Crystallography Open Database

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Searching journal of publication like 'Green Chemistry' volume of publication is 20

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7230303 CIFC36 H56 O6P 1 21/c 112.9802; 8.6558; 32.2944
90; 94.115; 90
3619.1Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi
Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process
Green Chemistry, 2018, 20, 1998
7230313 CIFC18 H29 Cl2 Ir N4 O2P -19.1521; 9.681; 11.7658
88.195; 86.069; 89.089
1039.4Lu, Sheng-Mei; Wang, Zhijun; Wang, Jijie; Li, Jun; Li, Can
Hydrogen generation from formic acid decomposition on a highly efficient iridium catalyst bearing a diaminoglyoxime ligand
Green Chemistry, 2018, 20, 1835
7230342 CIFC22 H25 N5 O4P -19.324; 9.76; 12.772
75.736; 70.173; 77.227
1047.6Zhang, Furen; Li, Chunmei; Liang, Xuezheng
Solid acid-catalyzed domino cyclization reaction: regio- and diastereoselective synthesis of pyrido[2,3-d]pyrimidine derivatives bearing three contiguous stereocenters
Green Chemistry, 2018, 20, 2057
7230380 CIFC116 H88 Cl6 N8C 1 2/c 143.317; 23.984; 28.932
90; 117.762; 90
26598Ishizuka, Tomoya; Ohkawa, Shumpei; Ochiai, Hidemi; Hashimoto, Muneaki; Ohkubo, Kei; Kotani, Hiroaki; Sadakane, Masahiro; Fukuzumi, Shunichi; Kojima, Takahiko
A supramolecular photocatalyst composed of a polyoxometalate and a photosensitizing water-soluble porphyrin diacid for the oxidation of organic substrates in water
Green Chemistry, 2018, 20, 1975
7230471 CIFC23 H18 N2 O5 SP -19.1495; 11.0385; 11.775
68.418; 81.041; 68.191
1026.46Yao, Xinghui; Weng, Xin; Wang, Kaixuan; Xiang, Haifeng; Zhou, Xiangge
Transition metal free oxygenation of 8-aminoquinoline amides in water
Green Chemistry, 2018, 20, 2472
7230499 CIFC14 H10 N2 OP 1 21/c 112.105; 7.6772; 11.507
90; 97.73; 90
1059.7Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua
Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage
Green Chemistry, 2018, 20, 2449
7230500 CIFC19 H14 N2 O2P 1 21/c 110.351; 11.378; 12.992
90; 106.17; 90
1469.6Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua
Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage
Green Chemistry, 2018, 20, 2449
7230578 CIFC12 H14 O4P 1 21/n 15.8802; 25.3608; 8.2156
90; 109.663; 90
1153.72Yang, Da; Liu, Huan; Wang, Dong-Liang; Luo, Zhoujie; Lu, Yong; Xia, Fei; Liu, Ye
Co-catalysis over a bi-functional ligand-based Pd-catalyst for tandem bis-alkoxycarbonylation of terminal alkynes
Green Chemistry, 2018, 20, 2588
7230581 CIFC15 H0 Br N OC 1 c 129.72; 5.675; 7.425
90; 95.29; 90
1247Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones
Green Chemistry, 2018, 20, 2722
7230582 CIFC20 H16 F3 NP -18.585; 9.869; 10.0994
91.079; 103.819; 90.728
830.6Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones
Green Chemistry, 2018, 20, 2722
7230705 CIFC13 H10 Cl N O SP 1 21/n 110.4863; 9.6208; 12.383
90; 111.484; 90
1162.48Ma, Yan-Na; Guo, Chen-Yang; Zhao, Qianyi; Zhang, Jie; Chen, Xuenian
Synthesis of dibenzothiazines from sulfides by one-pot N,O-transfer and intramolecular C‒H amination
Green Chemistry, 2018, 20, 2953
7230721 CIFC80 H70 Cl2 N6 O11F d d 221.758; 50.304; 13.416
90; 90; 90
14684Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent
Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles
Green Chemistry, 2018, 20, 2775
7230722 CIFC48 H49 Cl2 N3 O4P -112.043; 13.174; 13.616
98.819; 97.641; 98.079
2087Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent
Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles
Green Chemistry, 2018, 20, 2775
7230738 CIFC11 H10 O4P 21 21 217.22158; 9.60997; 13.4791
90; 90; 90
935.44Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230739 CIFC13 H11 N O5P 1 21 18.36693; 7.08624; 19.5336
90; 93.2815; 90
1156.25Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230740 CIFC15 H14 O3P 6513.5583; 13.5583; 45.7998
90; 90; 120
7291.3Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230741 CIFC11 H10 O3 SP 21 21 216.32713; 10.32552; 15.23806
90; 90; 90
995.516Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230742 CIFC13 H12 O4P 21 21 219.50457; 9.59528; 11.4776
90; 90; 90
1046.75Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230743 CIFC14 H14 O3P 21 21 216.47958; 7.89044; 22.4589
90; 90; 90
1148.25Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230744 CIFC13 H11 Cl O3P 1 21 15.94601; 5.17983; 18.2456
90; 94.739; 90
560.03Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423

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