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
7206035 CIFC7 H10 N2 O2P 21 21 215.8353; 9.651; 12.8178
90; 90; 90		721.85Nonappa,; 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
7206036 CIFC12 H18 N2 O2P 1 21/c 16.0475; 7.8473; 11.2904
90; 97.541; 90		531.17Nonappa,; 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
7206037 CIFC4 H6 N2 O2P 1 21/c 13.9045; 11.5645; 5.1679
90; 96.461; 90		231.87Nonappa,; 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
7206038 CIFC10 H11 N O5P 21 21 214.6835; 9.2616; 23.4038
90; 90; 90		1015.18Czarnecki, Paweł; Plutecka, Agnieszka; Gawroński, Jacek; Kacprzak, Karol
Simple and practical direct asymmetric aldol reaction of hydroxyacetone catalyzed by 9-amino Cinchona alkaloid tartrates
Green Chemistry, 2011, 13, 1280
7206164 CIFC52 H48 N12 O Ru2P n a 2118.7033; 25.8907; 9.8896
90; 90; 90		4789Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.
Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands
Green Chemistry, 2011, 13, 1885
7206165 CIFC48 H40 N12 Ru2P n a 2118.7417; 25.884; 9.8779
90; 90; 90		4791.9Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.
Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands
Green Chemistry, 2011, 13, 1885
7206166 CIFC52 H44 Cl N8 O5.25 Ru2P 4/n c c :215.028; 15.028; 21.962
90; 90; 90		4959.9Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.
Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands
Green Chemistry, 2011, 13, 1885
7206167 CIFC60 H60 Cl N8 O8 Ru2P c c n14.2592; 14.2608; 30.4171
90; 90; 90		6185.2Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.
Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands
Green Chemistry, 2011, 13, 1885
7206348 CIFC25 H18 N2P -18.8589; 10.2068; 11.4469
64.251; 84.5; 74.527		898.24Rustagi, Vineeta; Aggarwal, Trapti; Verma, Akhilesh K.
Highly efficient Ag(i)-catalyzed regioselective tandem synthesis of diversely substituted quinoxalines and benzimidazoles in water
Green Chemistry, 2011, 13, 1640
7206349 CIFC25 H18 N2P 1 21/c 19.309; 28.239; 7.304
90; 102.501; 90		1874.5Rustagi, Vineeta; Aggarwal, Trapti; Verma, Akhilesh K.
Highly efficient Ag(i)-catalyzed regioselective tandem synthesis of diversely substituted quinoxalines and benzimidazoles in water
Green Chemistry, 2011, 13, 1640
7206445 CIFC15 H27 Cl3 N4 O2 PdP b c a9.163; 15.148; 29.339
90; 90; 90		4072Zhou, Chunshan; Wang, Jinyun; Li, Liuyi; Wang, Ruihu; Hong, Maochun
A palladium chelating complex of ionic water-soluble nitrogen-containing ligand: the efficient precatalyst for Suzuki‒Miyaura reaction in water
Green Chemistry, 2011, 13, 2100
7206446 CIFC15 H7 Cl N2 OP 1 21/c 113.4701; 3.835; 25.5
90; 117.94; 90		1163.7Cheng, Chuang; Jiang, Bo; Tu, Shu-Jiang; Li, Guigen
[4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives
Green Chemistry, 2011, 13, 2107
7206447 CIFC22 H19 N O9P 1 21/c 114.9522; 18.8553; 7.6472
90; 102.114; 90		2108Cheng, Chuang; Jiang, Bo; Tu, Shu-Jiang; Li, Guigen
[4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives
Green Chemistry, 2011, 13, 2107
7206448 CIFC24 H60 N8 O24 P4 Zn3C 1 2/c 114.9192; 8.4607; 34.445
90; 102.271; 90		4248.5Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein
Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates
Green Chemistry, 2011, 13, 2000
7206449 CIFC20 H52 N8 O22 P4 Zn3C 1 2/c 115.0025; 8.6854; 30.5449
90; 97.181; 90		3948.9Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein
Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates
Green Chemistry, 2011, 13, 2000
7206450 CIFC21 H22 N2 O12 P2 Zn2P n a 219.974; 9.1804; 27.5385
90; 90; 90		2521.6Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein
Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates
Green Chemistry, 2011, 13, 2000
7206451 CIFC21 H22 N2 O12 P2 Zn2P 1 21/c 127.6213; 9.1189; 9.9954
90; 92.211; 90		2515.7Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein
Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates
Green Chemistry, 2011, 13, 2000
7206452 CIFC21 H34 N2 O12 P2 Zn2P 1 21/c 110.8928; 8.7917; 27.7665
90; 101.051; 90		2609.79Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein
Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates
Green Chemistry, 2011, 13, 2000
7206453 CIFC25 H22 N2 O2P 21 21 216.4801; 15.4593; 19.1885
90; 90; 90		1922.26El Asri, Zhor; Génisson, Yves; Guillen, Frédéric; Baslé, Olivier; Isambert, Nicolas; del Mar Sanchez Duque, Maria; Ladeira, Sonia; Rodriguez, Jean; Constantieux, Thierry; Plaquevent, Jean-Christophe
Multicomponent reactions in ionic liquids: convenient and ecocompatible access to the 2,6-DABCO core
Green Chemistry, 2011, 13, 2549
7206583 CIFC28 H24 Cl NP -19.3488; 9.504; 13.036
74.37; 72.819; 84.648		1065.5Chitra, Selvam; Paul, Nidhin; Muthusubramanian, Shanmugam; Manisankar, Paramasivam
A facile, water mediated, microwave-assisted synthesis of 4,6-diaryl-2,3,3a,4-tetrahydro-1H-pyrido[3,2,1-jk]carbazoles by a domino Fischer indole reaction‒intramolecular cyclization sequence
Green Chemistry, 2011, 13, 2777
7206768 CIFC11 H24 I NI 41/a :214.081; 14.081; 27.303
90; 90; 90		5413.49Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Nockemann, Peter; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith
Azepanium ionic liquids
Green Chemistry, 2011, 13, 3137
7206769 CIFC15 H28 F6 N2 O4 S2P 1 21/c 19.7447; 10.72; 21.453
90; 101.948; 90		2192.5Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Nockemann, Peter; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith
Azepanium ionic liquids
Green Chemistry, 2011, 13, 3137
7206770 CIFC16 H19 N O4P -17.236; 9.233; 12.061
85.83; 82.48; 73.52		765.5Choudhary, Garima; Peddinti, Rama Krishna
Introduction of a clean and promising protocol for the synthesis of β-amino-acrylates and 1,4-benzoheterocycles: an emerging innovation
Green Chemistry, 2011, 13, 3290
7206771 CIFC18 H16 O3P 1 21/n 17.9077; 10.7341; 17.41
90; 93.758; 90		1474.6Fan, Xuesen; He, Yan; Cui, Liangyan; Zhang, Xinying; Wang, Jianji
Tandem reaction of 1,2-allenic ketone with α-halo ketone or α-halo ester in water: an efficient and sustainable synthesis of 1,3,4′-tricarbonyl compounds
Green Chemistry, 2011, 13, 3218
7206772 CIFC27 H16 F N3 O2P 1 21/c 110.5755; 22.6797; 8.8593
90; 100.329; 90		2090.46Michael Rajesh, Stephen; Bala, Balasubramanian Devi; Perumal, Subbu; Menéndez, J. Carlos
l-Proline-catalysed sequential four-component “on water” protocol for the synthesis of structurally complex heterocyclic ortho-quinones
Green Chemistry, 2011, 13, 3248
7207279 CIFC17 H12 O5.5 ZnC 1 2/c 131.97; 6.334; 20.49
90; 120.078; 90		3590Ibarra, Ilich A.; Bayliss, Peter A.; Pérez, Eduardo; Yang, Sihai; Blake, Alexander J.; Nowell, Harriott; Allan, David R.; Poliakoff, Martyn; Schröder, Martin
Near-critical water, a cleaner solvent for the synthesis of a metal‒organic framework
Green Chemistry, 2012, 14, 117
7207280 CIFC26.5 H27 Cl2 N O P RhP -19.7477; 11.3212; 12.8467
72.948; 88.665; 65.903		1229.69Makhubela, Banothile C. E.; Jardine, Anwar; Smith, Gregory S.
Rh(i) complexes supported on a biopolymer as recyclable and selective hydroformylation catalysts
Green Chemistry, 2012, 14, 338
7207690 CIFC15 H33 N3R -3 :H10.3969; 10.3969; 28.4886
90; 90; 120		2666.9Mercer, Sean M.; Robert, Tobias; Dixon, Daniel V.; Chen, Chien-Shun; Ghoshouni, Zahra; Harjani, Jitendra R.; Jahangiri, Soran; Peslherbe, Gilles H.; Jessop, Philip G.
Design, synthesis, and solution behaviour of small polyamines as switchable water additives
Green Chemistry, 2012, 14, 832
7207691 CIFC20 H18 N2 O3 SP -18.096; 8.432; 14.387
85.32; 88.539; 62.728		870Wen, Li-Rong; Li, Zhao-Rui; Li, Ming; Cao, Han
Solvent-free and efficient synthesis of imidazo[1,2-a]pyridine derivatives via a one-pot three-component reaction
Green Chemistry, 2012, 14, 707
7207692 CIFC11 H13 N3 OP b c a10.4; 12.165; 15.37
90; 90; 90		1944.6Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong
Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium
Green Chemistry, 2012, 14, 945
7207693 CIFC12 H14 Br N3 OP 1 21/c 110.591; 12.359; 9.116
90; 97.951; 90		1181.8Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong
Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium
Green Chemistry, 2012, 14, 945
7207694 CIFC23 H28 Cl N3 O2P -18.355; 10.746; 12.843
98.611; 99.924; 110.707		1034.3Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong
Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium
Green Chemistry, 2012, 14, 945
7207695 CIFC26 H17 Cl N2 O2P 1 21/n 19.8188; 15.916; 13.4755
90; 100.875; 90		2068.08Gunasekaran, Pethaiah; Balamurugan, Kamaraj; Sivakumar, Sathiyamoorthi; Perumal, Subbu; Menéndez, J. Carlos; Almansour, Abdulrahman I.
Domino reactions in water: diastereoselective synthesis of densely functionalized indolyldihydrofuran derivatives
Green Chemistry, 2012, 14, 750
7207696 CIFC16 H18 N2 OP 1 21/c 18.715; 11.09; 13.771
90; 90.303; 90		1330.9Jida, Mouhamad; Soueidan, Olivier-Mohamad; Deprez, Benoit; Laconde, Guillaume; Deprez-Poulain, Rebecca
Racemic and diastereoselective construction of indole alkaloids under solvent- and catalyst-free microwave-assisted Pictet‒Spengler condensation
Green Chemistry, 2012, 14, 909
7207697 CIFC40 H58 Br2 N2 OP 1 21/c 111.814; 21.2181; 14.6684
90; 95.337; 90		3661Doherty, Simon; Knight, Julian G.; Ellison, Jack R.; Weekes, David; Harrington, Ross W.; Hardacre, Christopher; Manyar, Haresh
An efficient recyclable peroxometalate-based polymer-immobilised ionic liquid phase (PIILP) catalyst for hydrogen peroxide-mediated oxidation
Green Chemistry, 2012, 14, 925
7207893 CIFC15 H13 N O5P 1 21/n 19.394; 9.114; 16.558
90; 104.714; 90		1371.2Li, Jian; Liu, Yuejin; Li, Chunju; Jie, Haohua; Jia, Xueshun
Atom-economical synthesis of the functionalized spirocyclic oxindole-butenolide via three-component [2 + 2 + 1] cycloaddition strategy
Green Chemistry, 2012, 14, 1314
7207894 CIFC29 H33 Cl N2 O4P -18.897; 12.592; 13.863
99.404; 108.029; 95.241		1440Li, Jian; Liu, Yuejin; Li, Chunju; Jie, Haohua; Jia, Xueshun
Atom-economical synthesis of the functionalized spirocyclic oxindole-butenolide via three-component [2 + 2 + 1] cycloaddition strategy
Green Chemistry, 2012, 14, 1314
7207895 CIFC50 H56 I4 O18C 1 2/c 124.11; 17.011; 33.45
90; 91.57; 90		13714Dohi, Toshifumi; Fukushima, Kei-ichiro; Kamitanaka, Tohru; Morimoto, Koji; Takenaga, Naoko; Kita, Yasuyuki
An excellent dual recycling strategy for the hypervalent iodine/nitroxyl radical mediated selective oxidation of alcohols to aldehydes and ketones
Green Chemistry, 2012, 14, 1493
7207896 CIFC20 H19 N3P -19.4865; 9.9343; 10.5514
114.009; 113.796; 90.405		813.5Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda
Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads
Green Chemistry, 2012, 14, 1376
7207897 CIFC19 H15 N5 O2C 1 2/c 125.1335; 12.37744; 13.4158
90; 119.443; 90		3634.47Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda
Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads
Green Chemistry, 2012, 14, 1376
7207898 CIFC20 H14 N4P 1 21/n 120.561; 7.228; 24.638
90; 112.873; 90		3373.7Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda
Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads
Green Chemistry, 2012, 14, 1376
7207899 CIFC24 H20 N4 O2P -111.7899; 14.3124; 14.5079
64.617; 78.242; 76.142		2133.06Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda
Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads
Green Chemistry, 2012, 14, 1376
7208024 CIFC5 H6 O4P 21 21 214.25566; 10.2167; 12.2711
90; 90; 90		533.53Tomczyk, Karolina M.; Guńka, Piotr A.; Parzuchowski, Paweł G.; Zachara, Janusz; Rokicki, Gabriel
Intramolecular etherification of five-membered cyclic carbonates bearing hydroxyalkyl groups
Green Chemistry, 2012, 14, 1749
7208025 CIFC8 H8 O7P 21 21 217.9412; 10.0129; 10.831
90; 90; 90		861.22Tomczyk, Karolina M.; Guńka, Piotr A.; Parzuchowski, Paweł G.; Zachara, Janusz; Rokicki, Gabriel
Intramolecular etherification of five-membered cyclic carbonates bearing hydroxyalkyl groups
Green Chemistry, 2012, 14, 1749
7208130 CIFC18 H14 Ag N5 O5P 1 21/n 112.142; 10.509; 13.907
90; 106.101; 90		1704.9Sheykhan, Mehdi; Rashidi Ranjbar, Zohreh; Morsali, Ali; Heydari, Akbar
Minimisation of E-Factor in the synthesis of N-hydroxylamines: the role of silver(i)-based coordination polymers
Green Chemistry, 2012, 14, 1971
7208131 CIFC21 H18 F3 N O4P 1 21/c 113.6247; 8.6852; 17.0833
90; 112.949; 90		1861.5Reddy, T. Ram; Reddy, L. Srinivasula; Reddy, G. Rajeshwar; Yarbagi, Kaviraj; Lingappa, Y.; Rambabu, D.; Krishna, G. Rama; Reddy, C. Malla; Kumar, K. Shiva; Pal, Manojit
Construction of a quinoline ring via a 3-component reaction in water: crystal structure analysis and H-bonding patterns of a 2-aryl quinoline
Green Chemistry, 2012, 14, 1870
7208410 CIFC34 H28 Cl6 N2 O5P -111.373; 11.8524; 13.975
95.484; 112.666; 91.976		1725.1Khurana, Jitender M.; Chaudhary, Ankita; Lumb, Anshika; Nand, Bhaskara
An expedient four-component domino protocol for the synthesis of novel benzo[a]phenazine annulated heterocycles and their photophysical studies
Green Chemistry, 2012, 14, 2321
7208597 CIFC15 H13 N2 SI 4114.933; 14.933; 12.2771
90; 90; 90		2737.7Rout, Saroj Kumar; Guin, Srimanta; Nath, Jayashree; Patel, Bhisma K.
An “on-water” exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles
Green Chemistry, 2012, 14, 2491
7208598 CIFC11 H12 N2 S2P 1 21/c 110.13; 8.1511; 13.6
90; 93.902; 90		1120.4Rout, Saroj Kumar; Guin, Srimanta; Nath, Jayashree; Patel, Bhisma K.
An “on-water” exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles
Green Chemistry, 2012, 14, 2491
7208599 CIFC13 H18 N2 O SC 1 c 110.493; 14.6391; 9.0779
90; 113.021; 90		1283.39Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208600 CIFC11 H14 N2 S2P 1 21/c 111.5813; 9.3856; 10.8926
90; 101.21; 90		1161.41Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208601 CIFC13 H10 F2 N2 SP n m a8.3457; 26.4224; 5.3071
90; 90; 90		1170.29Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208602 CIFC11 H13 N3 O3 SP 1 21/n 110.2252; 10.5172; 11.1949
90; 90.788; 90		1203.79Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208603 CIFC11 H13 N3 O3 SP c a 2121.2213; 8.0908; 28.6471
90; 90; 90		4918.6Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208604 CIFC15 H16 N2 SP 1 21/n 112.67213; 9.79731; 12.10093
90; 115.223; 90		1359.12Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208605 CIFC14 H14 N2 O SP 1 21/c 128.4936; 5.55569; 8.14303
90; 90.7479; 90		1288.94Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208606 CIFC14 H13 N3 O2 SP n a 2114.50439; 13.62318; 7.14076
90; 90; 90		1410.99Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav
A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents
Green Chemistry, 2012, 14, 2462
7208607 CIFC31 H25 Br F N O7P -110.8539; 11.5075; 12.5661
97.508; 102.88; 113.095		1365.14Devi Bala, Balasubramanian; Michael Rajesh, Stephen; Perumal, Subbu
An eco-friendly sequential catalyst- and solvent-free four-component stereoselective synthesis of novel 1,4-pyranonaphthoquinones
Green Chemistry, 2012, 14, 2484
7208841 CIFC11 H10 N2 O5 SP 1 21/c 110.788; 16.5308; 7.1104
90; 106.861; 90		1213.52Paladhi, Sushovan; Chauhan, Ajay; Dhara, Kalyan; Tiwari, Ashwani Kumar; Dash, Jyotirmayee
An uncatalyzed aldol reaction of thiazolidinediones
Green Chemistry, 2012, 14, 2990
7208842 CIFC8 H6 Br2 N2 O4 S2P 1 21/c 120.804; 11.9934; 10.9684
90; 102.666; 90		2670.1Paladhi, Sushovan; Chauhan, Ajay; Dhara, Kalyan; Tiwari, Ashwani Kumar; Dash, Jyotirmayee
An uncatalyzed aldol reaction of thiazolidinediones
Green Chemistry, 2012, 14, 2990
7208843 CIFC27 H22 N2 O4P 1 21/n 117.188; 14.671; 17.44
90; 93.406; 90		4390Ghosh, Partha Pratim; Pal, Gargi; Paul, Sanjay; Das, Asish R.
Design and synthesis of benzylpyrazolyl coumarin derivatives via a four-component reaction in water: investigation of the weak interactions accumulating in the crystal structure of a signified compound
Green Chemistry, 2012, 14, 2691
7208844 CIFC25 H16 Cl2 F N O3P 1 21/n 110.017; 7.789; 27.003
90; 95.507; 90		2097.1Indumathi, Sethuraman; Perumal, Subbu; Anbananthan, Natarajan
A facile eco-friendly three-component protocol for the regio- and stereoselective synthesis of functionalized trans-dihydrofuro[3,2-c]-quinolin-4(2H)-ones
Green Chemistry, 2012, 14, 3361
7208845 CIFC25 H25 N3 O8P 1 21/c 110.8016; 23.0207; 9.9117
90; 111.566; 90		2292.11Lu, Qing; Song, Gonghua; Jasinski, Jerry P.; Keeley, Amanda C.; Zhang, Wei
One-pot double [3 + 2] cycloaddition for diastereoselective synthesis of tetracyclic pyrrolidine compounds
Green Chemistry, 2012, 14, 3010
7208846 CIFC28 H28 Cl2 N4 O8 SP 1 21/c 111.5934; 23.9267; 12.5474
90; 116.043; 90		3127.1Lu, Qing; Song, Gonghua; Jasinski, Jerry P.; Keeley, Amanda C.; Zhang, Wei
One-pot double [3 + 2] cycloaddition for diastereoselective synthesis of tetracyclic pyrrolidine compounds
Green Chemistry, 2012, 14, 3010
7208847 CIFC13 H7 F4 I N4 O2P 1 21 17.2406; 6.3111; 16.211
90; 98.719; 90		732.2Chen, Hao; Ni, Ben-Bo; Gao, Fan; Ma, Yuguo
Pressure-accelerated copper-free cycloaddition of azide and alkyne groups pre-organized in the crystalline state at room temperature
Green Chemistry, 2012, 14, 2703
7208848 CIFC15 H10 F4 N4 O3P -15.7206; 10.897; 12.306
86.6; 84.86; 80.87		753.6Chen, Hao; Ni, Ben-Bo; Gao, Fan; Ma, Yuguo
Pressure-accelerated copper-free cycloaddition of azide and alkyne groups pre-organized in the crystalline state at room temperature
Green Chemistry, 2012, 14, 2703
7208849 CIFC16 H14 F N O2P 1 21/c 19.5984; 9.3308; 14.7806
90; 100.934; 90		1299.73Griesbeck, Axel G.; Nazarov, Nestor; Neudörfl, Jörg M.; Heffen, Maria
Intermolecular photodecarboxylation of electron-deficient substrates by phthalimides in water: efficiency, selectivity and online monitoring
Green Chemistry, 2012, 14, 3004
7208850 CIFC17 H14 F3 N O2P 1 21/c 115.6286; 8.625; 10.8601
90; 96.661; 90		1454.02Griesbeck, Axel G.; Nazarov, Nestor; Neudörfl, Jörg M.; Heffen, Maria
Intermolecular photodecarboxylation of electron-deficient substrates by phthalimides in water: efficiency, selectivity and online monitoring
Green Chemistry, 2012, 14, 3004
7208851 CIFC10 H10 N2P c a 218.5482; 10.7471; 9.6662
90; 90; 90		888.02Zhang, Chun; Zhang, Liangren; Jiao, Ning
Catalyst free approach to benzimidazoles using air as the oxidant at room temperature
Green Chemistry, 2012, 14, 3273
7209200 CIFC10 H11 N O2P 21 21 215.955; 7.46; 19.878
90; 90; 90		883.1Ueno, Atsushi; Kayaki, Yoshihito; Ikariya, Takao
Cycloaddition of tertiary aziridines and carbon dioxide using a recyclable organocatalyst, 1,3-di-tert-butylimidazolium-2-carboxylate: straightforward access to 3-substituted 2-oxazolidones
Green Chemistry, 2013, 15, 425
7209250 CIFC25 H20 N2 O2C 1 2/c 120.8671; 10.4343; 18.53
90; 101.947; 90		3947.2Xu, Shengtao; Zhou, Yu; Xu, Jinyi; Jiang, Hualiang; Liu, Hong
Gold-catalyzed Michael addition/intramolecular annulation cascade: an effective pathway for the chemoselective- and regioselective synthesis of tetracyclic indole derivatives in water
Green Chemistry, 2013, 15, 718
7209293 CIFC37 H56 Cu I N4 O2P n m a16.9; 27.54; 8.179
90; 90; 90		3807Wang, Wenlong; Zhang, Guodong; Lang, Rui; Xia, Chungu; Li, Fuwei
pH-Responsive N-heterocyclic carbene copper(i) complexes: syntheses and recoverable applications in the carboxylation of arylboronic esters and benzoxazole with carbon dioxide
Green Chemistry, 2013, 15, 635
7209840 CIFC10 H8 N2 O S2P -17.4617; 7.5189; 9.84
109.76; 90.103; 90.706		519.5Singh, Maya Shankar; Nagaraju, Anugula; Verma, Girijesh Kumar; Shukla, Gaurav; Verma, Rajiv Kumar; Srivastava, Abhijeet; Raghuvanshi, Keshav
Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions
Green Chemistry, 2013, 15, 954
7209841 CIFC11 H10 N2 O2 S2P -18.0015; 8.1903; 9.1812
85.565; 75.327; 86.509		579.79Singh, Maya Shankar; Nagaraju, Anugula; Verma, Girijesh Kumar; Shukla, Gaurav; Verma, Rajiv Kumar; Srivastava, Abhijeet; Raghuvanshi, Keshav
Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions
Green Chemistry, 2013, 15, 954
7209842 CIFC16 H12 N2 OP 1 21/c 19.5564; 16.83; 7.9596
90; 98.532; 90		1266Shen, Shao-Chun; Sun, Xing-Wen; Lin, Guo-Qiang
An eco-benign and highly efficient access to 3-heterocyclic-substituted isoindolinones in ammonia water
Green Chemistry, 2013, 15, 896
7210021 CIFC21 H18 Br N O SP 1 21/n 15.569; 24.721; 13.606
90; 101.183; 90		1837.6Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda
A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties
Green Chemistry, 2013, 15, 1910
7210022 CIFC29 H26 N2 O3P 1 21/c 119.1534; 10.4617; 12.4228
90; 104.23; 90		2412.9Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda
A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties
Green Chemistry, 2013, 15, 1910
7210023 CIFC24 H23 N2 O3C 1 c 116.0558; 13.068; 11.5754
90; 122.419; 90		2050.2Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda
A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties
Green Chemistry, 2013, 15, 1910
7210450 CIFC8 H12 N4 O6 SP 21 21 216.4063; 8.1667; 23.311
90; 90; 90		1219.6Mottillo, Cristina; Lu, Yuneng; Pham, Minh-Hao; Cliffe, Matthew J.; Do, Trong-On; Friščić, Tomislav
Mineral neogenesis as an inspiration for mild, solvent-free synthesis of bulk microporous metal‒organic frameworks from metal (Zn, Co) oxides
Green Chemistry, 2013, 15, 2121
7210451 CIFC8 H6 Cl N O2P 1 21/n 17.3073; 7.1368; 15.6263
90; 91.452; 90		814.66Deadman, Benjamin J.; Battilocchio, Claudio; Sliwinski, Eric; Ley, Steven V.
