, Xinmiao; Liu, Renhua; Advanced Synthesis and Catalysis; vol. 352; nb. 1; (2010); p. 113 - 118, View in Reaxys; Uyanik, Muhammet; Fukatsu, Ryota; Ishihara, Kazuaki; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 456 - 460, View in Reaxys; Chu, Guobiao; Li, Chunbao; Organic and Biomolecular Chemistry; vol. 8; nb. 20; (2010); p. 4716 - 4719, View in Reaxys; TuckerSchwartz, Alexander K.; Garrell, Robin L.; Chemistry - A European Journal; vol. 16; nb. 42; (2010); p. 12718 - 12726, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 74 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy)

92/464

2016-04-07 09:00:27

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 - 2685, View in Reaxys; Uyanik, Muhammet; Fukatsu, Ryota; Ishihara, Kazuaki; Chemistry - An Asian Journal; vol. 5; nb. 3; (2010); p. 456 - 460, View in Reaxys; Tucker-Schwartz, Alexander K.; Garrell, Robin L.; Chemistry A European Journal; vol. 16; nb. 42; (2010); p. 12718 - 12726, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 75 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Miao, Cheng-Xia; He, Liang-Nian; Wang, Jin-Quan; Wang, Jing-Lun; Advanced Synthesis and Catalysis; vol. 351; nb. 13; (2009); p. 2209 - 2216, View in Reaxys; Miao, Cheng-Xia; He, Liang-Nian; Wang, Jing-Lun; Wu, Fang; Journal of Organic Chemistry; vol. 75; nb. 1; (2010); p. 257 - 260, View in Reaxys; Miao, Cheng-Xia; Yu, Bing; He, Liang-Nian; Green Chemistry; vol. 13; nb. 3; (2011); p. 541 - 544, View in Reaxys; Sun, Hua-Yin; Hua, Qing; Guo, Feng-Feng; Wang, Zhi-Yong; Huang, Wei-Xin; Advanced Synthesis and Catalysis; vol. 354; nb. 4; (2012); p. 569 573, View in Reaxys 76 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

300

Singh, Savita J.; Jayaram, Radha V.; Synthetic Communications; vol. 42; nb. 3; (2012); p. 299 - 308, View in Reaxys 78 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

93/464

2016-04-07 09:00:27

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

100.6

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 79 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

600

Location

supporting information

Hamasaki, Akiyuki; Kuwada, Hideyuki; Tokunaga, Makoto; Tetrahedron Letters; vol. 53; nb. 7; (2012); p. 811 - 814, View in Reaxys 80 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

150

Location

supporting information

Hamasaki, Akiyuki; Kuwada, Hideyuki; Tokunaga, Makoto; Tetrahedron Letters; vol. 53; nb. 7; (2012); p. 811 - 814, View in Reaxys 81 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

125.8

Location

supporting information

Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei; Journal of the American Chemical Society; vol. 134; nb. 8; (2012); p. 3643 - 3646, View in Reaxys; Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei; Angewandte Chemie - International Edition; vol. 51; nb. 51; (2012); p. 12790 - 12794; Angew. Chem.; (2012); p. 12962 - 12966, View in Reaxys 82 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Bekhradnia, Ahmad R.; Arshadi, Sattar; Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry; vol. 42; nb. 5; (2012); p. 705 - 710, View in Reaxys

94/464

2016-04-07 09:00:27

83 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

22.5

Bekhradnia, Ahmad R.; Arshadi, Sattar; Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry; vol. 42; nb. 5; (2012); p. 705 - 710, View in Reaxys 84 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Coupling Nuclei

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Original Text (NMR Spectroscopy)

δH: 2.42 (s, 3H, CH3), 7.31 (d, 2H, J = 7.8 Hz, Ar-H), 7.76 (d, 2H, J = 7.6 Hz, Ar-H), 9.95 (s, 1H, CH=O) ppm

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 85 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Original Text (NMR Spectroscopy)

δC: 22.0, 129.7, 129.8, 134.2, 145.5, 191.9 ppm

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 86 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

150

Location

supporting information

Yuan, Yu; Shi, Xiao; Liu, Wei; Synlett; nb. 4; (2011); p. 559 - 564; Art.No: W17710ST, View in Reaxys 87 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy)

95/464

2016-04-07 09:00:27

Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys 88 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Mamros, Audrey N.; Sharrow, Phillip R.; Weller, William E.; Luderer, Mark R.; Fair, Justin D.; Pazehoski, Kristina O.; Luderer, Matthew R.; Arkivoc; vol. 2011; nb. 5; (2011); p. 23 - 33, View in Reaxys 89 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Hong, Haiyan; Hu, Lei; Li, Min; Zheng, Junwei; Sun, Xuhui; Lu, Xinhua; Cao, Xueqin; Lu, Jianmei; Gu, Hongwei; Chemistry - A European Journal; vol. 17; nb. 31; (2011); p. 8726 - 8730, View in Reaxys 90 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]

Frequency (NMR Spectroscopy) [MHz]

100

Location

supporting information

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys; Dadhania, Abhishek N.; Patel, Vaibhav K.; Raval, Dipak K.; Journal of the Brazilian Chemical Society; vol. 22; nb. 3; (2011); p. 511 - 516, View in Reaxys 92 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Location

supporting information

Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao; Chemistry - A European Journal; vol. 14; nb. 9; (2008); p. 2679 - 2685, View in Reaxys; Moorthy, Jarugu Narasimha; Senapati, Kalyan; Parida, Keshaba Nanda; Jhulki,

96/464

2016-04-07 09:00:27

Samik; Sooraj, Kunnikuruvan; Nair, Nisanth N.; Journal of Organic Chemistry; vol. 76; nb. 23; (2011); p. 9593 9601, View in Reaxys 93 of 163

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- [D3]acetonitrile scopy) Location

supporting information

Ohkubo, Kei; Mizushima, Kentaro; Iwata, Ryosuke; Souma, Kazunori; Suzuki, Nobuo; Fukuzumi, Shunichi; Chemical Communications; vol. 46; nb. 4; (2010); p. 601 - 603, View in Reaxys 94 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 95 of 163

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 96 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 97 of 163

Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Frequency (NMR Spectroscopy) [MHz]

Location

supporting information

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 98 of 163

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- [(2)H6]acetone scopy)

97/464

2016-04-07 09:00:27

Original Text (NMR Spectroscopy)

9.99 (1H, s), 7.82 (2H, d), 7.42 (2H, d), 2.44 (3H, s).

Comment (NMR Spectroscopy)

Signals given

Patent; SYRACUSE UNIVERSITY; US2009/43134; (2009); (A1) English, View in Reaxys 99 of 163

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- [D3]acetonitrile scopy) Original Text (NMR Spectroscopy)

9.99 (1H, s), 7.78 (2H, d), 7.39 (2H, d), 2.41 (3H, s)

Comment (NMR Spectroscopy)

Signals given

Patent; SYRACUSE UNIVERSITY; US2009/43134; (2009); (A1) English, View in Reaxys 100 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Frequency (NMR Spectroscopy) [MHz]

400

Location

supporting information

Srogl, Jiri; Voltrova, Svatava; Organic Letters; vol. 11; nb. 4; (2009); p. 843 - 845, View in Reaxys 101 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Sato, Kazuhiko; Aoki, Masao; Takagi, Junko; Zimmermann, Klaus; Noyori, Ryoji; Bulletin of the Chemical Society of Japan; vol. 72; nb. 10; (1999); p. 2287 - 2306, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Organic Letters; vol. 7; nb. 17; (2005); p. 3689 - 3692, View in Reaxys; Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 - 6292, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7087 - 7090, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 72; nb. 18; (2007); p. 7030 - 7033, View in Reaxys; Wang, Guangjun; Li, Zhengwei; Ha, Chengyong; Ding, Ke; Synthetic Communications; vol. 38; nb. 10; (2008); p. 1629 - 1637, View in Reaxys 102 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Sato, Kazuhiko; Aoki, Masao; Takagi, Junko; Zimmermann, Klaus; Noyori, Ryoji; Bulletin of the Chemical Society of Japan; vol. 72; nb. 10; (1999); p. 2287 - 2306, View in Reaxys; Su, Weike; Jin, Can; Journal of Chemical Research; nb. 3; (2004); p. 188 - 189, View in Reaxys; Liu, Renhua; Dong, Chunyan; Liang, Xinmiao; Wang, Xiujuan; Hu, Xinquan; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 729 - 731, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Organic Letters; vol. 7; nb. 17; (2005); p. 3689 - 3692, View in Reaxys; Cooper, Thea; Novak, Andrew; Humphreys, Luke D.; Walker, Matthew D.; Woodward, Simon; Advanced Synthesis and Catalysis; vol. 348; nb. 6; (2006); p. 686 - 690, View in Reaxys; Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 - 6292, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7087 - 7090, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 72; nb. 18; (2007); p. 7030 - 7033, View in Reaxys; Moorthy, Jarugu Narasimha; Singhal, Nidhi; Senapati, Kalyan; Organic and Biomolecular Chemistry; vol. 5; nb. 5; (2007); p. 767 - 771, View in Reaxys; Wang,

98/464

2016-04-07 09:00:27

Guangjun; Li, Zhengwei; Ha, Chengyong; Ding, Ke; Synthetic Communications; vol. 38; nb. 10; (2008); p. 1629 1637, View in Reaxys 103 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Lermontov; Yurkova; Russian Chemical Bulletin; vol. 57; nb. 12; (2008); p. 2561 - 2563, View in Reaxys 104 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys 105 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys 106 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

500

Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys 107 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys 108 of 163 Description (NMR Spec- Spectrum troscopy)

99/464

2016-04-07 09:00:27

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

125

Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys 109 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

54.6

Podder, Susmita; Choudhury, Joyanta; Roy, Ujjal Kanti; Roy, Sujit; Journal of Organic Chemistry; vol. 72; nb. 8; (2007); p. 3100 - 3103, View in Reaxys 110 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

54.6

Podder, Susmita; Choudhury, Joyanta; Roy, Ujjal Kanti; Roy, Sujit; Journal of Organic Chemistry; vol. 72; nb. 8; (2007); p. 3100 - 3103, View in Reaxys 111 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

-273.16

Frequency (NMR Spectroscopy) [MHz]

300.26

Gregg, Brian T.; Golden, Kathryn C.; Quinn, John F.; Journal of Organic Chemistry; vol. 72; nb. 15; (2007); p. 5890 - 5893, View in Reaxys 112 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

