Crystallography Open Database

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1519680 CIFC49 H42 Au2 Cl2 N2 O4 P4 S2C 1 2/c 125.848; 11.2564; 20.6909
90; 122.413; 90
5082.2Vidal, C.; Merz, L.; García-Álvarez, J.
Deep eutectic solvents: biorenewable reaction media for Au( <scp>i</scp> )-catalysed cycloisomerisations and one-pot tandem cycloisomerisation/Diels–Alder reactions
Green Chemistry, 2015, 17, 3870-3878
1550815 CIFC30 H30 N2 O2 SP 21 21 215.7205; 19.9636; 21.5679
90; 90; 90
2463.09Yao, Wei-Wei; Li, Ran; Li, Jiang-Fei; Sun, Juan; Ye, Mengchun
NHC ligand-enabled Ni-catalyzed reductive coupling of alkynes and imines using isopropanol as a reductant
Green Chemistry, 2019, 21, 2240
1550819 CIFC21 H19 N O4P 1 21/c 17.5364; 20.5621; 11.4782
90; 94.877; 90
1772.27Li, Qing-Zhu; Zhang, Xiang; Xie, Ke; Dai, Qing-Song; Zeng, Rong; Liu, Yan-Qing; Jia, Zhi-Qiang; Feng, Xin; Li, Jun-Long
Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes
Green Chemistry, 2019, 21, 2375
1550820 CIFC24 H19 N3 O3P 1 21/n 113.6825; 10.7919; 14.7575
90; 108.476; 90
2066.8Li, Qing-Zhu; Zhang, Xiang; Xie, Ke; Dai, Qing-Song; Zeng, Rong; Liu, Yan-Qing; Jia, Zhi-Qiang; Feng, Xin; Li, Jun-Long
Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes
Green Chemistry, 2019, 21, 2375
7200176 CIFC22 H13 Cl2 F N2 O S2P -19.896; 10.256; 11.128
89.64; 73.71; 82.42
1074Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing
Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route
Green Chemistry, 2009, 11, 215
7200177 CIFC23 H17 Br N2 O S2P -16.3729; 12.941; 13.413
108.64; 96.27; 96.96
1027.5Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing
Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route
Green Chemistry, 2009, 11, 215
7200178 CIFC22 H13 Cl N2 O S2P 1 21/c 111.497; 7.537; 22.384
90; 103.64; 90
1884.9Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing
Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route
Green Chemistry, 2009, 11, 215
7200179 CIFC22 H14 Cl2 N2 O S2P -110.084; 10.331; 10.414
87.6; 85.58; 78.1
1058.1Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing
Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route
Green Chemistry, 2009, 11, 215
7200280 CIFC11 H13 N O3 SP 1 21/c 117.1392; 6.0512; 10.9857
90; 93.007; 90
1137.79Hota, Sandip K.; Chatterjee, Amrita; Bhattacharya, Pranab K.; Chattopadhyay, Partha
A green chemical approach for the N-alkylation of aldoximes to form nitrones in organized aqueous media and their in situ cycloaddition with olefins
Green Chemistry, 2009, 11, 169
7200610 CIFC8 H12 F4 N2 O3 SP 1 21/n 18.77; 9.766; 14.282
90; 95.363; 90
1217.9Harmer, Mark A.; Junk, Christopher P.; Rostovtsev, Vsevolod V.; Marshall, William J.; Grieco, Liane M.; Vickery, Jemma; Miller, Robert; Work, Stella
Catalytic reactions using superacids in new types of ionic liquids
Green Chemistry, 2009, 11, 517
7200611 CIFC10 H11 F9 N2 O3 SP 1 21/c 19.178; 34.444; 10.022
90; 91.711; 90
3167Harmer, Mark A.; Junk, Christopher P.; Rostovtsev, Vsevolod V.; Marshall, William J.; Grieco, Liane M.; Vickery, Jemma; Miller, Robert; Work, Stella
Catalytic reactions using superacids in new types of ionic liquids
Green Chemistry, 2009, 11, 517
7201002 CIFC19 H13 N O2 S2P -18.655; 9.619; 10.727
83.143; 72.938; 64.907
773.2Saha, Pritam; Naskar, Subhendu; Paira, Priyankar; Hazra, Abhijit; Sahu, Krishnendu B.; Paira, Rupankar; Banerjee, Sukdeb; Mondal, Nirup B.
