Crystallography Open Database

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Searching journal of publication like 'Green Chem.' volume of publication is 18

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7223441 CIFC23 H26 N2 O2P 1 21/c 19.0471; 17.5709; 12.943
90; 109.25; 90
1942.5Harvey, Benjamin G.; Guenthner, Andrew J.; Koontz, Thomas A.; Storch, Perrin J.; Reams, Josiah T.; Groshens, Thomas J.
Sustainable hydrophobic thermosetting resins and polycarbonates from turpentine
Green Chem., 2016, 18, 2416
7223442 CIFC28 H24 N2 O3 SP -19.0258; 11.0099; 12.4506
79.449; 76.11; 80.803
1172Dandia, Anshu; Parewa, Vijay; Kumari, Sukhbeer; Bansal, Sarika; Sharma, Amit
Imposed hydrophobic interactions by NaCl: accountable attribute for the synthesis of spiro[acenaphthylene-1,5′-pyrrolo[1,2-c]thiazole] derivatives via 1,3-dipolar cycloaddition reaction in aqueous medium
Green Chem., 2016, 18, 2488
7223600 CIFC38 H48 Cl Cu N4 O S2P -111.443; 12.452; 15.01
71.585; 84.083; 68.386
1886.3Barman, Milan Kr.; Sinha, Ashish Kumar; Nembenna, Sharanappa
An efficient and recyclable thiourea-supported copper(i) chloride catalyst for azide‒alkyne cycloaddition reactions
Green Chem., 2016, 18, 2534
7223770 CIFC75 H47 N5 O9 Zn2C 1 2/c 128.525; 29.966; 14.784
90; 109.02; 90
11947.1Liu, Yue; Chen, Dashu; Li, Xingyu; Yu, Ziyang; Xia, Qiansu; Liang, Desheng; Xing, Hongzhu
Visible-light-induced controlled radical polymerization of methacrylates mediated by a pillared-layer metal‒organic framework
Green Chem., 2016, 18, 1475
7223872 CIFC26 H34 O3 SP 21 21 29.7748; 36.406; 6.5704
90; 90; 90
2338.2Huang, Mingming; Hu, Liangzhen; Shen, Hang; Liu, Qing; Hussain, Muhammad Ijaz; Pan, Jing; Xiong, Yan
Sulfination of alcohols with sodium sulfinates promoted by BF3·OEt2: an unexpected access
Green Chem., 2016, 18, 1874
7224061 CIFC20 H22 OP -18.4061; 8.6026; 12.582
91.647; 102.618; 112.149
816.1Wang, Kuai; Meng, Ling-Guo; Zhang, Qi; Wang, Lei
Direct construction of 4-aryl tetralones via visible-light-induced cyclization of styrenes with molecular oxygen
Green Chem., 2016, 18, 2864
7224113 CIFC14 H14 N2 O2P 1 21 17.5292; 5.7936; 13.9668
90; 93.766; 90
607.93Chaudhary, Priyanka; Gupta, Surabhi; Muniyappan, Nalluchamy; Sabiah, Shahulhameed; Kandasamy, Jeyakumar
An efficient synthesis of N-nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite
Green Chem., 2016, 18, 2323
7224294 CIFC18 H13 Cl N4 O PdP 1 21/c 113.0361; 12.7404; 20.0773
90; 94.398; 90
3324.7Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj
Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step
Green Chem., 2016, 18, 3295
7224295 CIFC17 H12 Cl N3 O2 PdP n a 2118.2644; 9.0854; 19.045
90; 90; 90
3160.3Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj
Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step
Green Chem., 2016, 18, 3295
7224493 CIFC17 H12 N2 SP 1 21/c 112.247; 13.34; 8.315
90; 77.29; 90
1325Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav
Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles
Green Chem., 2016, 18, 2666
7224494 CIFC15 H12 N2 SP 21/c 1 15.873; 9.367; 22.93
91.31; 90; 90
1261.1Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav
Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles
Green Chem., 2016, 18, 2666
7224566 CIFC20 H21 N5 O4P 1 21/n 19.9263; 15.4568; 12.4445
90; 96.737; 90
1896.16Zhang, Xiaofeng; Zhi, Sanjun; Wang, Wei; Liu, Shuai; Jasinski, Jerry P.; Zhang, Wei
A pot-economical and diastereoselective synthesis involving catalyst-free click reaction for fused-triazolobenzodiazepines
Green Chem., 2016, 18, 2642
7224593 CIFC19 H16 F N O4P -18.747; 11.406; 16.58
80.72; 85.21; 85.46
1623.2Ahankar, Hamideh; Ramazani, Ali; Ślepokura, Katarzyna; Lis, Tadeusz; Joo, Sang Woo
Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation
Green Chem., 2016, 18, 3582
7224743 CIFC25 H25 N O9P 1 21/c 123.7419; 8.0217; 31.6881
90; 127.152; 90
4810.1Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K.
Water – the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides
Green Chem., 2016, 18, 2961
7224744 CIFC21 H17 N O8P -18.133; 11.671; 11.708
63.061; 84.432; 75.914
960.8Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K.
Water – the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides
Green Chem., 2016, 18, 2961
7225073 CIFC20 H22 N2P 1 21/c 110.815; 19.201; 7.858
90; 104.8; 90
1577.6Cai, Jinhui; Li, Feifei; Deng, Guo-Jun; Ji, Xiaochen; Huang, Huawen
The cyclopropylimine rearrangement/Povarov reaction cascade for the assembly of pyrrolo[3,2-c]quinoline derivatives
Green Chem., 2016, 18, 3503
7225077 CIFC20 H21 N4 O2.5P b c n15.4558; 18.7716; 26.327
90; 90; 90
7638.3Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang
Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions
Green Chem., 2016, 18, 4216
7225078 CIFC20 H11 N3 O4P -110.3603; 13.054; 14.655
75.239; 84.652; 69.915
1800Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang
Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions
Green Chem., 2016, 18, 4216
7225170 CIFC50 H68 N14 O16 Zn2I m -328.6573; 28.6573; 28.6573
90; 90; 90
23534.5Han, Yun-Hu; Zhou, Zhong-Yuan; Tian, Chong-Bin; Du, Shao-Wu
A dual-walled cage MOF as an efficient heterogeneous catalyst for the conversion of CO2under mild and co-catalyst free conditions
Green Chem., 2016, 18, 4086
7225274 CIFC19 H21 N3 OC 1 2/c 111.725; 17.259; 16.041
90; 90.789; 90
3245.8Lezana, Nicolás; Matus-Pérez, Massiel; Galdámez, Antonio; Lühr, Susan; Vilches-Herrera, Marcelo
Highly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels–Alder reaction under microwave irradiation in water
Green Chem., 2016, 18, 3712

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