A prototype device for evaporation in batch and flow chemical processes
Green Chemistry, 2013, 15, 2050
7210452 CIFC9 H14 Cl3 N6 O P S3P b c a15.0238; 11.6122; 20.9195
90; 90; 90		3649.6García-Álvarez, Rocío; Zablocka, Maria; Crochet, Pascale; Duhayon, Carine; Majoral, Jean-Pierre; Cadierno, Victorio
Thiazolyl-phosphine hydrochloride salts: effective auxiliary ligands for ruthenium-catalyzed nitrile hydration reactions and related amide bond forming processes in water
Green Chemistry, 2013, 15, 2447
7211311 CIFC21 H21 N4 O5P -18.1356; 10.6065; 12.462
91.571; 105.781; 100.384		1014.5Prasanna, Pitchaimani; Perumal, Subbu; Menéndez, J. Carlos
Chemodivergent, multicomponent domino reactions in aqueous media: l-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials
Green Chemistry, 2013, 15, 1292
7211312 CIFC24 H23 N4 O4P 1 21/n 112.2016; 13.6995; 15.4526
90; 110.166; 90		2424.65Prasanna, Pitchaimani; Perumal, Subbu; Menéndez, J. Carlos
Chemodivergent, multicomponent domino reactions in aqueous media: l-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials
Green Chemistry, 2013, 15, 1292
7211313 CIFC30 H36 Cl6 O8P 21 21 219.7594; 18.5524; 18.8335
90; 90; 90		3410Haldar, Saikat; Kolet, Swati P.; Thulasiram, Hirekodathakallu V.
Biocatalysis: fungi mediated novel and selective 12β- or 17β-hydroxylation on the basic limonoid skeleton
Green Chemistry, 2013, 15, 1311
7211314 CIFC19 H33 Cl Ni O3 P2C 1 2/c 118.8143; 18.2714; 14.9031
90; 117.805; 90		4531.61Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit
Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel
Green Chemistry, 2013, 15, 3188
7211315 CIFC20 H33 Cl Ni O4 P2P 1 21/c 115.908; 13.0746; 11.134
90; 91.464; 90		2315Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit
Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel
Green Chemistry, 2013, 15, 3188
7211316 CIFC26 H47 Cl Ni O2 P2P 1 21/n 110.4275; 14.033; 20.573
90; 101.18; 90		2953.3Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit
Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel
Green Chemistry, 2013, 15, 3188
7211317 CIFC38 H38 O10P -110.293; 11.524; 15.213
78.18; 84.68; 76.56		1715.9Forsythe, W. Graham; Garrett, Mark D.; Hardacre, Christopher; Nieuwenhuyzen, Mark; Sheldrake, Gary N.
An efficient and flexible synthesis of model lignin oligomers
Green Chemistry, 2013, 15, 3031
7211318 CIFC33 H27 N9 O3P 1 21/n 116.032; 11.544; 32.695
90; 90.772; 90		6050Zhao, Chao-Wei; Ma, Jian-Ping; Liu, Qi-Kui; Yu, Yang; Wang, Peng; Li, Yan-An; Wang, Kui; Dong, Yu-Bin
A self-assembled Pd6L8 nanoball for Suzuki‒Miyaura coupling reactions in both homogeneous and heterogeneous formats
Green Chemistry, 2013, 15, 3150
7211319 CIFC25 H20 Cl6 Fe N O4P b c a17.2201; 15.7615; 19.2134
90; 90; 90		5214.8Taherimehr, Masoumeh; Al-Amsyar, Syed M.; Whiteoak, Christopher J.; Kleij, Arjan W.; Pescarmona, Paolo P.
High activity and switchable selectivity in the synthesis of cyclic and polymeric cyclohexene carbonates with iron amino triphenolate catalysts
Green Chemistry, 2013, 15, 3083
7211320 CIFC16 H18 O4P 1 21/n 17.7968; 21.1512; 9.1046
90; 114.189; 90		1369.63Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.
Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones
Green Chemistry, 2013, 15, 2830
7211321 CIFC15 H16 O4P b c a12.8287; 7.9789; 24.2643
90; 90; 90		2483.67Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.
Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones
Green Chemistry, 2013, 15, 2830
7211322 CIFC16 H18 O5P 1 21/c 115.7243; 5.0123; 18.5815
90; 107.285; 90		1398.36Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.
Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones
Green Chemistry, 2013, 15, 2830
7211491 CIFC32 H26 Cl N O7C 1 2/c 129.861; 10.2141; 21.675
90; 117.455; 90		5866.4Wang, Huiyan; Liu, Xuecheng; Feng, Xian; Huang, Zhibin; Shi, Daqing
GAP chemistry for pyrrolyl coumarin derivatives: a highly efficient one-pot synthesis under catalyst-free conditions
Green Chemistry, 2013, 15, 3307
7211496 CIFC15 H22 N2 O3P b c a12.2357; 7.5855; 31.232
90; 90; 90		2898.8Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.
Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis
Green Chemistry, 2010, 12, 1036
7211497 CIFC15 H21 Br N2 O3P 21 21 217.0621; 13.9243; 16.421
90; 90; 90		1614.8Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.
Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis
Green Chemistry, 2010, 12, 1036
7211498 CIFC23 H38 N2 O3P 1 21/n 111.637; 10.801; 19.312
90; 103.443; 90		2361Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.
Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis
Green Chemistry, 2010, 12, 1036
7211499 CIFC14 H21 N3 O2P 1 21/c 115.067; 10.15; 9.665
90; 104.544; 90		1430.7Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.
Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis
Green Chemistry, 2010, 12, 1036
7212125 CIFC8 H14 N2 O3P 1 21/n 16.8805; 11.6254; 11.9614
90; 96.229; 90		951.13Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.
New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores
Green Chemistry, 2010, 12, 491
7212126 CIFC7 H14 N2 O4P 1 21/n 17.479; 13.289; 9.636
90; 95.011; 90		954Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.
New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores
Green Chemistry, 2010, 12, 491
7212127 CIFC7 H15 N O3P 1 21/n 16.6199; 13.9451; 9.2587
90; 101.76; 90		836.78Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.
New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores
Green Chemistry, 2010, 12, 491
7212281 CIFC18 H20 N2 O2P 1 21 18.4078; 8.3744; 11.4399
90; 98.698; 90		796.22Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume
Solvent-free microwave-assisted Meyers’ lactamization
Green Chemistry, 2010, 12, 961
7212282 CIFC12 H17 N O4C 1 2 117.5352; 7.6758; 10.0025
90; 113.78; 90		1232Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume
Solvent-free microwave-assisted Meyers’ lactamization
Green Chemistry, 2010, 12, 961
7212362 CIFC20 H15 N O2C 1 2/c 122.045; 9.268; 17.8038
90; 124.751; 90		2988.74Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa
‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)
Green Chemistry, 2010, 12, 1090
7212363 CIFC15 H17 N O6P 1 21/n 17.1337; 26.8903; 7.6505
90; 90.614; 90		1467.49Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa
‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)
Green Chemistry, 2010, 12, 1090
7212364 CIFC13 H13 N O2P c a b9.1168; 13.8294; 17.2443
90; 90; 90		2174.16Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa
‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)
Green Chemistry, 2010, 12, 1090
7212365 CIFC11 H13 N O5P 21 21 218.449; 11.2583; 12.0738
90; 90; 90		1148.5Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa
‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)
Green Chemistry, 2010, 12, 1090
7212382 CIFC13 H16 O2P 1 21/n 113.286; 5.6083; 15.808
90; 95.142; 90		1173.1Liu, Pei Nian; Xia, Fei; Wang, Qing Wei; Ren, Yu Jie; Chen, Jun Qin
Triflic acid adsorbed on silica gel as an efficient and recyclable catalyst for the addition of β-dicarbonyl compounds to alcohols and alkenes
Green Chemistry, 2010, 12, 1049
7212399 CIFC13 H17 N O2P -15.7313; 11.8701; 18.407
72.324; 85.809; 79.963		1174.6Feng, Li-Chun; Sun, Ya-Wei; Tang, Wei-Jun; Xu, Li-Jin; Lam, Kim-Lung; Zhou, Zhongyuan; Chan, Albert S. C.
Highly efficient chemoselective construction of 2,2-dimethyl-6-substituted 4-piperidones via multi-component tandem Mannich reaction in ionic liquids
Green Chemistry, 2010, 12, 949
7212674 CIFC48 H32 F8 N12 Ru2P 1 21/c 19.6596; 38.8963; 12.5248
90; 102.989; 90		4585.4Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Urbanos, Francisco A.
First microwave synthesis of multiple metal-metal bond paddlewheel compounds
Green Chemistry, 2010, 12, 965
7212698 CIFC48 H93 Cl5 Cu2 N6P -18.8041; 12.5714; 25.282
89.005; 89.757; 86.052		2791.1Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg
Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation
Green Chemistry, 2010, 12, 1589
7212699 CIFC60 H112 Cu F6 N8 PP -111.7007; 13.6056; 21.043
91.893; 94.239; 100.766		3278.2Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg
Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation
Green Chemistry, 2010, 12, 1589
7212700 CIFC90 H168 Cu6 I6 N12P -19.7553; 13.5795; 20.6572
106.873; 94.154; 95.814		2590.3Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg
Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation
Green Chemistry, 2010, 12, 1589
7212701 CIFC64 H124 Br8 Cu4 N8P -110.3068; 16.172; 25.595
73.875; 87.515; 87.742		4092.9Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg
Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation
Green Chemistry, 2010, 12, 1589
7212702 CIFC30 H56 Br2 Cu2 N4P -19.002; 9.454; 20.757
85.74; 87.75; 78.95		1728.4Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg
Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation
Green Chemistry, 2010, 12, 1589
7212731 CIFC22 H19 N O2P -19.2376; 14.5788; 14.9383
66.775; 74.994; 74.785		1756.3Zhou, Yu; Zhai, Yun; Li, Jian; Ye, Deju; Jiang, Hualiang; Liu, Hong
Metal-free tandem reaction in water: An efficient and regioselective synthesis of 3-hydroxyisoindolin-1-ones
Green Chemistry, 2010, 12, 1397
7212732 CIFC14 H14 B Bi F4 O SP 1 21/c 113.8004; 11.5529; 9.8253
90; 93.005; 90		1564.34Qiu, Renhua; Qiu, Yimiao; Yin, Shuangfeng; Song, Xingxing; Meng, Zhengong; Xu, Xinhua; Zhang, Xiaowen; Luo, Shenglian; Au, Chak-Tong; Wong, Wai-Yeung
Facile separation catalyst system: direct diastereoselective synthesis of (E)-α,β-unsaturated ketones catalyzed by an air-stable Lewis acidic/basic bifunctional organobismuth complex in ionic liquids
Green Chemistry, 2010, 12, 1767
7212907 CIFC20 H26 O4 SP 21 21 219.3439; 13.2412; 15.8279
90; 90; 90		1958.3Rosini, Goffredo; Paolucci, Claudio; Boschi, Francesca; Marotta, Emanuela; Righi, Paolo; Tozzi, Francesco
Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
Green Chemistry, 2010, 12, 1747
7212908 CIFC26 H26 F2 N2 O6 SP 1 21/c 114.6241; 20.681; 8.745
90; 90.538; 90		2644.7Ma, Ning; Jiang, Bo; Zhang, Ge; Tu, Shu-Jiang; Wever, Walter; Li, Guigen
New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines
Green Chemistry, 2010, 12, 1357
7212909 CIFC20 H44 Cu F6 N8 O4 P5 S2P -110.4612; 11.6733; 15.4745
80.696; 70.225; 83.182		1750.69García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José
A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles
Green Chemistry, 2010, 12, 2127
7212910 CIFC15 H12 I N3 SP 1 21/c 114.5177; 7.2359; 14.3593
90; 101.588; 90		1477.68García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José
A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles
Green Chemistry, 2010, 12, 2127
7212911 CIFC20 H22 F3 N2 O4.5R -3 :H35.238; 35.238; 8.3319
90; 90; 120		8959.8Yan, Shengjiao; Chen, Yulan; Liu, Lin; He, Nengqin; Lin, Jun
Three-component solvent-free synthesis of highly substituted bicyclic pyridines containing a ring-junction nitrogen
Green Chemistry, 2010, 12, 2043
7212939 CIFK0.7 Na0.3 Nb O3A m m 23.970162; 5.67111; 5.69467
90; 90; 90		128.217Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212940 CIFK0.7 Na0.3 Nb O3A m m 23.96867; 5.67069; 5.69626
90; 90; 90		128.195Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212941 CIFK0.7 Na0.3 Nb O3A m m 23.97024; 5.662; 5.68624
90; 90; 90		127.82Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212942 CIFK0.7 Na0.3 Nb O3A m m 23.96136; 5.65428; 5.68474
90; 90; 90		127.33Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212943 CIFK0.93 Na0.07 Nb O3A m m 23.98381; 5.689; 5.70757
90; 90; 90		129.356Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212944 CIFK0.903 Na0.097 Nb O3A m m 23.981973; 5.68731; 5.70733
90; 90; 90		129.252Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212945 CIFK0.86 Na0.14 Nb O3A m m 23.977443; 5.68725; 5.70678
90; 90; 90		129.091Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212946 CIFK0.84 Na0.16 Nb O3A m m 23.973479; 5.68046; 5.70266
90; 90; 90		128.716Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212947 CIFK0.83 Na0.17 Nb O3A m m 23.973479; 5.68046; 5.70266
90; 90; 90		128.716Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212948 CIFK0.77 Na0.23 Nb O3A m m 23.972623; 5.68015; 5.7037
90; 90; 90		128.705Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212949 CIFK0.73 Na0.27 Nb O3A m m 23.97304; 5.67576; 5.69703
90; 90; 90		128.468Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212950 CIFK0.75 Na0.25 Nb O3A m m 23.970626; 5.67573; 5.69855
90; 90; 90		128.424Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7212951 CIFK0.72 Na0.28 Nb O3A m m 23.96953; 5.6731; 5.69719
90; 90; 90		128.298Handoko, Albertus D.; Goh, Gregory K. L.
Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C
Green Chemistry, 2010, 12, 680
7214116 CIFC25 H19 N O5P 1 21/c 120.6371; 11.0516; 20.5751
90; 119.356; 90		4090Muthusaravanan, Sivasubramanian; Sasikumar, Chinnathambi; Devi Bala, Balasubramanian; Perumal, Subbu
An eco-friendly three-component regio- and stereoselective synthesis of highly functionalized dihydroindeno[1,2-b]pyrroles under grinding
Green Chemistry, 2014, 16, 1297
7214117 CIFC9 H21 N O3P c c n14.5983; 20.935; 8.5228
90; 90; 90		2604.7Vanderveen, Jesse R.; Durelle, Jeremy; Jessop, Philip G.
Design and evaluation of switchable-hydrophilicity solvents
Green Chemistry, 2014, 16, 1187
7214118 CIFC20 H14 N2 O3P 1 21/c 19.0629; 11.2174; 16.215
90; 104.835; 90		1593.5Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda
Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester
Green Chemistry, 2014, 16, 1426
7214119 CIFC21 H16 N2 OP 1 21 110.0929; 6.337; 12.8314
90; 100.192; 90		807.73Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda
Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester
Green Chemistry, 2014, 16, 1426
7214120 CIFC26 H17 N O5P -16.937; 11.638; 13.019
75.535; 89.874; 76.165		986.4Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda
Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester
Green Chemistry, 2014, 16, 1426
7214121 CIFC22 H27 N3 O3P -18.6867; 11.0032; 12.0059
70.06; 84.209; 76.001		1046.5Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda
Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester
Green Chemistry, 2014, 16, 1426
7214122 CIFC7 H5 Br2 O2 ReP 1 21/m 16.892; 8.967; 8.538
90; 112.7; 90		486.8Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav
A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes
Green Chemistry, 2014, 16, 1087
7214123 CIFC7 H5 Br2 O2 ReP 1 21/m 16.34; 12.504; 6.4937
90; 109.161; 90		486.27Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav
A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes
Green Chemistry, 2014, 16, 1087
7214124 CIFC7 H5 Cl2 O2 ReP 1 21/m 16.2456; 12.2155; 6.2656
90; 106.932; 90		457.3Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav
A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes
Green Chemistry, 2014, 16, 1087
7214125 CIFC7 H5 I2 O2 ReC 1 2/m 113.389; 9.29; 9.128
90; 107.669; 90		1081.8Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav
A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes
Green Chemistry, 2014, 16, 1087
7214126 CIFC23 H20 N2P 21 21 2110.2819; 10.7707; 15.6284
90; 90; 90		1730.7Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman
Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones
Green Chemistry, 2014, 16, 1120
7214127 CIFC28 H31 Cl N2 OP 1 21/n 15.7713; 16.573; 25.145
90; 92.354; 90		2403Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman
Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones
Green Chemistry, 2014, 16, 1120
7214128 CIFC8 H20 N2 O4P n a 2111.0906; 14.6981; 7.6029
90; 90; 90		1239.35Qi, Feng; Stein, Robin S.; Friščić, Tomislav
Mimicking mineral neogenesis for the clean synthesis of metal‒organic materials from mineral feedstocks: coordination polymers, MOFs and metal oxide separation
Green Chemistry, 2014, 16, 121
7214305 CIFC40 H86 Mo N2 O10P -19.7003; 10.0807; 26.1807
88.397; 82.073; 69.855		2379.99Chakravarthy, Rajan Deepan; Ramkumar, Venkatachalam; Chand, Dillip Kumar
A molybdenum based metallomicellar catalyst for controlled and selective sulfoxidation reactions in aqueous medium
Green Chemistry, 2014, 16, 2190
7214306 CIFC10 H16 N2 O S2P 1 21/n 110.7382; 10.2853; 11.9959
90; 114.837; 90		1202.35Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing
Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation
Green Chemistry, 2014, 16, 2266
7214307 CIFC10 H16 N2 O S2P 1 21/n 17.0242; 15.4761; 11.2508
90; 92.082; 90		1222.24Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing
Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation
Green Chemistry, 2014, 16, 2266
7214308 CIFC10 H19 N2 O5P b c n12.1669; 12.065; 19.2806
90; 90; 90		2830.3Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing
Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation
Green Chemistry, 2014, 16, 2266
7214309 CIFC23 H15 N OP c a 2122.439; 5.3555; 13.393
90; 90; 90		1609.5Rao, Yin; Li, Zhexian; Yin, Guodong
Clean and efficient assembly of functionalized benzofuro[2,3-c]pyridines via metal-free one-pot domino reactions
Green Chemistry, 2014, 16, 2213
7215076 CIFC23 H21 Cl N2 O2C 1 2/c 111.9856; 18.2571; 9.0361
90; 94.463; 90		1971.3Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S.
CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes
Green Chemistry, 2012, 14, 2912
7215077 CIFC28 H30 N2 O2 S2C 1 2/c 120.704; 12.3263; 21.8634
90; 113.463; 90		5118.3Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S.
CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes
Green Chemistry, 2012, 14, 2912
7215078 CIFC27 H28 N3 O2 P SP 1 21/c 19.7499; 30.5632; 8.5329
90; 101.967; 90		2487.44Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle
An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings
Green Chemistry, 2012, 14, 2807
7215079 CIFC28 H30 N3 O2 P SP 1 21/c 116.0609; 18.7305; 8.9676
90; 98.481; 90		2668.2Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle
An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings
Green Chemistry, 2012, 14, 2807
7215080 CIFC21 H23 N2 O2 P SP -18.7642; 10.8437; 12.1558
94.396; 106.808; 109.396		1023.87Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle
An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings
Green Chemistry, 2012, 14, 2807
7215081 CIFC25 H56 Cl6 N8 O5 P4 Pd2 S2P 1 21/c 112.8415; 13.0797; 28.1381
90; 109.006; 90		4468.5García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian
Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water
Green Chemistry, 2012, 14, 3190
7215082 CIFC17 H17 N3 O4P 1 21/n 111.6784; 5.6853; 23.4754
90; 96.479; 90		1548.7García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian
Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water
Green Chemistry, 2012, 14, 3190
7215777 CIFC18 H24 N2 O3 SiP -19.893; 10.366; 10.379
102.062; 105.681; 103.638		952.6Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi
Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides
Green Chemistry, 2008, 10, 327
7215778 CIFC15 H16 N2 O2P 1 21/c 114.092; 8.462; 11.276
90; 96.819; 90		1335.1Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi
Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides
Green Chemistry, 2008, 10, 327
7215812 CIFC11 H10 Br N O3P b c a12.936; 12.022; 14.578
90; 90; 90		2267.1Zou, You-Quan; Guo, Wei; Liu, Feng-Lei; Lu, Liang-Qiu; Chen, Jia-Rong; Xiao, Wen-Jing
Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism
Green Chemistry, 2014, 16, 3787
7216184 CIFC23 H19 NP -19.2869; 9.636; 11.202
84.187; 72.065; 64.104		857.3Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong
Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones
Green Chemistry, 2014, 16, 3715
7216185 CIFC20 H19 NP 1 21 17.859; 7.981; 23.406
90; 92.401; 90		1466.8Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong
Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones
Green Chemistry, 2014, 16, 3715
7216460 CIFC20 H20 Br N O4P 1 21/n 110.7001; 11.3758; 17.0795
90; 103.62; 90		2020.5Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah
Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction
Green Chemistry, 2014, 16, 3237
7216461 CIFC18 H18 N2 O3P 1 21/n 111.2762; 13.0441; 12.5041
90; 112.669; 90		1697.12Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah
Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction
Green Chemistry, 2014, 16, 3237
7216462 CIFC17 H15 N3 OP 1 21/c 114.9957; 7.6225; 11.9828
90; 91.022; 90		1369.47Li, Wenjun; Du, Zhiyun; Huang, Jiayao; Jia, Qianfa; Zhang, Kun; Wang, Jian
Direct access to 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of allyl ketones with azides
Green Chemistry, 2014, 16, 3003
7216643 CIFC27 H26 N2P 1 21/c 17.4217; 23.8402; 11.7942
90; 99.776; 90		2056.5Yasmin, Lyzu; Eggers, Paul K.; Skelton, Brian W.; Stubbs, Keith A.; Raston, Colin L.
Thin film microfluidic synthesis of fluorescent highly substituted pyridines
Green Chemistry, 2014, 16, 3450
7216644 CIFC28 H30 Cl2 N3 P RuP b c a11.8935; 13.1976; 33.9681
90; 90; 90		5331.8Li, Wei; Xie, Jian-Hua; Yuan, Ming-Lei; Zhou, Qi-Lin
Ruthenium complexes of tetradentate bipyridine ligands: highly efficient catalysts for the hydrogenation of carboxylic esters and lactones
Green Chemistry, 2014, 16, 4081
7218341 CIFC26 H18 Cu N2 O10C 1 2/c 110.118; 11.051; 21.051
90; 99.029; 90		2324.6Kathalikkattil, Amal Cherian; Kim, Dong-Woo; Tharun, Jose; Soek, Han-Geul; Roshan, Roshith; Park, Dae-Won
Aqueous-microwave synthesized carboxyl functional molecular ribbon coordination framework catalyst for the synthesis of cyclic carbonates from epoxides and CO2
Green Chemistry, 2014, 16, 1607
7229415 CIFC19 H19 N OP 1 21/c 114.0947; 5.86763; 18.4634
90; 97.511; 90		1513.87Karu, Ramesh; Gedu, Satyanarayana
Microwave assisted domino heck cyclization and alkynylation: synthesis of alkyne substituted dihydrobenzofurans
Green Chemistry, 2018, 20, 369
7229581 CIFC15 H15 N O3 SP 1 21/c 115.2479; 5.5541; 16.8079
90; 95.501; 90		1416.88Wang, Bin; Tang, Lin; Liu, Liyan; Li, Yanan; Yu, Yang; Wang, Zhiyong
Base-mediated tandem sulfonylation and oximation of alkenes in water
Green Chemistry, 2017
7229599 CIFC82 H78 F12 N2 O P6 Pd2 S4P -19.3104; 10.7032; 21.2565
86.197; 78.5; 88.333		2070.87Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James
From recovered metal waste to high-performance palladium catalysts
Green Chemistry, 2017
7229600 CIFC82 H78 F12 N2 O P6 Pd2 S4P 1 21/n 120.6104; 15.5218; 26.8129
90; 107.289; 90		8190.2Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James
From recovered metal waste to high-performance palladium catalysts
Green Chemistry, 2017
7229601 CIFC94 H88 F12 N2 O P6 Pd2 S4I 1 a 133.0045; 10.85381; 26.7343
90; 106.511; 90		9182Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James
From recovered metal waste to high-performance palladium catalysts
Green Chemistry, 2017
7229614 CIFC16 H15 N3 O5P -17.4889; 8.9633; 12.2743
98.953; 106.482; 98.679		763.71Qiao, Kai; Yuan, Xin; Wan, Li; Zheng, Mingwei; Zhang, Dong; Fan, Bingbing; Di, Zhechen; Fang, Zheng; Guo, Kai
Highly efficient synthesis of β-nitrate ester carboxamides through the ring-opening of 2-oxazolines
Green Chemistry, 2017
7229619 CIFC9 H8 Cl2 O2 SP 1 21 17.3712; 10.3338; 13.8683
90; 93.683; 90		1054.2Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.
Organic oxidations promoted in vortex driven thin films under continuous flow
Green Chemistry, 2018, 20, 118
7229620 CIFC14 H18 O2 SP 1 21/n 17.8477; 7.955; 20.8582
90; 96.801; 90		1292.98Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.
Organic oxidations promoted in vortex driven thin films under continuous flow
Green Chemistry, 2018, 20, 118
7229621 CIFC22 H16 F NP b c a19.293; 7.2555; 23.177
90; 90; 90		3244.3Ahmed, Waqar; Zhang, Sheng; Yu, Xiaoqiang; Yamamoto, Yoshinori; Bao, Ming
Brønsted acid-catalyzed metal- and solvent-free quinoline synthesis fromN-alkyl anilines and alkynes or alkenes
Green Chemistry, 2018, 20, 261
7229669 CIFC39 H31 N O2 P2P 1 21/n 111.651; 11.814; 23.05
90; 101.391; 90		3110.2Wen, Li-Rong; Sun, Yong-Xu; Zhang, Jin-Wei; Guo, Wei-Si; Li, Ming
Catalyst- and solvent-free bisphosphinylation of isothiocyanates: a practical method for the synthesis of bisphosphinoylaminomethanes
Green Chemistry, 2018, 20, 125
7229731 CIFC20 H20 O2 SP n m a6.2278; 37.44; 7.3546
90; 90; 90		1714.9Nguyen, Thanh Binh; Retailleau, Pascal
Sulfurative self-condensation of ketones and elemental sulfur: a three-component access to thiophenes catalyzed by aniline acid‒base conjugate pairs
Green Chemistry, 2018, 20, 387
7229831 CIFC42 H33 N3 OP -110.822; 12.45; 13.434
68.323; 84.539; 77.041		1639Albaladejo, María José; González-Soria, María José; Alonso, Francisco
Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes
Green Chemistry, 2018, 20, 701
7229832 CIFC44 H37 N3 O3P -112.1335; 12.3113; 12.6442
87.101; 86.513; 69.271		1762.4Albaladejo, María José; González-Soria, María José; Alonso, Francisco
Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes
Green Chemistry, 2018, 20, 701
7229843 CIFC11 H6 O2P -13.7722; 8.864; 25.643
86.384; 89.405; 81.479		846.27Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng
Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide
Green Chemistry, 2018, 20, 989
7229844 CIFC11 H5 O2P 1 21/c 13.8398; 6.201; 35.222
90; 91.034; 90		838.5Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng
Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide
Green Chemistry, 2018, 20, 989
7229845 CIFC32 H25 N O4 S2 Se3P 1 21/n 117.114; 11.241; 18.622
90; 116.978; 90		3192.6Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji
Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides
Green Chemistry, 2018, 20, 604
7229846 CIFC32 H25 N O4 S2 Se2P -19.3039; 11.2838; 15.363
110.126; 99.341; 93.707		1481.6Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji
Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides
Green Chemistry, 2018, 20, 604
7230013 CIFC18 H33 Mo12 N6 O40 PP -114.9687; 15.0798; 21.8498
86.944; 88.681; 85.622		4909.8Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230014 CIFC24 H45 Mo12 N6 O40 PP -112.9158; 21.2163; 21.6946
95.876; 105.285; 101.08		5553.7Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230015 CIFC30 H57 Mo12 N6 O40 PP b c a22.3846; 20.969; 26.0718
90; 90; 90		12237.7Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio
Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship
Green Chemistry, 2018, 20, 1042
7230209 CIFC7 H22 O3 Si3P -4 21 c17.5199; 17.5199; 10.0567
90; 90; 90		3086.9Arzumanyan, Ashot V.; Goncharova, Irina K.; Novikov, Roman A.; Milenin, Sergey A.; Boldyrev, Konstantin L.; Solyev, Pavel N.; Tkachev, Yaroslav V.; Volodin, Alexander D.; Smol'yakov, Alexander F.; Korlyukov, Alexander A.; Muzafarov, Aziz M.
Aerobic Co or Cu/NHPI-catalyzed oxidation of hydride siloxanes: synthesis of siloxanols
Green Chemistry, 2018, 20, 1467
7230285 CIFC24 H19 N OP -19.4619; 9.7534; 10.5387
68.185; 78.205; 88.782		882.26Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming
Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones
Green Chemistry, 2018, 20, 2007
7230286 CIFC25 H19 Cl3 N2P 1 21/c 110.6279; 15.8991; 13.4801
90; 100.33; 90		2240.9Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming
Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones
Green Chemistry, 2018, 20, 2007
7230301 CIFC16 H24 O3P -16.0145; 8.0625; 16.0814
96.122; 94.613; 100.073		759.5Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi
Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process
Green Chemistry, 2018, 20, 1998
7230302 CIFC17 H26 O3P 1 21/c 115.6175; 8.4961; 12.67
90; 96.193; 90		1671.3Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi
Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process
Green Chemistry, 2018, 20, 1998
7230303 CIFC36 H56 O6P 1 21/c 112.9802; 8.6558; 32.2944
90; 94.115; 90		3619.1Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi
Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process
Green Chemistry, 2018, 20, 1998
7230313 CIFC18 H29 Cl2 Ir N4 O2P -19.1521; 9.681; 11.7658
88.195; 86.069; 89.089		1039.4Lu, Sheng-Mei; Wang, Zhijun; Wang, Jijie; Li, Jun; Li, Can
Hydrogen generation from formic acid decomposition on a highly efficient iridium catalyst bearing a diaminoglyoxime ligand
Green Chemistry, 2018, 20, 1835
7230342 CIFC22 H25 N5 O4P -19.324; 9.76; 12.772
75.736; 70.173; 77.227		1047.6Zhang, Furen; Li, Chunmei; Liang, Xuezheng
Solid acid-catalyzed domino cyclization reaction: regio- and diastereoselective synthesis of pyrido[2,3-d]pyrimidine derivatives bearing three contiguous stereocenters
Green Chemistry, 2018, 20, 2057
7230380 CIFC116 H88 Cl6 N8C 1 2/c 143.317; 23.984; 28.932
90; 117.762; 90		26598Ishizuka, Tomoya; Ohkawa, Shumpei; Ochiai, Hidemi; Hashimoto, Muneaki; Ohkubo, Kei; Kotani, Hiroaki; Sadakane, Masahiro; Fukuzumi, Shunichi; Kojima, Takahiko
A supramolecular photocatalyst composed of a polyoxometalate and a photosensitizing water-soluble porphyrin diacid for the oxidation of organic substrates in water
Green Chemistry, 2018, 20, 1975
7230471 CIFC23 H18 N2 O5 SP -19.1495; 11.0385; 11.775
68.418; 81.041; 68.191		1026.46Yao, Xinghui; Weng, Xin; Wang, Kaixuan; Xiang, Haifeng; Zhou, Xiangge
Transition metal free oxygenation of 8-aminoquinoline amides in water
Green Chemistry, 2018, 20, 2472
7230499 CIFC14 H10 N2 OP 1 21/c 112.105; 7.6772; 11.507
90; 97.73; 90		1059.7Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua
Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage
Green Chemistry, 2018, 20, 2449
7230500 CIFC19 H14 N2 O2P 1 21/c 110.351; 11.378; 12.992
90; 106.17; 90		1469.6Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua
Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage
Green Chemistry, 2018, 20, 2449
7230578 CIFC12 H14 O4P 1 21/n 15.8802; 25.3608; 8.2156
90; 109.663; 90		1153.72Yang, Da; Liu, Huan; Wang, Dong-Liang; Luo, Zhoujie; Lu, Yong; Xia, Fei; Liu, Ye
Co-catalysis over a bi-functional ligand-based Pd-catalyst for tandem bis-alkoxycarbonylation of terminal alkynes
Green Chemistry, 2018, 20, 2588
7230581 CIFC15 H0 Br N OC 1 c 129.72; 5.675; 7.425
90; 95.29; 90		1247Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones
Green Chemistry, 2018, 20, 2722
7230582 CIFC20 H16 F3 NP -18.585; 9.869; 10.0994
91.079; 103.819; 90.728		830.6Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones
Green Chemistry, 2018, 20, 2722
7230705 CIFC13 H10 Cl N O SP 1 21/n 110.4863; 9.6208; 12.383
90; 111.484; 90		1162.48Ma, Yan-Na; Guo, Chen-Yang; Zhao, Qianyi; Zhang, Jie; Chen, Xuenian
Synthesis of dibenzothiazines from sulfides by one-pot N,O-transfer and intramolecular C‒H amination
Green Chemistry, 2018, 20, 2953
7230721 CIFC80 H70 Cl2 N6 O11F d d 221.758; 50.304; 13.416
90; 90; 90		14684Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent
Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles
Green Chemistry, 2018, 20, 2775
7230722 CIFC48 H49 Cl2 N3 O4P -112.043; 13.174; 13.616
98.819; 97.641; 98.079		2087Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent
Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles
Green Chemistry, 2018, 20, 2775
7230738 CIFC11 H10 O4P 21 21 217.22158; 9.60997; 13.4791
90; 90; 90		935.44Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230739 CIFC13 H11 N O5P 1 21 18.36693; 7.08624; 19.5336
90; 93.2815; 90		1156.25Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230740 CIFC15 H14 O3P 6513.5583; 13.5583; 45.7998
90; 90; 120		7291.3Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230741 CIFC11 H10 O3 SP 21 21 216.32713; 10.32552; 15.23806
90; 90; 90		995.516Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230742 CIFC13 H12 O4P 21 21 219.50457; 9.59528; 11.4776
90; 90; 90		1046.75Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230743 CIFC14 H14 O3P 21 21 216.47958; 7.89044; 22.4589
90; 90; 90		1148.25Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230744 CIFC13 H11 Cl O3P 1 21 15.94601; 5.17983; 18.2456
90; 94.739; 90		560.03Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230745 CIFC13 H12 O3P 1 21 111.11016; 9.04172; 15.58673
90; 95.3028; 90		1559.06Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.
Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)
Green Chemistry, 2018, 20, 4423
7230820 CIFC22 H16 O5 SP n a 217.7651; 16.4066; 14.1404
90; 90; 90		1801.5Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg
Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide
Green Chemistry, 2018, 20, 3059
7230821 CIFC21 H13 Cl O4 SP 1 c 112.8859; 5.6317; 25.025
90; 92.804; 90		1813.9Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg
Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide
Green Chemistry, 2018, 20, 3059
7230882 CIFC18 H19 N O2 SP -18.9159; 9.228; 10.159
105.035; 98.43; 102.959		767.8Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian
Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines
Green Chemistry, 2018, 20, 3191
7230883 CIFC14 H15 F6 N O3 SC 1 2/c 139.756; 6.2412; 31.125
90; 123.261; 90		6457.7Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian
Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines
Green Chemistry, 2018, 20, 3191
7230887 CIFC18 H21 N O6P -18.9121; 10.6028; 10.607
107.362; 95.433; 110.176		875.81Wang, Yinling; Du, Yiman; He, Jianghua; Zhang, Yuetao
Transformation of lignin model compounds to N-substituted aromatics via Beckmann rearrangement
Green Chemistry, 2018, 20, 3318
7230903 CIFC20 H18 OC 1 2/c 114.081; 14.4862; 16.112
90; 113.689; 90		3009.6Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230904 CIFC19 H16 O2P -16.3828; 10.3101; 11.896
104.198; 100.779; 97.652		732.2Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230905 CIFC12 H10 O3P 1 21/c 19.52; 13.2012; 8.3853
90; 112.716; 90		972.1Senadi, Gopal Chandru; Wang, Jeh-Jeng
p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy
Green Chemistry, 2018, 20, 3420
7230906 CIFC53 H44 Cl F6 N4 P3 RuI -428.6436; 28.6436; 13.5364
90; 90; 90		11106Chakrabarti, Kaushik; Mishra, Anju; Panja, Dibyajyoti; Paul, Bhaskar; Kundu, Sabuj
Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources
Green Chemistry, 2018, 20, 3339
7230942 CIFC42 H36 Br Cl2 N2 O5.5 S2P -110.1352; 13.2429; 16.5954
110.962; 96.295; 91.276		2062.93Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu
Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles
Green Chemistry, 2018, 20, 3271
7230943 CIFC25 H23 N O3 SP 1 21/c 118.5095; 10.9007; 10.3745
90; 103.857; 90		2032.3Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu
Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles
Green Chemistry, 2018, 20, 3271
7230944 CIFC31 H25 N O3 SP 1 21/n 111.7246; 12.2563; 16.5665
90; 98.55; 90		2354.15Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu
Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles
Green Chemistry, 2018, 20, 3271
7230945 CIFC21 H18 O4C 1 2/c 117.0463; 11.4307; 18.4621
90; 107.898; 90		3423.3Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo
Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols
Green Chemistry, 2018, 20, 3476
7230946 CIFC27 H23 N O3P 1 21/c 114.9117; 9.0532; 16.0374
90; 99.025; 90		2138.2Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo
Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols
Green Chemistry, 2018, 20, 3476
7231095 CIFC29 H29 N5P -19.7181; 11.6016; 12.0845
69.98; 78.308; 71.223		1205.45Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231096 CIFC22 H25 N5P -18.154; 14.767; 16.628
90.056; 100.409; 90.188		1969.2Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231097 CIFC26 H24 Cl N5 OP 1 21 19.5211; 11.9295; 20.9205
90; 100.11; 90		2339.3Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231098 CIFC26 H25 N5C 1 c 110.7702; 13.9788; 15.802
90; 109.391; 90		2244.11Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231099 CIFC26 H25 N5P 1 21/c 113.8953; 9.4127; 16.851
90; 97.186; 90		2186.67Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231100 CIFC1.61 H1.61 N0.3P 1 21/n 111.3769; 17.6453; 11.4216
90; 96.532; 90		2277.99Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231101 CIFC33 H31 N5 O2P 21 21 219.5012; 15.8064; 18.7456
90; 90; 90		2815.2Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.
C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines
Green Chemistry, 2018, 20, 3463
7231208 CIFC17 H14 N2 O2 SP -18.4181; 9.1433; 10.4688
74.013; 72.64; 69.444		706.85Chen, En; Shao, Jiaan; Tang, Pai; Shu, Ke; Chen, Wenteng; Yu, Yongping
Catalyst-free three-component sequencing for efficient assembly of [1,3] oxazine N-fused imidazole-2-thiones
Green Chemistry, 2018, 20, 3696
7231242 CIFC12 H14 N2 OP -15.8293; 9.3602; 10.5304
77.907; 80.183; 78.031		544.74Pelliccia, Sveva; Abbate, Vincenzo; Meneghetti, Fiorella; Frascione, Nunzianda; Hider, Robert Charles; Novellino, Ettore; Tron, Gian Cesare; Giustiniano, Mariateresa
On-water pyrrolidine-mediated domino synthesis of 2-iminoisatins
Green Chemistry, 2018, 20, 3912
7231243 CIFC90 H78 Cl N9 O5 P6 Ru2P 1 21/n 122.8345; 15.0703; 27.8444
90; 92.926; 90		9569.4Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei
Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes
Green Chemistry, 2018, 20, 4201
7231244 CIFC48 H40 N3 O P3 RuP -112.2479; 20.634; 25.309
106.192; 93.516; 106.236		5829.8Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei
Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes
Green Chemistry, 2018, 20, 4201
7231311 CIFC16 H14.5 F3 N3 O0.25P 1 21/c 15.6803; 22.15; 23.2022
90; 90.281; 90		2919.2Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231312 CIFC18 H23 N3 O4P 1 21 15.35503; 10.169; 32.73
90; 92.72; 90		1780.31Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231313 CIFC15 H12 F3 NP n a 2127.0703; 5.7522; 8.0156
90; 90; 90		1248.14Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231314 CIFC18 H23 N3 O2P 1 21/c 112.8362; 11.1053; 11.7668
90; 92.584; 90		1675.65Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231315 CIFC23 H21 N O2P 1 21 15.66625; 18.3197; 17.6253
90; 90.314; 90		1829.55Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231316 CIFC21 H19 N3 O2P 1 21/c 112.8553; 5.5968; 24.4632
90; 92.11; 90		1758.9Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia
Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents
Green Chemistry, 2018, 20, 4023
7231346 CIFC18 H26 Cl9 Ir N2 O4 SP b c a11.2915; 16.6242; 32.7927
90; 90; 90		6155.6Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.
Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water
Green Chemistry, 2018, 20, 4094
7231347 CIFC22 H27 Ir N2 O2P -18.592; 10.2464; 12.6648
78.655; 82.445; 67.017		1004.56Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.
Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water
Green Chemistry, 2018, 20, 4094
7231348 CIFC18 H29 Cl2 F6 Ir N2 O8 S2P 1 21/c 111.2529; 21.6653; 12.9575
90; 111.582; 90		2937.5Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.
Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water
Green Chemistry, 2018, 20, 4094
7231363 CIFC8 H19 N3 Si2P 1 21/c 16.7038; 9.1027; 21.146
90; 91.335; 90		1290Roshandel, Sahar; Suri, Suresh C.; Marcischak, Jacob C.; Rasul, Golam; Surya Prakash, G. K.