Basic alumina-supported highly effective Suzuki‒Miyaura cross-coupling reaction under microwave irradiation: application to fused tricyclic oxa-aza-quinolones
Green Chemistry, 2009, 11, 931
7201048 CIFC16 H14 N2 OP 1 21/c 111.3034; 13.2485; 8.9142
90; 97.277; 90
1324.2Ye, Deju; Wang, Jinfang; Zhang, Xu; Zhou, Yu; Ding, Xiao; Feng, Enguang; Sun, Haifeng; Liu, Guannan; Jiang, Hualiang; Liu, Hong
Gold-catalyzed intramolecular hydroamination of terminal alkynes in aqueous media: efficient and regioselective synthesis of indole-1-carboxamides
Green Chemistry, 2009, 11, 1201
7201240 CIFC11 H17 Cl2 N TiP 1 21/m 17.3084; 10.576; 8.5363
90; 102.7; 90
643.7Fletcher, Andrew E.D.; Hyatt, Jonathan D.; Ok, Kang Min; O'Hare, Dermot
Catalytic dechlorination of polychlorinated biphenyls (PCBs) using amine functionalised titanocenes
Green Chemistry, 2009, 11, 1343
7201469 CIFC11 H19 Cl2 O5 P RuP -16.985; 7.315; 16.94
80.825; 81.027; 63.636
762.05Lastra-Barreira, Beatriz; Díez, Josefina; Crochet, Pascale
Highly water-soluble arene-ruthenium(ii) complexes: application to catalytic isomerization of allylic alcohols in aqueous medium
Green Chemistry, 2009, 11, 1681
7201470 CIFC14 H25 Cl2 O5 P RuP 1 21/c 17.6034; 14.0769; 18.318
90; 109.371; 90
1849.63Lastra-Barreira, Beatriz; Díez, Josefina; Crochet, Pascale
Highly water-soluble arene-ruthenium(ii) complexes: application to catalytic isomerization of allylic alcohols in aqueous medium
Green Chemistry, 2009, 11, 1681
7201477 CIFC18 H16 F N O2 S2P -18.133; 10.9315; 11.3491
111.001; 103.328; 103.603
858.68Cohen, Anita; Crozet, Maxime D.; Rathelot, Pascal; Vanelle, Patrice
An efficient aqueous microwave-assisted Suzuki‒Miyaura cross-coupling reaction in the thiazole series
Green Chemistry, 2009, 11, 1736
7201484 CIFC15 H31 F3 N2 O3 SP 21 21 217.6593; 12.5747; 20.4376
90; 90; 90
1968.4Lin, Jin-Hong; Zhang, Cheng-Pan; Xiao, Ji-Chang
Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water
Green Chemistry, 2009, 11, 1750
7201610 CIFC13 H21 B F N O2P 1 21/c 113.748; 7.701; 13.781
90; 110.97; 90
1362.4Arnold, Kenny; Batsanov, Andrei S.; Davies, Bryan; Whiting, Andrew
Synthesis, evaluation and application of novel bifunctional N,N-di-isopropylbenzylamineboronic acid catalysts for direct amide formation between carboxylic acids and amines
Green Chemistry, 2008, 10, 124
7201611 CIFC14 H21 B F3 N O2P 1 21/c 115.4653; 7.7851; 13.2548
90; 105.71; 90
1536.2Arnold, Kenny; Batsanov, Andrei S.; Davies, Bryan; Whiting, Andrew
Synthesis, evaluation and application of novel bifunctional N,N-di-isopropylbenzylamineboronic acid catalysts for direct amide formation between carboxylic acids and amines
Green Chemistry, 2008, 10, 124
7202028 CIFC22 H20 O3P 1 21/c 116.0672; 14.9408; 7.1505
90; 96.855; 90
1704.26Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Platform technology for dienone and phenol‒formaldehyde architectures
Green Chemistry, 2008, 10, 842
7202029 CIFC26 H26 O5P 1 21/n 111.446; 15.395; 12.411
90; 92.07; 90
2185.5Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Platform technology for dienone and phenol‒formaldehyde architectures
Green Chemistry, 2008, 10, 842
7202030 CIFC28 H30 O4P 1 21/n 114.1051; 5.984; 14.3719
90; 114.297; 90
1105.61Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Platform technology for dienone and phenol‒formaldehyde architectures
Green Chemistry, 2008, 10, 842
7202031 CIFC45.5 H44.5 Cl1.5 O7P 1 21/n 115.1785; 15.078; 16.5313
90; 97.645; 90
3749.75Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Platform technology for dienone and phenol‒formaldehyde architectures
Green Chemistry, 2008, 10, 842
7202032 CIFC94 H90 Cl6 O14P 1 21/c 112.115; 22.3638; 30.838
90; 92.377; 90
8348Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Platform technology for dienone and phenol‒formaldehyde architectures
Green Chemistry, 2008, 10, 842
7202237 CIFC15 H12 N2 O SP b c a10.9047; 10.0696; 24.2827
90; 90; 90
2666.39Yella, Ramesh; Ghosh, Harisadhan; Patel, Bhisma K.
