Crystallography Open Database
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|---|---|---|---|---|---|---|
| 1540034 | CIF | C32 H28 F6 N8 O4 Zn | P -1 | 8.8018; 9.2775; 11.3673 82.433; 68.031; 67.635 | 796 | Nakatake, 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 | CIF | C40 H44 F6 N8 O4 Zn | P 1 21/n 1 | 14.5768; 8.9341; 15.9047 90; 103.294; 90 | 2015.8 | Nakatake, 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 | CIF | C18 H14 F6 N4 O4 Zn | P -1 | 9.7675; 11.262; 11.576 98.815; 107.953; 112.944 | 1059.8 | Nakatake, 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 |
| 7204165 | CIF | C80 H98 N2 O16 | P -1 | 11.2391; 12.889; 14.478 90.734; 110.956; 112.21 | 1786.49 | Brett A. Roberts; Gareth W. V. Cave; Colin L. Raston; Janet L. Scott Solvent-free synthesis of calix[4]resorcinarenes Green Chem., 3, 280-284 |
| 7204653 | CIF | C15 H12 O3 | P b c 21 | 5.912; 8.043; 25.07 90; 90; 90 | 1192.1 | Kazuhiro Yoshizawa; Shinji Toyota; Fumio Toda; Ingeborg Csöregh Preparative and mechanistic studies of solvent-free Rap–Stoermer reactions Green Chem., 2003, 5, 353-356 |
| 7217280 | CIF | C86.5 H113 Al Cl5 O4 P | C 1 2/c 1 | 27.1582; 28.5362; 24.0085 90; 113.869; 90 | 17015 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217281 | CIF | C77 H122 Al Cl2 Li O8 | P 1 21/n 1 | 16.4252; 16.4896; 29.6929 90; 102.666; 90 | 7846.5 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217282 | CIF | C76 H120 Al Na O8 | P -1 | 14.1898; 14.7188; 19.354 83.112; 89.299; 71.328 | 3800.35 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217283 | CIF | C77 H126 Al Cl2 N O4 | P b c a | 24.3711; 24.6465; 25.3492 90; 90; 90 | 15226.3 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217284 | CIF | C34 H52 N2 O2 | P -1 | 5.9662; 10.201; 14.27 101.025; 93.011; 104.712 | 819.8 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217285 | CIF | C94 H142 Al Au N2 O4 S | P c a 21 | 24.5162; 14.2702; 27.0151 90; 90; 90 | 9451.3 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217286 | CIF | C68 H104 Al Na O6 | C 1 2/c 1 | 11.081; 23.961; 24.439 90; 101.533; 90 | 6358 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217287 | CIF | C25 H27 Br O | P 1 21/c 1 | 9.971; 11.013; 19.557 90; 94.091; 90 | 2142.1 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217288 | CIF | C34 H54 O2 | I 41/a | 23.87; 23.87; 10.781 90; 90; 90 | 6143 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217289 | CIF | C92 H124 Al O4 P | P -1 | 23.163; 27.127; 30.989 115.645; 99.092; 100.786 | 16604 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217290 | CIF | C66 H86 O6 | P -1 | 11.466; 11.745; 11.838 71.639; 75.918; 72.993 | 1426.7 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7217291 | CIF | C136 H152 Al Cl4 O4 P | P 1 21/c 1 | 14.8662; 33.789; 27.09 90; 94.019; 90 | 13574 | Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F. Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions Green Chem., 2014, 16, 4696 |
| 7218262 | CIF | C25 H25 N O4 S | P 1 21/c 1 | 12.2796; 11.7459; 15.808 90; 102.781; 90 | 2223.57 | Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar Catalyst-free one-pot four-component domino reactions in water‒PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds Green Chem., 2015, 17, 950 |