Catalyst and solvent free microwave-assisted synthesis of substituted 1,2,3-triazoles
Green Chemistry, 2018, 20, 3700
7231382 CIFC14 H7 F4 NP 1 21/c 113.274; 14.344; 6.1256
90; 101.518; 90		1142.8Charpe, Vaibhav Pramod; Hande, Aniket A.; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible-light induced copper(i)-catalysed denitrogenative oxidative coupling of hydrazinylpyridines with terminal alkynes
Green Chemistry, 2018, 20, 4859
7231389 CIFC15 H45 Cl9 N3 O4.5 Sn3C 1 c 115.459; 9.19; 23.79
90; 95.25; 90		3365.62Bayu, Asep; Yoshida, Akihiro; Karnjanakom, Surachai; Kusakabe, Katsuki; Hao, Xiaogang; Prakoso, Tirto; Abudula, Abuliti; Guan, Guoqing
Catalytic conversion of biomass derivatives to lactic acid with increased selectivity in an aqueous tin(ii) chloride/choline chloride system
Green Chemistry, 2018, 20, 4112
7231395 CIFC90 H101 N6 O12P -119.911; 20.945; 23.811
106.471; 107.031; 108.096		8223Zhu, Xin-Qi; Yuan, Han; Sun, Qing; Zhou, Bo; Han, Xiao-Qin; Zhang, Zhi-Xin; Lu, Xin; Ye, Long-Wu
Benign catalysis with zinc: atom-economical and divergent synthesis of nitrogen heterocycles by formal [3 + 2] annulation of isoxazoles with ynol ethers
Green Chemistry, 2018, 20, 4287
7231603 CIFC40 H45 B Cl2 F4 Ir N3 P2P -111.0544; 13.3742; 14.3388
84.204; 84.669; 72.812		2010.4Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A.
A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin
Green Chemistry, 2018, 20, 4875
7231604 CIFC38 H41 B Cl2 F4 Ir N3 P2P 1 21/n 115.5008; 11.5673; 21.116
90; 97.583; 90		3753Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A.
A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin
Green Chemistry, 2018, 20, 4875
7231651 CIFC20 H22 F3 N O3P -18.318; 11.515; 11.539
61.6; 78.05; 75.08		934.8He, Yu-Tao; Kang, Dahye; Kim, Inwon; Hong, Sungwoo
Metal-free photocatalytic trifluoromethylative pyridylation of unactivated alkenes
Green Chemistry, 2018, 20, 5209
7231666 CIFC13.75 H12.5 N1.25 O1.25 S0.25P 1 21/c 18.6319; 18.0068; 7.8624
90; 99.001; 90		1207.03Xing, Zhimin; Yang, Mingyang; Sun, Haiyu; Wang, Zemin; Chen, Peng; Liu, Lin; Wang, Xiaolei; Xie, Xingang; She, Xuegong
Visible-light promoted dithioacetalization of aldehydes with thiols under aerobic and photocatalyst-free conditions
Green Chemistry, 2018, 20, 5117
7231667 CIFC51 H37 F12 N5 O9 Zn2C 1 2/c 127.538; 7.887; 23.328
90; 99.24; 90		5000.9Joharian, Monika; Morsali, Ali; Azhdari Tehrani, Alireza; Carlucci, Lucia; Proserpio, Davide M.
Water-stable fluorinated metal‒organic frameworks (F-MOFs) with hydrophobic properties as efficient and highly active heterogeneous catalysts in aqueous solution
Green Chemistry, 2018, 20, 5336
7231688 CIFC114 H126 N24 Nd4 O42 Zn3R -3 c17.8928; 17.8928; 69.099
90; 90; 120		19158.4Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng
Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition
Green Chemistry, 2018
7231689 CIFC114 H126 Eu4 N24 O42 Zn3R -3 c17.8497; 17.8497; 68.762
90; 90; 120		18973.2Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng
Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition
Green Chemistry, 2018
7231775 CIFC12 H11 N O2 SP 1 21/c 111.1231; 11.9525; 8.5577
90; 99.993; 90		1120.48Wang, Ming; Fan, Qiaoling; Jiang, Xuefeng
Metal-free construction of primary sulfonamides through three diverse salts
Green Chemistry, 2018, 20, 5469
7231898 CIFC16 H12 N2 OP 1 21 13.9878; 12.0606; 24.7189
90; 93.93; 90		1186.07Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla
Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination
Green Chemistry, 2019, 21, 99
7231899 CIFC17 H14 N2P 1 21/c 113.2669; 11.5841; 16.4623
90; 100.794; 90		2485.2Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla
Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination
Green Chemistry, 2019, 21, 99
7231952 CIFC40 H36 N8 O4 S2P -110.651; 12.816; 14.137
100.211; 107.686; 101.151		1745.4Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.
A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer
Green Chemistry, 2019, 21, 69
7231953 CIFC26 H26 N4 O2C 1 2/c 120.3152; 14.7532; 16.39
90; 110.119; 90		4612.6Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.
A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer
Green Chemistry, 2019, 21, 69
7231954 CIFC22 H20 N4 O2P 1 21/c 110.9372; 9.1286; 35.781
90; 95.129; 90		3558.1Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.
A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer
Green Chemistry, 2019, 21, 69
7231992 CIFC20 H26 Cl F6 Ir N3 O PP n m a13.5409; 12.9814; 13.6168
90; 90; 90		2393.6Huang, Ming; Li, Yinwu; Liu, Jiahao; Lan, Xiao-Bing; Liu, Yan; Zhao, Cunyuan; Ke, Zhuofeng
A bifunctional strategy for N-heterocyclic carbene-stabilized iridium complex-catalyzed N-alkylation of amines with alcohols in aqueous media
Green Chemistry, 2019, 21, 219
7231993 CIFC37 H54 Cl N2 P2 RhR -3 c :H26.6194; 26.6194; 27.22
90; 90; 120		16703.8Lam, Raphael H.; McQueen, Caitlin M. A.; Pernik, Indrek; McBurney, Roy T.; Hill, Anthony F.; Messerle, Barbara A.
Selective formylation or methylation of amines using carbon dioxide catalysed by a rhodium perimidine-based NHC complex
Green Chemistry, 2019, 21, 538
7232134 CIFC8 H12 N2 O2P c a 2113.4813; 8.2397; 6.9346
90; 90; 90		770.31Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232135 CIFC13 H23 N3 O2P 1 21/n 110.9982; 9.2785; 14.3717
90; 105.714; 90		1411.77Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232136 CIFC12 H21 N3 O2P 1 21/c 19.3632; 18.2488; 8.129
90; 114.812; 90		1260.76Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232137 CIFC13 H19 N3P 21 21 219.9385; 10.0425; 24.7502
90; 90; 90		2470.25Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232138 CIFC8 H14 N2 O3P 1 21/n 17.7428; 11.1556; 10.4925
90; 98.844; 90		895.52Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232139 CIFC9 H17 N3 O3P 1 21/n 18.1469; 10.0659; 12.9174
90; 104.799; 90		1024.16Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232140 CIFC23 H29 N3P 1 21/n 112.5296; 8.0939; 19.7181
90; 98.5378; 90		1977.52Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232141 CIFC16 H29 N3 O2P 1 21/c 114.3302; 9.2194; 12.9756
90; 104.588; 90		1659.02Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232142 CIFC13 H23 N3 O2C 1 c 110.3765; 13.1188; 11.2806
90; 114.605; 90		1396.17Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232143 CIFC15 H30 B F4 N3P 1 21/c 115.2506; 10.8267; 10.8569
90; 90.09; 90		1792.62Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232144 CIFC8 H13 N3 O2P 1 21/c 16.6679; 14.6889; 9.6025
90; 104.13; 90		912.05Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232145 CIFC19.5 H31.5 N3 O2P 1 21/c 114.6071; 41.9109; 14.5422
90; 117.159; 90		7921.1Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232146 CIFC16 H29 N3 O2P 4111.8565; 11.8565; 24.0309
90; 90; 90		3378.2Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian
Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts
Green Chemistry, 2019, 21, 640
7232175 CIFC27 H31 N O3P 1 21/c 110.8693; 19.0667; 11.8343
90; 102.11; 90		2398Chen, Ke; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Metal-free synthesis of triarylated (Z)-nitrones via H2O-mediated 1,3-dipolar transfer under aerobic conditions
Green Chemistry, 2019, 21, 675
7232200 CIFC27 H20 Cl2 N O PP 1 21/n 19.594; 11.0586; 21.6374
90; 93.293; 90		2291.86Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen
Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions
Green Chemistry, 2019, 21, 792
7232201 CIFC30 H27 Cl N O PP 1 21/c 18.6081; 16.0745; 18.0657
90; 99.465; 90		2465.74Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen
Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions
Green Chemistry, 2019, 21, 792
7232299 CIFC14 H10 N2 OP 1 21/c 112.1056; 7.802; 11.6256
90; 97.574; 90		1088.43Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng
Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions
Green Chemistry, 2019, 21, 979
7232300 CIFC14 H9 F N2 OP 1 21/c 112.4895; 7.7667; 11.5802
90; 96.718; 90		1115.59Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng
Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions
Green Chemistry, 2019, 21, 979
7232306 CIFC13 H9 N O3P -16.561; 7.0809; 12.0629
89.067; 87.281; 78.757		549.03Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing
Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones
Green Chemistry, 2019, 21, 991
7232307 CIFC18 H12 F3 N O3P -16.7109; 9.819; 12.7318
75.919; 82.43; 80.639		799.18Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing
Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones
Green Chemistry, 2019, 21, 991
7232308 CIFC18 H15 N O4P b c a6.04; 19.12; 26.355
90; 90; 90		3043.6Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing
Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones
Green Chemistry, 2019, 21, 991
7232363 CIFC21 H14 F5 N3 O4P -18.2387; 9.1226; 15.647
78.884; 77.335; 63.875		1023.9Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao
An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group
Green Chemistry, 2019, 21, 1505
7232364 CIFC23 H19 F5 N2 O2P -18.6308; 9.4049; 13.955
78.895; 81.887; 74.726		1067.4Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao
An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group
Green Chemistry, 2019, 21, 1505
7232431 CIFC52 H28 Br16 N4 O9 VP c a b20.733; 26.304; 28.112
90; 90; 90		15331Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R.
Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media
Green Chemistry, 2019, 21, 1757
7232432 CIFC27.5 H22 N3 O5 V0.5P c c n13.829; 14.439; 26.153
90; 90; 90		5222Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R.
Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media
Green Chemistry, 2019, 21, 1757
7232441 CIFC17 H14 N2 O2P 1 21/c 111.954; 7.454; 15.468
90; 95.33; 90		1372.3Botla, Vinayak; Pilli, NavyaSree; Malapaka, Chandrasekharam
Uncatalyzed, on water oxygenative cleavage of inert C‒N bond with concomitant 8,7-amino shift in 8-aminoquinoline derivatives
Green Chemistry, 2019, 21, 1735
7232442 CIFC2 H4 N8 O4 ZnP 1 21/c 16.294; 10.6563; 5.5677
90; 95.069; 90		371.97Zhang, Qi; Chen, Dong; Jing, Dong; Fan, Guijuan; He, Liu; Li, Hongzhen; Wang, Wentao; Nie, Fude
Access to green primary explosives via constructing coordination polymers based on bis-tetrazole oxide and non-lead metals
Green Chemistry, 2019, 21, 1947
7232466 CIFC15 H12 O2P 1 21/n 19.6376; 8.3094; 14.8885
90; 92.042; 90		1191.6Tang, Zhi; Tong, Zhou; Xu, Zhihui; Au, Chak-Tong; Qiu, Renhua; Yin, Shuang-Feng
Recyclable nickel-catalyzed C‒H/O‒H dual functionalization of phenols with mandelic acids for the synthesis of 3-aryl benzofuran-2(3H)-ones under solvent-free conditions
Green Chemistry, 2019, 21, 2015
7232467 CIFC19 H26 Cl4 Ir N3 OP 1 21/n 112.768; 14.165; 13.588
90; 111.994; 90		2278.7Chakrabarti, Kaushik; Maji, Milan; Kundu, Sabuj
Cooperative iridium complex-catalyzed synthesis of quinoxalines, benzimidazoles and quinazolines in water
Green Chemistry, 2019, 21, 1999
7232468 CIFC13 H17 N2 O3P 1 21/c 19.9995; 10.3691; 12.6092
90; 101.192; 90		1282.53Sun, Zhen; Li, Zheng; Liao, Wei-Wei
An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins
Green Chemistry, 2019, 21, 1614
7232495 CIFC5 H10 O4P 21 21 215.01554; 7.52021; 15.90107
90; 90; 90		599.755Benhamou, Laure; Foster, Robert W.; Ward, David P.; Wheelhouse, Katherine; Sloan, Lisa; Tame, Christopher J.; Bučar, Dejan-Krešimir; Lye, Gary J.; Hailes, Helen C.; Sheppard, Tom D.
Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass
Green Chemistry, 2019, 21, 2035
7232496 CIFC12 H13 Br O4C 1 2 122.3597; 5.5295; 9.5976
90; 90.661; 90		1186.55Benhamou, Laure; Foster, Robert W.; Ward, David P.; Wheelhouse, Katherine; Sloan, Lisa; Tame, Christopher J.; Bučar, Dejan-Krešimir; Lye, Gary J.; Hailes, Helen C.; Sheppard, Tom D.
Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass
Green Chemistry, 2019, 21, 2035
7232514 CIFC12 H13 Cl O2P 21 21 217.1261; 8.1012; 18.5115
90; 90; 90		1068.67Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.
Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions
Green Chemistry, 2019, 21, 2952
7232515 CIFC13 H16 Cl N OP -16.7087; 8.9522; 10.805
76.216; 82.767; 72.956		601.45Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.
Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions
Green Chemistry, 2019, 21, 2952
7232516 CIFC13 H16 Cl N OP 1 21/c 110.0679; 8.2104; 28.6875
90; 98.842; 90		2343.17Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.
Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions
Green Chemistry, 2019, 21, 2952
7232523 CIFC7 H32 B18 Co NC 1 2/m 19.13; 10.446; 11.101
90; 106.63; 90		1014.4Bennour, Ines; Cioran, Ana M.; Teixidor, Francesc; Viñas, Clara
3,2,1 and stop! An innovative, straightforward and clean route for the flash synthesis of metallacarboranes
Green Chemistry, 2019, 21, 1925
7232541 CIFC15 H12 Br N SeP 1 21/n 112.469; 6.265; 17.738
90; 96.553; 90		1376.6Rathore, Vandana; Kumar, Sangit
Visible-light-induced metal and reagent-free oxidative coupling of sp2 C‒H bonds with organo-dichalcogenides: synthesis of 3-organochalcogenyl indoles
Green Chemistry, 2019, 21, 2670
7232571 CIFC11 H10 Br N3 O2P 21 21 215.9656; 12.4421; 16.3174
90; 90; 90		1211.15Yadav, Dolly; Singh, Nem; Kim, Tae Wu; Kim, Jae Young; Park, No-Joong; Baeg, Jin-Ook
Highly regioselective and sustainable solar click reaction: a new post-synthetic modified triazole organic polymer as a recyclable photocatalyst for regioselective azide‒alkyne cycloaddition reaction
Green Chemistry, 2019, 21, 2677
7232637 CIFC30 H40 Cl4 N8 Ni2 O2C 1 2/m 117.2098; 8.7962; 12.4668
90; 112.273; 90		1746.43Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232638 CIFC28 H34 I2 N8 Ni2P b c a15.1186; 18.4249; 23.5902
90; 90; 90		6571.3Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232639 CIFC28 H32 Br4 N8 Ni2C 1 2/m 115.109; 15.035; 10.6611
90; 116.24; 90		2172.2Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232640 CIFC30 H40 I4 N8 Ni2 O2P 1 21/n 119.061; 10.993; 19.32
90; 112.098; 90		3750.9Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232641 CIFC68 H65 B2 N7 NiP -111.5825; 13.5215; 19.6576
98.75; 101.464; 103.617		2867.7Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232642 CIFC38 H40 B2 N4 NiP 21 21 2111.1094; 15.0969; 18.9302
90; 90; 90		3174.9Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232643 CIFC88 H92 B2 N12 Ni2 O4P 1 21/n 116.7786; 11.9023; 21.251
90; 105.676; 90		4086.1Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232644 CIFC14 H21 N4 Ni O9 S1.5C 1 2/c 121.7139; 11.0715; 16.0808
90; 100.803; 90		3797.4Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232645 CIFC96 H94 B2 N12 Ni2 S2P -110.8252; 11.8798; 17.529
70.982; 72.243; 78.092		2015.3Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232646 CIFC15 H16 N4 Ni O3R -330.9603; 30.9603; 11.4869
90; 90; 120		9535.5Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232647 CIFC163 H151 B3 N12 Ni3 O7C 1 2 142.319; 22.6; 15.7228
90; 93.976; 90		15001.2Angamuthu, Raja; Raje, Sakthi
Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride
Green Chemistry, 2019
7232648 CIFC40 H26 Cl2 N2 O5P -19.9687; 14.9432; 24.3238
92.312; 97.145; 107.847		3410.4Shafiee, Behnaz; Duffield, Joseph; Timm, Rudy; Liyanage, Rohana; Lay, Jackson O.; Khosropour, Ahmad R.; Amiri Rudbari, Hadi; Beyzavi, M. Hassan
Metal-free and benign approach for the synthesis of dihydro-5′H-spiro[benzo[c]chromene-8,4′-oxazole]-5′,6(7H)-dione scaffolds as masked amino acids
Green Chemistry, 2019, 21, 2656
7232653 CIFC26 H24 N O4 P SP 1 21/n 110.393; 18.063; 12.568
90; 99.096; 90		2330Liu, Teng; Li, Yongqin; Cheng, Feixiang; Shen, Xianfu; Liu, Jianjun; Lin, Jun
Highly chemo- and regioselective C‒P cross-coupling reaction of quinone imine ketals with Ar2P(O)H to construct ortho-amino triarylphosphine derivatives
Green Chemistry, 2019, 21, 3536
7232654 CIFC27 H26 N O5 P SP 1 21/n 110.82; 17.6091; 14.0022
90; 105.494; 90		2570.9Liu, Teng; Li, Yongqin; Cheng, Feixiang; Shen, Xianfu; Liu, Jianjun; Lin, Jun
Highly chemo- and regioselective C‒P cross-coupling reaction of quinone imine ketals with Ar2P(O)H to construct ortho-amino triarylphosphine derivatives
Green Chemistry, 2019, 21, 3536
7232700 CIFC12 H12 O2P 1 21 16.7747; 6.9936; 10.2745
90; 99.508; 90		480.11Zhang, Ying-Qi; Zhu, Xin-Qi; Xu, Yin; Bu, Hao-Zhen; Wang, Jia-Le; Zhai, Tong-Yi; Zhou, Jin-Mei; Ye, Long-Wu
Synthesis of functionalized 3-isochromanones via metal-free intramolecular alkoxylation-initiated cascade cyclization
Green Chemistry, 2019, 21, 3023
7232726 CIFC33 H27 N3 O2P 1 21/n 120.2486; 6.7682; 20.858
90; 118.296; 90		2517Li, Chunmei; Zhang, Furen; Qi, Chenze
A multicomponent two-step strategy for the synthesis of polysubstituted pyrrolo[3,2-c]pyridin-4-ones using a solid acid as a recyclable catalyst
Green Chemistry, 2019, 21, 3109
7232772 CIFC13 H15 Br OP 1 21/n 110.5578; 7.5212; 15.993
90; 108.303; 90		1205.7Chen, Chao; Kang, Jun-Chen; Mao, Chen; Dong, Jia-Wei; Xie, Yu-Yang; Ding, Tong-Mei; Tu, Yong-Qiang; Chen, Zhi-Min; Zhang, Shu-Yu
Electrochemical halogenation/semi-pinacol rearrangement of allylic alcohols using inorganic halide salt: an eco-friendly route to the synthesis of β-halocarbonyls
Green Chemistry, 2019, 21, 4014
7232793 CIFC12 H11 Br F3 N O2C 1 2/c 121.525; 9.597; 14.745
90; 121.67; 90		2592.4Zou, Long; Li, Pinhua; Wang, Bin; Wang, Lei
Visible-light-induced radical cyclization of N-allylbenzamides with CF3SO2Na to trifluoromethylated dihydroisoquinolinones in water at room temperature
Green Chemistry, 2019, 21, 3362
7232836 CIFC24 H29 N O3P 1 21/c 112.3821; 8.3089; 21.5533
90; 105.353; 90		2138.3Gong, Ming; Kim, Jung Keun; Zhao, Xiuli; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie
Visible-light-induced α-oxyamination of 1,3-dicarbonyls with TEMPO via a photo(electro)catalytic process applying a DSSC anode or in a DSSC system
Green Chemistry, 2019, 21, 3615
7232870 CIFC29 H23 F3 O2 Se2P 1 21/n 114.2456; 11.4003; 15.7834
90; 104.488; 90		2481.8Ma, Xian-Li; Wang, Qian; Feng, Xi-Yuan; Mo, Zu-Yu; Pan, Ying-Ming; Chen, Yan-Yan; Xin, Mao; Xu, Yan-Li
Metal-free visible-light induced cyclization/substitution cascade reaction of alkyne-tethered cyclohexadienones and diselenides: access to 5-hydroxy-3-selenyl-4a,8a-dihydro-2H-chromen-6(5H)-ones
Green Chemistry, 2019, 21, 3547
7232871 CIFC23 H19 F3 O3 SeP 1 21/c 111.2346; 13.8269; 13.8545
90; 112.472; 90		1988.7Ma, Xian-Li; Wang, Qian; Feng, Xi-Yuan; Mo, Zu-Yu; Pan, Ying-Ming; Chen, Yan-Yan; Xin, Mao; Xu, Yan-Li
Metal-free visible-light induced cyclization/substitution cascade reaction of alkyne-tethered cyclohexadienones and diselenides: access to 5-hydroxy-3-selenyl-4a,8a-dihydro-2H-chromen-6(5H)-ones
Green Chemistry, 2019, 21, 3547
7232918 CIFC16 H24 Cl2 N2 O3P n a 2111.1568; 17.163; 9.1319
90; 90; 90		1748.6Wu, Han-Qing; Yang, Kai; Chen, Xiao-Yun; Arulkumar, Mani; Wang, Neng; Chen, Si-Hong; Wang, Zhao-Yang
A 3,4-dihalo-2(5H)-furanone initiated ring-opening reaction of DABCO in the absence of a metal catalyst and additive and its application in a one-pot two-step reaction
Green Chemistry, 2019, 21, 3782
7232949 CIFC22 H19 N O2P 1 21/n 111.4902; 9.6989; 15.4453
90; 91.189; 90		1720.89Kong, Xianqiang; Liu, Yulong; Lin, Long; Chen, Qianjin; Xu, Bo
Electrochemical synthesis of enaminones via a decarboxylative coupling reaction
Green Chemistry, 2019, 21, 3796
7232950 CIFC22 H21 N3 O4 S2P -112.0153; 12.5845; 15.2028
77.758; 85.3; 72.021		2136.5Zhang, Yu-Zhen; Mo, Zu-Yu; Wang, Heng-Shan; Wen, Xiao-An; Tang, Hai-Tao; Pan, Ying-Ming
Electrochemically enabled chemoselective sulfonylation and hydrazination of indoles
Green Chemistry, 2019, 21, 3807
7232995 CIFC22 H35 Al N2P 1 21/n 115.4104; 18.6531; 15.4547
90; 96.747; 90		4411.7Liu, Wenqing; Ding, Yi; Jin, Da; Shen, Qiumiao; Yan, Ben; Ma, Xiaoli; Yang, Zhi
Organic aluminum hydrides catalyze nitrile hydroboration
Green Chemistry, 2019, 21, 3812
7232996 CIFC31 H47 Al N2C 1 2 127.963; 16.952; 12.983
90; 107.713; 90		5862.6Liu, Wenqing; Ding, Yi; Jin, Da; Shen, Qiumiao; Yan, Ben; Ma, Xiaoli; Yang, Zhi
Organic aluminum hydrides catalyze nitrile hydroboration
Green Chemistry, 2019, 21, 3812
7233001 CIFC19 H15 N O2P 1 21 13.9198; 25.3323; 7.1542
90; 97.305; 90		704.63Liang, Yaofeng; Teng, Lili; Wang, Yajun; He, Qiuxing; Cao, Hua
A visible-light-induced intermolecular [3 + 2] alkenylation‒cyclization strategy: metal-free construction of pyrrolo[2,1,5-cd]indolizine rings
Green Chemistry, 2019, 21, 4025
7233071 CIFC10 H9 N3 OP b c a10.5391; 9.15; 19.861
90; 90; 90		1915.3Zhang, Dongsheng; Fan, Yingzhu; Yan, Zhongliang; Nie, Yi; Xiong, Xingquan; Gao, Lizhu
Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles
Green Chemistry, 2019, 21, 4211
7233234 CIFC19 H16 N2 O2P 1 21/c 117.9538; 13.0669; 21.0038
90; 96.8682; 90		4892.14Kong, Yanyan; Li, Yabo; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
An electrochemical off‒on method for pyrimidin-2(1H)-one synthesis via three-component cyclization
Green Chemistry, 2019, 21, 4495
7233311 CIFC23 H16 O3 SeP 1 21/c 17.9403; 17.1323; 14.1867
90; 103.315; 90		1878Hua, Jiawei; Fang, Zheng; Xu, Jia; Bian, Mixue; Liu, ChengKou; He, Wei; Zhu, Ning; Yang, Zhao; Guo, Kai
Electrochemical oxidative cyclization of activated alkynes with diselenides or disulfides: access to functionalized coumarins or quinolinones
Green Chemistry, 2019, 21, 4706
7233375 CIFC15 H13 N3 O4P 4/n :219.766; 19.766; 7.7429
90; 90; 90		3025.1Shi, Taoda; Teng, Shenghan; Wei, Yajie; Guo, Xin; Hu, Wenhao
Synthesis of spiro[2,3-dihydrofuran-3,3′-oxindole] derivatives via a multi-component cascade reaction of α-diazo esters, water, isatins and malononitrile/ethyl cyanoacetate
Green Chemistry, 2019, 21, 4936
7233403 CIFC19 H14 F3 N OP 1 21/c 19.5181; 21.4287; 7.5942
90; 111.404; 90		1442.09Gao, Cai; Li, Bin; Geng, Xueyang; Zhou, Qianting; Zhang, Xinying; Fan, Xuesen
Two birds with one stone: one-pot simultaneous synthesis of 2,2,2-trifluoroethylphenanthridines and benzochromenones featuring the utilization of the byproduct of Togni's reagent
Green Chemistry, 2019, 21, 5113
7233413 CIFC42 H38 Cl2 O4 P2 Pd SP 1 21/n 116.7161; 13.9805; 19.1927
90; 105.636; 90		4319.34Yang, Da; Liu, Huan; Liu, Lei; Guo, Wen-Di; Lu, Yong; Liu, Ye
Co-catalysis over a tri-functional ligand modified Pd-catalyst for hydroxycarbonylation of terminal alkynes towards α,β-unsaturated carboxylic acids
Green Chemistry, 2019, 21, 5336
7233576 CIFC8 H8 O2P -17.308; 7.452; 7.833
96.059; 108.374; 117.853		341.3Hwang, Kuo Chu; Sagadevan, Arunachalam; Kundu, Pradip
Sustainable Room Temperature Conversion of p-Xylene to Terephthalic Acid using Ozone and UV Irradiation
Green Chemistry, 2019
7233577 CIFC12 H14 O4P 1 21/n 14.206; 15.399; 9.109
90; 92.854; 90		589.2Hwang, Kuo Chu; Sagadevan, Arunachalam; Kundu, Pradip
Sustainable Room Temperature Conversion of p-Xylene to Terephthalic Acid using Ozone and UV Irradiation
Green Chemistry, 2019
7233620 CIFC23 H22 O3P 1 21/n 19.2617; 17.7294; 11.9398
90; 100.901; 90		1925.19Xie, Peizhong; Wo, Xiangyang; Yang, Xiaobo; Cai, Xinying; Li, Shuangshuang; Gao, Cuiqing; Fu, Weishan; Sun, Zuolian; Loh, Teck-Peng
Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds
Green Chemistry, 2019, 21, 5207
7233621 CIFC23 H22 O3P 1 21/n 111.367; 15.8302; 11.4198
90; 114.025; 90		1876.9Xie, Peizhong; Wo, Xiangyang; Yang, Xiaobo; Cai, Xinying; Li, Shuangshuang; Gao, Cuiqing; Fu, Weishan; Sun, Zuolian; Loh, Teck-Peng
Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds
Green Chemistry, 2019, 21, 5207
7233731 CIFC15 H30 O6P 14.8349; 5.364; 16.1843
81.706; 89.469; 86.953		414.75Manhas, Sanjay; Lin, Yu Chen; Wang, Grace; Kyne, Luke T.; Taylor, Mark S.