100/464

2016-04-07 09:00:27

Liu, Renhua; Dong, Chunyan; Liang, Xinmiao; Wang, Xiujuan; Hu, Xinquan; Journal of Organic Chemistry; vol. 70; nb. 2; (2005); p. 729 - 731, View in Reaxys; Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 - 6292, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7087 - 7090, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 72; nb. 18; (2007); p. 7030 - 7033, View in Reaxys 113 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys; Moorthy, Jarugu Narasimha; Singhal, Nidhi; Senapati, Kalyan; Organic and Biomolecular Chemistry; vol. 5; nb. 5; (2007); p. 767 - 771, View in Reaxys 114 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Moorthy, Jarugu Narasimha; Singhal, Nidhi; Senapati, Kalyan; Organic and Biomolecular Chemistry; vol. 5; nb. 5; (2007); p. 767 - 771, View in Reaxys 115 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Reynolds, Kelly A.; Finn; Journal of Organic Chemistry; vol. 62; nb. 8; (1997); p. 2574 - 2593, View in Reaxys; Shaikh, Tanveer Mahammad Ali; Emmanuvel, Lourdusamy; Sudalai, Arumugam; Journal of Organic Chemistry; vol. 71; nb. 13; (2006); p. 5043 - 5046, View in Reaxys 116 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Baillargeon,V.P.; Stille,J.K.; Journal of the American Chemical Society; vol. 108; (1986); p. 452, View in Reaxys; Bromilow, John; Brownlee, Robert T. C.; Craik, David J.; Sadek, Maruse; Taft, Robert W.; Journal of Organic Chemistry; vol. 45; nb. 12; (1980); p. 2429 - 2438, View in Reaxys; Bromilow, John; Brownlee, Robert T. C.; Craik, David J.; Fiske, Peter R.; Rowe, Jeffrey E.; Sadek, Maruse; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 753 - 759, View in Reaxys; Lijser, H. J. P. de; Arnold, Donald R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1997); p. 1369 - 1380, View in Reaxys; Peterson, Karl P.; Larock, Richard C.; Journal of Organic Chemistry; vol. 63; nb. 10; (1998); p. 3185 - 3189, View in Reaxys; Nyquist, R. A.; Hasha, D. L.; Applied Spectroscopy; vol. 45; nb. 5; (1991); p. 849 - 859, View in Reaxys; Shaikh, Tanveer Mahammad Ali; Emmanuvel, Lourdusamy; Sudalai, Arumugam; Journal of Organic Chemistry; vol. 71; nb. 13; (2006); p. 5043 - 5046, View in Reaxys 117 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

400

101/464

2016-04-07 09:00:27

View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Journal of Organic Chemistry; vol. 71; nb. 18; (2006); p. 7087 7090, View in Reaxys 118 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Lai; Lee; Synthesis; nb. 11; (2001); p. 1645 - 1648, View in Reaxys; Shaikh, Tanveer Mahammad Ali; Emmanuvel, Lourdusamy; Sudalai, Arumugam; Journal of Organic Chemistry; vol. 71; nb. 13; (2006); p. 5043 - 5046, View in Reaxys 119 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

200

Lai; Lee; Synthesis; nb. 11; (2001); p. 1645 - 1648, View in Reaxys; Shaikh, Tanveer Mahammad Ali; Emmanuvel, Lourdusamy; Sudalai, Arumugam; Journal of Organic Chemistry; vol. 71; nb. 13; (2006); p. 5043 - 5046, View in Reaxys 120 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys 121 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

100

Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 - 6292, View in Reaxys 122 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Shaikh, Tanveer Mahammad Ali; Emmanuvel, Lourdusamy; Sudalai, Arumugam; Journal of Organic Chemistry; vol. 71; nb. 13; (2006); p. 5043 - 5046, View in Reaxys 123 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

102/464

2016-04-07 09:00:27

Gogoi, Pranjal; Hazarika, Parasa; Konwar, Dilip; Journal of Organic Chemistry; vol. 70; nb. 5; (2005); p. 1934 - 1936, View in Reaxys 124 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Ali; Wiggin; Synthetic Communications; vol. 31; nb. 9; (2001); p. 1389 - 1397, View in Reaxys; Dijksman; MarinoGonzalez; Payeras; Arends; Sheldon; Journal of the American Chemical Society; vol. 123; nb. 28; (2001); p. 6826 - 6833, View in Reaxys; Ohkubo, Kei; Suga, Kyou; Morikawa, Kohei; Fukuzumi, Shunichi; Journal of the American Chemical Society; vol. 125; nb. 42; (2003); p. 12850 - 12859, View in Reaxys; Dijksman, Arne; Arends, Isabel W C E; Sheldon, Roger A; Organic and biomolecular chemistry; vol. 1; nb. 18; (2003); p. 3232 - 3237, View in Reaxys; Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys 125 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

300

Ali; Wiggin; Synthetic Communications; vol. 31; nb. 9; (2001); p. 1389 - 1397, View in Reaxys; Dijksman; MarinoGonzalez; Payeras; Arends; Sheldon; Journal of the American Chemical Society; vol. 123; nb. 28; (2001); p. 6826 - 6833, View in Reaxys; Dijksman, Arne; Arends, Isabel W C E; Sheldon, Roger A; Organic and biomolecular chemistry; vol. 1; nb. 18; (2003); p. 3232 - 3237, View in Reaxys; Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys 126 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- tetradeuteriomethanol scopy) Frequency (NMR Spectroscopy) [MHz]

500

Sheu, Ming-Thau; Wu, Jender; Chen, Chih-Jui; Chao, Su-Hui; Wu, An-Bang; Tetrahedron Letters; vol. 45; nb. 43; (2004); p. 8107 - 8109, View in Reaxys 127 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- tetradeuteriomethanol scopy) Sheu, Ming-Thau; Wu, Jender; Chen, Chih-Jui; Chao, Su-Hui; Wu, An-Bang; Tetrahedron Letters; vol. 45; nb. 43; (2004); p. 8107 - 8109, View in Reaxys 128 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- various solvent(s) scopy) Tan, Jianwen; Bednarek, Pawel; Liu, Jikai; Schneider, Bernd; Svatos, Ales; Hahlbrock, Klaus; Phytochemistry; vol. 65; nb. 6; (2004); p. 691 - 699, View in Reaxys

103/464

2016-04-07 09:00:27

129 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Baillargeon,V.P.; Stille,J.K.; Journal of the American Chemical Society; vol. 108; (1986); p. 452, View in Reaxys; Turro, Nicholas J.; Mattay, Jochen; Journal of the American Chemical Society; vol. 103; nb. 14; (1981); p. 4200 4204, View in Reaxys; Goetz-Schatowitz, P.-R.; Struth, G.; Voss, J.; Wiegand, G.; Journal fuer Praktische Chemie/ Chemiker-Zeitung; vol. 335; nb. 3; (1993); p. 230 - 234, View in Reaxys; Shul'pin, G. B.; Nizova, G. V.; Serdobov, M. V.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 2; (1987); p. 461 - 464,402 - 404, View in Reaxys; Oshima, Takumi; Nagai, Toshikazu; Bulletin of the Chemical Society of Japan; vol. 53; nb. 3; (1980); p. 726 - 730, View in Reaxys; Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys; Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys; Baudin, Jean-Bernard; Commenil, Marie-Gabrielle; Julia, Sylvestre A.; Lome, Robert; Ruel, Odile; Bulletin de la Societe Chimique de France; vol. 133; nb. 11; (1996); p. 1127 - 1141, View in Reaxys; Lijser, H. J. P. de; Arnold, Donald R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1997); p. 1369 - 1380, View in Reaxys; Nyquist, R. A.; Hasha, D. L.; Applied Spectroscopy; vol. 45; nb. 5; (1991); p. 849 - 859, View in Reaxys; Koo, Bon-Suk; Lee, Chang Keun; Lee, Kee-Jung; Synthetic Communications; vol. 32; nb. 14; (2002); p. 2115 - 2123, View in Reaxys 131 of 163 Nucleus (NMR Spectroscopy) Coupling Nuclei

1H 1H

Solvents (NMR Spectro- CDCl3 scopy) Koo, Bon-Suk; Lee, Chang Keun; Lee, Kee-Jung; Synthetic Communications; vol. 32; nb. 14; (2002); p. 2115 - 2123, View in Reaxys 132 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

Ali; Wiggin; Synthetic Communications; vol. 31; nb. 9; (2001); p. 1389 - 1397, View in Reaxys 133 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

Lai; Lee; Synthesis; nb. 11; (2001); p. 1645 - 1648, View in Reaxys 134 of 163 Description (NMR Spec- Spectrum troscopy)

104/464

2016-04-07 09:00:27

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- tetrahydrofuran scopy) Temperature (NMR Spectroscopy) [°C]

-60

Reynolds, Kelly A.; Finn; Journal of Organic Chemistry; vol. 62; nb. 8; (1997); p. 2574 - 2593, View in Reaxys 135 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- tetrahydrofuran scopy) Reynolds, Kelly A.; Finn; Journal of Organic Chemistry; vol. 62; nb. 8; (1997); p. 2574 - 2593, View in Reaxys 136 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- CCl4 scopy) Temperature (NMR Spectroscopy) [°C]

Dahn, Hans; Pechy, Peter; Van Toan, Vien; Magnetic Resonance in Chemistry; vol. 35; nb. 9; (1997); p. 589 - 592, View in Reaxys 137 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Comment (NMR Spectroscopy)

1H-1H

Baillargeon,V.P.; Stille,J.K.; Journal of the American Chemical Society; vol. 108; (1986); p. 452, View in Reaxys; Turro, Nicholas J.; Mattay, Jochen; Journal of the American Chemical Society; vol. 103; nb. 14; (1981); p. 4200 4204, View in Reaxys; Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 578, View in Reaxys; Baudin, Jean-Bernard; Commenil, Marie-Gabrielle; Julia, Sylvestre A.; Lome, Robert; Ruel, Odile; Bulletin de la Societe Chimique de France; vol. 133; nb. 11; (1996); p. 1127 - 1141, View in Reaxys 138 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3; CD2Cl2 scopy) Temperature (NMR Spectroscopy) [°C]

-78

Yamataka, Hiroshi; Nishikawa, Kazuyoshi; Takatsuka, Tsutomu; Hanafusa, Terukiyo; Journal of Physical Organic Chemistry; vol. 8; (1995); p. 35 - 40, View in Reaxys 139 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

-50

105/464

2016-04-07 09:00:27

Mayr, Herbert; Gorath, Gorden; Journal of the American Chemical Society; vol. 117; nb. 30; (1995); p. 7862 - 7867, View in Reaxys 140 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Abraham, Raymond J.; Angiolini, Simone; Edgar, Mark; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1973 - 1980, View in Reaxys 141 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Abraham, Raymond J.; Angiolini, Simone; Edgar, Mark; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1973 - 1980, View in Reaxys 142 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

-50

Comment (NMR Spectroscopy)

1H-1H.

