Crystallography Open Database

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Searching journal of publication like 'Green Chemistry' volume of publication is 22

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7239764 CIFC23 H22 O4P 1 21/c 115.0906; 7.9886; 15.7975
90; 95.544; 90
1895.52Zhang, Zhipeng; Yu, Yang; Huang, Fei; Yi, Xiangyan; Xu, Yao; He, Yide; Baell, Jonathan B.; Huang, He
Catalytic O‒H bond insertion reactions using surface modified sewage sludge as a catalyst
Green Chemistry, 2020, 22, 1594-1604
7239784 CIFC12 H10 Mn N3 O5P -17.594; 8.5623; 13.088
97.266; 95.849; 95.577
834.5Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias
Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights
Green Chemistry, 2020, 22, 913-920
7239785 CIFC11 H9 Br Mn N3 O3P 1 21/n 17.9845; 12.118; 14.112
90; 100.181; 90
1343.9Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias
Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights
Green Chemistry, 2020, 22, 913-920
7239835 CIFC15 H13 F N2 SP -18.6772; 9.0145; 9.9691
110.22; 107.146; 97.596
674.97Wen, Jiangwei; Niu, Cong; Yan, Kelu; Cheng, Xingda; Gong, Ruike; Li, Mengqian; Guo, Yongqiang; Yang, Jianjing; Wang, Hua
Electrochemical-induced regioselective C-3 thiomethylation of imidazopyridines via a three-component cross-coupling strategy
Green Chemistry, 2020, 22, 1129-1133
7239951 CIFC33 H27 N O6P -112.6327; 15.2434; 15.98
102.027; 105.432; 112.595
2566.4Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239952 CIFC17 H17 NP -15.6742; 8.7921; 13.5713
103.259; 95.099; 95.624
651.48Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239953 CIFC16 H14 N2P -110.388; 10.8621; 11.9356
103.368; 111.316; 90.267
1214.77Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239961 CIFC9 H5 N O SP 1 21/c 18.398; 7.421; 13.749
90; 99.9; 90
844.1He, Dongdong; Yao, Jiaojiao; Ma, Boling; Wei, Jinghao; Hao, Guangguo; Tuo, Xun; Guo, Shengmei; Fu, Zhengjiang; Cai, Hu
An electrochemical method for deborylative seleno/thiocyanation of arylboronic acids under catalyst- and oxidant-free conditions
Green Chemistry, 2020, 22, 1559-1564
7239973 CIFC15 H13 Cl N2 OP 1 21/c 111.3479; 10.0774; 11.9461
90; 98.694; 90
1350.43Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying
Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination
Green Chemistry, 2020, 22, 1837-1841
7239974 CIFC16 H15 Cl N2 OP 1 21/c 112.8233; 10.2114; 12.0326
90; 116.906; 90
1405Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying
Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination
Green Chemistry, 2020, 22, 1837-1841
7239983 CIFC8 H11 N O3P b c a11.7246; 8.3285; 16.9656
90; 90; 90
1656.66Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239984 CIFC10 H11 N O2P 1 21/m 17.1931; 7.0581; 8.4454
90; 92.515; 90
428.36Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239985 CIFC14 H13 N O5P 21 21 217.1964; 11.9878; 14.751
90; 90; 90
1272.55Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239986 CIFC60 H84 N4 O24P 1 21/n 124.7484; 10.706; 26.2577
90; 115.723; 90
6267.71Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7240053 CIFC20 H19 N O4P 1 21/c 18.4606; 16.9137; 35.129
90; 90.02; 90
5027Zhao, Yong-Long; Tang, Yong-Qin; Fei, Xing-Hai; Yang, Fen-Fen; Cao, Zhuo-Xian; Duan, Dong-Zhu; Zhao, Qing-Jie; Yang, Yuan-Yong; Zhou, Meng; He, Bin
Direct C(sp3)‒H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI
Green Chemistry, 2020, 22, 2354-2358
7240065 CIFC11 H16 B3 N O7P 1 21/c 18.43; 17.184; 9.073
90; 93.26; 90
1312.2Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240066 CIFC27 H34 B3 N O8P -19.549; 11.307; 13.26
100.88; 92.261; 105.79
1346.6Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240067 CIFC19 H32 B3 N O7P -111.314; 11.98; 17.961
72.586; 79.494; 72.755
2207Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240089 CIFC36 H28 Cl2 F12 N6 P2 RuP -112.8944; 12.8937; 12.963
82.985; 66.987; 88.659
1968.1Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo
The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst
Green Chemistry, 2020, 22, 2279-2287
7240090 CIFC37 H31 F6 N5 O2 P RuP -111.159; 12.3059; 14.8631
67.875; 68.045; 86.116
1747.3Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo
The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst
Green Chemistry, 2020, 22, 2279-2287

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