Crystallography Open Database
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Result: there are 594 entries in the selection
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Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 17
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7156596 | CIF | C2.53 H2.27 N0.13 O0.13 | P b c a | 16.7527; 9.2802; 19.428 90; 90; 90 | 3020.4 | Xiao, Jun-An; Cheng, Xiu-Liang; Li, Yu-Chun; He, Yi-Miao; Li, Jin-Lian; Liu, Zhi-Ping; Xia, Peng-Ju; Su, Wei; Yang, Hua Palladium-catalysed ring-opening [3 + 2]-annulation of spirovinylcyclopropyl oxindole to diastereoselectively access spirooxindoles. Organic & biomolecular chemistry, 2018, 17, 103-107 |
| 7156597 | CIF | C54 H46 Cl2 N4 O6 | P -1 | 8.9496; 9.6224; 14.1054 100.823; 90.1216; 110.257 | 1116.34 | Xiao, Jun-An; Cheng, Xiu-Liang; Li, Yu-Chun; He, Yi-Miao; Li, Jin-Lian; Liu, Zhi-Ping; Xia, Peng-Ju; Su, Wei; Yang, Hua Palladium-catalysed ring-opening [3 + 2]-annulation of spirovinylcyclopropyl oxindole to diastereoselectively access spirooxindoles. Organic & biomolecular chemistry, 2018, 17, 103-107 |
| 7156598 | CIF | C10 H7 Br I N | P b c a | 10.5281; 7.794; 25.907 90; 90; 90 | 2125.8 | Wang, Fang; Zhang, Xinying; He, Yan; Fan, Xuesen Selective synthesis of pyrrolidin-2-ones and 3-iodopyrroles via the ring contraction and deformylative functionalization of piperidine derivatives. Organic & biomolecular chemistry, 2018, 17, 156-164 |
| 7156599 | CIF | C16 H12 Br N | P b c n | 13.856; 6.4827; 28.807 90; 90; 90 | 2587.6 | Gattu, Radhakrishna; Mondal, Santa; Ali, Saghir; Khan, Abu T. Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes. Organic & biomolecular chemistry, 2019, 17, 347-353 |
| 7156600 | CIF | C24 H22 N2 O3 | P 1 21 1 | 11.6212; 6.9157; 12.8041 90; 109.534; 90 | 969.82 | Motaghi, Milad; Khosravi, Hormoz; Balalaie, Saeed; Rominger, Frank Catalytic formal [4 + 1] isocyanide-based cycloaddition: an efficient strategy for the synthesis of 1H-cyclopenta[b]quinolin-1-one derivatives. Organic & biomolecular chemistry, 2019, 17, 275-282 |
| 7156601 | CIF | C16 H12 Br N | P b c n | 13.856; 6.4827; 28.807 90; 90; 90 | 2587.6 | Carlos, Andressa M. M.; Stieler, Rafael; Lüdtke, Diogo S Catalytic asymmetric synthesis of 3-aryl phthalides enabled by arylation-lactonization of 2-formylbenzoates. Organic & biomolecular chemistry, 2019, 17, 283-289 |
| 7156602 | CIF | C29 H27 N O5 S2 | P 1 21/n 1 | 14.943; 10.893; 16.259 90; 90.199; 90 | 2646.5 | Undeela, Sridhar; Chandra, Rajesh; Nanubolu, Jagadeesh Babu; Menon, Rajeev S. Gold-catalysed regioselective cascade cycloisomerisation reactions of aza-enediynes for the synthesis of substituted benzoisoquinoline derivatives. Organic & biomolecular chemistry, 2019, 17, 369-373 |
| 7156603 | CIF | C27 H39 N3 O6 | P 1 21 1 | 10.8594; 7.3763; 15.5152 90; 92.469; 90 | 1241.65 | Alkayar, Ziad T. I.; Coldham, Iain Cascade cyclization and intramolecular nitrone dipolar cycloaddition and formal synthesis of 19-hydroxyibogamine. Organic & biomolecular chemistry, 2018, 17, 66-73 |
| 7156604 | CIF | C25 H24 Br N3 O | P 1 21/n 1 | 10.1801; 10.2257; 21.1176 90; 103.581; 90 | 2136.8 | Wang, Kai-Kai; Li, Yan-Li; Wang, Zhan-Yong; Hu, Meng-Wei; Qiu, Ting-Ting; Zhu, Bao-Ku Cross 1,3-dipolar cycloadditions of C,N-cyclic azomethine imines with an N-benzyl azomethine ylide: facile access to fused tricyclic 1,2,4-hexahydrotriazines. Organic & biomolecular chemistry, 2019, 17, 244-247 |
| 7156605 | CIF | C11.5 H10.5 N1.5 O | P 1 21 1 | 10.5966; 7.8609; 11.8783 90; 114.143; 90 | 902.899 | Liu, Zhiwen; Ma, Liang; Zhang, Liping; Zhang, Wenjun; Zhu, Yiguang; Chen, Yuchan; Zhang, Weimin; Zhang, Changsheng Functional characterization of the halogenase SpmH and discovery of new deschloro-tryptophan dimers. Organic & biomolecular chemistry, 2019, 17, 1053-1057 |
