Crystallography Open Database
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Result: there are 136 entries in the selection
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Searching journal of publication like 'Organic Chemistry Frontiers' volume of publication is 2
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
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1553138 | CIF | C17 H18 N2 O3 | P -1 | 6.8879; 8.282; 14.4023 104.655; 94.121; 91.668 | 791.85 | Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols Organic Chemistry Frontiers, 2015, 2, 951 |
1553139 | CIF | C20 H26 N O2 S | P -1 | 8.6248; 9.8158; 11.6537 99.05; 101.411; 96.596 | 944.1 | Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation Organic Chemistry Frontiers, 2015, 2, 792 |
1553140 | CIF | C30 H31 N O2 S | P 1 21/n 1 | 8.5768; 10.2978; 28.986 90; 90.183; 90 | 2560.1 | Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation Organic Chemistry Frontiers, 2015, 2, 792 |
1553141 | CIF | C21 H22 Br N3 O5 | P 1 21 1 | 9.8915; 9.4814; 11.942 90; 102.048; 90 | 1095.31 | Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base Organic Chemistry Frontiers, 2015, 2, 968 |
1553142 | CIF | C14 H15 Br N2 O3 | P n a 21 | 7.1573; 21.4898; 9.4975 90; 90; 90 | 1460.8 | Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base Organic Chemistry Frontiers, 2015, 2, 968 |
1553143 | CIF | C70 H66 Cl34 N8 P2 Ru2 | P 1 21/n 1 | 13.25; 16.9695; 23.3436 90; 103.948; 90 | 5093.95 | Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties Organic Chemistry Frontiers, 2015, 2, 936 |
1553144 | CIF | C32 H35 Cl2 N4 O5 P Ru | P 1 21/c 1 | 18.2792; 11.74106; 17.1049 90; 117.389; 90 | 3259.49 | Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties Organic Chemistry Frontiers, 2015, 2, 936 |
1553145 | CIF | C26 H17 O3 P | P 21 21 21 | 8.4926; 12.013; 19.248 90; 90; 90 | 1963.7 | Xu, Guangqing; Li, Minghong; Wang, Shouliang; Tang, Wenjun Efficient synthesis of P-chiral biaryl phosphonates by stereoselective intramolecular cyclization Organic Chemistry Frontiers, 2015, 2, 1342 |
1553146 | CIF | C25 H23 Au I N3 O | C 1 2/c 1 | 32.577; 10.964; 15.077 90; 101.267; 90 | 5281.3 | Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes Organic Chemistry Frontiers, 2015, 2, 1475 |
1553147 | CIF | C23 H19 Au I N3 O | P 21 21 21 | 10.3025; 16.0231; 26.3966 90; 90; 90 | 4357.5 | Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes Organic Chemistry Frontiers, 2015, 2, 1475 |
1553148 | CIF | C24 H34 O10 | P 21 21 21 | 5.8507; 14.177; 30.834 90; 90; 90 | 2557.5 | Huang, Xin; Xue, Can; Fu, Chunling; Ma, Shengming A concise construction of carbohydrate-tethered axially chiral allenes via copper catalysis Organic Chemistry Frontiers, 2015, 2, 1040 |
1553149 | CIF | C21 H19 N O6 | P 21 21 21 | 10.8569; 14.913; 23.1808 90; 90; 90 | 3753.2 | Duan, Jindian; Cheng, Jing; Li, Pengfei Enantioselective construction of spiro-1,3-indandiones with three stereocenters via organocatalytic Michael-aldol reaction of 2-arylideneindane-1,3-diones and nitro aldehydes Organic Chemistry Frontiers, 2015, 2, 1048 |
1553150 | CIF | C72 H74 I2 N36 O16 | P n a 21 | 13.093; 25.621; 27.14 90; 90; 90 | 9104 | Zhou, Tian-You; Qi, Qiao-Yan; Zhang, Ying; Xu, Xiao-Na; Zhao, Xin A thermally stable pH-responsive “supramolecular buckle” based on the encapsulation of 4-(4-aminophenyl)-N-methylpyridinium by cucurbit[8]uril Organic Chemistry Frontiers, 2015, 2, 1030 |
1553151 | CIF | C18 H19 N O2 | C 1 2/c 1 | 20.293; 6.84225; 22.5979 90; 90.8593; 90 | 3137.36 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553152 | CIF | C18 H19 N O2 | P 1 21/c 1 | 7.63367; 29.2305; 6.84862 90; 102.295; 90 | 1493.12 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553153 | CIF | C19 H21 N O2 | P b c a | 12.4972; 14.1613; 17.5538 90; 90; 90 | 3106.61 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553154 | CIF | C16 H17 N O3 | P 21 21 21 | 6.86998; 15.21957; 27.0563 90; 90; 90 | 2828.96 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553155 | CIF | C19 H21 N O3 | P -1 | 6.98428; 15.3845; 16.6168 110.497; 97.0023; 102.274 | 1596.16 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553156 | CIF | C18 H20 N2 O3 | P -1 | 6.8071; 15.0202; 15.8559 90.798; 101.156; 100.035 | 1564.3 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553157 | CIF | C11 H14 N2 O2 | P -1 | 7.5414; 11.8446; 12.2635 80.154; 88.093; 88.519 | 1078.48 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
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