Crystallography Open Database
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Searching journal of publication like 'Green Chem.'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 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 |
| 7224494 | CIF | C15 H12 N2 S | P 21/c 1 1 | 5.873; 9.367; 22.93 91.31; 90; 90 | 1261.1 | 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 |
| 7224566 | CIF | C20 H21 N5 O4 | P 1 21/n 1 | 9.9263; 15.4568; 12.4445 90; 96.737; 90 | 1896.16 | Zhang, 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 | CIF | C19 H16 F N O4 | P -1 | 8.747; 11.406; 16.58 80.72; 85.21; 85.46 | 1623.2 | Ahankar, 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 | CIF | C25 H25 N O9 | P 1 21/c 1 | 23.7419; 8.0217; 31.6881 90; 127.152; 90 | 4810.1 | Samai, 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 | CIF | C21 H17 N O8 | P -1 | 8.133; 11.671; 11.708 63.061; 84.432; 75.914 | 960.8 | Samai, 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 | CIF | C20 H22 N2 | P 1 21/c 1 | 10.815; 19.201; 7.858 90; 104.8; 90 | 1577.6 | Cai, 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 | CIF | C20 H21 N4 O2.5 | P b c n | 15.4558; 18.7716; 26.327 90; 90; 90 | 7638.3 | Singh, 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 | CIF | C20 H11 N3 O4 | P -1 | 10.3603; 13.054; 14.655 75.239; 84.652; 69.915 | 1800 | Singh, 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 | CIF | C50 H68 N14 O16 Zn2 | I m -3 | 28.6573; 28.6573; 28.6573 90; 90; 90 | 23534.5 | Han, 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 | CIF | C19 H21 N3 O | C 1 2/c 1 | 11.725; 17.259; 16.041 90; 90.789; 90 | 3245.8 | Lezana, 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 | CIF | C55 H81 N2 Nd O5 | P -1 | 13.61; 15.446; 15.506 98.661; 107.06; 112.68 | 2743.8 | Qin, 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 | CIF | C55 H79 N2 O4 Y | P 1 21/n 1 | 15.2272; 14.1936; 24.434 90; 99.252; 90 | 5212.2 | Qin, 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 | CIF | C142 H214 N4 Nd2 O10 Zn | C 1 2/c 1 | 25.713; 25.211; 25.54 90; 115.838; 90 | 14901 | Qin, 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 | CIF | C18 H33 B2 F8 Ir N4 O2 | P -1 | 8.6729; 11.3034; 13.751 85.039; 74.421; 78.507 | 1271.7 | Lu, 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 | CIF | C10 H10 O5 | P 1 21/c 1 | 10.6927; 7.81215; 10.6458 90; 95.5149; 90 | 885.16 | Bai, 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 | CIF | C15 H11 N O | P 1 21/n 1 | 13.2486; 7.0891; 13.5496 90; 114.155; 90 | 1161.2 | Shi, 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 | CIF | C17 H17 Br O2 | P -1 | 9.5598; 9.6393; 18.0624 75.207; 81.884; 72.871 | 1533.97 | Chen, 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 | CIF | C16 H8 F3 I N0 O2 | P 1 21/c 1 | 10.392; 15.7128; 9.0091 90; 102.556; 90 | 1435.9 | Ni, 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 | CIF | C17 H12 O2 | P -1 | 7.1649; 7.1976; 25.276 92.384; 92.571; 90.05 | 1301 | Zhang, 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 | CIF | C32 H27 Br Cl3 O P | P 1 21/c 1 | 12.9435; 13.19; 17.35 90; 96.085; 90 | 2945.4 | Liu, 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 |
