Crystallography Open Database
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Searching journal of publication like 'The Journal of Organic Chemistry' volume of publication is 79
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4030160 | CIF | C15 H20.65 N O5.32 | P -1 | 9.9202; 11.6625; 15.0194 111.87; 97.172; 103.982 | 1519.64 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030161 | CIF | C16 H22 Cl2 N O5 | P 1 21/c 1 | 17.2369; 7.8216; 14.1194 90; 104.169; 90 | 1845.7 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030162 | CIF | C15 H23 N3 O5 | P -1 | 8.7313; 10.5992; 10.6362 60.424; 74.354; 71.334 | 803.55 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030163 | CIF | C19 H19 N O5 | P 1 21/c 1 | 14.035; 9.2967; 12.787 90; 93.461; 90 | 1665.4 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030164 | CIF | C21 H25 N O6 | P 1 21/c 1 | 13.287; 10.538; 14.009 90; 101.32; 90 | 1923 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030165 | CIF | C17 H21 N O7 | P 21 21 21 | 7.5487; 13.271; 16.861 90; 90; 90 | 1689.1 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030166 | CIF | C15 H21 N3 O4 | P n a 21 | 19.694; 13.615; 5.587 90; 90; 90 | 1498.1 | Helmy, Sameh; Oh, Saemi; Leibfarth, Frank A.; Hawker, Craig J.; Read de Alaniz, Javier Design and synthesis of donor-acceptor Stenhouse adducts: a visible light photoswitch derived from furfural. The Journal of organic chemistry, 2014, 79, 11316-11329 |
4030167 | CIF | C18 H21 Br N2 O3 | P 1 21 1 | 7.425; 29.523; 8.348 90; 107.871; 90 | 1741.7 | Xu, Changming; Zhang, Long; Luo, Sanzhong Asymmetric enamine catalysis with β-ketoesters by chiral primary amine: divergent stereocontrol modes. The Journal of organic chemistry, 2014, 79, 11517-11526 |
4030168 | CIF | C19 H15 Cl N2 O4 | P 1 21/n 1 | 11.2411; 7.7513; 19.5834 90; 103.11; 90 | 1661.89 | Imbri, Dennis; Netz, Natalie; Kucukdisli, Murat; Kammer, Lisa Marie; Jung, Philipp; Kretzschmann, Annika; Opatz, Till One-pot synthesis of pyrrole-2-carboxylates and -carboxamides via an electrocyclization/oxidation sequence. The Journal of organic chemistry, 2014, 79, 11750-11758 |
4030169 | CIF | C22 H23 F N2 O2 | P -1 | 11.7244; 13.1147; 13.1273 80.454; 84.455; 76.543 | 1932.3 | Imbri, Dennis; Netz, Natalie; Kucukdisli, Murat; Kammer, Lisa Marie; Jung, Philipp; Kretzschmann, Annika; Opatz, Till One-pot synthesis of pyrrole-2-carboxylates and -carboxamides via an electrocyclization/oxidation sequence. The Journal of organic chemistry, 2014, 79, 11750-11758 |
4030170 | CIF | C22 H16 Cl N O2 | C 1 2/c 1 | 32.745; 6.2347; 17.488 90; 96.92; 90 | 3544.3 | Chen, Zhi-Wei; Zhu, Yi-Zhou; Ou, Jin-Wang; Wang, Ya-Ping; Zheng, Jian-Yu Metal-free iodine(III)-promoted synthesis of isoquinolones. The Journal of organic chemistry, 2014, 79, 10988-10998 |
4030171 | CIF | C23 H19 N O3 | P -1 | 9.953; 12.581; 15.107 90.32; 97.35; 99.51 | 1849.7 | Chen, Zhi-Wei; Zhu, Yi-Zhou; Ou, Jin-Wang; Wang, Ya-Ping; Zheng, Jian-Yu Metal-free iodine(III)-promoted synthesis of isoquinolones. The Journal of organic chemistry, 2014, 79, 10988-10998 |