It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride
Green Chemistry, 2008, 10, 1307
7202238 CIFC15 H10 Cl2 N2 O SP b c a12.9; 10.035; 24.251
90; 90; 90
3139.3Yella, Ramesh; Ghosh, Harisadhan; Patel, Bhisma K.
It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride
Green Chemistry, 2008, 10, 1307
7202277 CIFC14 H16 Cl N S2P 1 21/c 110.704; 15.143; 8.924
90; 100.006; 90
1424.5Bhadra, Sukalyan; Saha, Amit; Ranu, Brindaban C.
One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: high diastereoselectivity achieved for vinyl dithiocarbamates
Green Chemistry, 2008, 10, 1224
7202470 CIFC18 H52 N6 O16 P4P 1 21/n 120.45; 7.329; 10.31
90; 99.28; 90
1525Shastri, Kirtida; Cheng, Eileen W. C.; Motevalli, Majid; Schofield, John; Wilkinson, Jennifer S.; Watkinson, Michael
Investigations into the efficacy of methyhlphosphonic acid functionalised 1,4,7-triazacyclononane ligands in bleaching catalysis
Green Chemistry, 2007, 9, 996
7202471 CIFC9 H28 Br2 N3 O5 PP -17.603; 9.1105; 13.0353
89.455; 75.731; 86.145
873.06Shastri, Kirtida; Cheng, Eileen W. C.; Motevalli, Majid; Schofield, John; Wilkinson, Jennifer S.; Watkinson, Michael
Investigations into the efficacy of methyhlphosphonic acid functionalised 1,4,7-triazacyclononane ligands in bleaching catalysis
Green Chemistry, 2007, 9, 996
7202474 CIFC6 H11 N3 O6P -16.43; 6.715; 11.544
87.486; 80.11; 80.82
484.7Smiglak, Marcin; Holbrey, John D.; Griffin, Scott T.; Reichert, W. Matthew; Swatloski, Richard P.; Katritzky, Alan R.; Yang, Hongfang; Zhang, Dazhi; Kirichenko, Kostyantyn; Rogers, Robin D.
Ionic liquids via reaction of the zwitterionic 1,3-dimethylimidazolium-2-carboxylate with protic acids. Overcoming synthetic limitations and establishing new halide free protocols for the formation of ILs
Green Chemistry, 2007, 9, 90
7202475 CIFC6 H9 N3 O5P 1 21/n 16.628; 11.91; 11.538
90; 104.508; 90
881.8Smiglak, Marcin; Holbrey, John D.; Griffin, Scott T.; Reichert, W. Matthew; Swatloski, Richard P.; Katritzky, Alan R.; Yang, Hongfang; Zhang, Dazhi; Kirichenko, Kostyantyn; Rogers, Robin D.