| 7225884 | CIF | C22 H18 O2 | P 1 21/c 1 | 8.8686; 6.9699; 27.0903 90; 98.69; 90 | 1655.32 | Zhang, Zhenbei; Sun, Qiangsheng; Xu, Daqian; Xia, Chungu; Sun, Wei Direct halogenative dearomatization of 2-naphthols by NXS (X = Cl, Br) in water Green Chem., 2016, 18, 5485 |
| 7225942 | CIF | C16 H13 Br Cl F3 N2 | I 1 2/a 1 | 22.7475; 11.3014; 27.0251 90; 104.181; 90 | 6735.9 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225943 | CIF | C9 H10 Br I N2 | C 1 2/c 1 | 16.4865; 10.7791; 13.0845 90; 110.686; 90 | 2175.3 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225944 | CIF | C9 H11 Br N2 | C 1 2/c 1 | 16.7925; 8.3062; 15.0809 90; 108.294; 90 | 1997.2 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225945 | CIF | C9 H11 Br N2 | P 1 21/c 1 | 7.4282; 14.952; 8.9188 90; 94.547; 90 | 987.46 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225946 | CIF | C8 H7 Br N2 | P 1 21/c 1 | 3.9883; 17.853; 11.2011 90; 91.622; 90 | 797.23 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225947 | CIF | C8 H8 Br I N2 | P 1 21/c 1 | 6.0553; 14.8323; 12.439 90; 103.295; 90 | 1087.25 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225948 | CIF | C12 H11 Br Cl F3 N2 | P -1 | 11.0563; 11.1805; 12.0711 98.874; 103.353; 103.781 | 1375 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225949 | CIF | C9 H6 Cl F3 N2 | I 1 2/a 1 | 12.0869; 8.1608; 19.776 90; 102.192; 90 | 1906.7 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7225950 | CIF | C8 H7 N3 O2 | R -3 | 24.304; 24.304; 6.8579 90; 90; 120 | 3508.1 | Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N. Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions Green Chem., 2016, 18, 4623 |
| 7226057 | CIF | C8 H8 O2 | P 1 21/n 1 | 6.6884; 7.6318; 12.9438 90; 100.414; 90 | 649.83 | Tšupova, Svetlana; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K. Synthesis of phenols from hydroxymethylfurfural (HMF) Green Chem., 2016, 18, 5800 |
| 7226058 | CIF | C11 H14 O3 | P 1 21/c 1 | 4.5985; 20.751; 10.2612 90; 91.893; 90 | 978.6 | Tšupova, Svetlana; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K. Synthesis of phenols from hydroxymethylfurfural (HMF) Green Chem., 2016, 18, 5800 |
| 7226098 | CIF | C8 H12 O6 | P 1 21/c 1 | 7.8642; 4.0675; 14.5155 90; 96.896; 90 | 460.96 | Sølvhøj, Amanda; Taarning, Esben; Madsen, Robert Methyl vinyl glycolate as a diverse platform molecule Green Chem., 2016, 18, 5448 |
| 7226477 | CIF | C13 H13 N3 O | P 1 21/n 1 | 13.5515; 3.9004; 20.9865 90; 94.725; 90 | 1105.5 | Sousa, Ana Catarina; Piedade, M. Fátima M. M.; Martins, Lígia O.; Robalo, M. Paula Eco-friendly synthesis of indo dyes mediated by a bacterial laccase Green Chem., 2016, 18, 6063 |
| 7226516 | CIF | C27 H18 N2 O7 Zn | P 21 21 2 | 15.7341; 19.19; 8.3925 90; 90; 90 | 2534 | Liu, Bo; Zhou, Hui-Fang; Guan, Zheng-Hui; Hou, Lei; Cui, Bin; Wang, Yao-Yu Cleavage of a C‒C σ bond between two phenyl groups under mild conditions during the construction of Zn(ii) organic frameworks Green Chem., 2016, 18, 5418 |
| 7226517 | CIF | C28 H18 N2 O8 Zn2 | P 4/m m m | 10.8088; 10.8088; 16.283 90; 90; 90 | 1902.3 | Liu, Bo; Zhou, Hui-Fang; Guan, Zheng-Hui; Hou, Lei; Cui, Bin; Wang, Yao-Yu Cleavage of a C‒C σ bond between two phenyl groups under mild conditions during the construction of Zn(ii) organic frameworks Green Chem., 2016, 18, 5418 |