Mayr, Herbert; Gorath, Gorden; Journal of the American Chemical Society; vol. 117; nb. 30; (1995); p. 7862 - 7867, View in Reaxys 143 of 163 Description (NMR Spec- NMR with shift reagents troscopy) Abraham, Raymond J.; Angiolini, Simone; Edgar, Mark; Sancassan, Fernando; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 11; (1995); p. 1973 - 1980, View in Reaxys 144 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- aq. H2SO4 scopy) Freiberg, W.; Roth, H.; Becken, B.; Kroeger, C. -F.; Journal fuer Praktische Chemie/Chemiker-Zeitung; vol. 335; nb. 6; (1993); p. 563 - 565, View in Reaxys 145 of 163 Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CS2; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

106/464

2016-04-07 09:00:27

Schaefer, Ted; Sebastian, Rudy; Canadian Journal of Chemistry; vol. 70; nb. 10; (1992); p. 2555 - 2557, View in Reaxys 146 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CDCl3; various solvent(s) scopy) Yamamoto, Yoshinori; Nakada, Tomohisa; Nemoto, Hisao; Journal of the American Chemical Society; vol. 114; nb. 1; (1992); p. 121 - 125, View in Reaxys 147 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3; various solvent(s) scopy) Yamamoto, Yoshinori; Nakada, Tomohisa; Nemoto, Hisao; Journal of the American Chemical Society; vol. 114; nb. 1; (1992); p. 121 - 125, View in Reaxys 148 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- acetone-d6 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Schaefer, Ted; Sebastian, Rudy; Canadian Journal of Chemistry; vol. 70; nb. 10; (1992); p. 2555 - 2557, View in Reaxys 149 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- CS2; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Schaefer, Ted; Sebastian, Rudy; Canadian Journal of Chemistry; vol. 70; nb. 10; (1992); p. 2555 - 2557, View in Reaxys 150 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CS2; cyclohexane-d12 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Comment (NMR Spectroscopy)

1H-1H.

Schaefer, Ted; Sebastian, Rudy; Canadian Journal of Chemistry; vol. 70; nb. 10; (1992); p. 2555 - 2557, View in Reaxys 151 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- acetone-d6 scopy)

107/464

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Temperature (NMR Spectroscopy) [°C]

23.9

Comment (NMR Spectroscopy)

1H-1H.

Schaefer, Ted; Sebastian, Rudy; Canadian Journal of Chemistry; vol. 70; nb. 10; (1992); p. 2555 - 2557, View in Reaxys 152 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- neat (no solvent) scopy) Antony, T. V.; Xavier, N.; Arulraj, S. J.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 27; nb. 1-12; (1988); p. 158 - 159, View in Reaxys 153 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Solvents (NMR Spectro- acetonitrile scopy) Temperature (NMR Spectroscopy) [°C]

Boykin, D. W.; Balakrishnan, P.; Baumstark, A. L.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 248 - 250, View in Reaxys 154 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Temperature (NMR Spectroscopy) [°C]

Comment (NMR Spectroscopy)

13C-13C.

Krishnamurthy, V. V.; Prakash, G. K. Surya; Iyer, Pradeep S.; Olah, George A.; Journal of the American Chemical Society; vol. 106; nb. 23; (1984); p. 7068 - 7073, View in Reaxys 155 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

Solvents (NMR Spectro- liquid HF; various solvent(s) scopy) Rimmelin, Paul; Schwartz, Sylvie; Sommer, Jean; Organic Magnetic Resonance; vol. 16; nb. 2; (1981); p. 160 163, View in Reaxys 156 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- 1,1,2-trichloro-1,2,2-trifluoro-ethane scopy) Temperature (NMR Spectroscopy) [°C]

-142

Drakenberg, Torbjoern; Sommer, Jean; Jost, Roland; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 363 - 369, View in Reaxys

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157 of 163 Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- acetone-d6 scopy) Nakai, Yoshimi; Takabayashi, Tetsuo; Yamada, Fukiko; Organic Magnetic Resonance; vol. 13; nb. 2; (1980); p. 94 - 96, View in Reaxys 158 of 163 Description (NMR Spec- NMR troscopy) Schiess,P.; Fuenfschilling,P.; Helvetica Chimica Acta; vol. 59; (1976); p. 1745 - 1755, View in Reaxys; Olah,G.A.; Forsyth,D.A.; Journal of the American Chemical Society; vol. 97; nb. 11; (1975); p. 3137 - 3141, View in Reaxys; van Putten; Pavlik; Tetrahedron; vol. 27; (1941); p. 3007, View in Reaxys; Garwood et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1975); p. 2471, View in Reaxys; Klinck; Stothers; Canadian Journal of Chemistry; vol. 40; (1962); p. 1071,1073, View in Reaxys; Nikki; Nakagawa; Bulletin of the Chemical Society of Japan; vol. 51; (1978); p. 3267,3269, View in Reaxys; Salomon; Reuter; Journal of the American Chemical Society; vol. 99; (1977); p. 4372,4377, View in Reaxys; Stothers; Lauterbur; Canadian Journal of Chemistry; vol. 42; (1964); p. 1563,1572, View in Reaxys; Inamoto et al.; Tetrahedron Letters; (1977); p. 737,739, View in Reaxys; Drakenberg; Journal of the Chemical Society, Chemical Communications; (1974); p. 1011, View in Reaxys; Jost et al.; Journal of the Chemical Society [Section] D: Chemical Communications; (1971); p. 879, View in Reaxys; Anteunis; Rommelaere; Bulletin des Societes Chimiques Belges; vol. 75; (1966); p. 89, View in Reaxys; Cartledge; Riedel; Journal of Organometallic Chemistry; vol. 34; (1972); p. 11,13, View in Reaxys; Rabinowitz; Grinvald; Journal of the American Chemical Society; vol. 94; (1972); p. 2724,2725, View in Reaxys; Inamoto et al.; Chemistry Letters; (1972); p. 107,109, View in Reaxys; Engel; Nathan; Journal of the Chemical Society [Section] C: Organic; (1971); p. 3844, View in Reaxys; Grinvald; Rabinovitz; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1974); p. 94, View in Reaxys; Yamamoto et al.; Analytical Chemistry; vol. 44; (1972); p. 1794, View in Reaxys; Grindley et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1975); p. 443, View in Reaxys; Beistel; Edwards; Journal of Physical Chemistry; vol. 80; (1976); p. 2023, View in Reaxys; Crampton; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1975); p. 185, View in Reaxys; Klinck; Stothers; Canadian Journal of Chemistry; vol. 40; (1962); p. 2329,2331, View in Reaxys; Fritz; Kreiter; Journal of Organometallic Chemistry; vol. 7; (1967); p. 427,429, View in Reaxys 159 of 163 Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

13C

Inamoto et al.; Tetrahedron Letters; (1976); p. 3707, View in Reaxys 160 of 163 Description (NMR Spec- Spin-spin coupling constants troscopy) Bildsoe; Schaumburg; Journal of Magnetic Resonance (1969-1992); vol. 14; (1974); p. 223, View in Reaxys; Hammel; Smith; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1970); p. 1852, View in Reaxys; Sommer et al.; Journal of Magnetic Resonance (1969-1992); vol. 21; (1976); p. 93,96, View in Reaxys; Yoder et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 385, View in Reaxys; Fritz; Kreiter; Journal of Organometallic Chemistry; vol. 7; (1967); p. 427,429, View in Reaxys 161 of 163 Description (NMR Spec- Chemical shifts troscopy) Bildsoe; Schaumburg; Journal of Magnetic Resonance (1969-1992); vol. 14; (1974); p. 223, View in Reaxys 162 of 163 Description (NMR Spec- Spectrum troscopy) Yoder et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 539, View in Reaxys 163 of 163 Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

graph.

Kowalewski; Kowalewski; Anales de la Asociacion Quimica Argentina (1921-2001); vol. 48; (1960); p. 157,160, View in Reaxys IR Spectroscopy (37)

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2016-04-07 09:00:27

1 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Location

supporting information

Gonzalez-De-Castro, Angela; Xiao, Jianliang; Journal of the American Chemical Society; vol. 137; nb. 25; (2015); p. 8206 - 8218, View in Reaxys; Bosco, A. John; Lawrence; Christopher; Radhakrishnan; Joseph Rosario, A. Arul; Raja; Vasudevan; Journal of Physical Organic Chemistry; vol. 28; nb. 9; (2015); p. 591 - 595, View in Reaxys 2 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Larrea, Edurne S.; Fernndez De Luis, Roberto; Orive, Joseba; Iglesias, Marta; Arriortua, Mara I.; European Journal of Inorganic Chemistry; vol. 2015; nb. 28; (2015); p. 4699 - 4707, View in Reaxys 3 of 37

Description (IR Spectroscopy)

Bands

Original Text (IR Spectroscopy)

IR (film, cm-1): 2926, 1702, 1605, 1168, 808

Comment (IR Spectroscopy)

film

Signals [cm-1]

2926; 1702; 1605; 1168; 808

Zhao, Hong; Chen, Qiurong; Wei, Li; Jiang, Yuanyuan; Cai, Mingzhong; Tetrahedron; vol. 71; nb. 46; (2015); p. 8725 - 8731; Art.No: 27151, View in Reaxys 4 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 772 - 780, View in Reaxys 5 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

film

Jiang, Jianwen; Wang, Pingping; Cai, Mingzhong; Journal of Chemical Research; vol. 38; nb. 4; (2014); p. 218 222, View in Reaxys 6 of 37

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Tabata, Masayuki; Moriyama, Katsuhiko; Togo, Hideo; European Journal of Organic Chemistry; vol. 2014; nb. 16; (2014); p. 3402 - 3410, View in Reaxys 7 of 37

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands

Solvent (IR Spectroscopy)

neat liquid

Moriyama, Katsuhiko; Takemura, Misato; Togo, Hideo; Journal of Organic Chemistry; vol. 79; nb. 13; (2014); p. 6094 - 6104, View in Reaxys 8 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

chloroform

Location

supporting information

110/464

2016-04-07 09:00:27

Walsh, Katie; Sneddon, Helen F.; Moody, Christopher J.; Organic Letters; vol. 16; nb. 19; (2014); p. 5224 - 5227, View in Reaxys 9 of 37