Ionic liquids via reaction of the zwitterionic 1,3-dimethylimidazolium-2-carboxylate with protic acids. Overcoming synthetic limitations and establishing new halide free protocols for the formation of ILs
Green Chemistry, 2007, 9, 90
7202477 CIFC22 H18 N2P 1 21/n 117.365; 9.9287; 20.981
90; 113.4; 90
3319.9Palimkar, Sanjay S.; Lahoti, Rajgopal J.; Srinivasan, Kumar V.
A novel one-pot three-component synthesis of 2,4-disubstituted-3 H-benzo[ b][1,4]diazepines in water
Green Chemistry, 2007, 9, 146
7202516 CIFC21 H26 N2 O3P -19.4031; 9.3855; 11.006
78.01; 84.307; 82.744
939.84Iván Kanizsai; Szilvia Gyónfalvi; Zsolt Szakonyi; Reijo Sillanpää; Ferenc Fülöp
Synthesis of bi- and tricyclic ?-lactam libraries in aqueous medium
Green Chemistry, 2007, 9, 357
7202585 CIFC23 H39 N O5 SP 21 21 217.1563; 13.1156; 27.469
90; 90; 90
2578.2Rosini, Goffredo; Ayoub, Claudia; Borzatta, Valerio; Marotta, Emanuela; Mazzanti, Andrea; Righi, Paolo
The same and not the same. Similarities and differences in the resolution of trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols
Green Chemistry, 2007, 9, 441
7202586 CIFC22 H35 N O4 SP 1 21 19.994; 7.8004; 15.8597
90; 106.301; 90
1186.68Rosini, Goffredo; Ayoub, Claudia; Borzatta, Valerio; Marotta, Emanuela; Mazzanti, Andrea; Righi, Paolo
The same and not the same. Similarities and differences in the resolution of trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols
Green Chemistry, 2007, 9, 441
7202699 CIFC36 H56 Mo8 N4 O26P 1 21/n 111.6255; 15.2552; 15.2882
90; 92.341; 90
2709.1Ming-Lin, Guo; Hui-Zhen, Li
Selective oxidation of benzyl alcohol to benzaldehyde with hydrogen peroxide over tetra-alkylpyridinium octamolybdate catalysts
Green Chemistry, 2007, 9, 421
7202710 CIFC23 H20 N3 O0.5C 1 2 125.39; 5.557; 13.342
90; 93.826; 90
1878.3Smith, Nicole M.; Raston, Colin L.; Smith, Christopher B.; Sobolev, Alexandre N.
PEG mediated synthesis of amino-functionalised 2,4,6-triarylpyridines
Green Chemistry, 2007, 9, 1185
7202843 CIFC11 H17 F3 N2 O4 SP 1 21/n 18.5166; 10.879; 16.006
90; 103; 90
1445Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine
Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation
Green Chemistry, 2007, 9, 1097
7202844 CIFC14 H20 F6 N4 O6 S2P -18.6516; 10.1699; 12.195
87.354; 85.474; 83.36
1061.7Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine
Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation
Green Chemistry, 2007, 9, 1097
7202845 CIFC27 H51 F6 N3 O7 S2P -19.5883; 9.7729; 19.198
85.627; 88.693; 88.563
1792.8Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine
Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation
Green Chemistry, 2007, 9, 1097
7202913 CIFC79 H122 Na2 O7P 1 21/n 116.035; 19.797; 24.936
90; 104.979; 90
7647Chen, Hsuan-Ying; Zhang, Jubo; Lin, Chu-Chieh; Reibenspies, Joseph H.; Miller, Stephen A.
Efficient and controlled polymerization of lactide under mild conditions with a sodium-based catalyst
Green Chemistry, 2007, 9, 1038
7202999 CIFC14 H20 N2P -18.952; 10.126; 14.757
70.511; 79.526; 76.96
1220.2Waldemar M. Czaplik; Jörg-M. Neudörfl; Axel Jacobi von Wangelin
On the quantitative recycling of Raney‒Nickel catalysts on a lab-scale
Green Chemistry, 2007, 9, 1163
7203081 CIFC16 H27 N O7 P2P -19.955; 10.404; 10.839
97.689; 98.771; 111.382
1011Zhang, Jianfeng; Cui, Zhanwei; Wang, Fei; Wang, Yadan; Miao, Zhiwei; Chen, Ruyu
Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions—synthesis of N-phosphoramino α-aminophosphonates
Green Chemistry, 2007, 9, 1341
7203136 CIFC16 H18 N2 O2P 1 21/n 19.4647; 9.9534; 15.7079
90; 98.509; 90
1463.49van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.
