Crystallography Open Database
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Result: there are 625 entries in the selection
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Searching journal of publication like 'Organic letters' volume of publication is 12
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1503154 | CIF | C14 H11 Cl N2 O | P -1 | 5.7679; 8.2804; 12.9064 74.09; 88.512; 85.529 | 590.99 | Urgaonkar, Sameer; Cortese, Joseph F.; Barker, Robert H.; Cromwell, Mandy; Serrano, Adelfa E.; Wirth, Dyann F.; Clardy, Jon; Mazitschek, Ralph A concise silylamine approach to 2-amino-3-hydroxy-indoles with potent in vivo antimalaria activity. Organic letters, 2010, 12, 3998-4001 |
| 1503155 | CIF | C42 H37 N4 Ni O4 | P 21 21 21 | 11.937; 14.935; 19.399 90; 90; 90 | 3458.4 | Dong, Zhenzhen; Plampin, 3rd, James N; Yap, Glenn P. A.; Fox, Joseph M. Minimalist end groups for control of absolute helicity in salen- and salophen-based metallofoldamers. Organic letters, 2010, 12, 4002-4005 |
| 1503156 | CIF | C43 H44 Cl2 N4 Ni O4 | P 1 | 12.3092; 12.3128; 12.973 90.061; 102.664; 98.557 | 1895.9 | Dong, Zhenzhen; Plampin, 3rd, James N; Yap, Glenn P. A.; Fox, Joseph M. Minimalist end groups for control of absolute helicity in salen- and salophen-based metallofoldamers. Organic letters, 2010, 12, 4002-4005 |
| 1503157 | CIF | C21 H33 N3 O5 S Si | P 1 21 1 | 7.6795; 8.1287; 21.2564 90; 99.965; 90 | 1306.9 | Kelley, Brandon T.; Joullié, Madeleine M Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines. Organic letters, 2010, 12, 4244-4247 |
| 1503158 | CIF | C22 H35 N3 O6 S Si | C 1 2 1 | 31.131; 7.805; 22.844 90; 110.163; 90 | 5210.4 | Kelley, Brandon T.; Joullié, Madeleine M Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines. Organic letters, 2010, 12, 4244-4247 |
| 1503159 | CIF | C19 H28 N2 O5 S Si | P 1 21 1 | 7.2155; 7.3686; 21.8244 90; 91.207; 90 | 1160.11 | Kelley, Brandon T.; Joullié, Madeleine M Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines. Organic letters, 2010, 12, 4244-4247 |
| 1503160 | CIF | C26 H22 N2 O4 | P 1 21/c 1 | 10.513; 21.209; 19.5593 90; 90.309; 90 | 4361.1 | Gao, Meng; Yang, Yan; Wu, Yan-Dong; Deng, Cong; Shu, Wen-Ming; Zhang, Dong-Xue; Cao, Li-Ping; She, Neng-Fang; Wu, An-Xin An efficient synthesis of hydantoins via sustainable integration of coupled domino processes. Organic letters, 2010, 12, 4026-4029 |
| 1503161 | CIF | C27 H23 N2 O4.5 | P b c n | 11.301; 17.774; 22.517 90; 90; 90 | 4522.9 | Gao, Meng; Yang, Yan; Wu, Yan-Dong; Deng, Cong; Shu, Wen-Ming; Zhang, Dong-Xue; Cao, Li-Ping; She, Neng-Fang; Wu, An-Xin An efficient synthesis of hydantoins via sustainable integration of coupled domino processes. Organic letters, 2010, 12, 4026-4029 |
| 1503162 | CIF | C124 H106 N8 O9 | P 1 21 1 | 20.312; 9.5308; 26.2849 90; 107.355; 90 | 4856.8 | Wiedner, Susan D.; Vedejs, Edwin Aziridinomitosanes via lactam cyclization. Organic letters, 2010, 12, 4030-4033 |
| 1503163 | CIF | C46 H45 N2 O7.5 | P 21 21 21 | 12.8063; 13.3599; 48.7876 90; 90; 90 | 8347.1 | Wiedner, Susan D.; Vedejs, Edwin Aziridinomitosanes via lactam cyclization. Organic letters, 2010, 12, 4030-4033 |
