Crystallography Open Database

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Searching journal of publication like 'Green Chemistry' volume of publication is 23

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7242163 CIFC15 H22 N2 O4P b c a9.448; 11.423; 30.49
90; 90; 90
3291Morita, Shunya; Yoshimura, Tomoyuki; Matsuo, Jun-ichi
Catalytic intermolecular aldol reactions of transient amide enolates in domino Michael/aldol reactions of nitroalkanes, acrylamides, and aldehydes
Green Chemistry, 2021, 23, 1160-1164
7242201 CIFC21 H32 Cl N O2 RuP 1 21/n 114.7118; 9.3818; 14.7793
90; 91.266; 90
2039.39Phearman, Alexander S.; Moore, Jewelianna M.; Bhagwandin, Dayanni D.; Goldberg, Jonathan M.; Heinekey, D. Michael; Goldberg, Karen I.
(Hexamethylbenzene)Ru catalysts for the Aldehyde-Water Shift reaction
Green Chemistry, 2021, 23, 1609-1615
7242202 CIFC25 H36 B2 O4P 1 21/n 16.5462; 27.28; 14.4106
90; 90.549; 90
2573.3Zhang, Yahui; Zhao, Xiangyu; Bi, Ce; Lu, Wenqi; Song, Mengyuan; Wang, Dongdong; Qing, Guangyan
Selective electrocatalytic hydroboration of aryl alkenes
Green Chemistry, 2021, 23, 1691-1699
7242218 CIFC10 H11 Cl F3 N O2P -15.6416; 5.8788; 18.0049
95.374; 95.693; 96.475
587.08Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242219 CIFC12 H16 Cl N O2P 1 21/c 16.099; 7.7041; 25.2722
90; 94.075; 90
1184.47Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242220 CIFC10 H13 N O2P 1 21/c 15.7769; 7.6286; 21.5338
90; 96.167; 90
943.5Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242221 CIFC8 H8 N2 O2C 1 2/c 118.9356; 3.81317; 21.672
90; 101.702; 90
1532.29Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242222 CIFC12 H14 Cl N O2P -15.7548; 10.5744; 10.5916
110.243; 102.912; 100.879
563.94Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242223 CIFC11 H13 N O2P 1 21/c 19.0379; 10.044; 11.0835
90; 99.123; 90
993.4Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242224 CIFC7 H12 O6P -17.6334; 8.7609; 14.2366
81.705; 88.677; 73.562
903.45Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242249 CIFC20 H19 N5 OP 1 21/n 16.7011; 9.1071; 28.951
90; 92.176; 90
1765.5Akulov, Alexey A.; Varaksin, Mikhail V.; Tsmokalyuk, Anton N.; Charushin, Valery N.; Chupakhin, Oleg N.
Blue-light-promoted radical Cā€’H azolation of cyclic nitrones enabled by Selectfluor®
Green Chemistry, 2021, 23, 2049-2057
7242297 CIFC7 H6 Cl N O2C 1 2/c 115.5231; 3.8267; 23.9744
90; 93.432; 90
1421.58Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng
Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids
Green Chemistry, 2021, 23, 2986-2991
7242298 CIFC17 H26 N2 O4P 21 21 217.9048; 11.2276; 19.3205
90; 90; 90
1714.73Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng
Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids
Green Chemistry, 2021, 23, 2986-2991
7242323 CIFC19 H18 N2 O2P 1 21/n 110.6894; 10.6948; 13.7194
90; 91.046; 90
1568.2Xu, Jun; Huang, Lin; He, Lei; Ni, Zhigang; Shen, Jiabin; Li, Xiaoling; Chen, Kaixian; Li, Wanmei; Zhang, Pengfei
A combination of heterogeneous catalysis and photocatalysis for the olefination of quinoxalin-2(1H)-ones with ketones in water: a green and efficient route to (Z)-enaminones
Green Chemistry, 2021, 23, 2123-2129
7242329 CIFC17 H18 O3 SP 1 21/n 115.40316; 7.20606; 15.43887
90; 116.871; 90
1528.62Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao
Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides
Green Chemistry, 2021, 23, 2420-2426
7242330 CIFC16 H14 O2 SP 21 21 218.5976; 10.8141; 15.2294
90; 90; 90
1416Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao
Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides
Green Chemistry, 2021, 23, 2420-2426
7242405 CIFC36 H32 Br2 N6 O4 S2P b c a15.138; 10.099; 22.516
90; 90; 90
3442.2Jiang, Shuai; Cao, Wen-Bin; Li, Hai-Yan; Xu, Xiao-Ping; Ji, Shun-Jun
Convenient synthesis of spiroindolenines from tryptamine-derived isocyanides and organic azides by cobalt catalysis in pure water
Green Chemistry, 2021, 23, 2619-2623
7242512 CIFC25 H22 Cl N O4 SP -112.3598; 12.8606; 15.4574
81.976; 75.455; 70.669
2239.9Liu, Chengkou; Lin, Yang; Cai, Chen; Yuan, Chengcheng; Fang, Zheng; Guo, Kai
Continuous-flow electro-oxidative coupling of sulfides with activated methylene compounds leading to sulfur ylides
Green Chemistry, 2021, 23, 2956-2961
7242526 CIFC38 H49 Bi O8P -112.5878; 12.6544; 13.1098
106.319; 105.558; 107.521
1763.44Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ā€’ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242527 CIFC54 H96 Bi2 Li4 N2 O20P 1 21/n 113.3571; 14.0806; 18.593
90; 95.0534; 90
3483.3Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ā€’ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755

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