Crystallography Open Database
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Result: there are 1034 entries in the selection
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Searching journal of publication like 'The Journal of organic chemistry' volume of publication is 80
COD ID ![]() |
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Cell parameters | Cell volume ![]() |
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4030464 | CIF | C17 H22 Cl3 N O3 S | C 1 2 1 | 20.259; 5.923; 17.597 90; 115.345; 90 | 1908.3 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030465 | CIF | C16 H21 N O3 S | P 21 21 21 | 11.1849; 11.7522; 47.233 90; 90; 90 | 6208.6 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030466 | CIF | C10 H11 N O3 S | P 21 21 21 | 6.364; 12.235; 13.112 90; 90; 90 | 1020.9 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030467 | CIF | C18 H24 Cl3 N O4 S | P -1 | 6.036; 10.487; 17.295 92.01; 92.12; 105.04 | 1055.4 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030468 | CIF | C22 H24 Cl3 N O3 S | P b c a | 9.746; 21.034; 22.8338 90; 90; 90 | 4680.9 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030469 | CIF | C20 H22 N2 O4 S | P 1 21/c 1 | 14.712; 11.439; 11.175 90; 94; 90 | 1876.1 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030470 | CIF | C17 H23 N O3 S | P 1 21 1 | 10.489; 7.978; 10.912 90; 115.008; 90 | 827.5 | Martinand-Lurin, Elodie; Gruber, Raymond; Retailleau, Pascal; Fleurat-Lessard, Paul; Dauban, Philippe Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes. The Journal of organic chemistry, 2015, 80, 1414-1426 |
4030471 | CIF | C22 H25 Cl Ir N3 | P -1 | 8.299; 10.7164; 11.8135 95.36; 91.437; 106.618 | 1000.88 | Wu, Yunxiang; Yang, Yaxi; Zhou, Bing; Li, Yuanchao Iridium(III)-Catalyzed C-7 Selective C-H Alkynylation of Indolines at Room Temperature. The Journal of organic chemistry, 2015, 80, 1946-1951 |
4030472 | CIF | C78 H10 O | P 1 21/c 1 | 10.9318; 17.8483; 20.0007 90; 102.883; 90 | 3804.2 | Chang, Wei-Wei; Li, Zong-Jun; He, Fa-Gui; Sun, Tao; Gao, Xiang Electronic vs Steric Effects on the Stability of Anionic Species: A Case Study on the Ortho and Para Regioisomers of Organofullerenes. The Journal of organic chemistry, 2015, 80, 1557-1563 |
4030473 | CIF | C74 H62 Br2 Cl2 N6 O4 | P 1 21 1 | 9.0626; 14.5164; 12.4684 90; 106.449; 90 | 1573.16 | Li, Xin; Tan, Wei; Gong, Yu-Xin; Shi, Feng Catalyst-controlled chemoselective reaction of 3-indolylmethanols with cyclic enaminones leading to c2-functionalized indoles. The Journal of organic chemistry, 2015, 80, 1841-1848 |
4030536 | CIF | C23 H38 O4 | C 1 2/c 1 | 32.0238; 16.1168; 8.624 90; 101.794; 90 | 4357.1 | Yang, Wei; Cao, Jingming; Zhang, Mengxun; Lan, Rongfeng; Zhu, Lizhi; Du, Guangyan; He, Shuzhong; Lee, Chi-Sing Systemic Study on the Biogenic Pathways of Yezo'otogirins: Total Synthesis and Antitumor Activities of (±)-Yezo'otogirin C and Its Structural Analogues. The Journal of organic chemistry, 2014, 80, 836 |
4030537 | CIF | C21 H34 O5 | P b c n | 23.5047; 13.3187; 13.1615 90; 90; 90 | 4120.2 | Yang, Wei; Cao, Jingming; Zhang, Mengxun; Lan, Rongfeng; Zhu, Lizhi; Du, Guangyan; He, Shuzhong; Lee, Chi-Sing Systemic Study on the Biogenic Pathways of Yezo'otogirins: Total Synthesis and Antitumor Activities of (±)-Yezo'otogirin C and Its Structural Analogues. The Journal of organic chemistry, 2014, 80, 836 |
4030538 | CIF | C29 H31 N O5 | P 1 21 1 | 5.8763; 9.3567; 22.8256 90; 95.152; 90 | 1249.94 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030539 | CIF | C20 H32 N2 O8 | P 21 21 21 | 9.2798; 11.1028; 22.049 90; 90; 90 | 2271.7 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030540 | CIF | C18 H23 N O5 | P 21 21 21 | 6.1419; 20.457; 27.077 90; 90; 90 | 3402.1 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030541 | CIF | C25 H29 N O5 | P 1 21 1 | 9.66; 10.965; 10.599 90; 96.916; 90 | 1114.5 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030542 | CIF | C18 H23 N O5 | P 21 21 21 | 5.906; 9.576; 29.275 90; 90; 90 | 1655.7 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030543 | CIF | C10 H17 N O4 | P 21 21 21 | 7.6184; 9.1016; 15.0206 90; 90; 90 | 1041.52 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030544 | CIF | C21 H27 N O6 | P 1 21 1 | 12.804; 5.996; 13.75 90; 108.29; 90 | 1002.3 | Das, Soumendra Nath; Chowdhury, Arpan; Tripathi, Neha; Jana, Prithwish K.; Mandal, Sukhendu B. Exploitation of in Situ Generated Sugar-Based Olefin Keto-Nitrones: Synthesis of Carbocycles, Heterocycles, and Nucleoside Derivatives. The Journal of organic chemistry, 2014, 80, 1136 |
4030545 | CIF | C21 H28 O Si | P 1 21/c 1 | 9.9503; 8.1458; 22.6084 90; 92.043; 90 | 1831.32 | Mori-Quiroz, Luis M; Maleczka, Jr, Robert E Stereoconvergent [1,2]- and [1,4]-Wittig Rearrangements of 2-Silyl-6-aryl-5,6-dihydropyrans: A Tale of Steric vs Electronic Regiocontrol of Divergent Pathways. The Journal of organic chemistry, 2015, 80, 1163 |
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