| 7226602 | CIF | C27 H22 N2 O | C 1 2/c 1 | 18.7062; 8.1149; 28.815 90; 106.281; 90 | 4198.7 | Mishra, Pawan K.; Verma, Akhilesh K. Metal-free regioselective tandem synthesis of diversely substituted benzimidazo-fused polyheterocycles in aqueous medium Green Chem., 2016, 18, 6367 |
| 7226670 | CIF | C36.75 H35 Br N2 O | P -1 | 9.5392; 12.9758; 13.6796 95.066; 96.544; 107.057 | 1595 | Sarkar, Piyali; Mukhopadhyay, Chhanda The synthesis of new 8-imino-1-one acridine derivatives catalyzed by a calix[4]arene mono-acid core Green Chem., 2016, 18, 6556 |
| 7226726 | CIF | C20 H17 P S | P 1 21/n 1 | 14.697; 6.6112; 17.826 90; 96.96; 90 | 1719.3 | Moglie, Yanina; González-Soria, María José; Martín-García, Iris; Radivoy, Gabriel; Alonso, Francisco Catalyst- and solvent-free hydrophosphination and multicomponent hydrothiophosphination of alkenes and alkynes Green Chem., 2016, 18, 4896 |
| 7226727 | CIF | C22 H27 O P | P 1 21 1 | 5.719; 17.9432; 9.0209 90; 99.0333; 90 | 914.22 | Moglie, Yanina; González-Soria, María José; Martín-García, Iris; Radivoy, Gabriel; Alonso, Francisco Catalyst- and solvent-free hydrophosphination and multicomponent hydrothiophosphination of alkenes and alkynes Green Chem., 2016, 18, 4896 |
| 7226749 | CIF | C9 H13 N3 O2 | P 1 21/c 1 | 7.3261; 20.1659; 13.1676 90; 102.555; 90 | 1898.8 | Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu. Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides Green Chem., 2016, 18, 6630 |
| 7226750 | CIF | C8 H10 Br N3 O | P 1 21/c 1 | 4.18964; 21.1953; 10.4364 90; 95.814; 90 | 921.99 | Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu. Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides Green Chem., 2016, 18, 6630 |
| 7226751 | CIF | C8 H10 Cl N3 O | P 1 21/c 1 | 4.1274; 20.8167; 10.4887 90; 95.909; 90 | 896.39 | Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu. Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides Green Chem., 2016, 18, 6630 |
| 7226790 | CIF | C30 H22 O2 | P n a 21 | 15.6898; 10.314; 13.7275 90; 90; 90 | 2221.45 | Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans Green Chem., 2016, 18, 6648 |
| 7226791 | CIF | C29 H19 F O | P -1 | 11.309; 12.473; 16.361 111.827; 92.561; 104.099 | 2054.3 | Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans Green Chem., 2016, 18, 6648 |
| 7226792 | CIF | C29 H19 Cl O | P 1 21/c 1 | 9.5556; 18.935; 11.627 90; 96.866; 90 | 2088.6 | Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans Green Chem., 2016, 18, 6648 |
| 7226822 | CIF | C27 H26 N4 O6 S | P 1 21/n 1 | 17.4184; 8.2542; 18.8202 90; 104.911; 90 | 2614.8 | Liu, Xihong; Yang, Dongxu; Wang, Kezhou; Zhang, Jinlong; Wang, Rui A catalyst-free 1,3-dipolar cycloaddition of C,N-cyclic azomethine imines and 3-nitroindoles: an easy access to five-ring-fused tetrahydroisoquinolines Green Chem., 2017, 19, 82 |
| 7226888 | CIF | C16 H11 N3 O | P 1 21 1 | 4.958; 21.437; 12.165 90; 98.132; 90 | 1280 | Xie, Yu-Yang; Wang, Ying-Chun; He, Yan; Hu, Da-Chao; Wang, Heng-Shan; Pan, Ying-Ming Catalyst-free synthesis of fused 1,2,3-triazole and isoindoline derivatives via an intramolecular azide‒alkene cascade reaction Green Chem., 2017, 19, 656 |