4030172 | CIF | C17 H13 N O3 | P 1 21/n 1 | 8.4145; 8.9482; 17.838 90; 102.12; 90 | 1313.2 | Chen, Zhi-Wei; Zhu, Yi-Zhou; Ou, Jin-Wang; Wang, Ya-Ping; Zheng, Jian-Yu Metal-free iodine(III)-promoted synthesis of isoquinolones. The Journal of organic chemistry, 2014, 79, 10988-10998 |
4030173 | CIF | C20 H15 N O2 S | P 1 21/n 1 | 11.395; 8.4405; 16.714 90; 91.37; 90 | 1607.1 | Chen, Zhi-Wei; Zhu, Yi-Zhou; Ou, Jin-Wang; Wang, Ya-Ping; Zheng, Jian-Yu Metal-free iodine(III)-promoted synthesis of isoquinolones. The Journal of organic chemistry, 2014, 79, 10988-10998 |
4030174 | CIF | C46 H50 Cl2 Cu N15 O16 | P -1 | 11.536; 13.186; 18.136 96.984; 100.355; 99.64 | 2642.6 | Saha, Subrata; Santra, Saikat; Akhuli, Bidyut; Ghosh, Pradyut [2]Rotaxane with multiple functional groups. The Journal of organic chemistry, 2014, 79, 11170-11178 |
4030175 | CIF | C19 H15 F3 N2 O S | C 1 2/c 1 | 23.049; 7.2946; 20.98 90; 99.77; 90 | 3476.3 | Wang, Yang; Zhao, Fei; Chi, Yue; Zhang, Wen-Xiong; Xi, Zhenfeng Substituent-controlled selective synthesis of N-acyl 2-aminothiazoles by intramolecular Zwitterion-mediated C-N bond cleavage. The Journal of organic chemistry, 2014, 79, 11146-11154 |
4030200 | CIF | C19 H13 Cl N2 O2 | C 1 2 1 | 24.266; 5.72; 13.017 90; 120.428; 90 | 1558 | Chu, Jean-Ho; Hsu, Wen-Ting; Wu, Yi-Hua; Chiang, Meng-Fan; Hsu, Nan-Hai; Huang, Hao-Ping; Wu, Ming-Jung Substituent electronic effects govern direct intramolecular C-N cyclization of N-(Biphenyl)pyridin-2-amines induced by hypervalent iodine(III) reagents. The Journal of organic chemistry, 2014, 79, 11395-11408 |
4030201 | CIF | C17 H11 Cl N2 | P 21 21 21 | 3.8405; 16.0573; 25.5787 90; 90; 90 | 1577.39 | Chu, Jean-Ho; Hsu, Wen-Ting; Wu, Yi-Hua; Chiang, Meng-Fan; Hsu, Nan-Hai; Huang, Hao-Ping; Wu, Ming-Jung Substituent electronic effects govern direct intramolecular C-N cyclization of N-(Biphenyl)pyridin-2-amines induced by hypervalent iodine(III) reagents. The Journal of organic chemistry, 2014, 79, 11395-11408 |
4030202 | CIF | C21 H13 Cl N4 | C 1 2/c 1 | 19.728; 12.427; 17.19 90; 124.311; 90 | 3481 | Zhang, Lei; Zheng, Liyao; Guo, Biao; Hua, Ruimao One-pot synthesis of multisubstituted 2-aminoquinolines from annulation of 1-aryl tetrazoles with internal alkynes via double C-H activation and denitrogenation. The Journal of organic chemistry, 2014, 79, 11541-11548 |
4030203 | CIF | C16 H14 N2 | P 1 21/c 1 | 9.362; 9.812; 14.178 90; 97.93; 90 | 1289.9 | Zhang, Lei; Zheng, Liyao; Guo, Biao; Hua, Ruimao One-pot synthesis of multisubstituted 2-aminoquinolines from annulation of 1-aryl tetrazoles with internal alkynes via double C-H activation and denitrogenation. The Journal of organic chemistry, 2014, 79, 11541-11548 |
4030204 | CIF | C40 H30 | P -1 | 9.5249; 10.3261; 16.1226 77.226; 82.154; 69.713 | 1447.5 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030205 | CIF | C46 H42 | P 1 21/c 1 | 14.6419; 15.164; 17.0369 90; 111.209; 90 | 3526.5 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030206 | CIF | C46.25 H42 Cl0.28 O6.12 | P -1 | 13.3327; 14.1261; 22.859 80.065; 79.996; 65.861 | 3844.3 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030207 | CIF | C40 H30 | P -1 | 10.1649; 14.5991; 19.9342 98.273; 104.589; 97.525 | 2789.5 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030208 | CIF | C46 H42 | P -1 | 9.8747; 11.2191; 17.2403 103.764; 97.167; 109.021 | 1710.7 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030209 | CIF | C46 H42 O6 | P -1 | 9.6352; 11.5649; 18.7317 97.6701; 103.632; 111.834 | 1825.52 | Freudenberg, Jan; Uptmoor, Andrea C.; Rominger, Frank; Bunz, Uwe H. F. Photolability of per-arylated butadienes: en route to dihydronaphthalenes. The Journal of organic chemistry, 2014, 79, 11787-11791 |
