Crystallography Open Database
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Searching journal of publication like 'Green Chem.'
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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 |
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