| 7226889 | CIF | C19 H13 N | P 1 21/n 1 | 8.4892; 17.7731; 9.0884 90; 107.345; 90 | 1308.9 | Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines Green Chem., 2016, 18, 6241 |
| 7226890 | CIF | C19 H12 Cl N | P -1 | 7.5233; 9.2661; 11.5013 109.068; 96.475; 105.036 | 714.5 | Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines Green Chem., 2016, 18, 6241 |
| 7226891 | CIF | C19 H17 N | P -1 | 9.0735; 9.1093; 9.1688 71.085; 75.202; 85.168 | 693.13 | Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines Green Chem., 2016, 18, 6241 |
| 7226892 | CIF | C19 H15 N O | P -1 | 8.2767; 8.6984; 11.4987 110.318; 90.656; 115.299 | 689.29 | Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines Green Chem., 2016, 18, 6241 |
| 7226984 | CIF | C13 H13 F O2 | P 1 21/c 1 | 14.2255; 6.0009; 13.9246 90; 114.398; 90 | 1082.53 | Tian, Qingshan; Chen, Bin; Zhang, Guozhu Silver-initiated radical ring expansion/fluorination of ethynyl cyclobutanols: efficient synthesis of monofluoroethenyl cyclopentanones Green Chem., 2016, 18, 6236 |
| 7226985 | CIF | C14 H13 N O3 | P 1 21/n 1 | 14.2032; 4.6426; 18.5046 90; 99.389; 90 | 1203.84 | Petronijević, Jelena; Bugarčić, Zorica; Bogdanović, Goran A.; Stefanović, Srđan; Janković, Nenad An enolate ion as a synthon in biocatalytic synthesis of 3,4-dihydro-2(1H)-quinoxalinones and 3,4-dihydro-1,4-benzoxazin-2-ones: lemon juice as an alternative to hazardous solvents and catalysts Green Chem., 2017, 19, 707 |
| 7227222 | CIF | C14 H9 Br F2 O3 | P -1 | 6.6847; 8.2593; 12.7076 71.172; 85.353; 72.077 | 631.7 | Gautam, Prashant; Kathe, Prasad; Bhanage, Bhalchandra M. Pd/C catalyzed phenoxycarbonylation using N-formylsaccharin as a CO surrogate in propylene carbonate, a sustainable solvent Green Chem., 2017, 19, 823 |
| 7227271 | CIF | C49 H44 Cl5 F6 Ir N4 O7 P2 S2 | P -1 | 12.1733; 12.9667; 19.521 93.601; 96.085; 111.847 | 2826.4 | Liu, Huan; Wang, Dong-Liang; Chen, Xia; Lu, Yong; Zhao, Xiao-Li; Liu, Ye Efficient and recyclable Ir(i)-catalysts with the involvement of π-acceptor phosphines for N-alkylation of aryl amines with alcohols Green Chem., 2017, 19, 1109 |
| 7227272 | CIF | C42 H34 Cl2 Ir N4 P2 | P 1 21/n 1 | 9.0997; 15.2322; 13.1977 90; 93.109; 90 | 1826.62 | Liu, Huan; Wang, Dong-Liang; Chen, Xia; Lu, Yong; Zhao, Xiao-Li; Liu, Ye Efficient and recyclable Ir(i)-catalysts with the involvement of π-acceptor phosphines for N-alkylation of aryl amines with alcohols Green Chem., 2017, 19, 1109 |
| 7227333 | CIF | C14 H18 Cl N3 O Se | R -3 | 25.4682; 25.4682; 12.316 90; 90; 120 | 6918.3 | Fang, Yi; Zhu, Zheng-Lin; Xu, Pei; Wang, Shun-Yi; Ji, Shun-Jun Aerobic radical-cascade cycloaddition of isocyanides, selenium and imidamides: facile access to 1,2,4-selenadiazoles under metal-free conditions Green Chem., 2017, 19, 1613 |
| 7227453 | CIF | C22 H21 N5 | P -1 | 9.2637; 10.3529; 10.4849 86.787; 75.671; 82.064 | 964.7 | Pharande, Shrikant G.; Corrales Escobosa, Alma Rosa; Gámez-Montaño, Rocío Endogenous water-triggered and ultrasound accelerated synthesis of 1,5-disubstituted tetrazoles via a solvent and catalyst-free Ugi-azide reaction Green Chem., 2017, 19, 1259 |
