Crystallography Open Database

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

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1540034 CIFC32 H28 F6 N8 O4 ZnP -18.8018; 9.2775; 11.3673
82.433; 68.031; 67.635
796Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540035 CIFC40 H44 F6 N8 O4 ZnP 1 21/n 114.5768; 8.9341; 15.9047
90; 103.294; 90
2015.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540036 CIFC18 H14 F6 N4 O4 ZnP -19.7675; 11.262; 11.576
98.815; 107.953; 112.944
1059.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
7221876 CIFC19 H11 N O2 SP 1 21/c 112.242; 11.566; 10.526
90; 93.08; 90
1488.2Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri
Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones
Green Chem., 2016, 18, 402
7221978 CIFC4 H6 O4P 1 21/c 110.6016; 9.5305; 10.7702
90; 119.312; 90
948.88Tryznowski, M.; Żołek-Tryznowska, Z.; Świderska, A.; Parzuchowski, P. G.
Synthesis, characterization and reactivity of a six-membered cyclic glycerol carbonate bearing a free hydroxyl group
Green Chem., 2016, 18, 802
7222111 CIFC18 H31 N O4P -19.384; 10.484; 11.281
102.829; 94.191; 113.456
976.4Maleki, Abbas; Nematollahi, Davood; Rasouli, Fereshteh; Zeinodini-Meimand, Azam
Electrode instead of catalyst and enzyme. A greener protocol for the synthesis of new 2-hydroxyacetamide derivatives containing a γ-lactone ring
Green Chem., 2016, 18, 672
7222916 CIFC7 H10 F N O3P 1 21 18.5224; 10.305; 9.1442
90; 90.3404; 90
803.06Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222917 CIFC7 H10 F N O3P 1 21 18.5211; 10.3039; 9.1547
90; 90.365; 90
803.77Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222918 CIFC8 H15 Cl F N O4P -15.821; 6.4875; 15.7485
100.738; 96.625; 94.612
577.23Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222919 CIFC7 H10 F N O3P 1 21/c 112.256; 6.72544; 10.4787
90; 113.193; 90
793.92Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222920 CIFC7 H13 Cl F N O4P 1 21/c 112.235; 11.3068; 7.6415
90; 100.289; 90
1040.12Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222921 CIFC6 H10 F N O4P -16.5648; 6.6759; 9.6206
98.163; 100.929; 101.047
399.3Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7223202 CIFC88 H72 Cd5 N6 O28P 1 21/c 114.6261; 23.2526; 15.7357
90; 107.099; 90
5115.1Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223203 CIFC96 H82 Cd5 N8 O28P 1 21/c 114.5196; 23.367; 15.6042
90; 107.475; 90
5049.8Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223204 CIFC88 H72 Cd3 Cu2 N6 O27P 1 21/c 114.3997; 23.362; 15.543
90; 106.309; 90
5018.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223205 CIFC90 H76 Cd5 N6 O28P 1 21/c 114.583; 23.241; 15.6338
90; 106.99; 90
5067.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223248 CIFC26 H16 N4 O8 ZnP 1 21/c 119.13; 26.34; 11.628
90; 90.671; 90
5859Gong, Le Le; Feng, Xue Feng; Luo, Feng; Yi, Xian Feng; Zheng, An Min
Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal‒organic framework
Green Chem., 2016, 18, 2047
7223249 CIFC36 H28 N4 P2P -18.8542; 12.9976; 14.0901
100.076; 90.969; 92.406
1594.63Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223250 CIFC40 H34 F6 N4 O6 P2 S2P -114.0858; 14.4866; 15.7112
67.615; 78.55; 62.44
2627Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223251 CIFC38 H33 Cl2 I N4 P2P 1 21/c 19.5438; 39.836; 10.6814
90; 116.464; 90
3635.4Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
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
7225275 CIFC55 H81 N2 Nd O5P -113.61; 15.446; 15.506
98.661; 107.06; 112.68
2743.8Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming
Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide
Green Chem., 2016, 18, 4270
7225276 CIFC55 H79 N2 O4 YP 1 21/n 115.2272; 14.1936; 24.434
90; 99.252; 90
5212.2Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming
Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide
Green Chem., 2016, 18, 4270
7225277 CIFC142 H214 N4 Nd2 O10 ZnC 1 2/c 125.713; 25.211; 25.54
90; 115.838; 90
14901Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming
Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide
Green Chem., 2016, 18, 4270
7225288 CIFC18 H33 B2 F8 Ir N4 O2P -18.6729; 11.3034; 13.751
85.039; 74.421; 78.507
1271.7Lu, Sheng-Mei; Wang, Zhijun; Li, Jun; Xiao, Jianliang; Li, Can
Base-free hydrogenation of CO2to formic acid in water with an iridium complex bearing a N,N′-diimine ligand
Green Chem., 2016, 18, 4553
7225401 CIFC10 H10 O5P 1 21/c 110.6927; 7.81215; 10.6458
90; 95.5149; 90
885.16Bai, Yinjuan; De bruyn, Mario; Clark, James H.; Dodson, Jennifer R.; Farmer, Thomas J.; Honoré, Mathilde; Ingram, Ian D. V.; Naguib, Mohamed; Whitwood, Adrian C.; North, Michael
Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol
Green Chem., 2016, 18, 3945
7225495 CIFC15 H11 N OP 1 21/n 113.2486; 7.0891; 13.5496
90; 114.155; 90
1161.2Shi, Qing; Li, Pinhua; Zhu, Xianjin; Wang, Lei
Decarboxylative/decarbonylative C3-acylation of indoles via photocatalysis: a simple and efficient route to 3-acylindoles
Green Chem., 2016, 18, 4916
7225644 CIFC17 H17 Br O2P -19.5598; 9.6393; 18.0624
75.207; 81.884; 72.871
1533.97Chen, Dao-Qian; Guo, Chun-Huan; Zhang, Heng-Rui; Jin, Dong-Po; Li, Xue-Song; Gao, Pin; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
A metal-free transformation of alkynes to carbonyls directed by remote OH group
Green Chem., 2016, 18, 4176
7225655 CIFC16 H8 F3 I N0 O2P 1 21/c 110.392; 15.7128; 9.0091
90; 102.556; 90
1435.9Ni, Shengyang; Cao, Jia; Mei, Haibo; Han, Jianlin; Li, Shuhua; Pan, Yi
Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N-iodosuccinimide: easy access to 3-iodocoumarins
Green Chem., 2016, 18, 3935
7225779 CIFC17 H12 O2P -17.1649; 7.1976; 25.276
92.384; 92.571; 90.05
1301Zhang, Wen-Zhen; Yang, Ming-Wang; Lu, Xiao-Bing
Carboxylative cyclization of substituted propenyl ketones using CO2: transition-metal-free synthesis of α-pyrones
Green Chem., 2016, 18, 4181
7225883 CIFC32 H27 Br Cl3 O PP 1 21/c 112.9435; 13.19; 17.35
90; 96.085; 90
2945.4Liu, Shiyao; Suematsu, Naoki; Maruoka, Keiji; Shirakawa, Seiji
Design of bifunctional quaternary phosphonium salt catalysts for CO2fixation reaction with epoxides under mild conditions
Green Chem., 2016, 18, 4611

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