Crystallography Open Database
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Searching journal of publication like 'Org. Chem. Front.'
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1553012 | CIF | C14 H10 N2 | P b c a | 11.876; 7.462; 24.973 90; 90; 90 | 2213.1 | You, Xu; Xie, Xin; Sun, Renhong; Chen, Haoyi; Li, Shi; Liu, Yuanhong Titanium-mediated cross-coupling reactions of 1,3-butadiynes with α-iminonitriles to 3-aminopyrroles: observation of an imino aza-Nazarov cyclization Org. Chem. Front., 2014, 1, 940 |
1553739 | CIF | C15 H9 F N2 | P b c a | 25.513; 13.881; 6.794 90; 90; 90 | 2406 | Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L. Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions Org. Chem. Front., 2017, 4, 1574 |
1552980 | CIF | C16 H13 F3 N2 O | P 1 21/c 1 | 9.805; 9.3144; 15.513 90; 97.91; 90 | 1403.3 | Yan, Xiaoyu; Yi, Xiangli; Xi, Chanjuan Direct cleavage of the NN bond of azobenzenes by MeOTf leading to N-arylbenzimidazoles Org. Chem. Front., 2014, 1, 657 |
1553740 | CIF | C16 H13 N2 | P b c a | 25.555; 14.1257; 6.8724 90; 90; 90 | 2480.8 | Panaka, Sangeetha; Trivedi, Rajiv; Sony, T.; Prabhakar, S.; Raju Chowhan, L. Silver(i) catalyzed intramolecular cyclization of N-(2-(alk-1-yn-1-yl))-1H-tetrazoles leading to the formation of N-cyano-2-substituted indoles under ambient conditions Org. Chem. Front., 2017, 4, 1574 |
1556393 | CIF | C16 H16 Br N3 O | P 21 21 21 | 9.466; 12.4249; 13.3396 90; 90; 90 | 1568.9 | Fu, Niankai; Zhang, Long; Luo, Sanzhong; Cheng, Jin-Pei Chiral primary amine catalysed asymmetric conjugate addition of azoles to α-substituted vinyl ketones Org. Chem. Front., 2014, 1, 68 |
1552977 | CIF | C16 H6 F4 N4 O2 | P 1 21/c 1 | 14.965; 8.119; 13.829 90; 116.87; 90 | 1498.8 | Liu, Yan-Hua; Zhang, Liang; Xu, Xiao-Na; Li, Zhi-Ming; Zhang, Dan-Wei; Zhao, Xin; Li, Zhan-Ting Intramolecular C‒H⋯F hydrogen bonding-induced 1,2,3-triazole-based foldamers Org. Chem. Front., 2014, 1, 494 |
1552979 | CIF | C17 H17 F3 N2 O3 S | P 1 21/c 1 | 13.555; 8.9872; 15.716 90; 112.99; 90 | 1762.5 | Yan, Xiaoyu; Yi, Xiangli; Xi, Chanjuan Direct cleavage of the NN bond of azobenzenes by MeOTf leading to N-arylbenzimidazoles Org. Chem. Front., 2014, 1, 657 |
1552972 | CIF | C17 H21 B Br O P | P 1 | 6.4951; 9.549; 15.501 81.333; 86.707; 74.351 | 915 | Li, Chun; Bian, Qing-Long; Xu, Sheng; Duan, Wei-Liang Palladium-catalyzed 1,4-addition of secondary alkylphenylphosphines to α,β-unsaturated carbonyl compounds for the synthesis of phosphorus- and carbon-stereogenic compounds Org. Chem. Front., 2014, 1, 541 |
1556391 | CIF | C18 H20 O2 | P 21 21 21 | 9.1769; 10.289; 14.62 90; 90; 90 | 1380.4 | Zhang, Shaoguang; Zhan, Ming; Wang, Qifeng; Wang, Chao; Zhang, Wen-Xiong; Xi, Zhenfeng Synthesis of semibullvalene derivatives via Co2(CO)8-mediated cyclodimerization of 1,4-dilithio-1,3-butadienes Org. Chem. Front., 2014, 1, 130 |
1553016 | CIF | C19 H15 Br F3 N O4 | P 1 21/c 1 | 24.855; 9.629; 15.692 90; 96.85; 90 | 3728.7 | Sang, Rui; Tang, Xiang-Ying; Shi, Min Ozonation of methylenecyclopropanes Org. Chem. Front., 2014, 1, 770 |