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 10 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Ali; Wiggin; Synthetic Communications; vol. 31; nb. 9; (2001); p. 1389 - 1397, View in Reaxys; Koo, Bon-Suk; Lee, Chang Keun; Lee, Kee-Jung; Synthetic Communications; vol. 32; nb. 14; (2002); p. 2115 - 2123, View in Reaxys; Jiang, Nan; Ragauskas, Arthur J.; Organic Letters; vol. 7; nb. 17; (2005); p. 3689 - 3692, View in Reaxys; Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys; Hong, BorCherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys; Moorthy, Jarugu Narasimha; Singhal, Nidhi; Senapati, Kalyan; Organic and Biomolecular Chemistry; vol. 5; nb. 5; (2007); p. 767 - 771, View in Reaxys; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron; vol. 69; nb. 14; (2013); p. 2961 - 2970, View in Reaxys 11 of 37

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys 12 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 24; nb. 13; (2013); p. 1707 - 1711; Art.No: ST-2013-U0386-L, View in Reaxys 13 of 37

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

neat liquid

Tucker-Schwartz, Alexander K.; Garrell, Robin L.; Chemistry - A European Journal; vol. 16; nb. 42; (2010); p. 12718 - 12726, View in Reaxys; Suzuki, Yusuke; Iinuma, Masataka; Moriyama, Katsuhiko; Togo, Hideo; Synlett; vol. 23; nb. 8; (2012); p. 1250 - 1256, View in Reaxys 14 of 37

Description (IR Spectroscopy)

Bands

Original Text (IR Spectroscopy)

IR (cm-1): 1686 (υC=O)

Signals [cm-1]

1686

Intensity

s (strong)

Ahmad, Jahir Uddin; Raeisaenen, Minna T.; Kemell, Marianna; Heikkilae, Mikko J.; Leskelae, Markku; Repo, Timo; Applied Catalysis A: General; vol. 449; (2012); p. 153 - 162, View in Reaxys 15 of 37

Description (IR Spectroscopy)

Bands

111/464

2016-04-07 09:00:27

Solvent (IR Spectroscopy)

potassium bromide

Location

supporting information

Yuan, Yu; Shi, Xiao; Liu, Wei; Synlett; nb. 4; (2011); p. 559 - 564; Art.No: W17710ST, View in Reaxys 16 of 37

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

Zhang, Li; Zha, Zhenggen; Wang, Zhiyong; Synlett; nb. 13; (2010); p. 1915 - 1918, View in Reaxys 17 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Comment (IR Spectroscopy)

neat liquid

Lin, Cheng-Kun; Lu, Ta-Jung; Tetrahedron; vol. 66; nb. 51; (2010); p. 9688 - 9693, View in Reaxys 18 of 37

Description (IR Spectroscopy)

Mid IR (MIR); Bands

Solvent (IR Spectroscopy)

potassium bromide

Bratulescu, George; Synthetic Communications; vol. 38; nb. 16; (2008); p. 2748 - 2752, View in Reaxys 19 of 37

Description (IR Spectroscopy)

Bands

Miller et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 891,894, View in Reaxys; Ono; Ueda; Chemical and Pharmaceutical Bulletin; vol. 22; (1974); p. 390,392, 396, View in Reaxys; Rao et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 685,686, View in Reaxys; Lewis; Australian Journal of Chemistry; vol. 17; (1964); p. 814, View in Reaxys; Silver; Wood; Transactions of the Faraday Society; vol. 60; (1964); p. 5, View in Reaxys; Cogrossi; Annali di Chimica (Rome, Italy); vol. 56; (1966); p. 270,278, 279, 282, View in Reaxys; Su, Weike; Jin, Can; Journal of Chemical Research; nb. 3; (2004); p. 188 - 189, View in Reaxys; Sheu, Ming-Thau; Wu, Jender; Chen, Chih-Jui; Chao, Su-Hui; Wu, AnBang; Tetrahedron Letters; vol. 45; nb. 43; (2004); p. 8107 - 8109, View in Reaxys; Podder, Susmita; Choudhury, Joyanta; Roy, Ujjal Kanti; Roy, Sujit; Journal of Organic Chemistry; vol. 72; nb. 8; (2007); p. 3100 - 3103, View in Reaxys 20 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Jain, Nidhi; Kumar, Anil; Chauhan, Shive M.S.; Tetrahedron Letters; vol. 46; nb. 15; (2005); p. 2599 - 2602, View in Reaxys; Gogoi, Pranjal; Hazarika, Parasa; Konwar, Dilip; Journal of Organic Chemistry; vol. 70; nb. 5; (2005); p. 1934 - 1936, View in Reaxys 21 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

dimethylsulfoxide

Velcheva, Evelina A.; Juchnovski, Ivan N.; Binev, Ivan G.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 59; nb. 8; (2003); p. 1745 - 1749, View in Reaxys 22 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

Lai; Lee; Synthesis; nb. 11; (2001); p. 1645 - 1648, View in Reaxys

112/464

2016-04-07 09:00:27

23 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1690 cm**(-1)

Varma, Rajender S.; Dahiya, Rajender; Tetrahedron Letters; vol. 38; nb. 12; (1997); p. 2043 - 2044, View in Reaxys 24 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

2960 - 808 cm**(-1)

Niestroj, Michael; Neumann, Wilhelm P.; Chemische Berichte; vol. 129; nb. 1; (1996); p. 45 - 51, View in Reaxys 25 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

1713 cm**(-1)

Freiberg, W.; Roth, H.; Becken, B.; Kroeger, C. -F.; Journal fuer Praktische Chemie/Chemiker-Zeitung; vol. 335; nb. 6; (1993); p. 563 - 565, View in Reaxys 26 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CCl4

Nyquist, R. A.; Hasha, D. L.; Applied Spectroscopy; vol. 45; nb. 5; (1991); p. 849 - 859, View in Reaxys 27 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1700 - 1690 cm**(-1)

Kolb, Vera M.; Stupar, Joseph W.; Janota, Timothy E.; Duax, William L.; Journal of Organic Chemistry; vol. 54; nb. 10; (1989); p. 2341 - 2346, View in Reaxys 28 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1690 - 810 cm**(-1)

Alcantara, A. R.; Marinas, J. Ma.; Sinisterra, J. V.; Tetrahedron Letters; vol. 28; nb. 14; (1987); p. 1515 - 1518, View in Reaxys 29 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

2725 - 1705 cm**(-1)

Baillargeon,V.P.; Stille,J.K.; Journal of the American Chemical Society; vol. 108; (1986); p. 452, View in Reaxys 30 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gas

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Comment (IR Spectroscopy)

3150 - 800 cm**(-1)

Bandow, Hiroshi; Washida, Nobuaki; Bulletin of the Chemical Society of Japan; vol. 58; nb. 9; (1985); p. 2541 - 2548, View in Reaxys 31 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1690 - 810 cm**(-1)

Gupton, John T.; Polk, Dale E.; Synthetic Communications; vol. 11; nb. 7; (1981); p. 571 - 578, View in Reaxys 32 of 37

Description (IR Spectroscopy)

Schiess,P.; Fuenfschilling,P.; Helvetica Chimica Acta; vol. 59; (1976); p. 1745 - 1755, View in Reaxys; Seguin,J.P. et al.; Bulletin de la Societe Chimique de France; (1974); p. 167 - 172, View in Reaxys; Garwood et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1975); p. 2471, View in Reaxys; Perjessy et al.; Collection of Czechoslovak Chemical Communications; vol. 37; (1972); p. 3302,3304, View in Reaxys; Broxton et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 6845,6848, View in Reaxys; Olah; Welch; Synthesis; (1977); p. 419, View in Reaxys; Rabinowitz; Grinvald; Journal of the American Chemical Society; vol. 94; (1972); p. 2724,2725, View in Reaxys; Penzias; Analytical Chemistry; vol. 45; (1973); p. 890,895, View in Reaxys; Berthelot et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 1771,1772,1774,1776, View in Reaxys; Grinvald; Rabinovitz; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1974); p. 94, View in Reaxys; Wright; Robson; Nature (London, United Kingdom); vol. 222; (1969); p. 290, View in Reaxys; Okada et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 1395,1396,1400, View in Reaxys; Green; Harrison; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 1279,1284,1285, View in Reaxys; Rao et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 685,686, View in Reaxys; Singh; Singh; Indian Journal of Physics (1926-1976); vol. 42; (1968); p. 266, View in Reaxys 33 of 37

Description (IR Spectroscopy)

Spectrum

English,P.J.Q. et al.; Journal of the American Chemical Society; vol. 90; nb. 7; (1968); p. 1767 - 1774, View in Reaxys; Powers et al.; Analytical Chemistry; vol. 32; (1960); p. 1287, View in Reaxys; Saier et al.; Analytical Chemistry; vol. 34; (1962); p. 824, View in Reaxys 34 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CH2Cl2

Comment (IR Spectroscopy)

3333 - 769 cm**(-1)

Blanc; Helvetica Chimica Acta; vol. 41; (1958); p. 625,632, View in Reaxys 35 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

3333 - 769 cm**(-1)

Blanc; Helvetica Chimica Acta; vol. 41; (1958); p. 625,632, View in Reaxys 36 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

Intensitaet der CO-Valenzschwingungsbande bei 1708 cmE-1.

