Crystallography Open Database
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Result: there are 907 entries in the selection
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Searching journal of publication like 'Organic letters' volume of publication is 16
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1513423 | CIF | C24 H22 N2 O2 S | P 1 21/c 1 | 8.6482; 22.5718; 11.0285 90; 104.935; 90 | 2080.1 | Xing, Yanpeng; Sheng, Guorong; Wang, Jing; Lu, Ping; Wang, Yanguang Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors. Organic letters, 2014, 16, 1244-1247 |
| 1513424 | CIF | C29 H25 N3 O2 S | P 1 21/c 1 | 12.2997; 13.4444; 15.1233 90; 103.646; 90 | 2430.23 | Xing, Yanpeng; Sheng, Guorong; Wang, Jing; Lu, Ping; Wang, Yanguang Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors. Organic letters, 2014, 16, 1244-1247 |
| 1513425 | CIF | C25 H22 N2 O2 S | P 1 21/c 1 | 11.4322; 22.0069; 8.2441 90; 98.244; 90 | 2052.7 | Xing, Yanpeng; Sheng, Guorong; Wang, Jing; Lu, Ping; Wang, Yanguang Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors. Organic letters, 2014, 16, 1244-1247 |
| 1513426 | CIF | C46 H40 N O5 P | P 21 21 21 | 11.4547; 13.3323; 48.8967 90; 90; 90 | 7467.4 | Morin, Marie S. T.; Arndtsen, Bruce A. Chiral phosphorus-based 1,3-dipoles: a modular approach to enantioselective 1,3-dipolar cycloaddition and polycyclic 2-pyrroline synthesis. Organic letters, 2014, 16, 1056-1059 |
| 1513427 | CIF | C20 H23 N O | P 1 21 1 | 15.7825; 5.8322; 18.8095 90; 113.102; 90 | 1592.51 | Morin, Marie S. T.; Arndtsen, Bruce A. Chiral phosphorus-based 1,3-dipoles: a modular approach to enantioselective 1,3-dipolar cycloaddition and polycyclic 2-pyrroline synthesis. Organic letters, 2014, 16, 1056-1059 |
| 1513428 | CIF | C26 H30 F6 Mn N6 O6 S2 | P 1 21 1 | 8.5432; 16.2125; 11.468 90; 90.352; 90 | 1588.36 | Shen, Duyi; Miao, Chengxia; Wang, Shoufeng; Xia, Chungu; Sun, Wei Efficient benzylic and aliphatic C-h oxidation with selectivity for methylenic sites catalyzed by a bioinspired manganese complex. Organic letters, 2014, 16, 1108-1111 |
| 1513429 | CIF | C24 H17 N S | P -1 | 9.953; 18.073; 18.081 116.66; 100.49; 100.58 | 2724.7 | Zhao, Peng; Yan, Xiaoyu; Yin, Hang; Xi, Chanjuan Alkyltriflate-Triggered Annulation of Arylisothiocyanates and Alkynes Leading to Multiply Substituted Quinolines through Domino Electrophilic Activation. Organic letters, 2014, 16, 1120-1123 |
| 1513430 | CIF | C16 H12 Br N S | P 1 21/n 1 | 11.406; 6.9954; 16.879 90; 91.93; 90 | 1346 | Zhao, Peng; Yan, Xiaoyu; Yin, Hang; Xi, Chanjuan Alkyltriflate-Triggered Annulation of Arylisothiocyanates and Alkynes Leading to Multiply Substituted Quinolines through Domino Electrophilic Activation. Organic letters, 2014, 16, 1120-1123 |
| 1513431 | CIF | C23 H20 N O S | C 1 2/c 1 | 22.58; 11.871; 16.728 90; 124.64; 90 | 3689.1 | Zhao, Peng; Yan, Xiaoyu; Yin, Hang; Xi, Chanjuan Alkyltriflate-Triggered Annulation of Arylisothiocyanates and Alkynes Leading to Multiply Substituted Quinolines through Domino Electrophilic Activation. Organic letters, 2014, 16, 1120-1123 |
| 1513432 | CIF | C20 H15 Cl N2 O | P 1 21/c 1 | 18.4649; 7.9164; 11.5345 90; 94.47; 90 | 1680.93 | Takahashi, Hiroki; Yasui, Seiji; Tsunoi, Shinji; Shibata, Ikuya Catalytic cycloaddition of 2-methyleneaziridines with 1,1-dicyanoalkenes. Organic letters, 2014, 16, 1192-1195 |