Benign approaches for the synthesis of bis-imine Schiff bases
Green Chemistry, 2006, 8, 50
7203137 CIFC16 H20 N4C 1 2/c 118.5478; 8.9189; 9.2148
90; 101.388; 90
1494.36van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.
Benign approaches for the synthesis of bis-imine Schiff bases
Green Chemistry, 2006, 8, 50
7203138 CIFC18 H20 N4C 1 2/c 135.5824; 5.701; 16.8318
90; 112.752; 90
3148.7van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.
Benign approaches for the synthesis of bis-imine Schiff bases
Green Chemistry, 2006, 8, 50
7203388 CIFC12 H10 F3 N O2P 1 21/a 17.925; 10.643; 13.886
90; 99.478; 90
1155.2Kayaki, Yoshihito; Yamamoto, Masafumi; Suzuki, Tomoyuki; Ikariya, Takao
Carboxylative cyclization of propargylamines with supercritical carbon dioxide
Green Chemistry, 2006, 8, 1019
7203394 CIFC21 H22 Cl N O2P 1 21/c 17.1209; 16.3999; 15.0997
90; 92.716; 90
1761.4Wang, Guan-Wu; Miao, Chun-Bao
Environmentally benign one-pot multi-component approaches to the synthesis of novel unsymmetrical 4-arylacridinediones
Green Chemistry, 2006, 8, 1080
7203399 CIFC27 H42 N2 O5P -17.936; 10.048; 17.864
91.753; 102.116; 106.858
1326.5Pernak, Juliusz; Smiglak, Marcin; Griffin, Scott T.; Hough, Whitney L.; Wilson, Timothy B.; Pernak, Anna; Zabielska-Matejuk, Jadwiga; Fojutowski, Andrzej; Kita, Kazimierz; Rogers, Robin D.
Long alkyl chain quaternary ammonium-based ionic liquids and potential applications
Green Chemistry, 2006, 8, 798
7203438 CIFC24 H26 O4P -111.219; 12.8515; 14.1651
82.272; 88.467; 75.715
1961.17Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203439 CIFC21 H19 N O4P -17.8646; 9.683; 11.3746
95.587; 102.801; 91.992
839.25Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203440 CIFC20 H18 Br N O2P 1 21/c 118.5748; 6.2641; 15.9337
90; 115.194; 90
1677.59Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203441 CIFC36 H38 Cl N OP -111.5683; 12.3023; 13.6088
98.825; 110.125; 111.483
1603.3Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203442 CIFC26 H31 N3 OP 1 21/n 110.0896; 13.29; 16.6649
90; 103.981; 90
2168.41Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203443 CIFC10 H15 N O2P b c a8.763; 10.924; 20.1019
90; 90; 90
1924.29Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.
A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones
Green Chemistry, 2006, 8, 1042
7203719 CIFC32 H40 O2 SnP 1 21 111.2787; 11.699; 11.696
90; 115.519; 90
1392.7John Fawcett; Eric G. Hope; Alison M. Stuart; Andrew J. West
Recycling of a perfluoroalkylated BINOL ligand using fluorous solid-phase extraction
Green Chemistry, 2005, 7, 316
7203730 CIFC9 H19 Cl2 N2 Na O6 S ZnP 1 21/c 118.3353; 7.6965; 12.7734
90; 104.148; 90
1747.88Liang, Hong-Chang; Das, Sanjib K.; Galvan, Juan R.; Sato, Suzanne M.; Zhang, Yonglian; Zakharov, Lev N.; Rheingold, Arnold L.
Syntheses of water-soluble N-donor ligands for aqueous catalysis using green, Michael-type addition reactions
Green Chemistry, 2005, 7, 410
7203755 CIFC24 H21 O6 PR 3 c :H19.1098; 19.1098; 10.2052
90; 90; 120
3227.5Ablan, Christopher D.; Sheppard, Daniel; Beckman, Eric J.; Olmstead, Marilyn M.; Jessop, Philip G.