| 7227474 | CIF | C24 H22 N4 O | P 1 21/c 1 | 44.778; 5.5195; 8.2452 90; 93.029; 90 | 2035 | Fang, Zheng; Hu, Wen-Li; Liu, De-Yong; Yu, Chu-Yi; Hu, Xiang-Guo Synthesis of tetrazines from gem-difluoroalkenes under aerobic conditions at room temperature Green Chem., 2017, 19, 1299 |
| 7227475 | CIF | C16 H12 Br2 N4 | P 1 21/n 1 | 4.8044; 34.603; 9.8785 90; 100.443; 90 | 1615.1 | Fang, Zheng; Hu, Wen-Li; Liu, De-Yong; Yu, Chu-Yi; Hu, Xiang-Guo Synthesis of tetrazines from gem-difluoroalkenes under aerobic conditions at room temperature Green Chem., 2017, 19, 1299 |
| 7227519 | CIF | C48 H72 Cu2 I2 N14 O23 Sm2 | P -1 | 11.0928; 12.4805; 15.1388 81.463; 83.416; 64.133 | 1862.06 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227520 | CIF | C48 H72 Cu2 Eu2 I2 N14 O23 | P -1 | 11.1874; 12.6; 15.1798 92.528; 96.837; 116.289 | 1893.5 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227521 | CIF | C48 H72 Cu2 Gd2 I2 N14 O23 | P -1 | 11.1994; 12.5884; 15.174 92.438; 96.979; 116.308 | 1892.3 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227522 | CIF | C48 H72 Cu2 I2 N14 O23 Tb2 | P -1 | 11.2008; 12.5798; 15.1576 92.291; 97.131; 116.347 | 1888.2 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227523 | CIF | C48 H72 Cu2 Dy2 I2 N14 O23 | P -1 | 11.1272; 12.4509; 15.132 81.365; 82.847; 63.926 | 1857.69 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227524 | CIF | C48 H72 Cu2 Ho2 I2 N14 O23 | P -1 | 11.1399; 12.4564; 15.1237 81.32; 82.723; 63.883 | 1858.5 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227525 | CIF | C48 H72 Cu2 Er2 I2 N14 O23 | P -1 | 11.2006; 12.5227; 15.113 92.084; 97.414; 116.45 | 1871.5 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227526 | CIF | C48 H72 Cu2 I2 N14 O23 Yb2 | P -1 | 11.1943; 12.4986; 15.077 91.996; 97.522; 116.512 | 1861.03 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227527 | CIF | C48 H72 Cu2 I2 N14 O23 Y2 | P -1 | 11.2135; 12.5387; 15.1202 92.092; 97.415; 116.389 | 1877.91 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227528 | CIF | C48 H40 Cu8 I8 N8 Na2 O25 Pr2 | C 2 2 21 | 17.8961; 31.932; 25.078 90; 90; 90 | 14331 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227529 | CIF | C48 H40 Cl0 Cu8 I8 N8 Na2 Nd2 O25 | C 2 2 21 | 17.889; 31.835; 24.831 90; 90; 90 | 14141 | Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework Green Chem., 2017, 19, 1250 |
| 7227553 | CIF | C21 H17 F N0 O2 S Se | P 1 21/n 1 | 7.1841; 18.013; 14.832 90; 95.33; 90 | 1911.1 | Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway Green Chem., 2017, 19, 1490 |
| 7227554 | CIF | C24 H24 N0 O2 S Se | P -1 | 8.7143; 10.963; 12.352 91.21; 95.23; 108.64 | 1111.9 | Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway Green Chem., 2017, 19, 1490 |
| 7227555 | CIF | C18 H18 N0 O2 S Se | C 1 2/c 1 | 14.693; 13.577; 17.032 90; 94.54; 90 | 3387 | Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway Green Chem., 2017, 19, 1490 |
| 7227670 | CIF | C23 H21 Cl N2 | P -1 | 6.0657; 11.6494; 14.2527 104.148; 102.007; 92.918 | 949.69 | Jamatia, Ramen; Gupta, Ajay; Dam, Binoyargha; Saha, Mithu; Pal, Amarta Kumar Graphite oxide: a metal free highly efficient carbocatalyst for the synthesis of 1,5-benzodiazepines under room temperature and solvent free heating conditions Green Chem., 2017, 19, 1576 |
