Crystallography Open Database
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Searching volume of publication is 15
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1508854 | CIF | C69 H52 S | P -1 | 10.4792; 13.4657; 20.0797 70.764; 77.704; 82.037 | 2606.7 | Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng Catalytic C-h and C-s bond activation of thiophenes. Organic letters, 2013, 15, 282-285 |
| 1508855 | CIF | C44 H35 F4 S | P 1 21/c 1 | 9.3242; 20.5863; 20.4716 90; 92.4025; 90 | 3926.09 | Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng Catalytic C-h and C-s bond activation of thiophenes. Organic letters, 2013, 15, 282-285 |
| 1508856 | CIF | C213 H201 S4 | P -1 | 16.0668; 16.7268; 18.1635 96.294; 99.037; 108.324 | 4510 | Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng Catalytic C-h and C-s bond activation of thiophenes. Organic letters, 2013, 15, 282-285 |
| 1508857 | CIF | C32 H29 Cl N2 O3 | P 21 21 21 | 8.3771; 10.29; 31.168 90; 90; 90 | 2686.69 | Shi, Feng; Xing, Gui-Juan; Zhu, Ren-Yi; Tan, Wei; Tu, Shujiang A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2'-quinoline] Scaffold. Organic letters, 2013, 15, 128-131 |
| 1508858 | CIF | C28 H25 N O4 | P 1 21 1 | 12.652; 5.3373; 17.942 90; 109.082; 90 | 1145 | Wu, Hua; He, Yu-Ping; Gong, Liu-Zhu Direct Access to Enantioenriched Spiroacetals through Asymmetric Relay Catalytic Three-Component Reaction. Organic letters, 2013, 15, 460-463 |
| 1508859 | CIF | C15 H19 N O3 | P -1 | 6.9397; 8.8694; 11.1168 97.572; 94.165; 92.775 | 675.33 | Reddy, B. V. Subba; Reddy, M. Ramana; Rao, Y. Gopal; Yadav, J. S.; Sridhar, B. Cu(OTf)(2)-Catalyzed Synthesis of 2,3-Disubstituted Indoles and 2,4,5-Trisubstituted Pyrroles from α-Diazoketones. Organic letters, 2013, 15, 464-467 |
| 1508860 | CIF | C14 H15 N O2 | P 1 21/n 1 | 11.7298; 9.2723; 11.8853 90; 103.883; 90 | 1254.91 | Reddy, B. V. Subba; Reddy, M. Ramana; Rao, Y. Gopal; Yadav, J. S.; Sridhar, B. Cu(OTf)(2)-Catalyzed Synthesis of 2,3-Disubstituted Indoles and 2,4,5-Trisubstituted Pyrroles from α-Diazoketones. Organic letters, 2013, 15, 464-467 |
| 1508861 | CIF | C34 H32 N4 | P 1 21/c 1 | 13.046; 18.896; 21.809 90; 91.007; 90 | 5375 | Chandra, Brijesh; Mahanta, Sanjeev P.; Pati, Narendra N.; Baskaran, Sambath; Kanaparthi, Ravi K.; Sivasankar, Chinnappan; Panda, Pradeepta K. Calix[2]bispyrrolylarenes: New Expanded Calix[4]pyrroles for Fluorometric Sensing of Anions via Extended π-Conjugation. Organic letters, 2013, 15, 306-309 |
| 1508862 | CIF | C24 H16 N2 | P 1 21 1 | 7.6144; 7.5543; 29.9948 90; 91.624; 90 | 1724.65 | Louillat, Marie-Laure; Patureau, Frederic W. Toward polynuclear ru-cu catalytic dehydrogenative C-N bond formation, on the reactivity of carbazoles. Organic letters, 2013, 15, 164-167 |
| 1508863 | CIF | C24 H24 O4 | P -1 | 9.2295; 10.3951; 11.3783 86.591; 69.851; 79.622 | 1008.07 | Qin, Changming; Davies, Huw M. L. Enantioselective Synthesis of 2-Arylbicyclo[1.1.0]butane Carboxylates. Organic letters, 2013, 15, 310-313 |
| 1508864 | CIF | C25 H25 N3 O3 | C 1 2 1 | 21.033; 9.9868; 10.2026 90; 102.928; 90 | 2088.8 | Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers. Organic letters, 2013, 15, 468-471 |
| 1508865 | CIF | C25 H24 Cl N3 O3 | P 21 21 21 | 8.1146; 9.2164; 35.493 90; 90; 90 | 2654.4 | Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers. Organic letters, 2013, 15, 468-471 |
| 1508866 | CIF | C12 H18 F6 N2 O2 | P 1 2/c 1 | 9.4219; 8.6467; 18.7345 90; 103.222; 90 | 1485.81 | Riofski, Mark V.; Hart, Allison D.; Colby, David A. Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate. Organic letters, 2013, 15, 208-211 |
| 1508867 | CIF | C25 H28 Cl N O6 | P 1 21/n 1 | 13.871; 11.664; 15.1202 90; 92.72; 90 | 2443.6 | Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L. Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals. Organic letters, 2013, 15, 350-353 |
| 1508868 | CIF | C29 H29 N O6 | P 1 21/c 1 | 9.4038; 10.7199; 24.4225 90; 99.093; 90 | 2431.04 | Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L. Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals. Organic letters, 2013, 15, 350-353 |
| 1508869 | CIF | C29 H29 N O6 | P -1 | 11.3123; 13.5731; 16.6509 78.645; 73.569; 86.82 | 2404.2 | Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L. Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals. Organic letters, 2013, 15, 350-353 |
| 1508870 | CIF | C27 H33 N O7 | P b c a | 19.1983; 10.9762; 23.4467 90; 90; 90 | 4940.8 | Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L. Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals. Organic letters, 2013, 15, 350-353 |
| 1508871 | CIF | C28 H33 N O7 | P -1 | 9.6224; 10.0813; 14.8728 103.357; 105.497; 103.944 | 1280.26 | Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L. Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals. Organic letters, 2013, 15, 350-353 |
| 1508872 | CIF | C30 H44 S4 Si4 | P 1 21/n 1 | 10.779; 6.217; 27.444 90; 93; 90 | 1836.6 | Wu, Tianjing; Shi, Jianwu; Li, Chunli; Song, Jinsheng; Xu, Li; Wang, Hua Synthesis of Dendrimers Based on Tetrakis(thiophene-2-yl)ethene as New Dendron. Organic letters, 2013, 15, 354-357 |
| 1508873 | CIF | C110 H140 S16 Si12 | P -1 | 12.183; 16.129; 16.62 100.265; 92.579; 90.124 | 3210 | Wu, Tianjing; Shi, Jianwu; Li, Chunli; Song, Jinsheng; Xu, Li; Wang, Hua Synthesis of Dendrimers Based on Tetrakis(thiophene-2-yl)ethene as New Dendron. Organic letters, 2013, 15, 354-357 |
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