| 7218263 | CIF | C31 H29 N O2 S | P n a 21 | 16.581; 11.236; 14.597 90; 90; 90 | 2719.5 | Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar Catalyst-free one-pot four-component domino reactions in water–PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds Green Chem., 2015, 17, 950 |
| 7218264 | CIF | C22 H25 N O2 S | P 1 21/n 1 | 6.4263; 12.9536; 23.9037 90; 97.062; 90 | 1974.74 | Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar Catalyst-free one-pot four-component domino reactions in water–PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds Green Chem., 2015, 17, 950 |
| 7218288 | CIF | C17 H24 N2 O | C 1 2/c 1 | 29.745; 5.802; 19.967 90; 112.103; 90 | 3193 | Xie, Yanjun; Cheng, Xiufang; Liu, Saiwen; Chen, Hui; Zhou, Wang; Yang, Luo; Deng, Guo-Jun Efficient 4,5-dihydro-1H-imidazol-5-one formation from amidines and ketones under transition-metal free conditions Green Chem., 2015, 17, 209 |
| 7218373 | CIF | C30 H26 I N O5 S | P -1 | 12.771; 14.579; 16.377 106.53; 105.21; 91.3 | 2805.1 | Xu, Shijie; Liu, Jianquan; Hu, Donghua; Bi, Xihe Metal-free hydroacyloxylation and hydration reactions of ynamides: synthesis of α-acyloxyenamides and N-acylsulfonamides Green Chem., 2015, 17, 184 |
| 7218396 | CIF | C22 H22 Cl N O2 | P 21 21 21 | 7.5759; 11.0478; 23.488 90; 90; 90 | 1965.9 | Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones Green Chem., 2015, 17, 188 |
| 7218397 | CIF | C18 H21 N O4 | P 1 21/n 1 | 10.0101; 10.7765; 15.5711 90; 93.9; 90 | 1675.8 | Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones Green Chem., 2015, 17, 188 |
| 7218398 | CIF | C24 H18 Cl N O4 | P -1 | 10.6004; 13.375; 16.069 82.836; 71.805; 89.343 | 2146.5 | Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones Green Chem., 2015, 17, 188 |
| 7218562 | CIF | C10 H8 Br N3 O2 | P c c n | 11.4437; 22.5577; 8.1293 90; 90; 90 | 2098.53 | Li, Wenjun; Du, Zhiyun; Zhang, Kun; Wang, Jian Organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated ketones with azides through iminium catalysis Green Chem., 2015, 17, 781 |
| 7218563 | CIF | C40 H0 Mo8 N8 O26 | P 1 21/n 1 | 16.4264; 10.8002; 17.5844 90; 96.397; 90 | 3100.2 | Zhou, Ming-Dong; Liu, Mei-Ju; Huang, Liang-Liang; Zhang, Jian; Wang, Jing-Yun; Li, Xue-Bing; Kühn, Fritz E.; Zang, Shu-Liang Olefin epoxidation with hydrogen peroxide using octamolybdate-based self-separating catalysts Green Chem., 2015, 17, 1186 |
| 7218564 | CIF | C44 H0 Mo8 N4 O27 | P 1 21/n 1 | 15.6345; 12.1211; 16.5893 90; 94.603; 90 | 3133.7 | Zhou, Ming-Dong; Liu, Mei-Ju; Huang, Liang-Liang; Zhang, Jian; Wang, Jing-Yun; Li, Xue-Bing; Kühn, Fritz E.; Zang, Shu-Liang Olefin epoxidation with hydrogen peroxide using octamolybdate-based self-separating catalysts Green Chem., 2015, 17, 1186 |
| 7218747 | CIF | C24 H40 B F4 Ir N4 O2 | P -1 | 10.1442; 11.7709; 15.044 109.125; 97.344; 109.259 | 1545.2 | Manas, Michael G.; Campos, Jesús; Sharninghausen, Liam S.; Lin, Elisa; Crabtree, Robert H. Selective catalytic oxidation of sugar alcohols to lactic acid Green Chem., 2015, 17, 594 |
| 7218933 | CIF | C6 H8 Cl0 Cu N14 O2 | P -1 | 7.1861; 7.5759; 7.6549 89.212; 63.414; 64.027 | 326.31 | Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance Green Chem., 2015, 17, 831-836 |
| 7218934 | CIF | C3 H Cu N7 O | P 1 21/n 1 | 7.404; 9.672; 9.341 90; 113.02; 90 | 615.7 | Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance Green Chem., 2015, 17, 831-836 |