| 1513433 | CIF | C18 H14 N2 O3 | P -1 | 6.0877; 10.9989; 11.2984 83.29; 87.571; 83.717 | 746.49 | Hao, Xin-Qi; Chen, Li-Juan; Ren, Baozeng; Li, Liu-Yan; Yang, Xin-Yan; Gong, Jun-Fang; Niu, Jun-Long; Song, Mao-Ping Copper-mediated direct aryloxylation of benzamides assisted by an n,o-bidentate directing group. Organic letters, 2014, 16, 1104-1107 |
| 1513434 | CIF | C24 H18 N2 O4 | P -1 | 7.2876; 12.0282; 12.8131 115.87; 93.712; 98.655 | 988.3 | Hao, Xin-Qi; Chen, Li-Juan; Ren, Baozeng; Li, Liu-Yan; Yang, Xin-Yan; Gong, Jun-Fang; Niu, Jun-Long; Song, Mao-Ping Copper-mediated direct aryloxylation of benzamides assisted by an n,o-bidentate directing group. Organic letters, 2014, 16, 1104-1107 |
| 1513435 | CIF | C37 H33 F3 N O4 Rh S | P -1 | 11.015; 12.485; 13.435 102.315; 110.462; 93.671 | 1672 | Yu, Songjie; Li, Xingwei Mild Synthesis of Chalcones via Rhodium(III)-Catalyzed C-C Coupling of Arenes and Cyclopropenones. Organic letters, 2014, 16, 1220-1223 |
| 1513436 | CIF | C26 H19 N O | P -1 | 10.7315; 13.8056; 14.032 89.874; 88.794; 68.616 | 1935.33 | Yu, Songjie; Li, Xingwei Mild Synthesis of Chalcones via Rhodium(III)-Catalyzed C-C Coupling of Arenes and Cyclopropenones. Organic letters, 2014, 16, 1220-1223 |
| 1513437 | CIF | C21 H18 O3 | P -1 | 8.9589; 9.9488; 10.2552 115.145; 98.6848; 96.7865 | 800.79 | Teo, Wan Teng; Rao, Weidong; Ng, Charmaine Jia Huan; Koh, Shaun Wei Yong; Chan, Philip Wai Hong Gold-Catalyzed Benzannulation of 5-Hydroxy-3-oxoalk-6-ynoate Esters to o-Phenolic Esters. Organic letters, 2014, 16, 1248-1251 |
| 1513438 | CIF | C12 H11 F3 N4 O2 S | P 1 21/c 1 | 9.7909; 9.9299; 15.0054 90; 108.195; 90 | 1385.92 | Qiao, Zongjun; Wei, Jianpeng; Jiang, Xuefeng Direct Cross-Coupling Access to Diverse Aromatic Sulfide: Palladium-Catalyzed Double C-S Bond Construction Using Na2S2O3 as a Sulfurating Reagent. Organic letters, 2014, 16, 1212-1215 |
| 1513439 | CIF | C17 H26 N2 O2 | P 1 21/c 1 | 13.224; 6.1677; 22.599 90; 118.413; 90 | 1621.2 | Luescher, Michael U.; Vo, Cam-Van T; Bode, Jeffrey W. SnAP Reagents for the Synthesis of Piperazines and Morpholines. Organic letters, 2014, 16, 1236-1239 |
| 1513440 | CIF | C13 H20 N2 O | P 1 21/c 1 | 9.62; 6.3559; 20.787 90; 107.642; 90 | 1211.2 | Luescher, Michael U.; Vo, Cam-Van T; Bode, Jeffrey W. SnAP Reagents for the Synthesis of Piperazines and Morpholines. Organic letters, 2014, 16, 1236-1239 |
| 1513441 | CIF | C20 H29 N3 O2 | P 21 21 21 | 10.1265; 10.6178; 18.064 90; 90; 90 | 1942.26 | Kapras, Vojtěch; Pohl, Radek; Císařová, Ivana; Jahn, Ullrich Asymmetric Domino Aza-Michael Addition/[3 + 2] Cycloaddition Reactions as a Versatile Approach to α,β,γ-Triamino Acid Derivatives. Organic letters, 2014, 16, 1088-1091 |
| 1513442 | CIF | C20 H29 N3 O2 | P 21 21 21 | 8.2352; 9.944; 23.9419 90; 90; 90 | 1960.62 | Kapras, Vojtěch; Pohl, Radek; Císařová, Ivana; Jahn, Ullrich Asymmetric Domino Aza-Michael Addition/[3 + 2] Cycloaddition Reactions as a Versatile Approach to α,β,γ-Triamino Acid Derivatives. Organic letters, 2014, 16, 1088-1091 |
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