Boronic acid-promoted site-selective Fischer esterifications of sugar alcohols
Green Chemistry, 2019, 21, 5363
7233764 CIFC31 H24 N2 O4P 1 21/n 118.5772; 6.9751; 19.5651
90; 90.586; 90		2535.1Zhou, Yuanyuan; Chen, Xianxiao; Ling, Xiangxiang; Rao, Weidong
Catalyst- and additive-free Baeyer‒Villiger-type oxidation of α-iodocyclopentenones to α-pyrones: using air as the oxidant
Green Chemistry, 2019, 21, 5611
7234157 CIFC29 H25 N O2P 1 21/c 113.123; 11.404; 16.76
90; 109.759; 90		2361Liao, Jun-Yi; Wu, Qing-Yan; Lu, Xiuqiang; Zou, Ning; Pan, Cheng-Xue; Liang, Cui; SU, Guifa; Mo, Dong-Liang
Copper-Catalyzed Diastereoselective O-Transfer Reaction of N-Vinyl-α,β-Unsaturated Nitrones with Ketenes into γ-Lactones through [5+2] Cycloaddition and N-O Bond Cleavage
Green Chemistry, 2019
7234611 CIFC26 H36 Cl2 Cu N10 OC 1 2/c 127.313; 9.409; 24.649
90; 107.956; 90		6026Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja
Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions
Green Chemistry, 2019
7234612 CIFC23 H31 N9I b a 221.678; 11.7948; 17.695
90; 90; 90		4524.4Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja
Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions
Green Chemistry, 2019
7234613 CIFC18 H31 Cl2 Cu F3 N8 O5 SP 1 21/n 114.918; 11.9455; 16.2476
90; 110.94; 90		2704.1Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja
Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions
Green Chemistry, 2019
7234614 CIFC25 H32 Cl Cu F6 N9 O6 S2P -18.4954; 11.7314; 19.281
100.763; 99.35; 108.877		1734.2Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja
Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions
Green Chemistry, 2019
7234615 CIFC25 H39 Cl2 Cu N9 O2P 1 21/n 18.1817; 15.7088; 24.5591
90; 95.921; 90		3139.6Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja
Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions
Green Chemistry, 2019
7234673 CIFC18 H34 N10 S2P 1 21/c 112.018; 22.054; 9.3
90; 101.617; 90		2414.4de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue
High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts
Green Chemistry, 2019
7234674 CIFC26 H42 N10 O8 S2P 1 21/c 118.132; 11.105; 16.92
90; 95.693; 90		3390.1de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue
High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts
Green Chemistry, 2019
7234675 CIFC13 H21 N5 O4 SP 1 21/c 18.53; 9.831; 22.657
90; 111.574; 90		1766.87de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue
High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts
Green Chemistry, 2019
7234676 CIFC13 H24 N5 O5.5 SP -18.825; 9.764; 12.08
107.075; 100.749; 96.427		962.04de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue
High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts
Green Chemistry, 2019
7234677 CIFC39 H63 N15 O12 S3P 1 21/c 113.495; 16.262; 23.781
90; 99.226; 90		5151.4de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue
High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts
Green Chemistry, 2019
7234745 CIFC23 H17 F3 O3P b c a17.2218; 13.242; 17.2998
90; 90; 90		3945.2Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo
Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process
Green Chemistry, 2019
7234746 CIFC17 H12 F3 N O2P -17.9917; 8.305; 11.875
107.623; 97.098; 91.682		743.55Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo
Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process
Green Chemistry, 2019
7234747 CIFC22 H15 Br N O2I 1 2/a 115.884; 7.23; 32.8613
90; 90.675; 90		3773.6Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo
Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process
Green Chemistry, 2019
7234809 CIFC13 H16 O10P 1 21/c 114.095; 9.4714; 11.1536
90; 102.69; 90		1452.6Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing
Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction
Green Chemistry, 2019
7234810 CIFC9 H8 O9P 21 21 215.709; 12.143; 14.775
90; 90; 90		1024.3Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing
Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction
Green Chemistry, 2019
7234811 CIFC13 H16 O10P b c a10.764; 11.06; 25.394
90; 90; 90		3023Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing
Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction
Green Chemistry, 2019
7234812 CIFC6 H6 O6P 1 21/n 111.6926; 5.2936; 12.0745
90; 118.255; 90		658.31Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing
Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction
Green Chemistry, 2019
7234813 CIFC15 H17 Cl3 O10P 21 21 218.238; 13.923; 17.649
90; 90; 90		2024Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing
Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction
Green Chemistry, 2019
7235236 CIFC23 H19 N OP 1 21/n 112.012; 9.465; 15.801
90; 91.447; 90		1795.9Zhao, Hong-Ping; Liang, Gui-Chao; Nie, Shu-Min; Lu, Xiuqiang; Pan, Cheng-Xue; Zhong, Xin-Xian; Su, Gui-Fa; Mo, Dong-Liang
Metal-free graphene oxide-catalyzed aza-semipinacol rearrangement to prepare 2-(indol-2-yl)phenols and benzofuro[3,2-b]indolines containing quaternary carbon centers
Green Chemistry, 2020, 22, 404-410
7235247 CIFC14 H13 N O2P 1 n 111.241; 5.7323; 17.696
90; 97.712; 90		1130Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu
Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines
Green Chemistry, 2020, 22, 1164-1170
7235248 CIFC18 H15 N O2P 1 21/c 112.2746; 9.2499; 14.751
90; 100.612; 90		1646.17Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu
Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines
Green Chemistry, 2020, 22, 1164-1170
7235249 CIFC13 H13 N O2 SP 1 21/n 114.568; 5.0757; 16.496
90; 102.818; 90		1189.4Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu
Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines
Green Chemistry, 2020, 22, 1164-1170
7235256 CIFC96 H56 Br12 N12 O5P 21 21 218.6559; 15.6308; 16.2787
90; 90; 90		2202.5Gohain, Shivanee Borpatra; Basumatary, Monika; Boruah, Purna K.; Das, Manash R.; Thakur, Ashim Jyoti
Nano Au/Pd-catalysed ‘on-water’ synthesis of C3‒C3′ diaryl-oxindole scaffolds via N2-selective dearomatization of indole
Green Chemistry, 2020, 22, 170-179
7235257 CIFC52 H46 Br2 F6 Ir N4 PC 1 2/c 114.8779; 25.5062; 15.6343
90; 104.511; 90		5743.6Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting
Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations
Green Chemistry, 2020, 22, 136-143
7235258 CIFC40 H38 Br2 Cl0.5 F9 Ir N4 P1.5P 1 2/n 111.3884; 14.5156; 14.8459
90; 105.062; 90		2369.9Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting
Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations
Green Chemistry, 2020, 22, 136-143
7235259 CIFC64 H56 F6 Ir N4 PP -112.1698; 14.9926; 16.2329
78.079; 89.769; 77.466		2826.3Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting
Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations
Green Chemistry, 2020, 22, 136-143
7237090 CIFC19 H16 Br O3 PP 1 21/c 114.87; 8.115; 15.295
90; 106.026; 90		1773.9Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao
Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols
Green Chemistry, 2018, 20, 5111
7237091 CIFC21 H21 O3 PA e a 232.26; 16.224; 7.12
90; 90; 90		3727Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao
Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols
Green Chemistry, 2018, 20, 5111
7237092 CIFC20 H19 O5 PP n a 2112.451; 18.5872; 7.9138
90; 90; 90		1831.48Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao
Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols
Green Chemistry, 2018, 20, 5111
7237093 CIFC19 H16 Br O3 PP b c a11.472; 17.116; 18.24
90; 90; 90		3582Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao
Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols
Green Chemistry, 2018, 20, 5111
7237094 CIFC20 H19 O3 PC 1 2/c 118.086; 11.245; 17.491
90; 98.109; 90		3522Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao
Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols
Green Chemistry, 2018, 20, 5111
7238046 CIFC9 H12 N2 OP 1 21/c 16.4219; 10.741; 13.507
90; 95.887; 90		926.8Kong, Lingbin; Huang, Rong; He, Haodan; Fan, Yunxiang; Lin, Jun; Yan, Shengjiao
Multi-component solvent-free cascade reaction of 2-cyanoacetamides: regioselective synthesis of pyridin-2-ones bearing quaternary centers
Green Chemistry, 2020, 22, 256-264
7238047 CIFC15 H16 N2 OP 1 21/c 17.3319; 11.5409; 16.169
90; 99.147; 90		1350.8Kong, Lingbin; Huang, Rong; He, Haodan; Fan, Yunxiang; Lin, Jun; Yan, Shengjiao
Multi-component solvent-free cascade reaction of 2-cyanoacetamides: regioselective synthesis of pyridin-2-ones bearing quaternary centers
Green Chemistry, 2020, 22, 256-264
7238048 CIFC46 H54 N8 O4P -14.7211; 13.737; 15.384
77.216; 86.717; 85.596		969.3Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.
Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching
Green Chemistry, 2019
7238049 CIFC31 H32 N4 O2P 1 21/c 121.6; 12.9539; 8.945
90; 90.508; 90		2502.8Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.
Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching
Green Chemistry, 2019
7238050 CIFC76 H98 N16 O8P 1 21/c 111.4759; 23.1694; 14.5016
90; 111.004; 90		3599.6Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.
Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching
Green Chemistry, 2019
7239605 CIFC20 H30 Cu2 N8 O14 V5C 1 2/c 122.7662; 12.1453; 24.9282
90; 98.796; 90		6811.6Tian, Hong-Rui; Liu, Yi-Wei; Zhang, Zhong; Liu, Shu-Mei; Dang, Tian-Yi; Li, Xiao-Hui; Sun, Xiu-Wei; Lu, Ying; Liu, Shu-Xia
A multicentre synergistic polyoxometalate-based metal‒organic framework for one-step selective oxidative cleavage of β-O-4 lignin model compounds
Green Chemistry, 2020, 22, 248-255
7239670 CIFC16 H13 N3 O4P -19.0134; 9.0528; 9.6602
70.923; 76.94; 75.474		712.15Saini, Sanjeev; Mayank,; Kaur, Navneet; Singh, Narinder
A cytochrome c-urea functionalized dipeptide conjugate: an efficient HBD framework to synthesize 4H-pyrans via one-pot multicomponent reaction
Green Chemistry, 2020, 22, 956-968
7239713 CIFC23 H20 O4 S SeP 1 21/c 18.486; 15.1787; 16.604
90; 97.43; 90		2120.7Chen, Shihao; Li, Yaping; Wang, Ming; Jiang, Xuefeng
General sulfone construction via sulfur dioxide surrogate control
Green Chemistry, 2020, 22, 322-326
7239714 CIFC11 H10 O2 SP b c a11.2374; 10.3578; 16.9587
90; 90; 90		1973.9Chen, Shihao; Li, Yaping; Wang, Ming; Jiang, Xuefeng
General sulfone construction via sulfur dioxide surrogate control
Green Chemistry, 2020, 22, 322-326
7239715 CIFC19 H16 F3 N O2P 1 21/c 115.4973; 10.5001; 9.92584
90; 90.3156; 90		1615.14Xu, Zhongnan; Huang, Zhixing; Li, Yueheng; Kuniyil, Rositha; Zhang, Chao; Ackermann, Lutz; Ruan, Zhixiong
Catalyst-free, direct electrochemical synthesis of annulated medium-sized lactams through C‒C bond cleavage
Green Chemistry, 2020, 22, 1099-1104
7239716 CIFC21 H22 N2 O2I 41/a :220.3378; 20.3378; 18.3367
90; 90; 90		7584.5Li, Jianxiao; Yu, Junsheng; Xiong, Wenfang; Tang, Hao; Hu, Miao; Wu, Wanqing; Jiang, Huanfeng
A palladium-catalyzed oxidative aminocarbonylation reaction of alkynone O-methyloximes with amines and CO in PEG-400
Green Chemistry, 2020, 22, 465-470
7239730 CIFC17 H24 N4 O7P 1 21/c 17.1396; 15.021; 17.652
90; 96.825; 90		1879.7Appiagyei, Benjamin; Bhatia, Souful; Keeney, Gabriela L.; Dolmetsch, Troy; Jackson, James E.
Electroactivated alkylation of amines with alcohols via both direct and indirect borrowing hydrogen mechanisms
Green Chemistry, 2020, 22, 860-869
7239750 CIFC40 H58 O4 Si2P 1 21/c 110.51; 11.377; 32.058
90; 93.828; 90		3824.7Ohno, Shohei; Avena, Ramon Francisco; Aoyama, Hiroshi; Fujioka, Hiromichi; Arisawa, Mitsuhiro
Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals
Green Chemistry, 2020, 22, 1220-1228
7239751 CIFC30 H25 N O2 S SeP 1 21/n 16.2629; 18.353; 22.063
90; 92.471; 90		2533.6Dutta, Shubham; Prabagar, B.; Vanjari, Rajeshwer; Gandon, Vincent; Sahoo, Akhila K.
An unconventional sulfur-to-selenium-to-carbon radical transfer: chemo-and regioselective cyclization of yne-ynamides
Green Chemistry, 2020, 22, 1113-1118
7239763 CIFC27 H25 Cl O4P 1 21/c 18.4738; 24.4748; 11.8708
90; 91.051; 90		2461.53Zhang, Zhipeng; Yu, Yang; Huang, Fei; Yi, Xiangyan; Xu, Yao; He, Yide; Baell, Jonathan B.; Huang, He
Catalytic O‒H bond insertion reactions using surface modified sewage sludge as a catalyst
Green Chemistry, 2020, 22, 1594-1604
7239764 CIFC23 H22 O4P 1 21/c 115.0906; 7.9886; 15.7975
90; 95.544; 90		1895.52Zhang, Zhipeng; Yu, Yang; Huang, Fei; Yi, Xiangyan; Xu, Yao; He, Yide; Baell, Jonathan B.; Huang, He
Catalytic O‒H bond insertion reactions using surface modified sewage sludge as a catalyst
Green Chemistry, 2020, 22, 1594-1604
7239784 CIFC12 H10 Mn N3 O5P -17.594; 8.5623; 13.088
97.266; 95.849; 95.577		834.5Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias
Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights
Green Chemistry, 2020, 22, 913-920
7239785 CIFC11 H9 Br Mn N3 O3P 1 21/n 17.9845; 12.118; 14.112
90; 100.181; 90		1343.9Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias
Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights
Green Chemistry, 2020, 22, 913-920
7239835 CIFC15 H13 F N2 SP -18.6772; 9.0145; 9.9691
110.22; 107.146; 97.596		674.97Wen, Jiangwei; Niu, Cong; Yan, Kelu; Cheng, Xingda; Gong, Ruike; Li, Mengqian; Guo, Yongqiang; Yang, Jianjing; Wang, Hua
Electrochemical-induced regioselective C-3 thiomethylation of imidazopyridines via a three-component cross-coupling strategy
Green Chemistry, 2020, 22, 1129-1133
7239951 CIFC33 H27 N O6P -112.6327; 15.2434; 15.98
102.027; 105.432; 112.595		2566.4Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239952 CIFC17 H17 NP -15.6742; 8.7921; 13.5713
103.259; 95.099; 95.624		651.48Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239953 CIFC16 H14 N2P -110.388; 10.8621; 11.9356
103.368; 111.316; 90.267		1214.77Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard
A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates
Green Chemistry, 2020, 22, 1894-1905
7239961 CIFC9 H5 N O SP 1 21/c 18.398; 7.421; 13.749
90; 99.9; 90		844.1He, Dongdong; Yao, Jiaojiao; Ma, Boling; Wei, Jinghao; Hao, Guangguo; Tuo, Xun; Guo, Shengmei; Fu, Zhengjiang; Cai, Hu
An electrochemical method for deborylative seleno/thiocyanation of arylboronic acids under catalyst- and oxidant-free conditions
Green Chemistry, 2020, 22, 1559-1564
7239973 CIFC15 H13 Cl N2 OP 1 21/c 111.3479; 10.0774; 11.9461
90; 98.694; 90		1350.43Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying
Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination
Green Chemistry, 2020, 22, 1837-1841
7239974 CIFC16 H15 Cl N2 OP 1 21/c 112.8233; 10.2114; 12.0326
90; 116.906; 90		1405Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying
Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination
Green Chemistry, 2020, 22, 1837-1841
7239983 CIFC8 H11 N O3P b c a11.7246; 8.3285; 16.9656
90; 90; 90		1656.66Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239984 CIFC10 H11 N O2P 1 21/m 17.1931; 7.0581; 8.4454
90; 92.515; 90		428.36Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239985 CIFC14 H13 N O5P 21 21 217.1964; 11.9878; 14.751
90; 90; 90		1272.55Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7239986 CIFC60 H84 N4 O24P 1 21/n 124.7484; 10.706; 26.2577
90; 115.723; 90		6267.71Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
Green Chemistry, 2020, 22, 1978-1984
7240053 CIFC20 H19 N O4P 1 21/c 18.4606; 16.9137; 35.129
90; 90.02; 90		5027Zhao, Yong-Long; Tang, Yong-Qin; Fei, Xing-Hai; Yang, Fen-Fen; Cao, Zhuo-Xian; Duan, Dong-Zhu; Zhao, Qing-Jie; Yang, Yuan-Yong; Zhou, Meng; He, Bin
Direct C(sp3)‒H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI
Green Chemistry, 2020, 22, 2354-2358
7240065 CIFC11 H16 B3 N O7P 1 21/c 18.43; 17.184; 9.073
90; 93.26; 90		1312.2Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240066 CIFC27 H34 B3 N O8P -19.549; 11.307; 13.26
100.88; 92.261; 105.79		1346.6Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240067 CIFC19 H32 B3 N O7P -111.314; 11.98; 17.961
72.586; 79.494; 72.755		2207Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.
Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4
Green Chemistry, 2020, 22, 2184-2190
7240089 CIFC36 H28 Cl2 F12 N6 P2 RuP -112.8944; 12.8937; 12.963
82.985; 66.987; 88.659		1968.1Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo
The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst
Green Chemistry, 2020, 22, 2279-2287
7240090 CIFC37 H31 F6 N5 O2 P RuP -111.159; 12.3059; 14.8631
67.875; 68.045; 86.116		1747.3Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo
The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst
Green Chemistry, 2020, 22, 2279-2287
7240091 CIFC43 H34 Cl3 F6 N5 P RuP -113.592; 13.6081; 14.0589
64.306; 73.922; 64.168		2096.6Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo
The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst
Green Chemistry, 2020, 22, 2279-2287
7240126 CIFC84 H90 N12 O6P 43 21 224.951; 24.951; 34.647
90; 90; 90		21570Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei
A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks
Green Chemistry, 2020, 22, 2498-2504
7240127 CIFC124 H144 N16 O8I 1 2 118.197; 18.1795; 23.1831
90; 100.957; 90		7529.4Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei
A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks
Green Chemistry, 2020, 22, 2498-2504
7240128 CIFC62 H80 N8 O8P 43 21 215.7706; 15.7706; 23.9901
90; 90; 90		5966.6Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei
A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks
Green Chemistry, 2020, 22, 2498-2504
7240160 CIFC30 H26 Cl7 N O2P 1 21 110.1043; 12.8257; 12.9176
90; 104.397; 90		1621.5Mandal, Susanta; Chhetri, Karan; Bhuyan, Samuzal; Roy, Biswajit G.
Efficient iron catalyzed ligand-free access to acridines and acridinium ions
Green Chemistry, 2020, 22, 3178-3185
7240161 CIFC27 H22 F N O2P -18.2718; 10.4182; 13.163
113.112; 93.907; 91.575		1039.06Mandal, Susanta; Chhetri, Karan; Bhuyan, Samuzal; Roy, Biswajit G.
Efficient iron catalyzed ligand-free access to acridines and acridinium ions
Green Chemistry, 2020, 22, 3178-3185
7240203 CIFC16.69 H18.62 N8 O0.83 Zn2P b c a15.6052; 15.8374; 18.1718
90; 90; 90		4491.1Thorne, Michael F.; Gómez, María Laura Ríos; Bumstead, Alice M.; Li, Shichun; Bennett, Thomas D.
Mechanochemical synthesis of mixed metal, mixed linker, glass-forming metal–organic frameworks
Green Chemistry, 2020, 22, 2505-2512
7240256 CIFC33 H48 Cl N OP 19.563; 12.5988; 25.0296
81.062; 88.375; 88.956		2977.5Xu, Biping; Shang, Yaping; Jie, Xiaoming; Zhang, Xiaofeng; Kan, Jian; Yedage, Subhash Laxman; Su, Weiping
Synthesis of α-enaminones from cyclic ketones and anilines using oxoammonium salt as an oxygen transfer reagent
Green Chemistry, 2020, 22, 1827-1831
7240266 CIFC22 H23 N O4P 1 21/c 113.2745; 7.8001; 24.2247
90; 129.278; 90		1941.6Gu, Guangmiao; Huang, Mengmeng; Kim, Jung Keun; Zhang, Jianye; Li, Yabo; Wu, Yangjie
Visible-light-induced photocatalyst-free C-3 functionalization of indoles with diethyl bromomalonate
Green Chemistry, 2020, 22, 2543-2548
7240283 CIFC20 H18 I N6 O2P -19.7382; 10.0324; 11.2964
73.551; 87.711; 74.719		1020.3Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli
A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization
Green Chemistry, 2020, 22, 3111-3116
7240284 CIFC22 H20 Cl I N6 O SP -17.6849; 11.331; 14.1776
94.684; 94.245; 106.982		1170.56Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli
A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization
Green Chemistry, 2020, 22, 3111-3116
7240285 CIFC22 H16 I N7P b c a21.618; 7.8792; 23.619
90; 90; 90		4023.1Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli
A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization
Green Chemistry, 2020, 22, 3111-3116
7240286 CIFC20 H15 I N6 OP 1 21/c 18.0435; 11.5711; 27.338
90; 95.054; 90		2534.5Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli
A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization
Green Chemistry, 2020, 22, 3111-3116
7240295 CIFC12 H11 N O3P -14.1648; 10.9613; 12.044
105.854; 90.015; 94.64		527.04Guo, Weiwei; Zhang, Qi; Cao, Yang; Cai, Kaihua; Zhang, Shengyong; Chai, Yonghai
Environmentally benign access to isoindolinones: synthesis, separation and resource recycling
Green Chemistry, 2020, 22, 2873-2878
7240308 CIFC15 H16 Cl N3 O4P -18.802; 9.0045; 10.8415
83.765; 86.631; 72.048		812.31Annes, Sesuraj Babiola; Saritha, Rajendhiran; Subramanian, Saravanan; Shankar, Bhaskaran; Ramesh, Subburethinam
Solvent-free and montmorillonite K10-catalyzed domino reactions for the synthesis of pyrazoles with alkynylester as a dual synthon
Green Chemistry, 2020, 22, 2388-2393
7240309 CIFC12 H12 N2 O2P 1 21/n 15.6602; 19.0351; 10.7528
90; 102.926; 90		1129.18Annes, Sesuraj Babiola; Saritha, Rajendhiran; Subramanian, Saravanan; Shankar, Bhaskaran; Ramesh, Subburethinam
Solvent-free and montmorillonite K10-catalyzed domino reactions for the synthesis of pyrazoles with alkynylester as a dual synthon
Green Chemistry, 2020, 22, 2388-2393
7240310 CIFC13 H14 N2 O SP 21 21 216.7032; 8.5139; 22.447
90; 90; 90		1281.1Gan, Ziyu; Li, Guoqing; Yan, Qiuli; Deng, Weiseng; Jiang, Yuan-Ye; Yang, Daoshan
Visible-light-promoted oxidative desulphurisation: a strategy for the preparation of unsymmetrical ureas from isothiocyanates and amines using molecular oxygen
Green Chemistry, 2020, 22, 2956-2962
7240311 CIFC11 H14 N2 O2P 1 21/c 18.1026; 15.7929; 8.4783
90; 104.183; 90		1051.84Gan, Ziyu; Li, Guoqing; Yan, Qiuli; Deng, Weiseng; Jiang, Yuan-Ye; Yang, Daoshan
Visible-light-promoted oxidative desulphurisation: a strategy for the preparation of unsymmetrical ureas from isothiocyanates and amines using molecular oxygen
Green Chemistry, 2020, 22, 2956-2962
7240411 CIFC20 H14 N2P 1 21/n 16.0178; 10.934; 22.509
90; 95.035; 90		1475.3Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature
Green Chemistry, 2020, 22, 4426-4432
7240412 CIFC14 H10 O2P 32 2 18.3601; 8.3601; 13.3968
90; 90; 120		810.88Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature
Green Chemistry, 2020, 22, 4426-4432
7240413 CIFC21 H15 N OP b c a19.711; 7.4314; 20.568
90; 90; 90		3012.8Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature
Green Chemistry, 2020, 22, 4426-4432
7240414 CIFC17 H14 O4C 1 2/c 123.502; 3.9358; 15.1235
90; 105.082; 90		1350.72Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature
Green Chemistry, 2020, 22, 4426-4432
7240415 CIFC23 H22 N2 O2 SP -19.3322; 10.0321; 11.8425
95.845; 105.956; 109.513		981.56Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu
Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature
Green Chemistry, 2020, 22, 4426-4432
7240416 CIFC11 H9 F O2P 1 21/c 18.2958; 7.8128; 14.5059
90; 98.757; 90		929.22Zhang, Zhipeng; Yu, Yang; Xie, Yuxing; Hughes, Timothy; Xu, Jun; Huang, Fei; Huang, He
Catalytic C‒C coupling of diazo compounds with arylboronic acids: using surface modified sewage sludge as catalyst
Green Chemistry, 2020, 22, 4165-4173
7240443 CIFC11 H11 N O4 SP n a 2138.544; 5.1102; 11.6487
90; 90; 90		2294.4Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander
Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity
Green Chemistry, 2020, 22, 2459-2467
7240444 CIFC11 H11 N O5P c a 2120.486; 3.9298; 13.6374
90; 90; 90		1097.89Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander
Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity
Green Chemistry, 2020, 22, 2459-2467
7240445 CIFC19 H23 N3 O3P 1 21/c 111.864; 11.162; 13.889
90; 99.31; 90		1815Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander
Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity
Green Chemistry, 2020, 22, 2459-2467
7240446 CIFC11 H9 N O4C 1 2/c 120.522; 3.8101; 26.193
90; 102.39; 90		2000.4Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander
Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity
Green Chemistry, 2020, 22, 2459-2467
7240449 CIFC35 H35 N O5P -19.3207; 10.8786; 14.8658
95.037; 96.282; 100.049		1466.5Ma, Xiao-Pan; Nong, Cai-Mei; Liang, Yu-Feng; Xu, Pei-Pei; Guo, Xiu-Yun; Liang, Cui; Pan, Cheng-Xue; Su, Gui-Fa; Mo, Dong-Liang
An Yb(OTf)3 and visible light relay catalyzed [3 + 2] cycloaddition/[3,3]-rearrangement/[4 + 2] cycloaddition in one pot to prepare oxazonine-fused endoperoxides
Green Chemistry, 2020, 22, 3827-3834
7240489 CIFC4 N O10 ScP 62 2 29.0093; 9.0093; 11.2503
90; 90; 120		790.82Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240490 CIFC6 H10 Na3 O18 ScI 1 2/a 117.851; 11.0413; 18.2806
90; 104.189; 90		3493.2Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240491 CIFC7 H12 K3.5 O20 ScC 1 2/c 115.8839; 11.4558; 22.7314
90; 92.19; 90		4133.2Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240492 CIFC4 N O9 YbP 1 2/n 19.0427; 6.09117; 7.8999
90; 90.182; 90		435.129Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240493 CIFC6 Eu K3 O15P -18.4883; 9.3894; 9.7552
98.255; 91.154; 96.544		763.89Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240494 CIFC6 H6 Gd K3 O15P -18.4795; 9.3708; 9.7323
98.377; 91.097; 96.629		759.45Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240495 CIFC3 Lu O9P -19.5867; 6.64358; 6.25859
98.1966; 99.4509; 75.113		377.889Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240496 CIFC6 H8 K3 O16 ScC 1 2/c 111.4151; 12.6781; 11.4093
90; 111.9; 90		1532.02Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav
Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium
Green Chemistry, 2020, 22, 4364-4375
7240578 CIFC96 H80 O28 P4 V10P 1 21/n 112.2892; 20.1324; 18.9867
90; 102.411; 90		4587.7Li, Chifeng; Mizuno, Noritaka; Murata, Kei; Ishii, Kazuyuki; Suenobu, Tomoyoshi; Yamaguchi, Kazuya; Suzuki, Kosuke
Selectivity switch in the aerobic oxygenation of sulfides photocatalysed by visible-light-responsive decavanadate
Green Chemistry, 2020, 22, 3896-3905
7240659 CIFC20 H34 O6P 1 21/n 17.8705; 10.1489; 23.9418
90; 93.881; 90		1908Bonjour, Olivier; Liblikas, Ilme; Pehk, Tõnis; Khai-Nghi, Truong; Rissanen, Kari; Vares, Lauri; Jannasch, Patric
Rigid biobased polycarbonates with good processability based on a spirocyclic diol derived from citric acid
Green Chemistry, 2020, 22, 3940-3951
7240671 CIFC22 H19 N O3 SP 1 21/n 19.15686; 13.9511; 14.2096
90; 101.125; 90		1781.14Wang, Ze-Shu; Chen, Yang-Bo; Wang, Kun; Xu, Zhou; Ye, Long-Wu
One-pot synthesis of 2-hydroxymethylindoles via photoredox-catalyzed ketyl‒ynamide coupling/1,3-allylic alcohol transposition
Green Chemistry, 2020, 22, 4483-4488
7240672 CIFC69 H56 Cu F6 N2 O3 P3C 1 c 125.4166; 16.5833; 14.6422
90; 105.981; 90		5933Forero-Cortés, Paola A.; Marx, Maximilian; Moustakas, Nikolaos G.; Brunner, Fabian; Housecroft, Catherine E.; Constable, Edwin C.; Junge, Henrik; Beller, Matthias; Strunk, Jennifer
Transferring photocatalytic CO2 reduction mediated by Cu(N^N)(P^P)+ complexes from organic solvents into ionic liquid media
Green Chemistry, 2020, 22, 4541-4549
7240682 CIFC33 H33 Cl N2 O4P 1 21/c 110.3143; 13.9869; 20.0442
90; 99.155; 90		2854.8Lei, Jie; Li, Yong; Xu, Jia; Tang, Dian-Yong; Shao, Jing-Wei; Li, Hong-yu; Chen, Zhong-Zhu; Xu, Zhi-Gang
An acid-catalyzed 1,4-addition isocyanide-based multicomponent reaction in neat water
Green Chemistry, 2020, 22, 3716-3720
7240708 CIFC27 H26 I O3.5 SP -19.783; 12.3051; 12.3219
62.429; 66.999; 79.648		1210.3Zhang, Tian-Shu; Hao, Wen-Juan; Wang, Rong; Wang, Shi-Chao; Tu, Shu-Jiang; Jiang, Bo
Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes
Green Chemistry, 2020, 22, 4259-4269
7240736 CIFC16 H14 O3P 1 21/c 113.6722; 21.2561; 8.9159
90; 95.877; 90		2577.5Akhtar, Muhammad Saeed; Thombal, Raju S.; Inductivo Tamargo, Ramuel John; Yang, Won-Guen; Kim, Sung Hong; Lee, Yong Rok
Eco-friendly organocatalyst- and reagent-controlled selective construction of diverse and multifunctionalized 2-hydroxybenzophenone frameworks for potent UV-A/B filters by cascade benzannulation
Green Chemistry, 2020, 22, 4523-4531
7240737 CIFC19 H14 O3P 1 21/c 17.3618; 7.4104; 25.4612
90; 95.2808; 90		1383.11Akhtar, Muhammad Saeed; Thombal, Raju S.; Inductivo Tamargo, Ramuel John; Yang, Won-Guen; Kim, Sung Hong; Lee, Yong Rok
Eco-friendly organocatalyst- and reagent-controlled selective construction of diverse and multifunctionalized 2-hydroxybenzophenone frameworks for potent UV-A/B filters by cascade benzannulation
Green Chemistry, 2020, 22, 4523-4531
7240755 CIFC18 H20 N2 O2P 1 21/c 111.8025; 6.6554; 19.9584
90; 90.687; 90		1567.63Liu, Yi; Meng, Ya-Nan; Huang, Xun-Jie; Qin, Fu-Hua; Wu, Dapeng; Shao, Qianjun; Guo, Zhiyong; Li, Qiang; Wei, Wen-Ting
Radical cyclization of 1,6-dienes with azobis(alkylcarbonitriles) on water under additive-free conditions
Green Chemistry, 2020, 22, 4593-4596
7240759 CIFC40 H84 Si5I 41/a :216.882; 16.882; 16.323
90; 90; 90		4652.1Herz, Fabian A. D.; Nobis, Matthias; Wendel, Daniel; Pahl, Philipp; Altmann, Philipp J.; Tillmann, Jan; Weidner, Richard; Inoue, Shigeyoshi; Rieger, Bernhard
Application of multifunctional silylenes and siliranes as universal crosslinkers for metal-free curing of silicones
Green Chemistry, 2020, 22, 4489-4497
7240768 CIFC17 H15 F3 N3 O S2P -17.145; 10.3161; 12.2769
101.41; 103.927; 93.498		855.32Li, Xiao-Yun; Liu, Yan; Chen, Xiao-Lan; Lu, Xin-Yuan; Liang, Xing-Xing; Zhu, Shan-Shan; Wei, Chuan-Wan; Qu, Ling-Bo; Yu, Bing
6π-Electrocyclization in water: microwave-assisted synthesis of polyheterocyclic-fused quinoline-2-thiones
Green Chemistry, 2020, 22, 4445-4449
7240806 CIFC6 H3 Co N18P 1 21/c 18.616; 8.888; 17.715
90; 96.499; 90		1347.9Wu, Shuo; Li, Min; Yang, Zhengyi; Xia, Zhengqiang; Liu, Bin; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Gao, Shengli; Lu, Jack Y.
Synthesis and characterization of a new energetic metal‒organic framework for use in potential propellant compositions
Green Chemistry, 2020, 22, 5050-5058
7240807 CIFC22 H35 Cl2 N4 O2.5P 43 21 211.2054; 11.2054; 83.0175
90; 90; 90		10423.8Esteve, Ferran; Altava, Belén; Burguete, M. Isabel; Bolte, Michael; García-Verdugo, Eduardo; Luis, Santiago V.
Pseudopeptidic macrocycles as cooperative minimalistic synzyme systems for the remarkable activation and conversion of CO2 in the presence of the chloride anion
Green Chemistry, 2020, 22, 4697-4705
7240814 CIFC7 H5 F2 N OP 1 21/c 14.352; 10.59; 14.532
90; 98.269; 90		662.8Jiang, Xiaolin; Huang, Zijun; Makha, Mohamed; Du, Chen-Xia; Zhao, Dongmei; Wang, Fang; Li, Yuehui
Tetracoordinate borates as catalysts for reductive formylation of amines with carbon dioxide
Green Chemistry, 2020, 22, 5317-5324
7240863 CIFC26 H18 F12 N2 O4 Se2P 1 21/n 110.4389; 21.5791; 14.669
90; 109.581; 90		3113.27Lei, Yingjie; Yang, Ju; Wang, Yawen; Wang, Hongying; Zhan, Yue; Jiang, Xianxing; Xu, Zhaoqing
Metal-free fluoroalkylfluoroalkylselenolation of unactivated alkenes: incorporation of two photoinduced processes
Green Chemistry, 2020, 22, 4878-4883
7240906 CIFC71 H76 O15 Ti4P 1 21/n 118.731; 16.579; 21.872
90; 100.786; 90		6672Li, Ning; Liu, Jing-Jing; Sun, Jia-Wei; Dong, Bao-Xia; Dong, Long-Zhang; Yao, Su-Juan; Xin, Zhifeng; Li, Shun-Li; Lan, Ya-Qian
Calix[8]arene-constructed stable polyoxo-titanium clusters for efficient CO2 photoreduction
Green Chemistry, 2020, 22, 5325-5332
7240907 CIFC68 H76 O24 Ti7C m c 2124.63; 19.1; 14.9
90; 90; 90		7009Li, Ning; Liu, Jing-Jing; Sun, Jia-Wei; Dong, Bao-Xia; Dong, Long-Zhang; Yao, Su-Juan; Xin, Zhifeng; Li, Shun-Li; Lan, Ya-Qian
Calix[8]arene-constructed stable polyoxo-titanium clusters for efficient CO2 photoreduction
Green Chemistry, 2020, 22, 5325-5332
7240916 CIFC24 H21 N O2P 1 21/c 19.1551; 11.365; 18.1448
90; 94.124; 90		1883.04Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng
Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis
Green Chemistry, 2020, 22, 5497-5503
7240917 CIFC24 H18 F3 N O2P 1 21/n 114.3957; 9.8622; 14.7627
90; 100.8; 90		2058.78Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng
Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis
Green Chemistry, 2020, 22, 5497-5503
7240918 CIFC24 H19 N O2P 1 21/c 110.6923; 11.1552; 15.2475
90; 97.358; 90		1803.67Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng
Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis
Green Chemistry, 2020, 22, 5497-5503
7240919 CIFC22 H25 N O2P 1 21/n 112.9186; 11.6675; 13.3986
90; 109.007; 90		1909.4Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng
Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis
Green Chemistry, 2020, 22, 5497-5503
7240920 CIFC21 H15 N OP 1 21/c 114.5135; 11.7884; 18.8103
90; 108.09; 90		3059.2Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng
Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis
Green Chemistry, 2020, 22, 5497-5503
7240963 CIFC15 H13 F3 N2 O2 SP 1 21/c 112.0991; 12.9247; 10.4969
90; 100.474; 90		1614.13Nadiveedhi, Maheshwara Reddy; Cirandur, Suresh Reddy; Akondi, Srirama Murthy
Visible-light-promoted photocatalyst- and additive-free intermolecular trifluoromethyl-thio(seleno)cyanation of alkenes
Green Chemistry, 2020, 22, 5589-5593
7241038 CIFC18 H30 Au Cl2 PP -18.6346; 11.4963; 11.874
65.995; 87.948; 71.81		1017.27Ingner, Fredric J. L.; Giustra, Zachary X.; Novosedlik, Sebastian; Orthaber, Andreas; Gates, Paul J.; Dyrager, Christine; Pilarski, Lukasz T.
Mechanochemical synthesis of (hetero)aryl Au(i) complexes
Green Chemistry, 2020, 22, 5648-5655
7241039 CIFC17 H29 Au Cl F N PP 1 21/n 18.6986; 18.586; 12.1084
90; 90.975; 90		1957.3Ingner, Fredric J. L.; Giustra, Zachary X.; Novosedlik, Sebastian; Orthaber, Andreas; Gates, Paul J.; Dyrager, Christine; Pilarski, Lukasz T.