Forbes; Mueller; Canadian Journal of Chemistry; vol. 35; (1957); p. 488,498, View in Reaxys 37 of 37

Description (IR Spectroscopy)

Bands

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Comment (IR Spectroscopy)

4000 cm**(-1)

Ellis; Journal of the American Chemical Society; vol. 51; (1929); p. 1386; Physical Review; vol. <2>32; (1928); p. 906; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1419, View in Reaxys Mass Spectrometry (28) Description (Mass Location Spectrometry)

References

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); electron impact (EI); spectrum

Lee, Jia Ying; Fan, Wai Yip; Mak, Kar Hang Garvin; Leong, Weng Kee; Journal of Organometallic Chemistry; vol. 724; (2013); p. 275 - 280, View in Reaxys; Gong, Jin-Long; Qi, Xinxin; Wei, Duo; Feng, Jian-Bo; Wu, Xiao-Feng; Organic and Biomolecular Chemistry; vol. 12; nb. 38; (2014); p. 7486 - 7488, View in Reaxys; Bai, Cuihua; Li, Aiqin; Yao, Xianfang; Liu, Hongli; Li, Yingwei; Green Chemistry; vol. 18; nb. 4; (2016); p. 1061 1069, View in Reaxys

spectrum

supporting information

electrospray ioni- supporting inforsation (ESI); time- mation of-flight mass spectra (TOFMS); high resolution mass spectrometry (HRMS); spectrum

Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 - 6575, View in Reaxys

electron impact (EI); spectrum

supporting information

Gu, Lijun; Jin, Cheng; Chemical Communications; vol. 51; nb. 30; (2015); p. 6572 - 6575, View in Reaxys

high resolution mass spectrometry (HRMS); CI (Chemical ionization); spectrum

supporting information

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

IT (ion trap); spectrum high resolution mass spectrometry (HRMS); electron impact (EI); time-of-flight mass spectra (TOFMS); spectrum

Mahmood, Shahid; Khalid, Azeem; Mahmood, Tariq; Arshad, Muhammad; LoyolaLicea, Juan Carlos; Crowley, David E.; RSC Advances; vol. 5; nb. 128; (2015); p. 106272 - 106279, View in Reaxys supporting information

Jiang, Jian-An; Du, Jia-Lei; Wang, Zhan-Guo; Zhang, Zhong-Nan; Xu, Xi; Zheng, GanLin; Ji, Ya-Fei; Tetrahedron Letters; vol. 55; nb. 10; (2014); p. 1677 - 1681, View in Reaxys

liquid chromatog- supporting inforraphy mass specmation trometry (LCMS); electrospray ionisation (ESI); timeof-flight mass spectra (TOFMS); spectrum

Jiang, Xiao; Wang, Jin-Mei; Zhang, Ying; Chen, Zhong; Zhu, Yong-Ming; Ji, ShunJun; Organic Letters; vol. 16; nb. 13; (2014); p. 3492 - 3495, View in Reaxys

liquid chromatography mass spectrometry (LCMS); APCI (atmospheric pressure chemical ionization); spectrum

Xu, Wenhao; Su, Weike; ; vol. 38; nb. 12; (2014); p. 710 - 714; Art.No: A3, View in Reaxys

high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

supporting information

Natte, Kishore; Dumrath, Andreas; Neumann, Helfried; Beller, Matthias; Angewandte Chemie - International Edition; vol. 53; nb. 38; (2014); p. 10090 - 10094; Angew. Chem.; vol. 126; nb. 38; (2015); p. 10254 - 10258,5, View in Reaxys

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electron impact (EI); spectrum

Sheu, Ming-Thau; Wu, Jender; Chen, Chih-Jui; Chao, Su-Hui; Wu, An-Bang; Tetrahedron Letters; vol. 45; nb. 43; (2004); p. 8107 - 8109, View in Reaxys; Rohitha; Kulkarni; Narender; Synthetic Communications; vol. 43; nb. 21; (2013); p. 2853 - 2866, View in Reaxys

gas chromatogra- supporting inforphy mass specmation trometry (GCMS); spectrum

Yuan, Rusheng; Fan, Shaolong; Zhou, Huaxi; Ding, Zhengxin; Lin, Sen; Li, Zhaohui; Zhang, Zizhong; Xu, Chao; Wu, Ling; Wang, Xuxu; Fu, Xianzhi; Angewandte Chemie International Edition; vol. 52; nb. 3; (2013); p. 1035 - 1039; Angew. Chem.; vol. 125; nb. 3; (2013); p. 1069 - 1073, View in Reaxys; Khumraksa, Bannarak; Phakhodee, Wong; Pattarawarapan, Mookda; Tetrahedron Letters; vol. 54; nb. 15; (2013); p. 1983 - 1986, View in Reaxys

gas chromatography mass spectrometry (GCMS); spectrum

Choi, Jongmyung; Kang, Donghyeon; Lee, Kyu Hyung; Lee, Byeongno; Kim, Kyung Joong; Hur, Nam Hwi; RSC Advances; vol. 3; nb. 24; (2013); p. 9402 - 9407, View in Reaxys; Chakraborty, Subrata; Blacque, Olivier; Fox, Thomas; Berke, Heinz; ACS Catalysis; vol. 3; nb. 10; (2013); p. 2208 - 2217, View in Reaxys

gas chromatography mass spectrometry (GCMS); time-of-flight mass spectra (TOFMS); spectrum

Hong, Saisai; Kang, Wenyu; Su, Yue; Guo, Yinlong; Chinese Journal of Chemistry; vol. 31; nb. 10; (2013); p. 1329 - 1335, View in Reaxys

high resolution supporting informass spectrome- mation try (HRMS); electrospray ionisation (ESI); spectrum

Nicklaus, Celine M.; Phua, Pim Huat; Buntara, Teddy; Noel, Sebastien; Heeres, Hero J.; De Vries, Johannes G.; Advanced Synthesis and Catalysis; vol. 355; nb. 14-15; (2013); p. 2839 - 2844, View in Reaxys

spectrum

Lijser, H. J. P. de; Arnold, Donald R.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1997); p. 1369 - 1380, View in Reaxys; D'Auria, Maurizio; Esposito, Vittorio; Gazzetta Chimica Italiana; vol. 127; nb. 9; (1997); p. 471 - 474, View in Reaxys; Farhadi, Saeid; Afshari, Mozhgan; Journal of Chemical Research; nb. 3; (2006); p. 188 - 191, View in Reaxys; Wiles, Charlotte; Watts, Paul; Haswell, Stephen J.; Tetrahedron Letters; vol. 47; nb. 30; (2006); p. 5261 5264, View in Reaxys; Hong, Bor-Cherng; Tseng, Hsing-Chang; Chen, Shang-Hung; Tetrahedron; vol. 63; nb. 13; (2007); p. 2840 - 2850, View in Reaxys; Lim, Chae Mi; Ha, Su Jeong; Lee, Jong Chan; Bulletin of the Korean Chemical Society; vol. 33; nb. 12; (2012); p. 4258 - 4260, View in Reaxys

EI (Electron impact); Spectrum

Singh, Savita J.; Jayaram, Radha V.; Synthetic Communications; vol. 42; nb. 3; (2012); p. 299 - 308, View in Reaxys

HRMS (High reso- supporting inforlution mass specmation trometry); Spectrum

Sun, Hua-Yin; Hua, Qing; Guo, Feng-Feng; Wang, Zhi-Yong; Huang, Wei-Xin; Advanced Synthesis and Catalysis; vol. 354; nb. 4; (2012); p. 569 - 573, View in Reaxys

EI (Electron imsupporting inforpact); GCMS (Gas mation chromatography mass spectrometry); Spectrum

Kamata, Keigo; Yamaura, Taiyo; Mizuno, Noritaka; Angewandte Chemie - International Edition; vol. 51; nb. 29; (2012); p. 7275 - 7278, View in Reaxys

EI (Electron impact); Spectrum

Yuan, Yu; Shi, Xiao; Liu, Wei; Synlett; nb. 4; (2011); p. 559 - 564; Art.No: W17710ST, View in Reaxys

supporting information

HRMS (High resolution mass spectrometry); Spectrum

Lin, Cheng-Kun; Lu, Ta-Jung; Tetrahedron; vol. 66; nb. 51; (2010); p. 9688 - 9693, View in Reaxys

Spectrum

Lin, Cheng-Kun; Lu, Ta-Jung; Tetrahedron; vol. 66; nb. 51; (2010); p. 9688 - 9693, View in Reaxys

GCMS (Gas chro- supporting informatography mass mation spectrometry); Spectrum

Du, Zhongtian; Sun, Zhiqiang; Zhang, Wei; Miao, Hong; Ma, Hong; Xu, Jie; Tetrahedron Letters; vol. 50; nb. 15; (2009); p. 1677 - 1680, View in Reaxys

spectrum; electron impact (EI)

Majima, Tetsuro; Tojo, Sachiko; Ishida, Akito; Takamuku, Setsuo; Journal of Organic Chemistry; vol. 61; nb. 22; (1996); p. 7793 - 7800, View in Reaxys; Kangani, Cyrous O.; Kelley, David E.; Day, Billy W.; Tetrahedron Letters; vol. 47; nb. 35; (2006); p. 6289 -

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2016-04-07 09:00:27

6292, View in Reaxys; Tan, Jianwen; Bednarek, Pawel; Liu, Jikai; Schneider, Bernd; Svatos, Ales; Hahlbrock, Klaus; Phytochemistry; vol. 65; nb. 6; (2004); p. 691 - 699, View in Reaxys electron impact (EI)

Koo, Bon-Suk; Lee, Chang Keun; Lee, Kee-Jung; Synthetic Communications; vol. 32; nb. 14; (2002); p. 2115 - 2123, View in Reaxys

spectrum; chemical ionization (CI)

Daishima, Shigeki; Iida, Yoshio; Kanda, Fujihiro; Organic Mass Spectrometry; vol. 26; nb. 5; (1991); p. 486 - 492, View in Reaxys

chemical ionization (CI); spectrum

Keough, T.; Analytical Chemistry; vol. 54; nb. 14; (1982); p. 2540 - 2547, View in Reaxys Salomon,R.G.; Reuter,J.M.; Journal of the American Chemical Society; vol. 99; nb. 13; (1977); p. 4372 - 4379, View in Reaxys; Kinlin et al.; Journal of Agricultural and Food Chemistry; vol. 20; (1972); p. 1021,1023, View in Reaxys; Migahed; Allam; Organic Mass Spectrometry; vol. 12; (1977); p. 695,696, View in Reaxys; Sakurai et al.; Bulletin of the Chemical Society of Japan; vol. 47; (1974); p. 2731,2732, View in Reaxys; Aczel; Lumpkin; Analytical Chemistry; vol. 33; (1961); p. 386,387-389, View in Reaxys

UV/VIS Spectroscopy (18) 1 of 18

Location

supporting information

Absorption Maxima (UV/ 263 VIS) [nm] Pratihar, Sanjay; Organic and Biomolecular Chemistry; vol. 12; nb. 30; (2014); p. 5781 - 5788, View in Reaxys 2 of 18

Solvent (UV/VIS Spectroscopy)

H2O

Absorption Maxima (UV/ 260 VIS) [nm] Anson; Novikova; Iozep; Russian Journal of Applied Chemistry; vol. 81; nb. 4; (2008); p. 647 - 650, View in Reaxys 3 of 18

Absorption Maxima (UV/ 203; 236 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

34; 21

Sheu, Ming-Thau; Wu, Jender; Chen, Chih-Jui; Chao, Su-Hui; Wu, An-Bang; Tetrahedron Letters; vol. 45; nb. 43; (2004); p. 8107 - 8109, View in Reaxys 4 of 18

Absorption Maxima (UV/ 290 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

14000

Ohkubo, Kei; Suga, Kyou; Morikawa, Kohei; Fukuzumi, Shunichi; Journal of the American Chemical Society; vol. 125; nb. 42; (2003); p. 12850 - 12859, View in Reaxys 5 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. H2SO4; various solvent(s)

Comment (UV/VIS Spectroscopy)