| 7227708 | CIF | C27 H23 N O2 | P -1 | 10.4147; 10.8221; 11.4326 63.221; 63.896; 74.519 | 1029.22 | Xiong, Wenfang; Qi, Chaorong; Guo, Tianzuo; Zhang, Min; Chen, Kai; Jiang, Huanfeng A copper-catalyzed oxidative coupling reaction of arylboronic acids, amines and carbon dioxide using molecular oxygen as the oxidant Green Chem., 2017, 19, 1642 |
| 7227831 | CIF | C21 H23 N O4 | P 1 21/c 1 | 10.2857; 22.5658; 7.71479 90; 97.8249; 90 | 1773.97 | Pagire, Santosh K.; Reiser, Oliver Tandem cyclisation of vinyl radicals: a sustainable approach to indolines utilizing visible-light photoredox catalysis Green Chem., 2017, 19, 1721 |
| 7227985 | CIF | C12 H10 F13 I N2 S | P -1 | 6.4269; 8.9443; 16.3677 85.57; 81.795; 86.766 | 927.49 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227986 | CIF | C12 H10 Cl F13 N2 S | P -1 | 6.3654; 9.2363; 16.0361 75.231; 83.709; 76.855 | 886.44 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227987 | CIF | C24 H20 F32 N4 S2 Si | P 1 21/c 1 | 18.463; 8.901; 11.595 90; 102.185; 90 | 1862.6 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227988 | CIF | C20 H10 F30 I2 N2 S | P -1 | 6.4954; 9.2039; 27.9195 94.848; 91.767; 95.367 | 1654.6 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227989 | CIF | C20 H13 F26 I N2 S | P -1 | 5.8881; 10.2741; 25.481 89.763; 87.419; 77.726 | 1504.69 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227990 | CIF | C15 H15 F13 N2 O3 S2 | P b c a | 8.6657; 10.1187; 48.601 90; 90; 90 | 4261.6 | Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids Green Chem., 2017 |
| 7227991 | CIF | C14 H13 N3 O4 | F d d 2 | 24.0182; 26.8445; 7.914 90; 90; 90 | 5102.6 | Ramakrishna, Seeram; nataraj, poomathi; Perumal, Paramasivan Thirumalai An efficient and eco-friendly synthesis of 2-pyridones and functionalized azaxanthone frameworks via indium triflate catalyzed domino reaction Green Chem., 2017 |
| 7227992 | CIF | C27 H22 Br N3 O4 S | P b c a | 14.158; 14.747; 23.048 90; 90; 90 | 4812 | Ramakrishna, Seeram; nataraj, poomathi; Perumal, Paramasivan Thirumalai An efficient and eco-friendly synthesis of 2-pyridones and functionalized azaxanthone frameworks via indium triflate catalyzed domino reaction Green Chem., 2017 |
| 7228109 | CIF | C26 H26 Br O3 P | P -1 | 6.0572; 12.7385; 16.2312 71.599; 85.516; 80.119 | 1170.35 | Xie, Peizhong; Wang, Jinyu; Fan, Jiang; Liu, Yanan; Wo, Xiangyang; Loh, Teck Peng The C-OH/P-H Dehydrative Cross-Coupling for the Construction of P-C Bond under Metal-free Conditions Green Chem., 2017 |
| 7228158 | CIF | C16 H14 N2 | P 1 21/n 1 | 10.0024; 6.9487; 17.5896 90; 98.794; 90 | 1208.2 | Jin, Jing; Guidi, Sandro; Abada, Zahra; Amara, Zacharias; Selva, Maurizio; George, Michael W.; Poliakoff, Martyn Continuous niobium phosphate catalysed Skraup reaction for quinoline synthesis from solketal Green Chem., 2017 |
| 7228229 | CIF | C12 H11 F3 N2 O2 | P 1 21/n 1 | 7.1752; 13.714; 12.346 90; 91.918; 90 | 1214.2 | Subramaniam, Palaniraja; Ramasubbu, Chandrasekaran; Athiramu, Selvaraj Exploiting Intramolecular Hydrogen Bond for Highly (Z)-Selective & Metal Free Synthesis of Amide Substituted β-aminoenones Green Chem., 2017 |