| 7218935 | CIF | C3 H2 Cu N7 | P 1 21/c 1 | 8.63; 9.867; 6.736 90; 108.297; 90 | 544.6 | Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance Green Chem., 2015, 17, 831-836 |
| 7218936 | CIF | C18 H16 N2 O4 | P 1 21/c 1 | 4.401; 12.3035; 14.8314 90; 97.593; 90 | 796.04 | Harvey, Benjamin G.; Guenthner, Andrew J.; Meylemans, Heather A.; Haines, Shannon R. L.; Lamison, Kevin R.; Groshens, Thomas J.; Cambrea, Lee R.; Davis, Matthew C.; Lai, William W. Renewable thermosetting resins and thermoplastics from vanillin Green Chem., 2015, 17, 1249 |
| 7218937 | CIF | C18 H14 N2 O4 | P 1 21/c 1 | 3.8765; 12.2303; 16.1995 90; 95.906; 90 | 763.95 | Harvey, Benjamin G.; Guenthner, Andrew J.; Meylemans, Heather A.; Haines, Shannon R. L.; Lamison, Kevin R.; Groshens, Thomas J.; Cambrea, Lee R.; Davis, Matthew C.; Lai, William W. Renewable thermosetting resins and thermoplastics from vanillin Green Chem., 2015, 17, 1249 |
| 7218993 | CIF | C14 H8 Cl N3 S | P c c n | 7.4354; 15.648; 21.424 90; 90; 90 | 2492.7 | Wen, Li-Rong; Li, Shou-Lei; Zhang, Jian; Li, Ming Convenient synthesis of benzo[4,5]thiazolo[2,3-c][1,2,4]triazoles with 1 mol% CuCl2·2H2O as catalyst in water Green Chem., 2015, 17, 1581 |
| 7219006 | CIF | C30 H31 N5 O2 | P -1 | 11.0519; 13.5682; 19.4863 107.546; 96.181; 109.124 | 2562.3 | Fu, Lei; Feng, Xian; Zhang, Juan-Juan; Hu, Jun-Die; Xun, Zhan; Wang, Jian-Jun; Huang, Zhi-Bin; Shi, Da-Qing Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation Green Chem., 2015, 17, 1535 |
| 7219007 | CIF | C31 H33 N5 O2 | P 1 21/c 1 | 18.6242; 10.3311; 29.295 90; 106.496; 90 | 5404.6 | Fu, Lei; Feng, Xian; Zhang, Juan-Juan; Hu, Jun-Die; Xun, Zhan; Wang, Jian-Jun; Huang, Zhi-Bin; Shi, Da-Qing Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation Green Chem., 2015, 17, 1535 |
| 7219041 | CIF | C12 H11 F N2 O2 | P 1 21/n 1 | 14.5192; 4.971; 16.4551 90; 106.074; 90 | 1141.21 | Marković, Violeta; Joksović, Milan D. “On water” synthesis of N-unsubstituted pyrazoles: semicarbazide hydrochloride as an alternative to hydrazine for preparation of pyrazole-3-carboxylate derivatives and 3,5-disubstituted pyrazoles Green Chem., 2015, 17, 842 |
| 7219093 | CIF | C88 H148 N6 Nd2 O9 Si4 | P -1 | 13.883; 14.024; 15.361 109.019; 106.371; 98.531 | 2616 | Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides Green Chem., 2015, 17, 1675 |
| 7219094 | CIF | C88 H148 La2 N6 O9 Si4 | P -1 | 13.963; 14.045; 15.374 108.936; 106.425; 98.499 | 2638.4 | Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides Green Chem., 2015, 17, 1675 |
| 7219095 | CIF | C88 H148 N6 O9 Si4 Y2 | P -1 | 13.74; 14; 15.31 109.27; 106.002; 98.57 | 2577 | Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides Green Chem., 2015, 17, 1675 |
| 7219176 | CIF | C18 H15 N O5 | P b c a | 12.291; 7.4147; 34.667 90; 90; 90 | 3159.3 | Sharma, Siddharth; Singh, Ajay K.; Singh, Devendra; Kim, Dong-Pyo Chemical fixation of carbon dioxide by copper catalyzed multicomponent reactions for oxazolidinedione syntheses Green Chem., 2015, 17, 1404 |
| 7219241 | CIF | C20 H62 Al3 Fe2 Li N4 O2 | P c a 21 | 15.4965; 16.8579; 12.6159 90; 90; 90 | 3295.8 | Gieshoff, Tim N.; Villa, Matteo; Welther, Alice; Plois, Markus; Chakraborty, Uttam; Wolf, Robert; Jacobi von Wangelin, Axel Iron-catalyzed olefin hydrogenation at 1 bar H2with a FeCl3‒LiAlH4catalyst Green Chem., 2015, 17, 1408 |