Remark: air-saturated solution; pH 3.7; ambient temperature

Anastasio; Faust; Rao; Environmental Science and Technology; vol. 31; nb. 1; (1997); p. 218 - 232, View in Reaxys 6 of 18

Solvent (UV/VIS Spectroscopy)

aq. H2SO4; various solvent(s)

Comment (UV/VIS Spectroscopy)

Remark: air-saturated solution; pH 3.7; ambient temperature

Absorption Maxima (UV/ 260 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

17000

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Anastasio; Faust; Rao; Environmental Science and Technology; vol. 31; nb. 1; (1997); p. 218 - 232, View in Reaxys 7 of 18

Description (UV/VIS Spectroscopy)

UV/VIS

Zhmurova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 42; (1972); p. 779,770,771, View in Reaxys; Bover; Zuman; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 786,788, View in Reaxys; Rabinowitz; Grinvald; Journal of the American Chemical Society; vol. 94; (1972); p. 2724,2725, View in Reaxys; Ostrovskii et al.; Zhurnal Organicheskoi Khimii; vol. 10; (1974); p. 2354,2365, View in Reaxys; van der Donckt; Vogels; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 1969,1971, 1973, View in Reaxys; Ching, Kallen; Journal of the American Chemical Society; vol. 100; (1978); p. 6119, View in Reaxys; Bover; Zumann; Journal of the American Chemical Society; vol. 95; (1973); p. 2531,2533-2536, View in Reaxys 8 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Bell,J.M. et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 4284 - 4292, View in Reaxys; Boyer; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 57; (1960); p. 381,382, View in Reaxys; Zalewski; Dunn; Canadian Journal of Chemistry; vol. 46; (1968); p. 2469, View in Reaxys; Davis et al.; Journal of Organic Chemistry; vol. 40; (1975); p. 1478,1480,1481, View in Reaxys; Ogata et al.; Kogyo Kagaku Zasshi; vol. 69; (1966); p. 901,902, View in Reaxys; Yates; Scott; Canadian Journal of Chemistry; vol. 41; (1963); p. 2320,2323, 2326, View in Reaxys 9 of 18

Description (UV/VIS Spectroscopy)

Singlet-triplet band

van der Donckt; Vogels; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 28; (1972); p. 1969,1971, 1973, View in Reaxys; Hayashi; Nagakura; Molecular Physics; vol. 27; (1974); p. 969,972,974,975,978, View in Reaxys 10 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Berlin,K.D.; Burpo,D.H.; Journal of Organic Chemistry; vol. 31; (1966); p. 1304 - 1306, View in Reaxys; Woeldike; Zeitschrift fuer Naturforschung; vol. 1; (1946); p. 566,571, View in Reaxys; Singh; Singh; Current Science; vol. 36; (1967); p. 603, View in Reaxys; Mitchell; Wan; Journal of Pharmaceutical Sciences; vol. 53; (1964); p. 1467, View in Reaxys 11 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

aq. H2SO4

Absorption Maxima (UV/ 264; 313 VIS) [nm] Yates; Stewart; Canadian Journal of Chemistry; vol. 37; (1959); p. 664,665, View in Reaxys 12 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

methanol

Absorption Maxima (UV/ 256 VIS) [nm] Santerre et al.; Journal of the American Chemical Society; vol. 80; (1958); p. 1254, View in Reaxys 13 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

H2SO4

Absorption Maxima (UV/ 310 VIS) [nm] Forbes et al.; Canadian Journal of Chemistry; vol. 35; (1957); p. 1049,1051, View in Reaxys 14 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane

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Absorption Maxima (UV/ 251; 257; 279; 326 VIS) [nm] Braude; Sondheimer; Journal of the Chemical Society; (1955); p. 3754,3765, View in Reaxys 15 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Grammaticakis; Bulletin de la Societe Chimique de France; (1953); p. 821,825, View in Reaxys 16 of 18

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

cyclohexane

Grammaticakis; Bulletin de la Societe Chimique de France; (1953); p. 821,825, View in Reaxys 17 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Waljaschko; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 42; (1910); p. 962,1013; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 1752, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 105; (1914); p. 2497, View in Reaxys; Grammaticakis; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 427,434; Bulletin de la Societe Chimique de France; (1949); p. 410,412, View in Reaxys 18 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

im Dampfzustand.

Purvis; Journal of the Chemical Society; vol. 105; (1914); p. 2497, View in Reaxys ESR Spectroscopy (1) 1 of 1

Description (ESR Spectroscopy)

ESR

Mao; Hirota; Molecular Physics; vol. 27; (1974); p. 309,312,313, View in Reaxys; Dubois; Dodin; Journal of the American Chemical Society; vol. 94; (1972); p. 7520, View in Reaxys Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Stark effect

Hossain; Hanson; Chemical Physics; vol. 30; (1978); p. 155, View in Reaxys; Koyanagi et al.; Chemical Physics Letters; vol. 52; (1977); p. 184, View in Reaxys

Raman Spectroscopy (2) Description (Ram- References an Spectroscopy) Raman

Green; Harrison; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 32; (1976); p. 1279,1284,1285, View in Reaxys

Spectrum

Kahovec; Kohlrausch; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 38; (1938); p. 119,138, View in Reaxys; Bonino; Manzoni Ansidei; Ricerca Scientifica; Mem. Accad. Bologna; vol. <9> 1; (1933); p. 349,27,29, View in Reaxys

Luminescence Spectroscopy (3) Description (Lumi- Comment (Luminescence Specnescence Spectroscopy) troscopy)

References

Luminescence quenching

Gorner, Helmut; Kuhn, Hans Jochen; Journal of Physical Chemistry; vol. 90; nb. 22; (1986); p. 5946 - 5955, View in Reaxys

Luminescence lifetime

Quenching with water

Mao; Hirota; Molecular Physics; vol. 27; (1974); p. 309,312,313, View in Reaxys; Deshpande; Suryanarayana Rao; Current Science; vol. 36; (1967); p. 429, View in Reaxys; Hayashi; Nagakura; Molecular Physics; vol. 27; (1974); p. 969,972,974,975,978,

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View in Reaxys; Harrigan; Hirota; Molecular Physics; vol. 31; (1976); p. 681,683,684,688,689, View in Reaxys Luminescence

Singh; Singh; Current Science; vol. 38; (1969); p. 491, View in Reaxys

Phosphorescence Spectroscopy (5) Description Solvent (PhosComment (Phos(Phosphoresphorescence phorescence cence SpectroSpectroscopy) Spectroscopy) scopy)

References

Triplet state energy

Lin, Zhong-Ping; Aue, Walter A.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 56; nb. 1; (2000); p. 111 - 117, View in Reaxys

Spectrum

xylene

396.1 - 395.88 nm McCauley E. M.; Lasko, C. L.; Tinti, D. S.; Journal of Physical Chemistry; vol. 96; nb. 3; (1992); p. 1146 - 1151, View in Reaxys

Maxima

acetonitrile

402 nm; 429 nm; 455 nm

Gorner, Helmut; Kuhn, Hans Jochen; Journal of Physical Chemistry; vol. 90; nb. 22; (1986); p. 5946 - 5955, View in Reaxys

Maxima

various solvent(s)

403 nm; 430 nm; 456 nm; 484 nm

Gorner, Helmut; Kuhn, Hans Jochen; Journal of Physical Chemistry; vol. 90; nb. 22; (1986); p. 5946 - 5955, View in Reaxys

Phosphorescence

Mao; Hirota; Molecular Physics; vol. 27; (1974); p. 309,312,313, View in Reaxys; Koyanagi; Goodman; Chemical Physics Letters; vol. 21; (1973); p. 1, View in Reaxys; Cheng; Hirota; Molecular Physics; vol. 27; (1974); p. 281,289,303,304, View in Reaxys; Hayashi; Nagakura; Molecular Physics; vol. 27; (1974); p. 969,972,974,975,978, View in Reaxys; Harrigan; Hirota; Molecular Physics; vol. 31; (1976); p. 681,683,684,688,689, View in Reaxys; Nishimura; Tinti; Chemical Physics Letters; vol. 13; (1972); p. 278, View in Reaxys; Koyanagi et al.; Chemical Physics Letters; vol. 52; (1977); p. 184, View in Reaxys

Other Spectroscopic Methods (1) Description (Other References Spectroscopic Methods) Photoelectron spectrum

Modelli, A.; Burrow, P. D.; Journal of Physical Chemistry; vol. 88; nb. 16; (1984); p. 3550 - 3554, View in Reaxys

Pharmacological Data (7) 1 of 7

Comment (Pharmacological Data)

Bioactivities present

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Mohammadnia, Majid; Research on Chemical Intermediates; vol. 42; nb. 3; (2016); p. 1899 - 1911, View in Reaxys; Khanapure, Sharanabasappa; Jagadale, Megha; Salunkhe, Rajashri; Rashinkar, Gajanan; Research on Chemical Intermediates; vol. 42; nb. 3; (2016); p. 2075 - 2085, View in Reaxys; Tayyebi Sabet Khomami, Narjes; Heshmatpour, Felora; Research on Chemical Intermediates; vol. 42; nb. 3; (2016); p. 2087 - 2099, View in Reaxys; Rostamizadeh, Shahnaz; Zekri, Negar; Research on Chemical Intermediates; vol. 42; nb. 3; (2016); p. 2329 - 2341, View in Reaxys; Hassanpour, Akbar; Hosseinzadeh-Khanmiri, Rahim; Babazadeh, Mirzaagha; Edjlali, Laden; Research on Chemical Intermediates; vol. 42; nb. 3; (2016); p. 2221 - 2231, View in Reaxys; Pang, Hai-Xia; Hui, Yong-Hai; Fan, Kui; Xing, Xue-Jian; Wu, Yang; Yang, Jing-Hui; Shi, Wei; Xie, Zheng-Feng; Chinese Chemical Letters; vol. 27; nb. 3; (2016); p. 335 - 339, View in Reaxys; Soliman, Hanan A.; Mubarak, Ahmed Y.; Elmorsy, Saad S.; Chinese Chemical Letters; vol. 27; nb. 3; (2016); p. 353 - 356, View in Reaxys; Bhosle, Manisha R.; Khillare, Lalit D.; Dhumal, Sambhaji T.; Mane, Ramrao A.; Chinese Chemical Letters; vol. 27; nb. 3; (2016); p. 370 - 374, View in Reaxys; Paul, Mitali; Shirase, Satoru; Morimoto, Yuma; Mathey, Laurent; Murugesapandian, Balasubramanian; Tanaka, Shinji; Itoh, Shinobu; Tsurugi, Hayato; Mashima, Kazushi; Chemistry - A European Journal; vol. 22; nb. 12; (2016); p. 4008 - 4014, View in Reaxys; Yang, Fengjuan; Zhang, Xiaowen; Li, Fengxi; Wang, Zhi; Wang, Lei; European Journal of Organic Chemistry; vol. 2016; nb. 7; (2016); p. 1251 - 1254, View in Reaxys 2 of 7