4030210 | CIF | C19 H16 Br N O | P 1 21 1 | 5.5979; 16.633; 8.6913 90; 101.74; 90 | 792.32 | Hua, Yuan-Zhao; Han, Xing-Wang; Yang, Xiao-Chao; Song, Xixi; Wang, Min-Can; Chang, Jun-Biao Enantioselective Friedel-Crafts alkylation of pyrrole with chalcones catalyzed by a dinuclear zinc catalyst. The Journal of organic chemistry, 2014, 79, 11690-11699 |
4030211 | CIF | C16 H17 N O | P 1 21 1 | 7.9007; 10.334; 8.6158 90; 111.72; 90 | 653.5 | Hua, Yuan-Zhao; Han, Xing-Wang; Yang, Xiao-Chao; Song, Xixi; Wang, Min-Can; Chang, Jun-Biao Enantioselective Friedel-Crafts alkylation of pyrrole with chalcones catalyzed by a dinuclear zinc catalyst. The Journal of organic chemistry, 2014, 79, 11690-11699 |
4030212 | CIF | C17 H20 O2 | P 1 21/c 1 | 9.5719; 8.5121; 17.2444 90; 97.11; 90 | 1394.22 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030213 | CIF | C26 H26 O3 | P -1 | 10.091; 14.27; 16.4485 64.623; 72.52; 80.615 | 2039.6 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030214 | CIF | C19 H24 O2 | P 1 21/n 1 | 12.1767; 7.0864; 18.9922 90; 105.033; 90 | 1582.73 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030215 | CIF | C23 H24 O2 | P 1 21/n 1 | 14.5496; 7.1138; 17.4167 90; 99.946; 90 | 1775.59 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030216 | CIF | C18 H22 O3 | P 1 21/c 1 | 11.1013; 8.4844; 15.9687 90; 95.724; 90 | 1496.56 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030217 | CIF | C11 H17 Cl O2 | P -1 | 5.9783; 7.2121; 13.006 77.36; 79.561; 89.748 | 537.76 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030218 | CIF | C18 H22 O2 | P -1 | 7.3582; 10.2308; 10.3868 95.5; 97.251; 101.113 | 755.3 | Lin, Hsin-Hui; Lee, Kuan-Yi; Chen, Yin-An; Liu, Chi-Fan; Yeh, Ming-Chang P Diastereoselective synthesis of 2-arylmethylene-6-hydroxyspiro[4.5]deca-7-ones via FeCl3·6H2O-catalyzed spiroannulation/hydride transfer of 6-(5-arylpent-4-yn-1-yl)-7-oxabicyclo[4.1.0]heptan-2-ols. The Journal of organic chemistry, 2014, 79, 11802-11811 |
4030219 | CIF | C15 H28 N2 O5 | P 1 21 1 | 8.836; 6.0632; 16.037 90; 100.167; 90 | 845.7 | Sánchez-Fernández, Elena M; Álvarez, Eleuterio; Ortiz Mellet, Carmen; García Fernández, José M Synthesis of multibranched australine derivatives from reducing castanospermine analogues through the Amadori rearrangement of gem-diamine intermediates: selective inhibitors of β-glucosidase. The Journal of organic chemistry, 2014, 79, 11722-11728 |
4030220 | CIF | C74.5 H65 O8.25 | P -1 | 18.6028; 19.681; 19.8332 114.23; 101.248; 94.91 | 6382.1 | Schwenger, Alexander; Gerlach, Claudia; Griesser, Helmut; Richert, Clemens Synthesis of eight-arm, branched oligonucleotide hybrids and studies on the limits of DNA-driven assembly. The Journal of organic chemistry, 2014, 79, 11558-11566 |