Solubility of several analogues of triphenylphosphine in carbon dioxide
Green Chemistry, 2005, 7, 590
7203759 CIFC15 H4 N4 O5P 1 21/n 114.169; 6.451; 15.238
90; 110.614; 90
1303.64Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc
Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions
Green Chemistry, 2005, 7, 413
7203760 CIFC29 H16 N4 O5 SP 1 21/n 17.731; 15.143; 21.152
90; 98.189; 90
2451Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc
Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions
Green Chemistry, 2005, 7, 413
7203761 CIFC13 H4 Br2 N2 O5P 1 21/c 110.366; 16.072; 8.312
90; 103.372; 90
1347.26Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc
Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions
Green Chemistry, 2005, 7, 413
7203787 CIFC12 H22 N Na O6P 6221.1806; 21.1806; 5.6912
90; 90; 120
2211.1Godinez-Salomon, Fernando; Hallen-Lopez, Jose M.; Höpfl, Herbert; Morales-Pacheco, Adela; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.
Strecker intermediates as non-pollutant scavengers for cyanides
Green Chemistry, 2005, 7, 716
7203796 CIFC20 H16 Cl2 OP 1 21/n 110.0665; 16.6372; 10.5634
90; 107.793; 90
1684.52Zhang, Lijun; Wang, Shaowu; Sheng, Enhong; Zhou, Shuangliu
A solvent-free synthesis of α,α′-bis(substituted benzylidene) cycloalkanones catalyzed by lanthanide amides [(Me3Si)2N]3Ln(µ-Cl)Li(THF)3 under microwave irradiation
Green Chemistry, 2005, 7, 683
7203832 CIFC18 H12 N2 S2P 1 c 120.312; 9.9902; 15.927
90; 108.289; 90
3068.7Smith, Christopher B.; Raston, Colin L.; Sobolev, Alexandre N.
Poly(ethyleneglycol)(PEG): a versatile reaction medium in gaining access to 4′-(pyridyl)-terpyridines
Green Chemistry, 2005, 7, 650
7203907 CIFC18 H16 O3P 1 21/n 16.9104; 15.8694; 13.2342
90; 103.602; 90
1410.61Raston, Colin L.; Scott, Janet L.
Chemoselective, solvent-free aldol condensation reaction
Green Chemistry, 2000, 2, 49
7203908 CIFC18 H14 OP -17.272; 7.5704; 12.3802
77.14; 89.263; 69.134
619.23Raston, Colin L.; Scott, Janet L.
Chemoselective, solvent-free aldol condensation reaction
Green Chemistry, 2000, 2, 49
7203909 CIFC21 H20 OP 1 21/c 112.2718; 7.8706; 16.1076
90; 102.299; 90
1520.07Raston, Colin L.; Scott, Janet L.
Chemoselective, solvent-free aldol condensation reaction
Green Chemistry, 2000, 2, 49
7203969 CIFC33 H36 O6P 1 21/n 114.4429; 8.0609; 24.3908
90; 99.51; 90
2800.62Scott, Janet L.; MacFarlane, Douglas R.; Raston, Colin L.; Teoh, Ching Mei
Clean, efficient syntheses of cyclotriveratrylene (CTV) and tris-(O-allyl)CTV in an ionic liquid
Green Chemistry, 2000, 2, 123
7204028 CIFC14 H14 O6P -15.9637; 9.123; 12.0646
99.666; 96.329; 95.837
638.28Scott, Janet L.; Raston, Colin L.
Solvent-free synthesis of 3-carboxycoumarins
Green Chemistry, 2000, 2, 245
7204029 CIFC11 H8 O5P 1 21/c 15.11; 19.5292; 9.4299
90; 99.909; 90
927.01Scott, Janet L.; Raston, Colin L.
Solvent-free synthesis of 3-carboxycoumarins
Green Chemistry, 2000, 2, 245
7204218 CIFC15 H17 N O5P n a 219.1435; 27.8109; 5.8488
90; 90; 90
1487.3Correa, Waldo H.; Scott, Janet L.