| 7219331 | CIF | C33 H33 N5 O | P 1 21/n 1 | 11.9187; 9.8408; 24.353 90; 102.942; 90 | 2783.8 | Sousa, Ana Catarina; Piedade, M. Fátima M. M.; Martins, Lígia O.; Robalo, M. Paula An enzymatic route to a benzocarbazole framework using bacterial CotA laccase Green Chem., 2015, 17, 1429 |
| 7219518 | CIF | C26 H21 N5 O2 | P -1 | 9.1187; 10.839; 12.4287 66.309; 88.214; 81.725 | 1112.7 | Feng, Xian; Wang, Jian-Jun; Zhang, Juan-Juan; Cao, Cheng-Pao; Huang, Zhi-Bin; Shi, Da-Qing Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions Green Chem., 2015, 17, 973 |
| 7219519 | CIF | C27 H23 N5 O2 | P -1 | 8.5318; 10.724; 13.1003 74.306; 87.632; 81.193 | 1140.3 | Feng, Xian; Wang, Jian-Jun; Zhang, Juan-Juan; Cao, Cheng-Pao; Huang, Zhi-Bin; Shi, Da-Qing Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions Green Chem., 2015, 17, 973 |
| 7219548 | CIF | C8 H7 N O | P b c a | 7.5044; 11.9291; 14.8473 90; 90; 90 | 1329.1 | Ren, Lanhui; Wang, Lianyue; Lv, Ying; Shang, Sensen; Chen, Bo; Gao, Shuang Synthesis of 6,7-dihydro-5H-cyclopenta[b]pyridin-5-one analogues through manganese-catalyzed oxidation of the CH2adjacent to pyridine moiety in water Green Chem., 2015, 17, 2369 |
| 7219929 | CIF | C5 H7 F O4 | P 1 21/c 1 | 6.1459; 10.5542; 9.5004 90; 93.777; 90 | 614.91 | Harsanyi, Antal; Sandford, Graham Fluorine gas for life science syntheses: green metrics to assess selective direct fluorination for the synthesis of 2-fluoromalonate esters Green Chem., 2015, 17, 3000 |
| 7220061 | CIF | C24 H26 N4 O3 | P -1 | 6.6676; 7.3731; 21.962 98.895; 91.912; 99.057 | 1051.5 | Schröder, Felix; Ojeda, Manuel; Erdmann, Nico; Jacobs, Jeroen; Luque, Rafael; Noël, Timothy; Van Meervelt, Luc; Van der Eycken, Johan; Van der Eycken, Erik V. Supported gold nanoparticles as efficient and reusable heterogeneous catalyst for cycloisomerization reactions Green Chem., 2015, 17, 3314 |
| 7220062 | CIF | C22 H16 F N5 O3 | P 1 21/c 1 | 13.3119; 10.7033; 13.8141 90; 91.8261; 90 | 1967.25 | Poomathi, Nataraj; Mayakrishnan, Sivakalai; Muralidharan, Doraiswamy; Srinivasan, Rajagopal; Perumal, Paramasivan T. Reaction of isatins with 6-amino uracils and isoxazoles: isatin ring-opening vs. annulations and regioselective synthesis of isoxazole fused quinoline scaffolds in water Green Chem., 2015, 17, 3362 |
| 7220063 | CIF | C30 H22 N4 O4.5 S0.5 | P 1 21/c 1 | 24.9048; 9.498; 22.2694 90; 110.723; 90 | 4926.9 | Poomathi, Nataraj; Mayakrishnan, Sivakalai; Muralidharan, Doraiswamy; Srinivasan, Rajagopal; Perumal, Paramasivan T. Reaction of isatins with 6-amino uracils and isoxazoles: isatin ring-opening vs. annulations and regioselective synthesis of isoxazole fused quinoline scaffolds in water Green Chem., 2015, 17, 3362 |
| 7220409 | CIF | C29 H25 Cl N2 O3 | P 21 21 21 | 11.88; 16.051; 26.14 90; 90; 90 | 4985 | Vivekanand, Thavaraj; Vinoth, Perumal; Agieshkumar, B.; Sampath, Natarajan; Sudalai, Arumugam; Menéndez, J. Carlos; Sridharan, Vellaisamy Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation‒Michael addition‒cyclization sequence under catalyst- and solvent-free conditions Green Chem., 2015, 17, 3415 |
| 7220410 | CIF | C13 H11 N3 O5 | P 1 21 1 | 8.6065; 7.1858; 11.184 90; 110.985; 90 | 645.794 | Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin “On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones Green Chem., 2015, 17, 3266 |