Mechanochemical synthesis of (hetero)aryl Au(i) complexes
Green Chemistry, 2020, 22, 5648-5655
7241086 CIFC13 H13 N OP -15.923; 8.454; 10.773
78.722; 76.248; 86.236		513.8Bi, Hong-Yan; Li, Cheng-Jing; Wei, Cui; Liang, Cui; Mo, Dong-Liang
Copper-catalyzed tri- or tetrafunctionalization of alkenylboronic acids to prepare tetrahydrocarbazol-1-ones and indolo[2,3-a]carbazoles
Green Chemistry, 2020, 22, 5815-5821
7241087 CIFC44 H36 Ir2 N8 Na2 O23 S4P -110.3801; 12.7791; 22.1745
92.814; 92.689; 104.376		2840.6Ainembabazi, Diana; Wang, Kai; Finn, Matthew; Ridenour, James; Voutchkova-Kostal, Adelina
Efficient transfer hydrogenation of carbonate salts from glycerol using water-soluble iridium N-heterocyclic carbene catalysts
Green Chemistry, 2020, 22, 6093-6104
7241129 CIFC21 H18 N2 O SP 1 21/n 111.37; 10.2878; 14.5801
90; 97.519; 90		1690.8Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming
Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade
Green Chemistry, 2020, 22, 6334-6339
7241130 CIFC22.75 H22 N3 O1.75 SP -14.9241; 14.209; 15.299
90.853; 96.934; 99.1		1048.6Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming
Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade
Green Chemistry, 2020, 22, 6334-6339
7241131 CIFC25 H20 N2 SP 21 21 215.6915; 12.7636; 26.8264
90; 90; 90		1948.78Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming
Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade
Green Chemistry, 2020, 22, 6334-6339
7241146 CIFC54 H52 F4 N4 O12P 18.5574; 9.8938; 14.8351
91.403; 93.658; 97.92		1240.8Babij, Nicholas R.; Choy, Nakyen; Cismesia, Megan A.; Couling, David J.; Hough, Nicole M.; Johnson, Peter L.; Klosin, Jerzy; Li, Xiaoyong; Lu, Yu; McCusker, Elizabeth O.; Meyer, Kevin G.; Renga, James M.; Rogers, Richard B.; Stockman, Kenneth E.; Webb, Nicola J.; Whiteker, Gregory T.; Zhu, Yuanming
Design and synthesis of florylpicoxamid, a fungicide derived from renewable raw materials
Green Chemistry, 2020, 22, 6047-6054
7241147 CIFC24 H36 Cl F2 N O4P 21 21 218.3081; 11.7497; 26.4644
90; 90; 90		2583.39Babij, Nicholas R.; Choy, Nakyen; Cismesia, Megan A.; Couling, David J.; Hough, Nicole M.; Johnson, Peter L.; Klosin, Jerzy; Li, Xiaoyong; Lu, Yu; McCusker, Elizabeth O.; Meyer, Kevin G.; Renga, James M.; Rogers, Richard B.; Stockman, Kenneth E.; Webb, Nicola J.; Whiteker, Gregory T.; Zhu, Yuanming
Design and synthesis of florylpicoxamid, a fungicide derived from renewable raw materials
Green Chemistry, 2020, 22, 6047-6054
7241185 CIFC19 H15 Cl F N O8P 1 21/n 18.1097; 14.367; 16.622
90; 98.194; 90		1916.9Chen, Li; Huang, Rong; Li, Kun; Yun, Xing-Han; Yang, Chang-Long; Yan, Sheng-Jiao
An environmentally benign cascade reaction of chromone-3-carboxaldehydes with ethyl 2-(pyridine-2-yl)acetate derivatives for highly site-selective synthesis of quinolizines and quinolizinium salts in water
Green Chemistry, 2020, 22, 6943-6953
7241224 CIFC21 H17 N O2P 21 21 219.61101; 10.7261; 15.5952
90; 90; 90		1607.69Zhu, Lixiang; Ren, Xiaoyu; Du, Juan; Wu, Jia-Hong; Tan, Jian-Ping; Che, Jixing; Pan, Jianke; Wang, Tianli
A transition-metal-free multicomponent reaction towards constructing chiral 2H-1,4-benzoxazine scaffolds
Green Chemistry, 2020, 22, 7506-7512
7241225 CIFC23 H19 N O2P 21 21 218.4921; 13.5753; 15.0981
90; 90; 90		1740.55Zhu, Lixiang; Ren, Xiaoyu; Du, Juan; Wu, Jia-Hong; Tan, Jian-Ping; Che, Jixing; Pan, Jianke; Wang, Tianli
A transition-metal-free multicomponent reaction towards constructing chiral 2H-1,4-benzoxazine scaffolds
Green Chemistry, 2020, 22, 7506-7512
7241226 CIFC44 H48 O20P 1 21 18.352; 5.7066; 22.623
90; 91.45; 90		1077.9Wang, Pei-Long; Shen, Hui-Zhi; Cheng, Hui-Hui; Gao, Hui; Li, Pin-Hua
Electrochemical esterification reaction of alkynes with diols via cleavage of carbon‒carbon triple bonds without catalyst and oxidant
Green Chemistry, 2020, 22, 6783-6791
7241227 CIFC22 H21 N O4 SP 1 21/n 18.7517; 11.7055; 19.7505
90; 101.925; 90		1979.64Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241228 CIFC23 H25 Cl2 N O5 SP 1 21/c 113.9122; 12.1203; 14.5292
90; 103.724; 90		2380Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241229 CIFC24 H25 Cl2 N O4 SP -110.7314; 10.99; 12.275
71.712; 69.196; 68.46		1230.5Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241230 CIFC22 H21 N O6 SP b c a9.5153; 17.8775; 24.2427
90; 90; 90		4123.9Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241231 CIFC16 H19 N O2 SP 1 21/c 112.239; 19.008; 20.975
90; 100.52; 90		4798Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241232 CIFC22 H19 N O3 SP 1 21/c 112.0121; 9.9422; 15.9636
90; 99.105; 90		1882.5Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241233 CIFC21 H19 N O4 SC 1 2/c 111.9374; 18.7941; 16.6525
90; 95.525; 90		3718.68Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241234 CIFC19 H23 N O4 SP -19.0842; 11.168; 11.3556
108.185; 106.055; 109.685		932Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241235 CIFC20 H23 N O4 SP -19.489; 10.341; 12.078
75.859; 82.328; 69.425		1074.5Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241236 CIFC19 H17 N O2 SP 21 21 214.9632; 9.9037; 33.603
90; 90; 90		1651.72Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai
Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study
Green Chemistry, 2020, 22, 6798-6803
7241295 CIFC18 H16 O6P -19.1121; 9.4374; 10.647
95.85; 104.17; 111.98		803.9Hu, Deqing; Yang, Lu; Wan, Jie-Ping
Biaryl and atropisomeric biaryl aldehyde synthesis by one-step, metal-free benzannulation of aryl enals and propiolates
Green Chemistry, 2020, 22, 6773-6777
7241315 CIFC24 H20 Cu2 N8 O6 V2P -111.6196; 12.0604; 12.2162
63.651; 75.955; 61.239		1343.91Tian, Hong-Rui; Zhang, Zhong; Liu, Shu-Mei; Dang, Tian-Yi; Li, Zhuo; Lu, Ying; Liu, Shu-Xia
A highly stable polyoxovanadate-based Cu(i)‒MOF for the carboxylative cyclization of CO2 with propargylic alcohols at room temperature
Green Chemistry, 2020, 22, 7513-7520
7241334 CIFC13 H11 B F4 N2 OP n a 2110.3539; 10.9951; 11.059
90; 90; 90		1258.98Gao, Wenjing; Wan, Yameng; Zhang, Zhiguo; Wu, Hao; Liu, Tongxin; Zhang, Guisheng
The Hofmann reaction involving annulation of o-(pyridin-2-yl)aryl amides selectively and rapidly leads to potential photocatalytically active 6H-pyrido[1,2-c]quinazolin-6-one derivatives
Green Chemistry, 2020, 22, 7955-7961
7241345 CIFC20 H44 Li2 N2 O4P -18.1303; 8.5936; 9.2306
88.833; 68.333; 89.254		599.23Yang, Hongzhi; Zeng, Tianying; Xi, Shuang; Hu, Shengkun; Wu, Yunfei; Tang, Yefeng
Photoinduced, strain-promoted cycloadditions of trans-cycloheptenones and azides
Green Chemistry, 2020, 22, 7023-7030
7241346 CIFC17 H21 N O2P 1 21/n 113.1208; 7.6644; 15.2725
90; 111.229; 90		1431.63Yang, Hongzhi; Zeng, Tianying; Xi, Shuang; Hu, Shengkun; Wu, Yunfei; Tang, Yefeng
Photoinduced, strain-promoted cycloadditions of trans-cycloheptenones and azides
Green Chemistry, 2020, 22, 7023-7030
7241383 CIFC21 H16 Cl N3 SP -18.4738; 9.6099; 12.106
88.37; 69.823; 84.352		920.81Wang, Guanjie; Wei, Chenlong; Hong, Xianfang; Fu, Zhenqian; Huang, Wei
Sodium pyruvate as a peroxide scavenger in aerobic oxidation under carbene catalysis
Green Chemistry, 2020, 22, 6819-6826
7241409 CIFC16 H20 N2 O2P n m a12.863; 7.173; 16.464
90; 90; 90		1519.1Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing
Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines
Green Chemistry, 2020, 22, 7832-7838
7241410 CIFC22 H28 N2 O2P 42 b c20.029; 20.029; 9.929
90; 90; 90		3983.1Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing
Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines
Green Chemistry, 2020, 22, 7832-7838
7241411 CIFC27 H47 N7 S2P 21 21 2111.9503; 12.9375; 19.6351
90; 90; 90		3035.7Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing
Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines
Green Chemistry, 2020, 22, 7832-7838
7241412 CIFC28 H49 N7 O2P 1 21/c 112.003; 19.823; 16.309
90; 111.59; 90		3608Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing
Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines
Green Chemistry, 2020, 22, 7832-7838
7241413 CIFC62 H115 N14 O9P -112.8442; 17.5019; 18.6407
63.996; 70.836; 69.475		3450.4Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing
Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines
Green Chemistry, 2020, 22, 7832-7838
7241648 CIFC45 H24 Cl N2 O3 ReP n m a7.2328; 19.384; 25.55
90; 90; 90		3582.1Qiu, Li-Qi; Chen, Kai-Hong; Yang, Zhi-Wen; He, Liang-Nian
A rhenium catalyst with bifunctional pyrene groups boosts natural light-driven CO2 reduction
Green Chemistry, 2020, 22, 8614-8622
7241649 CIFC17 H17 N3 O5 SP 1 21/n 17.1176; 16.5556; 14.6211
90; 98.965; 90		1701.85Cioc, Răzvan C.; Lutz, Martin; Pidko, Evgeny A.; Crockatt, Marc; van der Waal, Jan C.; Bruijnincx, Pieter C. A.
Direct Diels‒Alder reactions of furfural derivatives with maleimides
Green Chemistry, 2021, 23, 367-373
7241699 CIFC13 H11 Na O6 SP 1 21/c 116.2484; 11.3597; 8.2456
90; 100.148; 90		1498.14Zhang, Hui; Wang, Ming; Jiang, Xuefeng
Sustainable access to sulfonic acids from halides and thiourea dioxide with air
Green Chemistry, 2020, 22, 8238-8242
7241700 CIFC32 H30 Cl2 N2 O5C 1 2/c 116.8614; 19.0598; 8.8881
90; 103.357; 90		2779.1Zhang, Ming-Zhong; Liu, Long; Gou, Quan; Wang, Qi; Li, Yi; Li, Wan-Ting; Luo, Fei; Yuan, Min; Chen, Tieqiao; He, Wei-Min
Synthesis of hydroxyl-containing oxindoles and 3,4-dihydroquinolin-2-ones through oxone-mediated cascade arylhydroxylation of activated alkenes
Green Chemistry, 2020, 22, 8369-8374
7241884 CIFC10 H7 I N2 O SP 1 21/c 17.7399; 13.3332; 10.8147
90; 95.823; 90		1110.29Lu, Fangling; Zhang, Kan; Yao, Yanxiu; Yin, Ying; Chen, Jiafu; Zhang, Xinwei; Wang, Yin; Lu, Lijun; Gao, Ziwei; Lei, Aiwen
Electrochemical oxidative thiocyanation and amination of enaminones towards the synthesis of multi-substituted alkenes
Green Chemistry, 2021, 23, 763-766
7241885 CIFC9 H12 O5P 1 21/c 110.7742; 7.035; 12.0329
90; 101.619; 90		893.36Kirchhecker, Sarah; Dell'Acqua, Andrea; Angenvoort, Astrid; Spannenberg, Anke; Ito, Kenji; Tin, Sergey; Taden, Andreas; de Vries, Johannes G.
HMF‒glycerol acetals as additives for the debonding of polyurethane adhesives
Green Chemistry, 2021, 23, 957-965
7241886 CIFC20 H11 F5 O5 S4P -17.7476; 18.5104; 23.642
72.297; 85.352; 85.778		3215.1Cai, Song-Zhou; Ge, Danhua; Sun, Li-Wen; Rao, Weidong; Wang, Xin; Shen, Zhi-Liang; Chu, Xue-Qiang
Three-component heteroannulation for tetrasubstituted furan construction enabled by successive defluorination and dual sulfonylation relay
Green Chemistry, 2021, 23, 935-941
7241887 CIFC15 H16 F2 N2 OP 1 21/c 19.8524; 12.043; 12.4397
90; 112.982; 90		1358.85Niu, Kaikai; Hao, Yanke; Song, Lingyun; Liu, Yuxiu; Wang, Qingmin
Electro-oxidative C‒H alkylation of quinoxalin-2(1H)-ones with organoboron compounds
Green Chemistry, 2021, 23, 302-306
7241930 CIFC41 H49 Cl6 Cu N2P 1 21/c 110.624; 23.227; 17.226
90; 97.34; 90		4215.9Cervantes-Reyes, Alejandro; Farshadfar, Kaveh; Rudolph, Matthias; Rominger, Frank; Schaub, Thomas; Ariafard, Alireza; Hashmi, A. Stephen K.
Copper-catalysed synthesis of α-alkylidene cyclic carbonates from propargylic alcohols and CO2
Green Chemistry, 2021, 23, 889-897
7241931 CIFC18 H16 O4C 1 2/c 133.614; 6.0727; 14.459
90; 93.236; 90		2946.8Cervantes-Reyes, Alejandro; Farshadfar, Kaveh; Rudolph, Matthias; Rominger, Frank; Schaub, Thomas; Ariafard, Alireza; Hashmi, A. Stephen K.
Copper-catalysed synthesis of α-alkylidene cyclic carbonates from propargylic alcohols and CO2
Green Chemistry, 2021, 23, 889-897
7242054 CIFC24 H19 N O3P -19.099; 12.6543; 17.4953
69.761; 87.356; 78.198		1849.4Kong, Yanyan; Kim, Jung Keun; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie
An oxidant- and catalyst-free electrooxidative cross-coupling approach to 3-tetrahydroisoquinoline substituted coumarins
Green Chemistry, 2021, 23, 1274-1279
7242055 CIFC24 H20 N2 O2P 1 21/n 18.6666; 23.4805; 9.5853
90; 102.461; 90		1904.62Kong, Yanyan; Kim, Jung Keun; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie
An oxidant- and catalyst-free electrooxidative cross-coupling approach to 3-tetrahydroisoquinoline substituted coumarins
Green Chemistry, 2021, 23, 1274-1279
7242064 CIFC24 H27 Br3 N6R 3 m :H16.647; 16.647; 7.749
90; 90; 120		1859.7Ma, Shuai; Cui, Jing-Wang; Rao, Cai-Hui; Jia, Meng-Ze; Chen, Yun-Rui; Zhang, Jie
Boosting activity of molecular oxygen by pyridinium-based photocatalysts for metal-free alcohol oxidation
Green Chemistry, 2021, 23, 1337-1343
7242065 CIFC12 H6 F N O3P -14.7015; 7.5668; 13.7164
100.964; 91.553; 102.63		466.26Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242066 CIFC14 H12 F N O4 SP -16.182; 7.343; 15.4344
97.694; 93.323; 97.422		686.49Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242067 CIFC13 H9 N O4C 1 2/c 128.1572; 11.7989; 6.8522
90; 107.682; 90		2168.92Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242068 CIFC13 H8 F N O3P -17.7844; 7.8633; 9.9225
71.839; 82.19; 67.855		534.42Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242069 CIFC14 H11 N O3P 1 21/c 14.6906; 14.7537; 16.5416
90; 97.187; 90		1135.75Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242070 CIFC13 H8 Br N O3P 1 21/c 14.70525; 13.1424; 18.3356
90; 96.343; 90		1126.9Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242071 CIFC13 H9 N O3P -17.6718; 7.8925; 10.0037
71.388; 80.879; 66.502		526.1Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242072 CIFC14 H11 N O5P 1 21/n 114.4314; 4.4645; 18.5538
90; 90.744; 90		1195.3Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu
Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water
Green Chemistry, 2021, 23, 1136-1139
7242118 CIFC36 H46 Mn3 N10 O16P 1 21/n 113.2958; 10.0194; 16.6456
90; 106.404; 90		2127.2Asghar, Aisha; Iqbal, Naseem; Noor, Tayyaba; Kariuki, Benson M.; Kidwell, Luke; Easun, Timothy L.
Efficient electrochemical synthesis of a manganese-based metal‒organic framework for H2 and CO2 uptake
Green Chemistry, 2021, 23, 1220-1227
7242119 CIFC11 H11 Mn N O5P 1 21/c 113.4484; 10.1799; 17.656
90; 90.271; 90		2417.14Asghar, Aisha; Iqbal, Naseem; Noor, Tayyaba; Kariuki, Benson M.; Kidwell, Luke; Easun, Timothy L.
Efficient electrochemical synthesis of a manganese-based metal‒organic framework for H2 and CO2 uptake
Green Chemistry, 2021, 23, 1220-1227
7242163 CIFC15 H22 N2 O4P b c a9.448; 11.423; 30.49
90; 90; 90		3291Morita, Shunya; Yoshimura, Tomoyuki; Matsuo, Jun-ichi
Catalytic intermolecular aldol reactions of transient amide enolates in domino Michael/aldol reactions of nitroalkanes, acrylamides, and aldehydes
Green Chemistry, 2021, 23, 1160-1164
7242201 CIFC21 H32 Cl N O2 RuP 1 21/n 114.7118; 9.3818; 14.7793
90; 91.266; 90		2039.39Phearman, Alexander S.; Moore, Jewelianna M.; Bhagwandin, Dayanni D.; Goldberg, Jonathan M.; Heinekey, D. Michael; Goldberg, Karen I.
(Hexamethylbenzene)Ru catalysts for the Aldehyde-Water Shift reaction
Green Chemistry, 2021, 23, 1609-1615
7242202 CIFC25 H36 B2 O4P 1 21/n 16.5462; 27.28; 14.4106
90; 90.549; 90		2573.3Zhang, Yahui; Zhao, Xiangyu; Bi, Ce; Lu, Wenqi; Song, Mengyuan; Wang, Dongdong; Qing, Guangyan
Selective electrocatalytic hydroboration of aryl alkenes
Green Chemistry, 2021, 23, 1691-1699
7242218 CIFC10 H11 Cl F3 N O2P -15.6416; 5.8788; 18.0049
95.374; 95.693; 96.475		587.08Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242219 CIFC12 H16 Cl N O2P 1 21/c 16.099; 7.7041; 25.2722
90; 94.075; 90		1184.47Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242220 CIFC10 H13 N O2P 1 21/c 15.7769; 7.6286; 21.5338
90; 96.167; 90		943.5Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242221 CIFC8 H8 N2 O2C 1 2/c 118.9356; 3.81317; 21.672
90; 101.702; 90		1532.29Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242222 CIFC12 H14 Cl N O2P -15.7548; 10.5744; 10.5916
110.243; 102.912; 100.879		563.94Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242223 CIFC11 H13 N O2P 1 21/c 19.0379; 10.044; 11.0835
90; 99.123; 90		993.4Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242224 CIFC7 H12 O6P -17.6334; 8.7609; 14.2366
81.705; 88.677; 73.562		903.45Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.
A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Green Chemistry, 2021, 23, 2336-2351
7242249 CIFC20 H19 N5 OP 1 21/n 16.7011; 9.1071; 28.951
90; 92.176; 90		1765.5Akulov, Alexey A.; Varaksin, Mikhail V.; Tsmokalyuk, Anton N.; Charushin, Valery N.; Chupakhin, Oleg N.