Solvent-free, two-step synthesis of some unsymmetrical 4-aryl-1,4-dihydropyridines
Green Chemistry, 2001, 3, 296-301
7204407 CIFC14 H13 Br N2 OP 1 21/c 124.9478; 6.0316; 8.3285
90; 98.391; 90
1239.82Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204408 CIFC14 H14 N2P -19.436; 10.4454; 12.0165
99.837; 98.858; 101.754
1120.4Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204409 CIFC14 H13 N3 O2P 1 21/c 112.1392; 7.7897; 13.5753
90; 111.14; 90
1197.3Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204410 CIFC14 H14 N2 OP b c a11.3431; 8.7088; 23.4287
90; 90; 90
2314.4Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204411 CIFC21 H16 Br2 N2 O2P 1 21/c 124.8822; 4.6291; 16.5755
90; 106.263; 90
1832.81Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204412 CIFC16 H18 N2 O2P n a 2120.4722; 13.2281; 20.7521
90; 90; 90
5619.84Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204413 CIFC21 H18 N2 O2P 1 21/c 19.72; 14.037; 12.2058
90; 97.056; 90
1652.74Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.
Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines
Green Chemistry, 2002, 4, 245
7204584 CIFC16 H14 N4P b c a8.5187; 9.8623; 14.8684
90; 90; 90
1249.2Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn
Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/
Green Chemistry, 2003, 5, 187
7204585 CIFC20 H14 N4P 1 21/c 17.5866; 10.366; 9.7278
90; 107.895; 90
728Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn
Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/
Green Chemistry, 2003, 5, 187
7204586 CIFC20 H14 N4P b c n17.712; 8.7976; 9.7375
90; 90; 90
1517.3Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn
Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/
Green Chemistry, 2003, 5, 187
7204602 CIFC14 H24 F12 N4 O2 P2P 1 21/c 111.761; 16.685; 11.864
90; 90.504; 90
2328Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.
Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.
Green Chemistry, 2003, 5, 129
7204603 CIFC18 H32 F12 N4 P2P 1 21/c 16.4611; 16.5436; 12.1828
90; 99.445; 90
1284.56Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.
Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.
Green Chemistry, 2003, 5, 129
7204604 CIFC30 H44 Hg N4 O11 S2P -110.086; 12.459; 15.204
83.209; 84.16; 67.666
1751.5Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.
Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.
Green Chemistry, 2003, 5, 129
7204671 CIFC8 H17 F N2 OP 21 21 218.4317; 10.439; 11.313
90; 90; 90
995.8Swatloski, Richard P.; Holbrey, John D.; Rogers, Robin D.
Ionic liquids are not always green: hydrolysis of 1-butyl-3-methylimidazolium hexafluorophosphate
Green Chemistry, 2003, 5, 361
7204752 CIFC31 H33 B N2 OP -110.771; 11.201; 11.612
96.211; 111.392; 94.957
1284.7Holbrey, John D.; Turner, Megan B.; Reichert, W. Matthew; Rogers, Robin D.
New ionic liquids containing an appended hydroxyl functionality from the atom-efficient, one-pot reaction of 1-methylimidazole and acid with propylene oxide
Green Chemistry, 2003, 5, 731
7204761 CIFC12 H14 N2 O2C 1 2/c 119.764; 8.877; 15.763
90; 117.617; 90
2450.5Wang, Zhong-Xia; Qin, Hua-Li
Solventless syntheses of pyrazole derivativesElectronic supplementary information (ESI) available: analytical and spectroscopic data. See http://www.rsc.org/suppdata/gc/b3/b312833d/
Green Chemistry, 2004, 6, 90
7204801 CIFC78 H80 O4C 1 2/c 127.15; 14.785; 31.326
90; 91.02; 90
12573Makha, Mohamed; Raston, Colin L.; Skelton, Brian W.; White, Allan H.
A more benign approach to the synthesis of calixarenes
Green Chemistry, 2004, 6, 158
7205034 CIFC6 H12 N2 O4 SP 21 21 216.2418; 9.747; 15.951
90; 90; 90
970.4Holbrey, John D.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Pitner, William R.; Seddon, Kenneth R.; Rogers, Robin D.