| 7220411 | CIF | C16 H17 N3 O6 | P 1 21/n 1 | 13.5271; 7.4112; 16.501 90; 94.763; 90 | 1648.55 | Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin “On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones Green Chem., 2015, 17, 3266 |
| 7220412 | CIF | C13 H13 N3 O3 | P 1 21/c 1 | 6.3186; 11.7574; 16.3886 90; 95.537; 90 | 1211.83 | Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin “On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones Green Chem., 2015, 17, 3266 |
| 7220413 | CIF | C22 H24 N2 O4 S2 | P -1 | 8.1437; 11.826; 12.4 73.31; 88.33; 79.7 | 1125.2 | Khazalpour, Sadegh; Nematollahi, Davood Electrochemical and chemical synthesis of different types of sulfonamide derivatives of N,N-dimethyl-1,4-benzenediamine using 4-nitroso-N,N-dimethylaniline Green Chem., 2015, 17, 3508 |
| 7220414 | CIF | C29 H24 N2 O5 | P -1 | 9.441; 10.287; 13.246 100.627; 94.498; 108.144 | 1188.7 | Sarkar, Piyali; Mukhopadhyay, Chhanda Single step incorporation of carboxylic acid groups in the lower rim of calix[4]arenes: a recyclable catalyst towards assembly of diverse five ring fused acridines Green Chem., 2015, 17, 3452 |
| 7220488 | CIF | C19 H35 I O4 S | P -1 | 10.4883; 11.9211; 20.6101 93.874; 92.989; 115.747 | 2306.2 | Koh, Peng-Fei; Loh, Teck Peng Synthesis of Biologically Active Natural Products, Aspergillides A and B, Entirely from Biomass Derived Platform Chemicals Green Chem., 2015 |
| 7220569 | CIF | C11 H18 N2 O S | P 1 21/n 1 | 12.645; 15.1066; 13.214 90; 93.207; 90 | 2520.22 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation Green Chem., 2015 |
| 7220570 | CIF | C20 H28 N2 O S | P 1 21/c 1 | 10.4317; 15.4783; 11.9638 90; 102.189; 90 | 1888.19 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation Green Chem., 2015 |
| 7220571 | CIF | C11 H18 N2 S2 | P 1 21/n 1 | 7.9953; 15.115; 11.4875 90; 107.186; 90 | 1326.3 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation Green Chem., 2015 |
| 7220572 | CIF | C20 H28 N2 S2 | P 1 21/c 1 | 10.1668; 16.0775; 12.9862 90; 103.802; 90 | 2061.4 | Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation Green Chem., 2015 |
| 7220590 | CIF | C23 H14 Cl N O2 | P -1 | 8.686; 10.371; 11.293 109.138; 111.662; 92.379 | 877.8 | Koneni, Venkata Sashidhara; Palnati, Gopala Reddy; Singh, L. Ravithej; Upadhyay, Amit; Avula, Srinivasa Rao; kumar, Abdhesh; Kant, Ruchir Molecular Iodine Catalysed One-Pot Synthesis of Chromeno[4,3-b]quinolin-6-ones under Microwave Irradiation Green Chem., 2015 |
| 7220686 | CIF | C12 H12 N4 O2 | P 1 21/n 1 | 7.534; 10.682; 16.411 90; 102.32; 90 | 1290.3 | Ershov, O. V.; Ievlev, M. Yu.; Tafeenko, V. A.; Nasakin, O. E. Glycine catalyzed diastereoselective domino-synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in water Green Chem., 2015, 17, 4234 |
| 7220692 | CIF | C20 H17 N O6 | P 1 21/c 1 | 7.8241; 24.301; 9.1574 90; 93.76; 90 | 1737.4 | Xia, JIa-Ning; Yu, Bing; Guo, Chun-Xiang; He, Liang-Nian Copper(I)/phosphine-catalyzed tandem carboxylation/annulation of terminal alkynes with ambient pressure of CO2: one-pot access to 3a-hydroxyisoxazolo[3,2-a]isoindol-8(3aH)-ones Green Chem., 2015 |
| 7220977 | CIF | C20 H43 O4 P | P -1 | 9.6788; 9.6941; 12.4864 86.025; 86.707; 89.675 | 1166.81 | Anderson, Kris; Atkins, Martin P.; Estager, Julien; Kuah, Yongcheun; Ng, Shieling; Oliferenko, Alexander A.; Plechkova, Natalia V.; Puga, Alberto V.; Seddon, Kenneth R.; Wassell, David F. Carbon dioxide uptake from natural gas by binary ionic liquid‒water mixtures Green Chem., 2015, 17, 4340 |
