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
7220063 CIFC30 H22 N4 O4.5 S0.5P 1 21/c 124.9048; 9.498; 22.2694
90; 110.723; 90
4926.9Poomathi, 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 CIFC29 H25 Cl N2 O3P 21 21 2111.88; 16.051; 26.14
90; 90; 90
4985Vivekanand, 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 CIFC13 H11 N3 O5P 1 21 18.6065; 7.1858; 11.184
90; 110.985; 90
645.794Zhang, 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 CIFC16 H17 N3 O6P 1 21/n 113.5271; 7.4112; 16.501
90; 94.763; 90
1648.55Zhang, 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 CIFC13 H13 N3 O3P 1 21/c 16.3186; 11.7574; 16.3886
90; 95.537; 90
1211.83Zhang, 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 CIFC22 H24 N2 O4 S2P -18.1437; 11.826; 12.4
73.31; 88.33; 79.7
1125.2Khazalpour, 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 CIFC29 H24 N2 O5P -19.441; 10.287; 13.246
100.627; 94.498; 108.144
1188.7Sarkar, 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 CIFC19 H35 I O4 SP -110.4883; 11.9211; 20.6101
93.874; 92.989; 115.747
2306.2Koh, 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 CIFC11 H18 N2 O SP 1 21/n 112.645; 15.1066; 13.214
90; 93.207; 90
2520.22Wang, 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 CIFC20 H28 N2 O SP 1 21/c 110.4317; 15.4783; 11.9638
90; 102.189; 90
1888.19Wang, 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 CIFC11 H18 N2 S2P 1 21/n 17.9953; 15.115; 11.4875
90; 107.186; 90
1326.3Wang, 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 CIFC20 H28 N2 S2P 1 21/c 110.1668; 16.0775; 12.9862
90; 103.802; 90
2061.4Wang, 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 CIFC23 H14 Cl N O2P -18.686; 10.371; 11.293
109.138; 111.662; 92.379
877.8Koneni, 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 CIFC12 H12 N4 O2P 1 21/n 17.534; 10.682; 16.411
90; 102.32; 90
1290.3Ershov, 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 CIFC20 H17 N O6P 1 21/c 17.8241; 24.301; 9.1574
90; 93.76; 90
1737.4Xia, 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 CIFC20 H43 O4 PP -19.6788; 9.6941; 12.4864
86.025; 86.707; 89.675
1166.81Anderson, 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 CIFC34 H74 O6 P2P 1 21/c 110.569; 11.627; 31.826
90; 90.812; 90
3911Anderson, 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 CIFC20 H15 B F4 N2P b c a11.5582; 12.3717; 23.8099
90; 90; 90
3404.7de 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 CIFC26 H20 B F4 N3P -18.5758; 10.4878; 12.8368
75.32; 78.092; 74.019
1062.06de 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 CIFC15 H14 Cl2 N2 O2 RuP -17.668; 8.3022; 13.5405
83.606; 81.922; 70.403
802.11Gupta, 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 CIFC19 H22 Cl2 N2 RuP 1 21/c 117.072; 12.3086; 9.1013
90; 100.9; 90
1877.97Gupta, 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 CIFC19 H11 N O2 SP 1 21/c 112.242; 11.566; 10.526
90; 93.08; 90
1488.2Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri
Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones
Green Chem., 2016, 18, 402
7221978 CIFC4 H6 O4P 1 21/c 110.6016; 9.5305; 10.7702
90; 119.312; 90
948.88Tryznowski, 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 CIFC18 H31 N O4P -19.384; 10.484; 11.281
102.829; 94.191; 113.456
976.4Maleki, 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 CIFC19 H20 O6P n a 2123.0884; 10.4956; 7.3329
90; 90; 90
1776.96Wang, 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 CIFC19 H20 O6P n a 2122.9356; 10.4908; 7.3765
90; 90; 90
1774.88Wang, 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 CIFC7 H10 F N O3P 1 21 18.5224; 10.305; 9.1442
90; 90.3404; 90
803.06Willis, 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 CIFC7 H10 F N O3P 1 21 18.5211; 10.3039; 9.1547
90; 90.365; 90
803.77Willis, 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 CIFC8 H15 Cl F N O4P -15.821; 6.4875; 15.7485
100.738; 96.625; 94.612
577.23Willis, 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 CIFC7 H10 F N O3P 1 21/c 112.256; 6.72544; 10.4787
90; 113.193; 90
793.92Willis, 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 CIFC7 H13 Cl F N O4P 1 21/c 112.235; 11.3068; 7.6415
90; 100.289; 90
1040.12Willis, 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 CIFC6 H10 F N O4P -16.5648; 6.6759; 9.6206
98.163; 100.929; 101.047
399.3Willis, 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 CIFC88 H72 Cd5 N6 O28P 1 21/c 114.6261; 23.2526; 15.7357
90; 107.099; 90
5115.1Qiao, 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 CIFC96 H82 Cd5 N8 O28P 1 21/c 114.5196; 23.367; 15.6042
90; 107.475; 90
5049.8Qiao, 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 CIFC88 H72 Cd3 Cu2 N6 O27P 1 21/c 114.3997; 23.362; 15.543
90; 106.309; 90
5018.4Qiao, 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 CIFC90 H76 Cd5 N6 O28P 1 21/c 114.583; 23.241; 15.6338
90; 106.99; 90
5067.4Qiao, 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 CIFC26 H16 N4 O8 ZnP 1 21/c 119.13; 26.34; 11.628
90; 90.671; 90
5859Gong, 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 CIFC36 H28 N4 P2P -18.8542; 12.9976; 14.0901
100.076; 90.969; 92.406
1594.63Li, 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 CIFC40 H34 F6 N4 O6 P2 S2P -114.0858; 14.4866; 15.7112
67.615; 78.55; 62.44
2627Li, 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 CIFC38 H33 Cl2 I N4 P2P 1 21/c 19.5438; 39.836; 10.6814
90; 116.464; 90
3635.4Li, 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 CIFC23 H26 N2 O2P 1 21/c 19.0471; 17.5709; 12.943
90; 109.25; 90
1942.5Harvey, 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 CIFC28 H24 N2 O3 SP -19.0258; 11.0099; 12.4506
79.449; 76.11; 80.803
1172Dandia, 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 CIFC38 H48 Cl Cu N4 O S2P -111.443; 12.452; 15.01
71.585; 84.083; 68.386
1886.3Barman, 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 CIFC75 H47 N5 O9 Zn2C 1 2/c 128.525; 29.966; 14.784
90; 109.02; 90
11947.1Liu, 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 CIFC26 H34 O3 SP 21 21 29.7748; 36.406; 6.5704
90; 90; 90
2338.2Huang, 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 CIFC20 H22 OP -18.4061; 8.6026; 12.582
91.647; 102.618; 112.149
816.1Wang, 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 CIFC14 H14 N2 O2P 1 21 17.5292; 5.7936; 13.9668
90; 93.766; 90
607.93Chaudhary, 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 CIFC18 H13 Cl N4 O PdP 1 21/c 113.0361; 12.7404; 20.0773
90; 94.398; 90
3324.7Arumugam, 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 CIFC17 H12 Cl N3 O2 PdP n a 2118.2644; 9.0854; 19.045
90; 90; 90
3160.3Arumugam, 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 CIFC17 H12 N2 SP 1 21/c 112.247; 13.34; 8.315
90; 77.29; 90
1325Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav
Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles
Green Chem., 2016, 18, 2666

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