Efficient, halide free synthesis of new, low cost ionic liquids: 1,3-dialkylimidazolium salts containing methyl- and ethyl-sulfate anions
Green Chemistry, 2002, 4, 407
7205539 CIFC18 H16 F3 N3 O3 Ru SP -19.3778; 10.7852; 11.1818
101.718; 114.717; 102.712
944.94Thibault, Michelle E.; DiMondo, Domenico V.; Jennings, Michael; Abdelnur, Patrícia Verardi; Eberlin, Marcos N.; Schlaf, Marcel
Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium complexes as catalysts for the total deoxygenation of 1,2-hexanediol and glycerol
Green Chemistry, 2011, 13, 357
7205540 CIFC50 H46 Cl6 O4 P4 Pd2P 1 21/c 18.5469; 15.1743; 20.6543
90; 100.479; 90
2634.04Marziale, Alexander N.; Jantke, Dominik; Faul, Stefan H.; Reiner, Thomas; Herdtweck, Eberhardt; Eppinger, Jörg
An efficient protocol for the palladium-catalysed Suzuki‒Miyaura cross-coupling
Green Chemistry, 2011, 13, 169
7205541 CIFC36 H44 Cl2 O2 P2 Pd2P 4317.6026; 17.6026; 23.747
90; 90; 90
7358Marziale, Alexander N.; Jantke, Dominik; Faul, Stefan H.; Reiner, Thomas; Herdtweck, Eberhardt; Eppinger, Jörg
An efficient protocol for the palladium-catalysed Suzuki‒Miyaura cross-coupling
Green Chemistry, 2011, 13, 169
7205542 CIFC13 H24 F3 N O2P b n a12.284; 13.229; 18.391
90; 90; 90
2988.63Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith
New ionic liquids from azepane and 3-methylpiperidine exhibiting wide electrochemical windows
Green Chemistry, 2011, 13, 59
7205907 CIFC24 H36 N2 O6 SP -18.818; 10.459; 16.684
73.495; 82.566; 65.165
1338.8Shaabani, Ahmad; Sarvary, Afshin; Ghasemi, Sabrieh; Rezayan, Ali Hossein; Ghadari, Rahim; Ng, Seik Weng
An environmentally benign approach for the synthesis of bifunctional sulfonamide-amide compounds via isocyanide-based multicomponent reactions
Green Chemistry, 2011, 13, 582
7205908 CIFC24 H30 N2 O7 SP 1 21/c 111.2071; 23.3231; 11.1208
90; 117.989; 90
2566.8Shaabani, Ahmad; Sarvary, Afshin; Ghasemi, Sabrieh; Rezayan, Ali Hossein; Ghadari, Rahim; Ng, Seik Weng
An environmentally benign approach for the synthesis of bifunctional sulfonamide-amide compounds via isocyanide-based multicomponent reactions
Green Chemistry, 2011, 13, 582
7205909 CIFC9 H9 Cl2 N3 O2P 1 21/n 15.6284; 12.5878; 15.935
90; 98.913; 90
1115.35Li, Da-Peng; Zhang, Guang-Liang; An, Li-Tao; Zou, Jian-Ping; Zhang, Wei
Solvent- and catalyst-free synthesis of 2,3-dihydro-1H-benzo[d]imidazoles
Green Chemistry, 2011, 13, 594
7205910 CIFC7 H18 Cl N3C 1 2/m 113.622; 7.8211; 9.8987
90; 104.1; 90
1022.8Oelkers, Benjamin; Sundermeyer, Jörg
Pentaalkylmethylguanidinium methylcarbonates ‒ versatile precursors for the preparation of halide-free and metal-free guanidinium-based ILs
Green Chemistry, 2011, 13, 608
7206033 CIFC10 H18 N2 O6P 21 21 217.7534; 8.0651; 18.818
90; 90; 90
1176.7Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki
Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids
Green Chemistry, 2011, 13, 1203
7206034 CIFC18 H14 N2 O2P 1 21/c 110.5612; 8.4166; 15.8706
90; 107.86; 90
1342.7Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki
Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids
Green Chemistry, 2011, 13, 1203

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