1553032 | CIF | C20 H20 N2 O | P 1 21/n 1 | 11.245; 22.954; 26.071 90; 100.618; 90 | 6614 | Song, Junjie; Fan, Congbin; Liu, Gang; Qiu, Guanyinsheng Generation of 1-amino-isoquinoline-N-oxides via a tandem reaction of 2-alkynylbenzaldoxime with secondary amines in the presence of silver(i) and copper(i) Org. Chem. Front., 2014, 1, 1045 |
1556404 | CIF | C20 H21 N3 | P b c a | 15.3067; 12.1443; 18.1692 90; 90; 90 | 3377.5 | Kuang, Jinqiang; Chen, Bo; Ma, Shengming Copper-mediated efficient three-component synthesis of 1,2,4-triazoles from amines and nitriles Org. Chem. Front., 2014, 1, 186 |
1552973 | CIF | C20 H22 B Br N O P | P 21 21 21 | 6.2364; 17.7803; 18.9588 90; 90; 90 | 2102.2 | Li, Chun; Bian, Qing-Long; Xu, Sheng; Duan, Wei-Liang Palladium-catalyzed 1,4-addition of secondary alkylphenylphosphines to α,β-unsaturated carbonyl compounds for the synthesis of phosphorus- and carbon-stereogenic compounds Org. Chem. Front., 2014, 1, 541 |
1553029 | CIF | C20 H26 Cl2 Fe N2 | P 1 21/n 1 | 9.0055; 15.94; 14.422 90; 90.178; 90 | 2070.2 | Cao, Yanchun; Zhang, Yanlu; Zhang, Lei; Zhang, Dan; Leng, Xuebing; Huang, Zheng Selective synthesis of secondary benzylic (Z)-allylboronates by Fe-catalyzed 1,4-hydroboration of 1-aryl-substituted 1,3-dienes Org. Chem. Front., 2014, 1, 1101 |
1556405 | CIF | C21 H16 I N3 | P 1 21/c 1 | 12.2051; 18.0249; 8.7754 90; 110.387; 90 | 1809.6 | Kuang, Jinqiang; Chen, Bo; Ma, Shengming Copper-mediated efficient three-component synthesis of 1,2,4-triazoles from amines and nitriles Org. Chem. Front., 2014, 1, 186 |
1553034 | CIF | C21 H17 Br2 N O3 S | P 1 21 1 | 9.4812; 8.1107; 13.3671 90; 106.9; 90 | 983.53 | Liu, Cheng-Hang; Yu, Zhi-Xiang Gold(i)- and platinum(iv)-catalyzed intramolecular annulations of allenes towards furans Org. Chem. Front., 2014, 1, 1205 |
1556403 | CIF | C21 H22 O2 S | P -1 | 8.7371; 9.2269; 12.186 89.9; 72.14; 80.18 | 920 | Peng, Lingling; Zhang, Xiu; Ma, Jie; Wang, Jianbo Ru(ii)-catalyzed rearrangement of the allenic sulfide bearing propargyl moiety: efficient formation of benzene derivatives Org. Chem. Front., 2014, 1, 235 |
1556386 | CIF | C21 H27 N | P b c a | 9.2391; 17.1518; 22.2035 90; 90; 90 | 3518.53 | Qiu, Youai; Ma, Dengke; Kong, Wangqing; Fu, Chunling; Ma, Shengming Regiocontrolled 1,2-migration in cyclization of 1-(indol-2-yl)-3-alkyn-1-ols: (Ph3P)Au+vs. PtCl4 Org. Chem. Front., 2014, 1, 62 |
1556387 | CIF | C21 H27 N | P 1 21/c 1 | 13.1716; 8.3809; 20.39 90; 127.363; 90 | 1789 | Qiu, Youai; Ma, Dengke; Kong, Wangqing; Fu, Chunling; Ma, Shengming Regiocontrolled 1,2-migration in cyclization of 1-(indol-2-yl)-3-alkyn-1-ols: (Ph3P)Au+vs. PtCl4 Org. Chem. Front., 2014, 1, 62 |
1553033 | CIF | C21 H28 N4 O | P 32 | 13.204; 13.204; 11.5028 90; 90; 120 | 1736.78 | Ma, Gaoyuan; Sibi, Mukund P. Enantioselective allylic amination of MBH carbonates catalyzed by novel chiral 4-dialkylaminopyridine catalysts Org. Chem. Front., 2014, 1, 1152 |
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