| 7220978 | CIF | C34 H74 O6 P2 | P 1 21/c 1 | 10.569; 11.627; 31.826 90; 90.812; 90 | 3911 | Anderson, Kris; Atkins, Martin P.; Estager, Julien; Kuah, Yongcheun; Ng, Shieling; Oliferenko, Alexander A.; Plechkova, Natalia V.; Puga, Alberto V.; Seddon, Kenneth R.; Wassell, David F. Carbon dioxide uptake from natural gas by binary ionic liquid–water mixtures Green Chem., 2015, 17, 4340 |
| 7220979 | CIF | C20 H15 B F4 N2 | P b c a | 11.5582; 12.3717; 23.8099 90; 90; 90 | 3404.7 | de Robillard, Guillaume; Makni, Oumayma; Cattey, Hélène; Andrieu, Jacques; Devillers, Charles H. Towards sustainable synthesis of pyren-1-yl azoliums via electrochemical oxidative C–N coupling Green Chem., 2015, 17, 4669 |
| 7220980 | CIF | C26 H20 B F4 N3 | P -1 | 8.5758; 10.4878; 12.8368 75.32; 78.092; 74.019 | 1062.06 | de Robillard, Guillaume; Makni, Oumayma; Cattey, Hélène; Andrieu, Jacques; Devillers, Charles H. Towards sustainable synthesis of pyren-1-yl azoliums via electrochemical oxidative C–N coupling Green Chem., 2015, 17, 4669 |
| 7221692 | CIF | C15 H14 Cl2 N2 O2 Ru | P -1 | 7.668; 8.3022; 13.5405 83.606; 81.922; 70.403 | 802.11 | Gupta, Kavita; Tyagi, Deepika; Dwivedi, Ambikesh D.; Mobin, Shaikh M.; Singh, Sanjay K. Catalytic transformation of bio-derived furans to valuable ketoacids and diketones by water-soluble ruthenium catalysts Green Chem., 2015, 17, 4618 |
| 7221693 | CIF | C19 H22 Cl2 N2 Ru | P 1 21/c 1 | 17.072; 12.3086; 9.1013 90; 100.9; 90 | 1877.97 | Gupta, Kavita; Tyagi, Deepika; Dwivedi, Ambikesh D.; Mobin, Shaikh M.; Singh, Sanjay K. Catalytic transformation of bio-derived furans to valuable ketoacids and diketones by water-soluble ruthenium catalysts Green Chem., 2015, 17, 4618 |
| 7221876 | CIF | C19 H11 N O2 S | P 1 21/c 1 | 12.242; 11.566; 10.526 90; 93.08; 90 | 1488.2 | Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones Green Chem., 2016, 18, 402 |
| 7221978 | CIF | C4 H6 O4 | P 1 21/c 1 | 10.6016; 9.5305; 10.7702 90; 119.312; 90 | 948.88 | Tryznowski, 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 | CIF | C18 H31 N O4 | P -1 | 9.384; 10.484; 11.281 102.829; 94.191; 113.456 | 976.4 | Maleki, 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 |
| 7222112 | CIF | C19 H20 O6 | P n a 21 | 23.0884; 10.4956; 7.3329 90; 90; 90 | 1776.96 | Wang, Zhihan; Kastern, Brent; Randazzo, Katelyn; Ugrinov, Angel; Butz, Jonathan; Seals, David W.; Sibi, Mukund P.; Chu, Qianli R. Linear polyester synthesized from furfural-based monomer by photoreaction in sunlight Green Chem., 2015, 17, 4720 |
| 7222113 | CIF | C19 H20 O6 | P n a 21 | 22.9356; 10.4908; 7.3765 90; 90; 90 | 1774.88 | Wang, Zhihan; Kastern, Brent; Randazzo, Katelyn; Ugrinov, Angel; Butz, Jonathan; Seals, David W.; Sibi, Mukund P.; Chu, Qianli R. Linear polyester synthesized from furfural-based monomer by photoreaction in sunlight Green Chem., 2015, 17, 4720 |
