Crystallography Open Database

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1540034 CIFC32 H28 F6 N8 O4 ZnP -18.8018; 9.2775; 11.3673
82.433; 68.031; 67.635
796Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540035 CIFC40 H44 F6 N8 O4 ZnP 1 21/n 114.5768; 8.9341; 15.9047
90; 103.294; 90
2015.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540036 CIFC18 H14 F6 N4 O4 ZnP -19.7675; 11.262; 11.576
98.815; 107.953; 112.944
1059.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
7204165 CIFC80 H98 N2 O16P -111.2391; 12.889; 14.478
90.734; 110.956; 112.21
1786.49Brett 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 CIFC15 H12 O3P b c 215.912; 8.043; 25.07
90; 90; 90
1192.1Kazuhiro Yoshizawa; Shinji Toyota; Fumio Toda; Ingeborg Csöregh
Preparative and mechanistic studies of solvent-free Rap–Stoermer reactions
Green Chem., 2003, 5, 353-356
7217280 CIFC86.5 H113 Al Cl5 O4 PC 1 2/c 127.1582; 28.5362; 24.0085
90; 113.869; 90
17015Söhner, 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 CIFC77 H122 Al Cl2 Li O8P 1 21/n 116.4252; 16.4896; 29.6929
90; 102.666; 90
7846.5Söhner, 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 CIFC76 H120 Al Na O8P -114.1898; 14.7188; 19.354
83.112; 89.299; 71.328
3800.35Söhner, 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 CIFC77 H126 Al Cl2 N O4P b c a24.3711; 24.6465; 25.3492
90; 90; 90
15226.3Söhner, 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 CIFC34 H52 N2 O2P -15.9662; 10.201; 14.27
101.025; 93.011; 104.712
819.8Söhner, 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 CIFC94 H142 Al Au N2 O4 SP c a 2124.5162; 14.2702; 27.0151
90; 90; 90
9451.3Söhner, 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 CIFC68 H104 Al Na O6C 1 2/c 111.081; 23.961; 24.439
90; 101.533; 90
6358Söhner, 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 CIFC25 H27 Br OP 1 21/c 19.971; 11.013; 19.557
90; 94.091; 90
2142.1Söhner, 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 CIFC34 H54 O2I 41/a23.87; 23.87; 10.781
90; 90; 90
6143Söhner, 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 CIFC92 H124 Al O4 PP -123.163; 27.127; 30.989
115.645; 99.092; 100.786
16604Söhner, 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 CIFC66 H86 O6P -111.466; 11.745; 11.838
71.639; 75.918; 72.993
1426.7Söhner, 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 CIFC136 H152 Al Cl4 O4 PP 1 21/c 114.8662; 33.789; 27.09
90; 94.019; 90
13574Söhner, 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 CIFC25 H25 N O4 SP 1 21/c 112.2796; 11.7459; 15.808
90; 102.781; 90
2223.57Nagaraju, 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 CIFC31 H29 N O2 SP n a 2116.581; 11.236; 14.597
90; 90; 90
2719.5Nagaraju, 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 CIFC22 H25 N O2 SP 1 21/n 16.4263; 12.9536; 23.9037
90; 97.062; 90
1974.74Nagaraju, 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 CIFC17 H24 N2 OC 1 2/c 129.745; 5.802; 19.967
90; 112.103; 90
3193Xie, 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 CIFC30 H26 I N O5 SP -112.771; 14.579; 16.377
106.53; 105.21; 91.3
2805.1Xu, 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 CIFC22 H22 Cl N O2P 21 21 217.5759; 11.0478; 23.488
90; 90; 90
1965.9Ye, 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 CIFC18 H21 N O4P 1 21/n 110.0101; 10.7765; 15.5711
90; 93.9; 90
1675.8Ye, 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 CIFC24 H18 Cl N O4P -110.6004; 13.375; 16.069
82.836; 71.805; 89.343
2146.5Ye, 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 CIFC10 H8 Br N3 O2P c c n11.4437; 22.5577; 8.1293
90; 90; 90
2098.53Li, 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 CIFC40 H0 Mo8 N8 O26P 1 21/n 116.4264; 10.8002; 17.5844
90; 96.397; 90
3100.2Zhou, 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 CIFC44 H0 Mo8 N4 O27P 1 21/n 115.6345; 12.1211; 16.5893
90; 94.603; 90
3133.7Zhou, 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 CIFC24 H40 B F4 Ir N4 O2P -110.1442; 11.7709; 15.044
109.125; 97.344; 109.259
1545.2Manas, 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 CIFC6 H8 Cl0 Cu N14 O2P -17.1861; 7.5759; 7.6549
89.212; 63.414; 64.027
326.31Liu, 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 CIFC3 H Cu N7 OP 1 21/n 17.404; 9.672; 9.341
90; 113.02; 90
615.7Liu, 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 CIFC3 H2 Cu N7P 1 21/c 18.63; 9.867; 6.736
90; 108.297; 90
544.6Liu, 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 CIFC18 H16 N2 O4P 1 21/c 14.401; 12.3035; 14.8314
90; 97.593; 90
796.04Harvey, 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 CIFC18 H14 N2 O4P 1 21/c 13.8765; 12.2303; 16.1995
90; 95.906; 90
763.95Harvey, 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 CIFC14 H8 Cl N3 SP c c n7.4354; 15.648; 21.424
90; 90; 90
2492.7Wen, 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 CIFC30 H31 N5 O2P -111.0519; 13.5682; 19.4863
107.546; 96.181; 109.124
2562.3Fu, 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 CIFC31 H33 N5 O2P 1 21/c 118.6242; 10.3311; 29.295
90; 106.496; 90
5404.6Fu, 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 CIFC12 H11 F N2 O2P 1 21/n 114.5192; 4.971; 16.4551
90; 106.074; 90
1141.21Marković, 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 CIFC88 H148 N6 Nd2 O9 Si4P -113.883; 14.024; 15.361
109.019; 106.371; 98.531
2616Cheng, 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 CIFC88 H148 La2 N6 O9 Si4P -113.963; 14.045; 15.374
108.936; 106.425; 98.499
2638.4Cheng, 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 CIFC88 H148 N6 O9 Si4 Y2P -113.74; 14; 15.31
109.27; 106.002; 98.57
2577Cheng, 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 CIFC18 H15 N O5P b c a12.291; 7.4147; 34.667
90; 90; 90
3159.3Sharma, 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 CIFC20 H62 Al3 Fe2 Li N4 O2P c a 2115.4965; 16.8579; 12.6159
90; 90; 90
3295.8Gieshoff, 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 CIFC33 H33 N5 OP 1 21/n 111.9187; 9.8408; 24.353
90; 102.942; 90
2783.8Sousa, 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 CIFC26 H21 N5 O2P -19.1187; 10.839; 12.4287
66.309; 88.214; 81.725
1112.7Feng, 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 CIFC27 H23 N5 O2P -18.5318; 10.724; 13.1003
74.306; 87.632; 81.193
1140.3Feng, 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 CIFC8 H7 N OP b c a7.5044; 11.9291; 14.8473
90; 90; 90
1329.1Ren, 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 CIFC5 H7 F O4P 1 21/c 16.1459; 10.5542; 9.5004
90; 93.777; 90
614.91Harsanyi, 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 CIFC24 H26 N4 O3P -16.6676; 7.3731; 21.962
98.895; 91.912; 99.057
1051.5Schröder, 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 CIFC22 H16 F N5 O3P 1 21/c 113.3119; 10.7033; 13.8141
90; 91.8261; 90
1967.25Poomathi, 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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