Effect (Pharmacological Data)

inflammation; effect on

Species or Test-System (Pharmacological Data)

Kunming mouse

Sex

male

Route of Application

peroral

Concentration (Pharmacological Data)

20 mg/kg

Kind of Dosing (Pharma- title comp. suspended in carboxymethyl cellulose cological Data) Method (Pharmacological Data)

mice treated with title comp.; 30 min later xylene applied to anterior and posterior surfaces of ear; 2 h later xylene-induced ear edema weighed

Further Details (Pharma- 30 mg/kg aspirin used as reference compound cological Data) Comment (Pharmacological Data)

No effect

Gu, Keli; Bi, Lanrong; Zhao, Ming; Wang, Chao; Ju, Jingfang; Peng, Shiqi; Bioorganic and Medicinal Chemistry; vol. 15; nb. 14; (2007); p. 4775 - 4799, View in Reaxys 3 of 7

Effect (Pharmacological Data)

enzyme; inhib. of

Species or Test-System (Pharmacological Data)

DBA/2N/Kuo mouse liver microsomes CYP2A5

Sex

male and female

Method (Pharmacological Data)

enzymatic assay; coumarin used as a substrate; in the presence of NADPH; Tris-HCl buffer, pH 7.4; 37 deg C; 10 min incubation; coumarin 7-hydroxylation monitored by fluorescence measurements

Type (Pharmacological Data)

pIC50

Value of Type (Pharmacological Data)

4.68 dimensionless

Rahnasto, Minna; Raunio, Hannu; Poso, Antti; Wittekindt, Carsten; Juvonen, Risto O.; Journal of Medicinal Chemistry; vol. 48; nb. 2; (2005); p. 440 - 449, View in Reaxys 4 of 7

Effect (Pharmacological Data)

enzyme; inhib. of

Species or Test-System (Pharmacological Data)

human liver microsomes CYP2A6

Method (Pharmacological Data)

enzymatic assay; coumarin used as a substrate; in the presence of NADPH; Tris-HCl buffer, pH 7.4; 37 deg C; 10 min incubation; coumarin 7-hydroxylation monitored by fluorescence measurements

Type (Pharmacological Data)

pIC50

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Value of Type (Pharmacological Data)

4.88 dimensionless

Rahnasto, Minna; Raunio, Hannu; Poso, Antti; Wittekindt, Carsten; Juvonen, Risto O.; Journal of Medicinal Chemistry; vol. 48; nb. 2; (2005); p. 440 - 449, View in Reaxys 5 of 7

Effect (Pharmacological Data)

enzyme; examination of

Species or Test-System (Pharmacological Data)

recombinant pig testicular 20β-hydroxysteroid dehydrogenase

Concentration (Pharmacological Data)

0.3 - 10000 μmol/l

Method (Pharmacological Data)

in vitro; carbonyl reductase activity determined spectrophotometrically by measuring oxidation rate of NADPH; 80 mM NADPH; potassium phosphate buffer, pH 6.5; 37 deg C

Results

exhibited carbonyl reductase activity with Km of 0.584 mM and Vmax of 110 nmol/min/mg (Vmax/Km: 188)

Metabolite XRN (Pharmacological Data)

1856550

Metabolite (Pharmacological Data)

4-Methylbenzyl alcohol

Nakajin, Shizuo; Tamura, Fumihiro; Takase, Noriko; Toyoshima, Satoshi; Biological and Pharmaceutical Bulletin; vol. 20; nb. 11; (1997); p. 1215 - 1218, View in Reaxys 6 of 7

Effect (Pharmacological Data)

metabolic

Endpoint of Effect (Phar- enzyme; exam. of macological Data) Species or Test-System (Pharmacological Data)

rat hepatic microsomal aldehyde dehydrogenase

Method (Pharmacological Data)

in vitro; NAD; 37 deg C; pH 7.4; also with 30-min enzyme preincubation with its anti IgG; NADH levels determined spectrophotometrically

Results

metabolized to corresponding acid with Km: 1545 μM and Vmax: 3.69 nmol of NADH produced/min*μg of protein

Martini, Robert; Murray, Michael; Chemical Research in Toxicology; vol. 9; nb. 1; (1996); p. 268 - 276, View in Reaxys 7 of 7

Comment (Pharmacological Data)

antifungal activity at 27 deg C and 0.5-2.0 mM on growth of Blastomyces dermatitidis, Histoplasma capsulatum, Trichophyton rubrum (H), Fonsecaea pedrosoi (T), Aspergillus nidulans, Penicillium frequentans, Penicillium cyclopium

Kurita; Miyaji; Kurane; Takahara; Agricultural and Biological Chemistry; vol. 45; nb. 4; (1981); p. 945 - 952, View in Reaxys Ecotoxicology (5) 1 of 5

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Spirostomum ambiguum

Kind of Dosing (Ecotoxi- stock solution of title comp. diluted with Tyrod solution (1:64) cology) Exposure Period (Ecotoxicology)

24 h

Method (Ecotoxicology)

24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; lethal responses: spherical deformation and autolysis

Type (Ecotoxicology)

log LC50

Value of Type (Ecotoxicology)

0.034 dimensionless

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 395, View in Reaxys

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2 of 5

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Spirostomum ambiguum

Kind of Dosing (Ecotoxi- stock solution of title comp. diluted with Tyrod solution (1:64) cology) Exposure Period (Ecotoxicology)

24 h

Method (Ecotoxicology)

24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; test responses: morphological changes

Type (Ecotoxicology)

-log EC50

Value of Type (Ecotoxicology)

0.652 dimensionless

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 395, View in Reaxys 3 of 5

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Spirostomum ambiguum

Kind of Dosing (Ecotoxi- stock solution of title comp. diluted with Tyrod solution (1:64) cology) Exposure Period (Ecotoxicology)

48 h

Method (Ecotoxicology)

24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; test responses: morphological changes

Type (Ecotoxicology)

-log EC50

Value of Type (Ecotoxicology)

0.652 dimensionless

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 395, View in Reaxys 4 of 5

Effect (Ecotoxicology)

toxicity to invertebrates

Species or Test-System (Ecotoxicology)

Spirostomum ambiguum

Kind of Dosing (Ecotoxi- stock solution of title comp. diluted with Tyrod solution (1:64) cology) Exposure Period (Ecotoxicology)

48 h

Method (Ecotoxicology)

24-well microplates as test containers; Spirotox biotest; pH = 7.4; 3 replicates; incubated in the dark at 25 deg C; lethal responses: spherical deformation and autolysis

Type (Ecotoxicology)

log LC50

Value of Type (Ecotoxicology)

0.097 dimensionless

Nalcz-Jawecki; Sawicki; Archives of Environmental Contamination and Toxicology; vol. 42; nb. 4; (2002); p. 389 395, View in Reaxys 5 of 5

Effect (Ecotoxicology)

toxicity to bacteria

Endpoint of Effect (Ecotoxicology)

growth

Species or Test-System (Ecotoxicology)

Tetrahymena pyriformis

Exposure Period (Ecotoxicology)

Method (Ecotoxicology)

spectrophotometric, 540 nm; sterile medium; 27 deg C; pH 7.35; starting conc. of cells: ca. 2500 cells/ml

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Type (Ecotoxicology)

IC50

Value of Type (Ecotoxicology)

137.08 mg/l

Schultz; Bryant; Kissel; Bulletin of Environmental Contamination and Toxicology; vol. 56; nb. 1; (1996); p. 129 - 134, View in Reaxys Exposure Assessment (5) Exposure Sources

References

presence in air

as emission from Ban-Weiss, George A.; Mclaughlin, John P.; Harley, Robert A.; Kean, Andrew J.; gasoline powered Grosjean, Eric; Grosjean, Daniel; Environmental Science and Technology; vol. 42; nb. light-duty vehi11; (2008); p. 3944 - 3950, View in Reaxys cles; from Caldecott tunnel, San Francisco Bay area, California, USA during 2001; emission factor: 2.6 mg/kg fuel burned

presence in air

as emission from Ban-Weiss, George A.; Mclaughlin, John P.; Harley, Robert A.; Kean, Andrew J.; medium- (MD) Grosjean, Eric; Grosjean, Daniel; Environmental Science and Technology; vol. 42; nb. and heavy duty 11; (2008); p. 3944 - 3950, View in Reaxys (HD) diesel trucks; from Caldecott tunnel, San Francisco, California, USA during midday between JulyAugust 2006; MD/ HD emission factor: 6.1 mg/kg fuel burned

emissions from wood adhesive, unoccupied, new- latex print, Dougly constructed las fir, pine houses in different counties of California, U.S. in January 2006

Seaman, Vincent Y.; Bennett, Deborah H.; Cahill, Thomas M.; Environmental Science and Technology; vol. 41; nb. 20; (2007); p. 6940 - 6946, View in Reaxys

presence in clean Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, offgas; municipal View in Reaxys waste incineration plant; Germany Concentration in the Environment (21) 1 of 21

Media (Concentration in the Environment)

ambient air

Location

An-San and Si-Hung city, Korea

Contamination Concentration

0.07 - 104 ppb

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Method, Remarks (Con- emission conc.; samples collected from 195 man-made source units within 77 individual centration in the Environ- companies in Ban-Wall and Si-Hwa Industrial Complex between June 2004 and October ment) 2005; HPLC-UV; mean conc.: 3.14 ppb; median conc.: 0.32 ppb; table Kim, Ki-Hyun; Hong, Yoon-Jung; Pal, Raktim; Jeon, Eui-Chan; Koo, Yoon-Seo; Sunwoo, Young; Chemosphere; vol. 70; nb. 5; (2008); p. 807 - 820, View in Reaxys 2 of 21

Media (Concentration in the Environment)

light-duty gasoline emission, gas-phase

Location

El Monte, California

Contamination Concentration

26 - 150 μg/l

Method, Remarks (Con- gas-phase emissions collec. from low-emission and three catalyst-equipped vehicles at centration in the Environ- Haagen-Smit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/v) ment) 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 21

Media (Concentration in the Environment)

light-duty gasoline emission, particle-phase

Location

El Monte, California

Contamination Concentration

4 - 65 μg/l

Method, Remarks (Con- particle phase emissions collec. from low-emission, three catalyst-equipped vehicles at centration in the Environ- Haagen-Smit Laboratory during Aug.-Sep. 2002; ultrasonic extrac. in 1:1 hexane/DCM (v/ ment) v), methanol; derivatization by PFBHA for 24 h; HPLC-APCI-ITMS; GC-ITMS; table 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 4 of 21