| 7222916 | CIF | C7 H10 F N O3 | P 1 21 1 | 8.5224; 10.305; 9.1442 90; 90.3404; 90 | 803.06 | Willis, 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 | CIF | C7 H10 F N O3 | P 1 21 1 | 8.5211; 10.3039; 9.1547 90; 90.365; 90 | 803.77 | Willis, 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 | CIF | C8 H15 Cl F N O4 | P -1 | 5.821; 6.4875; 15.7485 100.738; 96.625; 94.612 | 577.23 | Willis, 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 | CIF | C7 H10 F N O3 | P 1 21/c 1 | 12.256; 6.72544; 10.4787 90; 113.193; 90 | 793.92 | Willis, 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 | CIF | C7 H13 Cl F N O4 | P 1 21/c 1 | 12.235; 11.3068; 7.6415 90; 100.289; 90 | 1040.12 | Willis, 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 | CIF | C6 H10 F N O4 | P -1 | 6.5648; 6.6759; 9.6206 98.163; 100.929; 101.047 | 399.3 | Willis, 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 | CIF | C88 H72 Cd5 N6 O28 | P 1 21/c 1 | 14.6261; 23.2526; 15.7357 90; 107.099; 90 | 5115.1 | Qiao, 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 | CIF | C96 H82 Cd5 N8 O28 | P 1 21/c 1 | 14.5196; 23.367; 15.6042 90; 107.475; 90 | 5049.8 | Qiao, 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 | CIF | C88 H72 Cd3 Cu2 N6 O27 | P 1 21/c 1 | 14.3997; 23.362; 15.543 90; 106.309; 90 | 5018.4 | Qiao, 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 | CIF | C90 H76 Cd5 N6 O28 | P 1 21/c 1 | 14.583; 23.241; 15.6338 90; 106.99; 90 | 5067.4 | Qiao, 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 | CIF | C26 H16 N4 O8 Zn | P 1 21/c 1 | 19.13; 26.34; 11.628 90; 90.671; 90 | 5859 | Gong, 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 | CIF | C36 H28 N4 P2 | P -1 | 8.8542; 12.9976; 14.0901 100.076; 90.969; 92.406 | 1594.63 | Li, 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 | CIF | C40 H34 F6 N4 O6 P2 S2 | P -1 | 14.0858; 14.4866; 15.7112 67.615; 78.55; 62.44 | 2627 | Li, 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 | CIF | C38 H33 Cl2 I N4 P2 | P 1 21/c 1 | 9.5438; 39.836; 10.6814 90; 116.464; 90 | 3635.4 | Li, 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 | CIF | C23 H26 N2 O2 | P 1 21/c 1 | 9.0471; 17.5709; 12.943 90; 109.25; 90 | 1942.5 | Harvey, 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 | CIF | C28 H24 N2 O3 S | P -1 | 9.0258; 11.0099; 12.4506 79.449; 76.11; 80.803 | 1172 | Dandia, 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 | CIF | C38 H48 Cl Cu N4 O S2 | P -1 | 11.443; 12.452; 15.01 71.585; 84.083; 68.386 | 1886.3 | Barman, 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 | CIF | C75 H47 N5 O9 Zn2 | C 1 2/c 1 | 28.525; 29.966; 14.784 90; 109.02; 90 | 11947.1 | Liu, 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 | CIF | C26 H34 O3 S | P 21 21 2 | 9.7748; 36.406; 6.5704 90; 90; 90 | 2338.2 | Huang, 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 | CIF | C20 H22 O | P -1 | 8.4061; 8.6026; 12.582 91.647; 102.618; 112.149 | 816.1 | Wang, 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 | CIF | C14 H14 N2 O2 | P 1 21 1 | 7.5292; 5.7936; 13.9668 90; 93.766; 90 | 607.93 | Chaudhary, 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 | CIF | C18 H13 Cl N4 O Pd | P 1 21/c 1 | 13.0361; 12.7404; 20.0773 90; 94.398; 90 | 3324.7 | Arumugam, 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 | CIF | C17 H12 Cl N3 O2 Pd | P n a 21 | 18.2644; 9.0854; 19.045 90; 90; 90 | 3160.3 | Arumugam, 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 | CIF | C17 H12 N2 S | P 1 21/c 1 | 12.247; 13.34; 8.315 90; 77.29; 90 | 1325 | Đud, 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 |
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