| 7228256 | CIF | C14 H13 Br O6 | P 21 21 21 | 9.0731; 9.3483; 17.357 90; 90; 90 | 1472.2 | Guo, Yan-Jun; Xia, Ai-Bao; Meng, Chen-Hong; Xu, Zhen Yuan; Xu, Danqian Direct Conversion of γ,γ-Dicarbonyl-Substituted Aldehydes into γ- Lactones with a Sodium Chlorite/DBDMH Combination Green Chem., 2017 |
| 7228288 | CIF | C22 H28 O2 | P 21 21 21 | 7.7777; 13.5678; 16.7615 90; 90; 90 | 1768.78 | Werner, Georg; Rodygin, Konstantin S.; Kostin, Anton A.; Gordeev, Evgeniy G.; Kashin, Alexey S.; Ananikov, Valentine P. A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols Green Chem., 2017 |
| 7228289 | CIF | C29 H48 O | P 1 21 1 | 12.6051; 8.5936; 13.0034 90; 117.576; 90 | 1248.55 | Werner, Georg; Rodygin, Konstantin S.; Kostin, Anton A.; Gordeev, Evgeniy G.; Kashin, Alexey S.; Ananikov, Valentine P. A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols Green Chem., 2017 |
| 7228294 | CIF | C22 H14 O3 S | P 1 21/c 1 | 8.1926; 16.181; 13.1852 90; 104.684; 90 | 1690.8 | Majee, Adinath; Mahato, Sachinta; Santra, Sougata; Chatterjee, Rana; Zyryanov, Grigory V.; Hajra, Alakananda Brønsted acidic ionic liquid-catalyzed tandem reaction: an efficient approach towards regioselective synthesis of pyrano[3,2-c]coumarins under solvent-free conditions bearing lower E-factors Green Chem., 2017 |
| 7228330 | CIF | C19 H17 N O3 | P 1 21/c 1 | 9.4992; 12.0176; 14.7148 90; 107.666; 90 | 1600.6 | Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water. Green Chem., 2017 |
| 7228331 | CIF | C20 H22 N2 O2 | P 1 21/n 1 | 10.0712; 9.0247; 19.0587 90; 99.811; 90 | 1706.9 | Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water. Green Chem., 2017 |
| 7228332 | CIF | C22 H17 N O | P -1 | 9.3178; 9.5222; 10.9385 68.404; 66.038; 66.642 | 789.02 | Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water. Green Chem., 2017 |
| 7228397 | CIF | C18 H38 Ca I2 N2 O8 | P -1 | 7.4395; 10.2984; 10.4052 118.125; 94.6199; 92.7499 | 697.42 | Steinbauer, J.; Spannenberg, A.; Werner, T. An in situ formed Ca2±-crown ether complex and its use in CO2-fixation reactions with terminal and internal epoxides Green Chem., 2017 |
| 7228398 | CIF | C10 H10 O4 | P 21 21 21 | 8.6487; 9.628; 10.6343 90; 90; 90 | 885.51 | Steinbauer, J.; Spannenberg, A.; Werner, T. An in situ formed Ca2±-crown ether complex and its use in CO2-fixation reactions with terminal and internal epoxides Green Chem., 2017 |
| 7228456 | CIF | C26 H43 B3 O6 | P -1 | 10.7089; 11.6927; 13.5483 114.506; 99.354; 104.113 | 1428.7 | Gao, Guoliang; Yan, Jianxiang; Yang, Kai; Chen, Fen er; Song, Qiuling Base-Controlled Highly Selective Synthesis of Alkyl 1,2-Bis(boronates) or 1,1,2-Tris(boronates) from Terminal Alkynes Green Chem., 2017 |
| 7228528 | CIF | C20 H24 F N2 O4.5 | P 1 c 1 | 12.3686; 15.9846; 9.9812 90; 113.591; 90 | 1808.4 | Ma, Yulu; Wang, Kai-Min; Huang, Rong; Lin, Jun; Yan, Sheng-Jiao An environmentally benign double Michael addition reaction of heterocyclic ketene aminals with quinone monoketals for diastereoselective synthesis of highly functionly morphan derivatives in water Green Chem., 2017 |
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