Media (Concentration in the Environment)

heavy-duty diesel emission, particle-phase

Location

California

Contamination Concentration

2.8 - 67 μg/l

Method, Remarks (Con- emissions from 1999 Freightliner Tractor operated under idle-creep, heavy heavy-duty diecentration in the Environ- sel truck driving cycle condition; June 2003; ultrasonic extrac. in 1:1 hexane/DCM (v/v), ment) 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 5 of 21

Media (Concentration in the Environment)

heavy-duty diesel emission, gas-phase

Location

California

Contamination Concentration

180 - 790 μg/l

Media (Concentration in the Environment)

ambient air

Location

Roseville, California, USA

Contamination Concentration

Ca. 2 - 10 pg/l

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Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- on-road diurnal samples collected from stationary site at California Air Resources Board on centration in the Environ- North Sunrise Blvd on July 17 during summer of 2006; derivatization with pentafluorohyment) droxylamine; extraction with hexane; GC/MS-NCI; figure Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 7 of 21

Media (Concentration in the Environment)

ambient air

Location

Roseville, California, USA

Contamination Concentration

0 - 28.8 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- diurnal samples collected from California Air Resources Board on North Sunrise Blvd during centration in the Environ- winter of 2006/2007; derivatization with pentafluorohydroxylamine; extraction with hexane; ment) GC/MS-NCI; median conc.: 3.6-5.3 ng/m3; table; figure Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 8 of 21

Media (Concentration in the Environment)

exhaust air

Location

Roseville, California, USA

Contamination Concentration

430000 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- average conc.; emission samples collected from 1997 Toyota Corolla car during 10 min at centration in the Environ- California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohyment) droxylamine; extraction with hexane; GC/MS-NCI Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 9 of 21

Media (Concentration in the Environment)

wood smoke

Location

Roseville, California, USA

Contamination Concentration

9200 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- average conc.; samples collected from Douglas fir fire during 3 min at California Air Recentration in the Environ- sources Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extracment) tion with hexane; GC/MS-NCI Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 10 of 21

Media (Concentration in the Environment)

wood smoke

Location

Roseville, California, USA

Contamination Concentration

7100 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- average conc.; samples collected from Blue Oak fire during 3 min at California Air Resources centration in the Environ- Board on North Sunrise Blvd; derivatization with pentafluorohydroxylamine; extraction with ment) hexane; GC/MS-NCI

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Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 11 of 21

Media (Concentration in the Environment)

exhaust air

Location

Roseville, California, USA

Contamination Concentration

18000 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- average conc.; emission samples collected from 1986 Ford Mustang jeep during 10 min at centration in the Environ- California Air Resources Board on North Sunrise Blvd; derivatization with pentafluorohyment) droxylamine; extraction with hexane; GC/MS-NCI Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 12 of 21

Media (Concentration in the Environment)

ambient air

Location

Roseville, California, USA

Contamination Concentration

0 - 36.8 pg/l

Background Concentration

0 - 5.6 pg/l

Method, Remarks (Con- diurnal samples collected from California Air Resources Board on North Sunrise Blvd during centration in the Environ- summer of 2006; derivatization with pentafluorohydroxylamine; extraction with hexane; GC/ ment) MS-NCI; median conc.: 2.1-7.5 ng/m3; table; figure Spada, Nicholas; Fujii, Erin; Cahill, Thomas M.; Environmental Science and Technology; vol. 42; nb. 19; (2008); p. 7084 - 7090, View in Reaxys 13 of 21

Media (Concentration in the Environment)

ambient air

Location

Athens, Greece

Contamination Concentration

2.3 ng/l

Method, Remarks (Con- 42 samples collected at site in Patission street (commercial area at city center) during Junecentration in the Environ- December 2000; title comp. analyzed using HPLC; mean conc. determined ment) Bakeas, Evangelos B.; Argyris, Dimitrios I.; Siskos, Panayotis A.; Chemosphere; vol. 52; nb. 5; (2003); p. 805 813, View in Reaxys 14 of 21

Media (Concentration in the Environment)

ambient air

Location

Copacabana, Brazil

Contamination Concentration

0.154 ng/l

Method, Remarks (Con- one sample collected for 2 h in the afternoon on October 2, 1999; sampling site located on centration in the Environ- the ninth floor of a building placed on Avenida Atlantica; HPLC and MS analyses ment) Grosjean, Daniel; Grosjean, Eric; Moreira, Lino F. R.; Environmental Science and Technology; vol. 36; nb. 7; (2002); p. 1389 - 1395, View in Reaxys 15 of 21

Media (Concentration in the Environment)

ambient air

Location

Rio de Janeiro, Brazil

Contamination Concentration

0.03 - 0.279 ng/l

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Method, Remarks (Con- 14 samples collected at a downtown location (ca. 23 deg S, 43 deg W), every two weeks centration in the Environ- during the period of May 3 to November 2, 2000; 3 h period of sampling from ca. 8 a.m. to ment) 11 a.m.; HPLC and MS analyses Grosjean, Daniel; Grosjean, Eric; Moreira, Lino F. R.; Environmental Science and Technology; vol. 36; nb. 7; (2002); p. 1389 - 1395, View in Reaxys 16 of 21

Media (Concentration in the Environment)

ambient air

Location

San Francisco, California, USA

Contamination Concentration

0.019 ng/l

Method, Remarks (Con- mean conc.; two samples collected at the Oakland-San Francisco Bay Bridge toll plaza on centration in the Environ- April 25, 2001, during rush hour traffic from 3:00 to 7:00 p.m.; derivatized sample; HRGC/ ment) ITMS analyses Destaillats, Hugo; Spaulding, Reggie S.; Charles, M. Judith; Environmental Science and Technology; vol. 36; nb. 10; (2002); p. 2227 - 2235, View in Reaxys 17 of 21

Media (Concentration in the Environment)

ambient air

Location

San Francisco, California, USA

Contamination Concentration

0.116 ng/l

Method, Remarks (Con- mean conc.; two samples collected at the Oakland-San Francisco Bay Bridge toll plaza on centration in the Environ- April 25, 2001, during rush hour traffic from 6:00 to 10:00 a.m.; derivatized sample; HRGC/ ment) ITMS analyses Destaillats, Hugo; Spaulding, Reggie S.; Charles, M. Judith; Environmental Science and Technology; vol. 36; nb. 10; (2002); p. 2227 - 2235, View in Reaxys 18 of 21

Media (Concentration in the Environment)

ambient air

Location

San Francisco, California, USA

Contamination Concentration

0.023 ng/l

Method, Remarks (Con- mean conc.; two samples collected at the Oakland-San Francisco Bay Bridge toll plaza on centration in the Environ- April 24, 2001, during rush hour traffic from 3:00 to 7:00 p.m.; derivatized sample; HRGC/ ment) ITMS analyses Destaillats, Hugo; Spaulding, Reggie S.; Charles, M. Judith; Environmental Science and Technology; vol. 36; nb. 10; (2002); p. 2227 - 2235, View in Reaxys 19 of 21

Media (Concentration in the Environment)

air

Location

Tuscarora Mountain Tunnel, PA

Contamination Concentration

0.014 - 0.147 ng/l

Method, Remarks (Con- average tunnel inlet and outlet conc., resp.; 10 experiments (1-h duration); May 18-21, 1999; centration in the Environ- av. emission factor: 0.28 mg/km; emission factors for light-duty and heavy-duty vehicles ment) determined; LC, UV and CIMS of 2,4-DNPH derivative analyses Grosjean, Daniel; Grosjean, Eric; Gertler, Alan W.; Environmental Science and Technology; vol. 35; nb. 1; (2001); p. 45 - 53, View in Reaxys 20 of 21

Media (Concentration in the Environment)

air

Location

Caldecott tunel, California, U.S.A.

Contamination Concentration

1.9 mg/l fuel burned

Method, Remarks (Con- emission factor for light-duty vehicles given as mean values over 8 days of sampling, excentration in the Environ- pressed per unit of volume of fuel burned; exit/entrance ratio: 17 (conc. at the tunnel exit ment) divided by the conc. at the entrance)

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Kean, Andrew J.; Grosjean, Eric; Grosjean, Daniel; Harley, Robert A.; Environmental Science and Technology; vol. 35; nb. 21; (2001); p. 4198 - 4204, View in Reaxys 21 of 21

Media (Concentration in the Environment)

clean offgas

Location

Germany

Contamination Concentration

0.96 ng/l

Method, Remarks (Con- municipal waste incineration plant; water vapor condensation; XAD-resin filters; adsorption/ centration in the Environ- thermodesorption; adsorption/elution; GC-FID analysis ment) Jay, K.; Stieglitz, L.; Chemosphere; vol. 30; nb. 7; (1995); p. 1249 - 1260, View in Reaxys Use (4) Use Pattern

Location

References

An elasmobranch repellent

Page/Page column 20

Patent; SHARK DEFENSE L.L.C.; US2010/16346; (2010); (A1) English, View in Reaxys

Compositions and personal care products

Patent; GIVAUDAN SA; WO2008/71027; (2008); (A1) English, View in Reaxys

flavor agent

Patent; Lee, Robert E.; Aldritt, Mary; US2006/39971; (2006); (A1) English, View in Reaxys

partially oxidized alkylaromatic intermediate for producing an aromatic carboxylic acid

Patent; Samsung General Chemicals Co., Ltd.; EP1173401; (2005); (B1) English, View in Reaxys

Isolation from Natural Product (2) Isolation from Nat- References ural Product ethanol extract of He, Zhi-Zhou; Yan, Ju-Fang; Song, Zhi-Jun; Ye, Fei; Liao, Xun; Peng, Shu-Lin; Ding, Li-Sheng; Journal aerial parts of Ar- of Natural Products; vol. 72; nb. 6; (2009); p. 1198 - 1201, View in Reaxys temisia minor; collected at Lhasa, in Tibet, China Dactylanthus taylorii

Ecroyd; Franich; Kroese; Steward; Phytochemistry; vol. 40; nb. 5; (1995); p. 1387 - 1389, View in Reaxys

Quantum Chemical Calculations (1) Calculated Prop- Method (Quantum Location erties Chemical Calculations) Molecular orbitals; Ab initio calcns. Electronic energy (LCAO, GO SCF, levels DIM, SAMO, X-à, Hartree-Fock)

supporting information

References

Pratihar, Sanjay; Organic and Biomolecular Chemistry; vol. 12; nb. 30; (2014); p. 5781 - 5788, View in Reaxys

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