| 7156606 | CIF | C20 H32 O11 | P 21 21 21 | 6.9268; 7.6212; 39.643 90; 90; 90 | 2092.8 | Wang, Junfeng; Qin, Li; Zhao, Biqing; Cai, Liang; Zhong, Zhenping; Liu, Yonghong; Zhou, Xiaojiang Crotonols A and B, two rare tigliane diterpenoid derivatives against K562 cells from Croton tiglium. Organic & biomolecular chemistry, 2018, 17, 195-202 |
| 7156607 | CIF | C15 H17 N O | P 21 21 21 | 7.1064; 10.3163; 15.973 90; 90; 90 | 1171 | Xu, Dawen; Kaiser, Felix; Li, Han; Reich, Robert M.; Guo, Hao; Kühn, Fritz E Highly selective AlCl<sub>3</sub> initiated intramolecular α-alkylation of α,β-unsaturated lactams and lactones. Organic & biomolecular chemistry, 2018, 17, 49-52 |
| 7156608 | CIF | C31 H51 N2 Sc Si2 | C 1 2/c 1 | 38.238; 10.441; 17.4643 90; 98.199; 90 | 6901.2 | Su, Jianhong; Zhou, Yiqun; Xu, Xin Hydroaminoalkylation of sterically hindered alkenes with N,N-dimethyl anilines using a scandium catalyst. Organic & biomolecular chemistry, 2019, 17, 2013-2019 |
| 7156609 | CIF | C15 H10 Br N O3 | P 1 21/c 1 | 11.436; 8.3742; 14.1928 90; 94.648; 90 | 1354.74 | da Silva, Vitor A. F.; da Silva, Gustavo P.; Matsuo, Bianca T.; Ali, Akbar; Davis, Rebecca L.; Zukerman-Schpector, Julio; Corrêa, Arlene G; Paixão, Márcio W Synthesis of (Z)-β-halo α,β-unsaturated carbonyl systems via the combination of halotrimethylsilane and tetrafluoroboric acid. Organic & biomolecular chemistry, 2019, 17, 519-526 |
| 7156610 | CIF | C25 H21 Br N2 O8 | P 1 21/a 1 | 8.5538; 28.5184; 9.9217 90; 104.085; 90 | 2347.5 | Bakthadoss, Manickam; Jayakumar, Srinivasan; Raman, Selvakumar; Devaraj, Anthonisamy; Sharada, Duddu S. A novel multicomponent quadruple/double quadruple domino reaction: highly efficient synthesis of polyheterocyclic architectures. Organic & biomolecular chemistry, 2019, 17, 3884-3893 |
| 7156611 | CIF | C22 H17 Br N2 O6 | P -1 | 8.0079; 10.6912; 12.9965 79.773; 82.666; 69.817 | 1025.11 | Bakthadoss, Manickam; Jayakumar, Srinivasan; Raman, Selvakumar; Devaraj, Anthonisamy; Sharada, Duddu S. A novel multicomponent quadruple/double quadruple domino reaction: highly efficient synthesis of polyheterocyclic architectures. Organic & biomolecular chemistry, 2019, 17, 3884-3893 |
| 7156612 | CIF | C16 H10 N2 O5 S | P -1 | 7.552; 8.2283; 12.801 74.726; 86.674; 72.819 | 732.95 | McCaw, Patrick G.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Collins, Stuart G. Synthesis of 1,2,5-oxathiazole-S-oxides by 1,3-dipolar cycloadditions of nitrile oxides to α-oxo sulfines. Organic & biomolecular chemistry, 2019, 17, 622-638 |
| 7156613 | CIF | C20 H19 N O3 S | P 1 21/c 1 | 11.0131; 11.9246; 14.5681 90; 107.106; 90 | 1828.55 | McCaw, Patrick G.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Collins, Stuart G. Synthesis of 1,2,5-oxathiazole-S-oxides by 1,3-dipolar cycloadditions of nitrile oxides to α-oxo sulfines. Organic & biomolecular chemistry, 2019, 17, 622-638 |
| 7156614 | CIF | C16 H9 F2 N O2 S | P 1 21/c 1 | 14.0083; 8.7108; 11.5419 90; 105.733; 90 | 1355.62 | McCaw, Patrick G.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Collins, Stuart G. Synthesis of 1,2,5-oxathiazole-S-oxides by 1,3-dipolar cycloadditions of nitrile oxides to α-oxo sulfines. Organic & biomolecular chemistry, 2019, 17, 622-638 |
| 7156615 | CIF | C17 H12 F N O3 S | P b c a | 15.237; 11.212; 17.948 90; 90; 90 | 3066.2 | McCaw, Patrick G.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Collins, Stuart G. Synthesis of 1,2,5-oxathiazole-S-oxides by 1,3-dipolar cycloadditions of nitrile oxides to α-oxo sulfines. Organic & biomolecular chemistry, 2019, 17, 622-638 |
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