Crystallography Open Database

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Searching journal of publication like 'Organic Chemistry Frontiers' volume of publication is 2

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1553158 CIFC46 H42 N2 OC 1 2/c 112.55604; 15.09459; 18.9643
90; 105.866; 90
3457.35Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553159 CIFC48 H46 N2 O3P -110.1705; 10.2903; 19.4528
99.778; 99.679; 106.888
1868.04Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553160 CIFC34 H34 N2 OP 1 21/c 111.9986; 10.6018; 20.9045
90; 104.851; 90
2570.36Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.
γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Organic Chemistry Frontiers, 2015, 2, 1445
1553161 CIFC15 H18 N2 O2P 1 21/n 118.06936; 17.802; 18.2203
90; 90.5295; 90
5860.69Huang, Pei-Qiang; Ou, Wei; Ye, Jian-Liang
Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines
Organic Chemistry Frontiers, 2015, 2, 1094
1553162 CIFC10 H9 F3 O2 S2P 1 21/n 19.4647; 5.7312; 22.1678
90; 100.283; 90
1183.16Yang, Hai-Bin; Fan, Xing; Wei, Yin; Shi, Min
Solvent-controlled nucleophilic trifluoromethylthiolation of Morita‒Baylis‒Hillman carbonates: dual roles of DABCO in activating the Zard's trifluoromethylthiolation reagent and the MBH carbonates
Organic Chemistry Frontiers, 2015, 2, 1088
1553163 CIFC23 H27 N O3P 1 21/c 110.695; 21.389; 9.1312
90; 99.66; 90
2059.2Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong
Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water
Organic Chemistry Frontiers, 2015, 2, 1326
1553164 CIFC22 H24 Cl N O4P b c a12.5003; 9.5999; 34.846
90; 90; 90
4181.6Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong
Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water
Organic Chemistry Frontiers, 2015, 2, 1326
1553165 CIFC30 H23 N O2P -18.8044; 9.6097; 13.3333
93.346; 95.699; 90.433
1120.5Guo, Tenglong; Jiang, Quanbin; Yu, Zhengkun
Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles
Organic Chemistry Frontiers, 2015, 2, 1361
1553166 CIFC10 H8 N4 OP b c a7.008; 13.515; 19.467
90; 90; 90
1843.8Li, Pan; Zhao, Jingjing; Xia, Chungu; Li, Fuwei
The development of carbene-stabilized N‒O radical coupling strategy in metal-free regioselective C‒H azidation of quinoline N-oxides
Organic Chemistry Frontiers, 2015, 2, 1313
1553167 CIFC25 H0 N24 O0.5P -110.974; 13.036; 14.337
68.085; 67.898; 73.316
1737Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553168 CIFC36 H40 O8C 1 2/c 18.621; 21.744; 18.379
90; 100.954; 90
3382.5Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553169 CIFC33 H41 N O9P 1 21/c 19.7518; 17.4971; 20.0458
90; 101.206; 90
3355.17Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu
Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes
Organic Chemistry Frontiers, 2015, 2, 1366
1553170 CIFC15 H14 O3 SP -18.503; 10.6762; 15.8607
76.75; 81.107; 88.437
1384.6Li, Siyu; Li, Xiang; Yang, Fan; Wu, Yangjie
Copper-catalyzed direct decarboxylative hydrosulfonylation of aryl propiolic acids with sulfonylhydrazides leading to vinylsulfones
Organic Chemistry Frontiers, 2015, 2, 1076
1553171 CIFC28 H29 N3 O4 S2P 1 21/n 110.2945; 18.1137; 14.6463
90; 105.831; 90
2627.5Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min
Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C‒H functionalization of indolyltriazoles
Organic Chemistry Frontiers, 2015, 2, 1516
1553172 CIFC27 H24 Cl3 N3 O4 S2P -111.3585; 11.981; 13.438
106.42; 108.985; 104.217
1539.6Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min
Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C‒H functionalization of indolyltriazoles
Organic Chemistry Frontiers, 2015, 2, 1516
1553173 CIFC26 H23 Cl F7 N OC 1 c 112.89225; 15.11065; 24.8076
90; 101.997; 90
4727.22Lao, Ye-Xing; Wu, Jia-Qiang; Chen, Yunyun; Zhang, Shang-Shi; Li, Qingjiang; Wang, Honggen
Palladium-catalyzed methylene C(sp3)‒H arylation of the adamantyl scaffold
Organic Chemistry Frontiers, 2015, 2, 1374
1553174 CIFC9 H6 F3 N3P 1 21/c 111.6048; 11.0429; 22.106
90; 94.237; 90
2825.2Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An
Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles
Organic Chemistry Frontiers, 2015, 2, 1468
1553175 CIFC11 H7 F6 N3P 1 21/c 110.63; 8.222; 13.645
90; 100.814; 90
1171.4Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An
Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles
Organic Chemistry Frontiers, 2015, 2, 1468
1553176 CIFC23 H19 Cl O2C 1 2/c 128.386; 9.195; 17.591
90; 125.324; 90
3746.1Li, Yang; Liu, Bang; Ouyang, Xuan-Hui; Song, Ren-Jie; Li, Jin-Heng
Alkylation/1,2-aryl migration of α-aryl allylic alcohols with α-carbonyl alkyl bromides using visible-light photoredox catalysis
Organic Chemistry Frontiers, 2015, 2, 1457
1553177 CIFC25 H27 Br2 N5 O2P -18.8674; 9.3784; 16.618
82.99; 87.24; 62.65
1218.3Zende, V. M.; Schulzke, C.; Kapdi, A. R.
Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki‒Miyaura arylation of bromoanthracene and related substrates
Organic Chemistry Frontiers, 2015, 2, 1397

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