| 1503164 | CIF | C32 H50 N6 O2 | P -1 | 6.897; 11.772; 20.837 78.683; 88.669; 73.136 | 1586.5 | Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions. Organic letters, 2010, 12, 3910-3913 |
| 1503165 | CIF | C32 H48 N6 O4 S | C m c 21 | 17.106; 16.317; 11.461 90; 90; 90 | 3199 | Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions. Organic letters, 2010, 12, 3910-3913 |
| 1503166 | CIF | C28 H42 N4 O7 S | P 1 21/c 1 | 19.123; 13.758; 11.749 90; 106.098; 90 | 2969.9 | Mani, Ganesan; Guchhait, Tapas; Kumar, Rajnish; Kumar, Shanish Macrocyclic and acyclic molecules synthesized from dipyrrolylmethanes: receptors for anions. Organic letters, 2010, 12, 3910-3913 |
| 1503167 | CIF | C17 H25 N O3 | P 21 21 21 | 9.1204; 11.6853; 14.1079 90; 90; 90 | 1503.54 | Zhao, Fu-Wei; Sun, Qian-Yun; Yang, Fu-Mei; Hu, Guang-Wan; Luo, Ji-Feng; Tang, Gui-Hua; Wang, Yue-Hu; Long, Chun-Lin Palhinine A, a novel alkaloid from Palhinhaea cernua. Organic letters, 2010, 12, 3922-3925 |
| 1503168 | CIF | C24 H24 N2 O4 | P -1 | 9.941; 10.774; 11.867 77.103; 66.061; 65.409 | 1054 | McCormack, Michael P.; Shalumova, Tamila; Tanski, Joseph M.; Waters, Stephen P. Development of a 2-aza-Cope-[3 + 2] dipolar cycloaddition strategy for the synthesis of quaternary proline scaffolds. Organic letters, 2010, 12, 3906-3909 |
| 1503169 | CIF | C23 H19 N O2 | P -1 | 8.0436; 10.604; 11.289 110.89; 95.92; 99.62 | 873 | Yang, Luo; Lei, Chuan-Hu; Wang, De-Xian; Huang, Zhi-Tang; Wang, Mei-Xiang Highly efficient and expedient synthesis of 5-hydroxy-1H-pyrrol-2-(5H)-ones from FeCl3-catalyzed tandem intramolecular enaminic addition of tertiary enamides to ketones and 1,3-hydroxy rearrangement. Organic letters, 2010, 12, 3918-3921 |
| 1503170 | CIF | C24 H21 N O2 | P 1 21/c 1 | 8.5467; 10.49; 21.228 90; 101.57; 90 | 1864.5 | Yang, Luo; Lei, Chuan-Hu; Wang, De-Xian; Huang, Zhi-Tang; Wang, Mei-Xiang Highly efficient and expedient synthesis of 5-hydroxy-1H-pyrrol-2-(5H)-ones from FeCl3-catalyzed tandem intramolecular enaminic addition of tertiary enamides to ketones and 1,3-hydroxy rearrangement. Organic letters, 2010, 12, 3918-3921 |
| 1503171 | CIF | C25 H23 Br N O3 P S | P 1 21/c 1 | 9.276; 22.735; 11.894 90; 110.871; 90 | 2343.7 | Xie, Peizhong; Huang, You; Chen, Ruyu Phosphine-catalyzed domino reaction: highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allylic carbonates. Organic letters, 2010, 12, 3768-3771 |
| 1503172 | CIF | C31 H27 Br N O3 P S | P 21 21 21 | 10.26; 8.486; 30.754 90; 90; 90 | 2677.6 | Xie, Peizhong; Huang, You; Chen, Ruyu Phosphine-catalyzed domino reaction: highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl N-thiophosphinyl imines and allylic carbonates. Organic letters, 2010, 12, 3768-3771 |
| 1503173 | CIF | C13 H7 B F5 N3 | P 1 21/c 1 | 8.39; 28.706; 20.46 90; 93.631; 90 | 4918 | Kubota, Yasuhiro; Tsuzuki, Toshihiro; Funabiki, Kazumasa; Ebihara, Masahiro; Matsui, Masaki Synthesis and fluorescence properties of a pyridomethene-BF2 complex. Organic letters, 2010, 12, 4010-4013 |
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