4030221 | CIF | C15 H11 F2 N O3 | P 1 21/n 1 | 15.83; 5.1326; 17.275 90; 107.501; 90 | 1338.6 | Smirnov, Vladimir O.; Struchkova, Marina I.; Arkhipov, Dmitry E.; Korlyukov, Alexander A.; Dilman, Alexander D. Synthesis of gem-difluorinated nitroso compounds. The Journal of organic chemistry, 2014, 79, 11819-11823 |
4030222 | CIF | C24 H19 F2 N O4 | P -1 | 8.5372; 10.4431; 12.236 81.804; 69.686; 82.905 | 1009.37 | Smirnov, Vladimir O.; Struchkova, Marina I.; Arkhipov, Dmitry E.; Korlyukov, Alexander A.; Dilman, Alexander D. Synthesis of gem-difluorinated nitroso compounds. The Journal of organic chemistry, 2014, 79, 11819-11823 |
4030223 | CIF | C20 H22 N2 O4 | C 1 2/c 1 | 22.0688; 6.4813; 25.2718 90; 104.499; 90 | 3499.62 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030224 | CIF | C22 H24 O8 | C 1 c 1 | 5.2895; 25.359; 15.0712 90; 98.909; 90 | 1997.2 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030225 | CIF | C14 H20 O4 | P 1 21/n 1 | 4.4393; 7.7069; 19.5385 90; 94.3771; 90 | 666.53 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030226 | CIF | C25 H27 N3 O6 | P 1 21/a 1 | 13.1801; 11.6477; 13.9929 90; 90.152; 90 | 2148.15 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030227 | CIF | C34 H28 | P 1 21/c 1 | 13.4959; 7.435; 24.6097 90; 93.1287; 90 | 2465.71 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030228 | CIF | C20 H22 N2 O4 | P 1 21 1 | 7.4676; 6.9456; 17.1815 90; 102.013; 90 | 871.64 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030229 | CIF | C28 H30 O12 | P 1 21/a 1 | 10.3961; 15.5192; 16.774 90; 91.4837; 90 | 2705.4 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030230 | CIF | C22 H44 Si4 | P 1 21 1 | 18.4241; 12.7737; 20.9954 90; 113.385; 90 | 4535.3 | Lindeboom, Erik J.; Willis, Anthony C.; Paddon-Row, Michael N; Sherburn, Michael S. Computational and synthetic studies with tetravinylethylenes. The Journal of organic chemistry, 2014, 79, 11496-11507 |
4030233 | CIF | C22 H16 N2 O S | P 1 21/n 1 | 7.699; 28.969; 8.335 90; 110.23; 90 | 1744.3 | Iwasaki, Masayuki; Kaneshika, Wataru; Tsuchiya, Yuta; Nakajima, Kiyohiko; Nishihara, Yasushi Palladium-catalyzed peri-selective chalcogenation of naphthylamines with diaryl disulfides and diselenides via C-H bond cleavage. The Journal of organic chemistry, 2014, 79, 11330-11338 |
4030234 | CIF | C38 H45 Cl N O10 | P 1 21/c 1 | 12.037; 12.9351; 23.784 90; 103.709; 90 | 3597.7 | Gromov, Sergey P.; Vedernikov, Artem I.; Lobova, Natalia A.; Kuz'mina, Lyudmila G.; Dmitrieva, Svetlana N.; Strelenko, Yuri A.; Howard, Judith A. K. Synthesis, structure, and properties of supramolecular photoswitches based on ammonioalkyl derivatives of crown ether styryl dyes. The Journal of organic chemistry, 2014, 79, 11416-11430 |
4030235 | CIF | C31 H46 Br2 N2 O9 | P -1 | 11.431; 11.6678; 14.7274 104.737; 95.77; 114.086 | 1687.2 | Gromov, Sergey P.; Vedernikov, Artem I.; Lobova, Natalia A.; Kuz'mina, Lyudmila G.; Dmitrieva, Svetlana N.; Strelenko, Yuri A.; Howard, Judith A. K. Synthesis, structure, and properties of supramolecular photoswitches based on ammonioalkyl derivatives of crown ether styryl dyes. The Journal of organic chemistry, 2014, 79, 11416-11430 |
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