Crystallography Open Database

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

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7229415 CIFC19 H19 N OP 1 21/c 114.0947; 5.86763; 18.4634
90; 97.511; 90
1513.87Karu, Ramesh; Gedu, Satyanarayana
Microwave assisted domino heck cyclization and alkynylation: synthesis of alkyne substituted dihydrobenzofurans
Green Chemistry, 2018, 20, 369
7229619 CIFC9 H8 Cl2 O2 SP 1 21 17.3712; 10.3338; 13.8683
90; 93.683; 90
1054.2Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.
Organic oxidations promoted in vortex driven thin films under continuous flow
Green Chemistry, 2018, 20, 118
7229620 CIFC14 H18 O2 SP 1 21/n 17.8477; 7.955; 20.8582
90; 96.801; 90
1292.98Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.
Organic oxidations promoted in vortex driven thin films under continuous flow
Green Chemistry, 2018, 20, 118
7229621 CIFC22 H16 F NP b c a19.293; 7.2555; 23.177
90; 90; 90
3244.3Ahmed, Waqar; Zhang, Sheng; Yu, Xiaoqiang; Yamamoto, Yoshinori; Bao, Ming
Brønsted acid-catalyzed metal- and solvent-free quinoline synthesis fromN-alkyl anilines and alkynes or alkenes
Green Chemistry, 2018, 20, 261
7229669 CIFC39 H31 N O2 P2P 1 21/n 111.651; 11.814; 23.05
90; 101.391; 90
3110.2Wen, Li-Rong; Sun, Yong-Xu; Zhang, Jin-Wei; Guo, Wei-Si; Li, Ming
Catalyst- and solvent-free bisphosphinylation of isothiocyanates: a practical method for the synthesis of bisphosphinoylaminomethanes
Green Chemistry, 2018, 20, 125
7229731 CIFC20 H20 O2 SP n m a6.2278; 37.44; 7.3546
90; 90; 90
1714.9Nguyen, Thanh Binh; Retailleau, Pascal
Sulfurative self-condensation of ketones and elemental sulfur: a three-component access to thiophenes catalyzed by aniline acid‒base conjugate pairs
Green Chemistry, 2018, 20, 387
7229831 CIFC42 H33 N3 OP -110.822; 12.45; 13.434
68.323; 84.539; 77.041
1639Albaladejo, María José; González-Soria, María José; Alonso, Francisco
Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes
Green Chemistry, 2018, 20, 701
7229832 CIFC44 H37 N3 O3P -112.1335; 12.3113; 12.6442
87.101; 86.513; 69.271
1762.4Albaladejo, María José; González-Soria, María José; Alonso, Francisco
Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes
Green Chemistry, 2018, 20, 701
7229843 CIFC11 H6 O2P -13.7722; 8.864; 25.643
86.384; 89.405; 81.479
846.27Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng
Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide
Green Chemistry, 2018, 20, 989
7229844 CIFC11 H5 O2P 1 21/c 13.8398; 6.201; 35.222
90; 91.034; 90
838.5Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng
Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide
Green Chemistry, 2018, 20, 989
7229845 CIFC32 H25 N O4 S2 Se3P 1 21/n 117.114; 11.241; 18.622
90; 116.978; 90
3192.6Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji
Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides
Green Chemistry, 2018, 20, 604
7229846 CIFC32 H25 N O4 S2 Se2P -19.3039; 11.2838; 15.363
110.126; 99.341; 93.707
1481.6Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji
Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides
Green Chemistry, 2018, 20, 604
7230013 CIFC18 H33 Mo12 N6 O40 PP -114.9687; 15.0798; 21.8498
86.944; 88.681; 85.622
4909.8Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230014 CIFC24 H45 Mo12 N6 O40 PP -112.9158; 21.2163; 21.6946
95.876; 105.285; 101.08
5553.7Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230015 CIFC30 H57 Mo12 N6 O40 PP b c a22.3846; 20.969; 26.0718
90; 90; 90
12237.7Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230209 CIFC7 H22 O3 Si3P -4 21 c17.5199; 17.5199; 10.0567
90; 90; 90
3086.9Arzumanyan, Ashot V.; Goncharova, Irina K.; Novikov, Roman A.; Milenin, Sergey A.; Boldyrev, Konstantin L.; Solyev, Pavel N.; Tkachev, Yaroslav V.; Volodin, Alexander D.; Smol'yakov, Alexander F.; Korlyukov, Alexander A.; Muzafarov, Aziz M.
Aerobic Co or Cu/NHPI-catalyzed oxidation of hydride siloxanes: synthesis of siloxanols
Green Chemistry, 2018, 20, 1467
7230285 CIFC24 H19 N OP -19.4619; 9.7534; 10.5387
68.185; 78.205; 88.782
882.26Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming
Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones
Green Chemistry, 2018, 20, 2007
7230286 CIFC25 H19 Cl3 N2P 1 21/c 110.6279; 15.8991; 13.4801
90; 100.33; 90
2240.9Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming
Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones
Green Chemistry, 2018, 20, 2007
7230301 CIFC16 H24 O3P -16.0145; 8.0625; 16.0814
96.122; 94.613; 100.073
759.5Wang, 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
7230302 CIFC17 H26 O3P 1 21/c 115.6175; 8.4961; 12.67
90; 96.193; 90
1671.3Wang, 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
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
7230745 CIFC13 H12 O3P 1 21 111.11016; 9.04172; 15.58673
90; 95.3028; 90
1559.06Hughes, 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
7230820 CIFC22 H16 O5 SP n a 217.7651; 16.4066; 14.1404
90; 90; 90
1801.5Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg
Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide
Green Chemistry, 2018, 20, 3059
7230821 CIFC21 H13 Cl O4 SP 1 c 112.8859; 5.6317; 25.025
90; 92.804; 90
1813.9Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg
Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide
Green Chemistry, 2018, 20, 3059
7230882 CIFC18 H19 N O2 SP -18.9159; 9.228; 10.159
105.035; 98.43; 102.959
767.8Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian
Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines
Green Chemistry, 2018, 20, 3191
7230883 CIFC14 H15 F6 N O3 SC 1 2/c 139.756; 6.2412; 31.125
90; 123.261; 90
6457.7Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian
Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines
Green Chemistry, 2018, 20, 3191
7230887 CIFC18 H21 N O6P -18.9121; 10.6028; 10.607
107.362; 95.433; 110.176
875.81Wang, Yinling; Du, Yiman; He, Jianghua; Zhang, Yuetao
Transformation of lignin model compounds to N-substituted aromatics via Beckmann rearrangement
Green Chemistry, 2018, 20, 3318
7230903 CIFC20 H18 OC 1 2/c 114.081; 14.4862; 16.112
90; 113.689; 90
3009.6Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230904 CIFC19 H16 O2P -16.3828; 10.3101; 11.896
104.198; 100.779; 97.652
732.2Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230905 CIFC12 H10 O3P 1 21/c 19.52; 13.2012; 8.3853
90; 112.716; 90
972.1Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230906 CIFC53 H44 Cl F6 N4 P3 RuI -428.6436; 28.6436; 13.5364
90; 90; 90
11106Chakrabarti, Kaushik; Mishra, Anju; Panja, Dibyajyoti; Paul, Bhaskar; Kundu, Sabuj
Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources
Green Chemistry, 2018, 20, 3339

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