Blue-light-promoted radical C‒H azolation of cyclic nitrones enabled by Selectfluor®
Green Chemistry, 2021, 23, 2049-2057
7242297 CIFC7 H6 Cl N O2C 1 2/c 115.5231; 3.8267; 23.9744
90; 93.432; 90		1421.58Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng
Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids
Green Chemistry, 2021, 23, 2986-2991
7242298 CIFC17 H26 N2 O4P 21 21 217.9048; 11.2276; 19.3205
90; 90; 90		1714.73Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng
Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids
Green Chemistry, 2021, 23, 2986-2991
7242323 CIFC19 H18 N2 O2P 1 21/n 110.6894; 10.6948; 13.7194
90; 91.046; 90		1568.2Xu, Jun; Huang, Lin; He, Lei; Ni, Zhigang; Shen, Jiabin; Li, Xiaoling; Chen, Kaixian; Li, Wanmei; Zhang, Pengfei
A combination of heterogeneous catalysis and photocatalysis for the olefination of quinoxalin-2(1H)-ones with ketones in water: a green and efficient route to (Z)-enaminones
Green Chemistry, 2021, 23, 2123-2129
7242329 CIFC17 H18 O3 SP 1 21/n 115.40316; 7.20606; 15.43887
90; 116.871; 90		1528.62Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao
Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides
Green Chemistry, 2021, 23, 2420-2426
7242330 CIFC16 H14 O2 SP 21 21 218.5976; 10.8141; 15.2294
90; 90; 90		1416Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao
Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides
Green Chemistry, 2021, 23, 2420-2426
7242405 CIFC36 H32 Br2 N6 O4 S2P b c a15.138; 10.099; 22.516
90; 90; 90		3442.2Jiang, Shuai; Cao, Wen-Bin; Li, Hai-Yan; Xu, Xiao-Ping; Ji, Shun-Jun
Convenient synthesis of spiroindolenines from tryptamine-derived isocyanides and organic azides by cobalt catalysis in pure water
Green Chemistry, 2021, 23, 2619-2623
7242512 CIFC25 H22 Cl N O4 SP -112.3598; 12.8606; 15.4574
81.976; 75.455; 70.669		2239.9Liu, Chengkou; Lin, Yang; Cai, Chen; Yuan, Chengcheng; Fang, Zheng; Guo, Kai
Continuous-flow electro-oxidative coupling of sulfides with activated methylene compounds leading to sulfur ylides
Green Chemistry, 2021, 23, 2956-2961
7242526 CIFC38 H49 Bi O8P -112.5878; 12.6544; 13.1098
106.319; 105.558; 107.521		1763.44Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242527 CIFC54 H96 Bi2 Li4 N2 O20P 1 21/n 113.3571; 14.0806; 18.593
90; 95.0534; 90		3483.3Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242528 CIFC58 H102 Bi2 Li4 N4 O20P 1 21/n 116.1427; 13.2582; 18.584
90; 110.087; 90		3735.47Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242529 CIFC64 H116 Bi2 Li4 N2 O20P 1 21/n 114.3713; 17.9791; 15.3608
90; 92.508; 90		3965.17Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242530 CIFC106 H119 Bi2 Li4 N3 O20P 1 21/c 124.0601; 18.8535; 22.3563
90; 92.989; 90		10127.4Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242531 CIFC104 H116 Bi2 Li4 N2 O20P 1 21/c 124.7978; 16.4792; 24.6871
90; 103.624; 90		9804.5Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian
Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds
Green Chemistry, 2021, 23, 2747-2755
7242532 CIFC24 H18 F3 N3 O2P 4/n :224.437; 24.437; 7.3579
90; 90; 90		4393.9Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin
Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations
Green Chemistry, 2021, 23, 2944-2949
7242533 CIFC23 H19 N3 O SP 1 21/n 18.754; 18.911; 11.952
90; 104.763; 90		1913.3Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin
Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations
Green Chemistry, 2021, 23, 2944-2949
7242534 CIFC23 H14 N3 O SP -113.632; 13.694; 22.48
98.57; 95.81; 92.8		4120Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin
Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations
Green Chemistry, 2021, 23, 2944-2949
7242571 CIFC32 H46 Cu2 Ge N12 O48 W12C 1 m 112.5419; 22.4521; 11.6246
90; 109.951; 90		3076.9Shen, Qingbo; Gómez-García, Carlos J.; Sun, Wenlong; Lai, Xiaoyong; Pang, Haijun; Ma, Huiyuan
Improving the photocatalytic H2 evolution activity of Keggin polyoxometalates anchoring copper-azole complexes
Green Chemistry, 2021, 23, 3104-3114
7242572 CIFC36 H32 Cu5 Ge N30 O44 W12P -112.203; 13.495; 14.262
104.873; 111.48; 105.681		1931.3Shen, Qingbo; Gómez-García, Carlos J.; Sun, Wenlong; Lai, Xiaoyong; Pang, Haijun; Ma, Huiyuan
Improving the photocatalytic H2 evolution activity of Keggin polyoxometalates anchoring copper-azole complexes
Green Chemistry, 2021, 23, 3104-3114
7242614 CIFC18 H13 N OP -17.1154; 9.6387; 10.8333
93.473; 98.583; 109.416		688.03Li, Wenjing; Li, Shun; Luo, Lihua; Ge, Yicen; Xu, Jiaqi; Zheng, Xueli; Yuan, Maolin; Li, Ruixiang; Chen, Hua; Fu, Haiyan
Visible-light-initiated catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes containing pyridyl motif under ambient conditions
Green Chemistry, 2021, 23, 3649-3655
7242618 CIFC26 H21 Cl4 N2 O4P 1 21/c 117.7729; 19.2994; 7.3793
90; 95.972; 90		2517.4Liu, Xu; Liu, Chang; Cheng, Xu
Ring-contraction of hantzsch esters and their derivatives to pyrroles via electrochemical extrusion of ethyl acetate out of aromatic rings
Green Chemistry, 2021, 23, 3468-3473
7242639 CIFC22 H20 Cl6 N4 Ni O2I 1 2/a 115.0319; 11.2984; 16.0579
90; 107.022; 90		2607.74Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242640 CIFC42 H64 N6 Ni O2I 1 2/a 112.7952; 18.3813; 18.9751
90; 109.067; 90		4217.96Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242641 CIFC30 H40 N6 Ni O2C 1 2/c 112.0724; 10.2682; 24.5315
90; 102.057; 90		2973.89Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242642 CIFC30 H24 N6 Ni O2P 1 21/n 17.7855; 14.7244; 22.189
90; 98.032; 90		2518.72Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242643 CIFC26 H34 N6 Ni O3P 1 21/n 112.8828; 18.5259; 22.3137
90; 98.798; 90		5262.85Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242644 CIFC36 H36 N6 Ni O2P 1 21/n 111.1131; 10.3896; 14.6952
90; 109.634; 90		1598.07Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin
Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
Green Chemistry, 2021, 23, 3365-3373
7242664 CIFC12 H11 N4 O1.5C 1 2/c 118.0472; 7.044; 16.9293
90; 96.096; 90		2139.96Niu, Kaikai; Ding, Ling; Zhou, Pan; Hao, Yanke; Liu, Yuxiu; Song, Hongjian; Wang, Qingmin
Electro-oxidative C‒H azolation of quinoxalin-2(1H)-ones
Green Chemistry, 2021, 23, 3246-3249
7242675 CIFC13 H12 O3 S2P -15.5069; 13.3044; 35.296
84.488; 88.558; 89.975		2573.2Pampana, V. Kishore Kumar; Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Das, Deb Kumar; Lin, Chun-Cheng; Hwu, Jih Ru; Hwang, Kuo Chu
Oxy-sulfonylation of terminal alkynes via C‒S coupling enabled by copper photoredox catalysis
Green Chemistry, 2021, 23, 3569-3574
7242676 CIFC14 H11 Cl O3 SP b c a13.3682; 7.2588; 26.6061
90; 90; 90		2581.78Pampana, V. Kishore Kumar; Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Das, Deb Kumar; Lin, Chun-Cheng; Hwu, Jih Ru; Hwang, Kuo Chu
Oxy-sulfonylation of terminal alkynes via C‒S coupling enabled by copper photoredox catalysis
Green Chemistry, 2021, 23, 3569-3574
7242866 CIFC32 H36 Ca3 O24C 1 2/c 123.4643; 11.4906; 16.2903
90; 122.775; 90		3692.95Pan, Yanxiong; Li, Hui; Lenertz, Mary; Han, Yulun; Ugrinov, Angel; Kilin, Dmitri; Chen, Bingcan; Yang, Zhongyu
One-pot synthesis of enzyme@metal‒organic material (MOM) biocomposites for enzyme biocatalysis
Green Chemistry, 2021, 23, 4466-4476
7242945 CIFC17 H8 F6 N2 O3C 1 2/c 131.1491; 7.2268; 13.9772
90; 92.13; 90		3144.2Brahmachari, Goutam; Karmakar, Indrajit; Karmakar, Pintu
Catalyst- and solvent-free Csp2‒H functionalization of 4-hydroxycoumarins via C-3 dehydrogenative aza-coupling under ball-milling
Green Chemistry, 2021, 23, 4762-4770
7243033 CIFC20 H21 N O2P -110.249; 11.657; 14.822
104.005; 92.306; 109.243		1608.2Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok
Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors
Green Chemistry, 2021, 23, 5113-5119
7243034 CIFC18 H17 N OP 1 21/n 15.8897; 19.96; 11.987
90; 103.094; 90		1372.5Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok
Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors
Green Chemistry, 2021, 23, 5113-5119
7243035 CIFC23 H21 NP b c n11.1052; 16.1802; 9.2208
90; 90; 90		1656.8Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok
Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors
Green Chemistry, 2021, 23, 5113-5119
7243062 CIFC20 H14 N2 O SP 1 21/n 13.8618; 33.708; 11.8039
90; 98.934; 90		1517.9Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu
Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes
Green Chemistry, 2021, 23, 5024-5030
7243063 CIFC21 H18 N2 O2 SP 1 21/c 19.3403; 17.0872; 10.882
90; 106.207; 90		1667.74Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu
Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes
Green Chemistry, 2021, 23, 5024-5030
7243064 CIFC22 H15 Cl N2 O2P 1 21/n 114.02; 8.187; 15.972
90; 104.692; 90		1773.4Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu
Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes
Green Chemistry, 2021, 23, 5024-5030
7243065 CIFC16 H11 N O4P b c a18.517; 6.9182; 38.2895
90; 90; 90		4905.05Bashir, Muhammad Adnan; Zhang, Yulong; Yu, Huaibin; Wang, Bofei; Zhao, Weining; Zhong, Fangrui
Bimetallic copper/cobalt-cocatalyzed double aerobic phenol oxidation/cyclization toward π-extended benzofuro[2,3-b]indoles as electron donors for electroluminescence
Green Chemistry, 2021, 23, 5031-5036
7243079 CIFC42 H36 N4P 1 21/n 115.6432; 13.2799; 17.6411
90; 114.078; 90		3345.9Luo, Zhenli; Pan, Yixiao; Yao, Zhen; Yang, Ji; Zhang, Xin; Liu, Xintong; Xu, Lijin; Fan, Qing-Hua
BF3·Et2O as a metal-free catalyst for direct reductive amination of aldehydes with amines using formic acid as a reductant
Green Chemistry, 2021, 23, 5205-5211
7243088 CIFC48 H55 N4 O2P -111.9297; 12.924; 13.666
75.136; 78.644; 89.902		1994Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai
Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage
Green Chemistry, 2021, 23, 5535-5541
7243089 CIFC25 H34 N2 O2R -3 :H34.3408; 34.3408; 10.4316
90; 90; 120		10653.7Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai
Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage
Green Chemistry, 2021, 23, 5535-5541
7243090 CIFC21 H25 Cl N2 OP 1 21/c 115.3242; 13.8242; 9.0303
90; 104.165; 90		1854.86Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai
Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage
Green Chemistry, 2021, 23, 5535-5541
7243091 CIFB5 H12 N O12A e a 211.3246; 11.0147; 9.1513
90; 90; 90		1141.51Kusy, Rafał; Grela, Karol
Ligand-free (Z)-selective transfer semihydrogenation of alkynes catalyzed by in situ generated oxidizable copper nanoparticles
Green Chemistry, 2021, 23, 5494-5502
7243119 CIFC16 H15 I O2 SP 21 21 215.4771; 9.0324; 31.6646
90; 90; 90		1566.49Lin, Li; Yang, Zhonglie; Liu, Jianchen; Wang, Jingxia; Zheng, Jiale; Li, Jun-Long; Zhang, Xiaobin; Liu, Xiang-Wei; Jiang, Hezhong; Li, Jiahong
Visible-light-induced surfactant-promoted sulfonylation of alkenes and alkynes with sulfonyl chloride by the formation of an EDA-complex with NaI in water at room temperature
Green Chemistry, 2021, 23, 5467-5473
7243124 CIFC17 H14 O2 SP 1 21/c 111.6106; 16.0508; 7.5624
90; 104.79; 90		1362.63Klöpfer, Viktor; Eckl, Robert; Floß, Johannes; Roth, Philippe M. C.; Reiser, Oliver; Barham, Joshua P.
Catalyst-free, scalable heterocyclic flow photocyclopropanation
Green Chemistry, 2021, 23, 6366-6372
7243270 CIFC20 H17 Br2 N3P 1 21/n 114.62006; 5.80584; 22.6165
90; 104.199; 90		1861.08Yang, Jingya; Song, Menghui; Zhou, Hongyan; Qi, Yanfang; Ma, Ben; Wang, Xi-Cun
Visible-light-promoted decarboxylative addition cyclization of N-aryl glycines and azobenzenes to access 1,2,4-triazolidines
Green Chemistry, 2021, 23, 5806-5811
7243271 CIFC20 H17 Br2 N3P 1 21/n 114.62006; 5.80584; 22.6165
90; 104.199; 90		1861.08Yang, Jingya; Song, Menghui; Zhou, Hongyan; Qi, Yanfang; Ma, Ben; Wang, Xi-Cun
Visible-light-promoted decarboxylative addition cyclization of N-aryl glycines and azobenzenes to access 1,2,4-triazolidines
Green Chemistry, 2021, 23, 5806-5811
7243278 CIFC22 H17 F3 O3 S2P -18.0894; 8.6805; 16.3072
80.083; 79.077; 79.493		1094.2Qin, Long-Zhou; Yuan, Xin; Liu, Jie; Wu, Meng-Yu; Sun, Qi; Duan, Xiu; Zhang, Xin-Peng; Qiu, Jiang-Kai; Guo, Kai
Continuous-flow processes for the S-alkynylation of cysteine-containing peptides and thioglycosides under catalyst-free, oxidant-free and mild conditions
Green Chemistry, 2021, 23, 6598-6603
7243303 CIFC18 H18 N2 O3P -18.4879; 9.8238; 10.6092
110.924; 95.681; 108.558		760.4Han, Zhi-Peng; Xu, Meng-Meng; Zhang, Rui-Ying; Xu, Xiao-Ping; Ji, Shun-Jun
Rh(iii)-Catalyzed C(sp2)‒H functionalization/cyclization cascade of N-carboxamide indole and iodonium reagents for access to indoloquinazolinone derivatives
Green Chemistry, 2021, 23, 6337-6340
7243507 CIFC27 H26 P4 PdP -18.4671; 10.5451; 14.4131
88.379; 80.098; 73.608		1215.92Xia, Shu-Mei; Yang, Zhi-Wen; Yao, Xiang-Yang; Chen, Kai-Hong; Qiu, Li-Qi; He, Liang-Nian
The synergistic copper/ppm Pd-catalyzed hydrocarboxylation of alkynes with formic acid as a CO surrogate as well as a hydrogen source: an alternative indirect utilization of CO2
Green Chemistry, 2021, 23, 8089-8095
7243508 CIFC17 H10 F6 O2P 1 21/c 15.5094; 15.212; 18.2863
90; 96.429; 90		1522.92Xia, Shu-Mei; Yang, Zhi-Wen; Yao, Xiang-Yang; Chen, Kai-Hong; Qiu, Li-Qi; He, Liang-Nian
The synergistic copper/ppm Pd-catalyzed hydrocarboxylation of alkynes with formic acid as a CO surrogate as well as a hydrogen source: an alternative indirect utilization of CO2
Green Chemistry, 2021, 23, 8089-8095
7243522 CIFC26 H47 N O2 SP 1 21/n 17.5329; 10.6912; 34.1
90; 95.908; 90		2731.7Bisz, Elwira; Koston, Martina; Szostak, Michal
N-Butylpyrrolidone (NBP) as a non-toxic substitute for NMP in iron-catalyzed C(sp2)‒C(sp3) cross-coupling of aryl chlorides
Green Chemistry, 2021
7243545 CIFC21 H16 Cl N3 O3 SP -18.3414; 10.8615; 11.6407
69.332; 87.543; 76.539		958.77Kumar, Navaneet; Bhadoria, Deepak; Kumar, Atul
Visible-light-promoted three-component cycloaddition reaction: synthesis of 4-functionalized 1,5-disubstituted 1,2,3-triazoles
Green Chemistry, 2021, 23, 7987-7995
7243613 CIFC19 H17 F8 N5 O3C 1 2 111.1446; 6.5924; 29.135
90; 93.968; 90		2135.4Ning, Yongquan; Wang, Hongwei; Sivaguru, Paramasivam; Li, Shuang; Zanoni, Giuseppe; Nolan, Steven P.; Bi, Xihe
Defluorinative [4 + 1] annulation of perfluoroalkyl N-mesylhydrazones with primary amines provides 5-fluoroalkyl 1,2,3-triazoles
Green Chemistry, 2021, 23, 7976-7981
7243618 CIFC19 H11 F2 NC 1 c 13.8635; 26.708; 12.5375
90; 90.609; 90		1293.63Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang
Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations
Green Chemistry, 2021, 23, 7950-7955
7243619 CIFC23 H21 NP b c n11.0913; 16.1163; 9.1839
90; 90; 90		1641.6Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang
Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations
Green Chemistry, 2021, 23, 7950-7955
7243620 CIFC19 H11 Cl2 NP -17.1916; 8.2658; 13.5299
87.021; 75.797; 68.795		726.3Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang
Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations
Green Chemistry, 2021, 23, 7950-7955
7243621 CIFC21 H17 N O2P 1 21/c 112.6441; 17.5664; 15.456
90; 114.037; 90		3135.26Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang
Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations
Green Chemistry, 2021, 23, 7950-7955
7243648 CIFC18 H12 Cl2 N2 OP 1 21/c 114.8126; 11.5893; 18.701
90; 91.746; 90		3208.9Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas
Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides
Green Chemistry, 2021
7243649 CIFC18 H12 F5 N3 OP b c a12.8826; 9.2515; 28.4963
90; 90; 90		3396.3Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas
Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides
Green Chemistry, 2021
7243650 CIFC18 H12 Cl2 F3 N3 OP 1 21/c 111.8929; 18.0476; 8.6239
90; 110.092; 90		1738.37Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas
Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides
Green Chemistry, 2021
7243651 CIFC21 H23 N3P 1 21/n 115.4459; 7.45856; 16.2431
90; 118.081; 90		1650.99Wang, Lin-Xuan; Qiu, Bin; An, Xiao-De; Dong, Pei-Zhen; Liu, Rui-Bin; Xiao, Jian
Organocatalytic cascade aldimine condensation/[1,6]-hydride transfer/Mannich-type cyclization: sustainable access to indole-2,3-fused diazocanes
Green Chemistry, 2021, 23, 8181-8186
7243704 CIFC21 H19 N3 O SP 21 21 217.2246; 11.8631; 20.815
90; 90; 90		1784Duan, Xiu; Sun, Qi; Yuan, Xin; Qin, Long-Zhou; Zhang, Xin-Peng; Liu, Jie; Wu, Meng-Yu; Zhu, Shan-Shan; Ma, Can-Liang; Qiu, Jiang-Kai; Guo, Kai
Photoinduced remote heteroaryl migration accompanied by cyanoalkylacylation in continuous flow
Green Chemistry, 2021, 23, 8916-8921
7243738 CIFC15 H13 F N2 O3P 1 21/c 112.35; 13.16; 8.567
90; 93; 90		1390Luo, Mu-Jia; Ouyang, Xuan-Hui; Zhu, Yan-Ping; Li, Yang; Li, Jin-Heng
Metal-free electrochemical [3 + 2] heteroannulation of anilines with pyridines enabled by dual C–H radical aminations
Green Chemistry, 2021, 23, 9024-9029
7243739 CIFC18 H48 B Cu3 K3 N24 O66 W12R -3 :H35.1668; 35.1668; 20.227
90; 90; 120		21663.5Chang, Shenzhen; Chen, Yanhong; An, Haiyan; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui
Polyoxometalate-based supramolecular porous frameworks with dual-active centers towards highly efficient synthesis of functionalized p-benzoquinones
Green Chemistry, 2021, 23, 8591-8603
7243740 CIFC18 H67 Cu3 K3 N24 O76 Si W12P -315.57; 15.57; 10.337
90; 90; 120		2170.2Chang, Shenzhen; Chen, Yanhong; An, Haiyan; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui
Polyoxometalate-based supramolecular porous frameworks with dual-active centers towards highly efficient synthesis of functionalized p-benzoquinones
Green Chemistry, 2021, 23, 8591-8603
7243782 CIFC21 H18 N O3 PP 1 21/n 19.52643; 14.88162; 12.71774
90; 90.7242; 90		1802.83Zhu, Yuan-Yuan; Zhang, Tao; Zhou, Linlin; Yang, Shang-Dong
Concise synthesis of N-phosphorylated amides through three-component reactions
Green Chemistry, 2021, 23, 9417-9421
7243783 CIFC26 H22 N O2 PP 1 21/c 115.6285; 9.3057; 14.6152
90; 95.164; 90		2116.92Zhu, Yuan-Yuan; Zhang, Tao; Zhou, Linlin; Yang, Shang-Dong
Concise synthesis of N-phosphorylated amides through three-component reactions
Green Chemistry, 2021, 23, 9417-9421
7243784 CIFC22 H18 N2P 1 21/c 19.87; 20.34; 8.95
90; 108.57; 90		1703Chen, Wei-Li; Li, Kun; Liao, Wei-Cong; Liang, Wang-Fu; Qiu, Pei-Wen; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
An iron(iii)-catalyzed dehydrogenative cross-coupling reaction of indoles with benzylamines to prepare 3-aminoindole derivatives
Green Chemistry, 2021, 23, 9610-9616
7243785 CIFC20 H14 N2P 1 21/n 17.9106; 10.4113; 18.0346
90; 98.689; 90		1468.28Chen, Wei-Li; Li, Kun; Liao, Wei-Cong; Liang, Wang-Fu; Qiu, Pei-Wen; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
An iron(iii)-catalyzed dehydrogenative cross-coupling reaction of indoles with benzylamines to prepare 3-aminoindole derivatives
Green Chemistry, 2021, 23, 9610-9616
7243842 CIFC23 H22 I N O4P 1 21/c 115.4121; 8.5604; 15.8404
90; 98.365; 90		2067.65Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong
I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines
Green Chemistry, 2021, 23, 9165-9171
7243843 CIFC25 H25 N O4P 1 21/n 19.216; 21.035; 10.878
90; 98.207; 90		2087.2Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong
I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines
Green Chemistry, 2021, 23, 9165-9171
7243844 CIFC23 H22 I N O4P 1 21/c 18.0055; 15.3728; 17.6184
90; 101.571; 90		2124.18Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong
I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines
Green Chemistry, 2021, 23, 9165-9171
7243855 CIFC22 H19 N O3 S SeP 1 21/n 19.4942; 18.7603; 11.8071
90; 112.137; 90		1948Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong
Visible-light-induced intermolecular aminoselenation of alkenes
Green Chemistry, 2021, 23, 9968-9973
7243856 CIFC24 H21 N O3 S SeP 1 21/c 114.6984; 11.124; 14.3493
90; 117.396; 90		2083.1Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong
Visible-light-induced intermolecular aminoselenation of alkenes
Green Chemistry, 2021, 23, 9968-9973
7243857 CIFC24 H29 N O2 S SeP 1 21 19.8465; 23.1935; 10.1145
90; 108.968; 90		2184.5Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong
Visible-light-induced intermolecular aminoselenation of alkenes
Green Chemistry, 2021, 23, 9968-9973
7243874 CIFC10 H13 N O4 S3P n a 2112.8766; 6.3085; 16.9497
90; 90; 90		1376.86Gong, Kai; Zhou, Yilin; Jiang, Xuefeng
From symmetrical tetrasulfides to trisulfide dioxides via photocatalysis
Green Chemistry, 2021, 23, 9865-9869
7243893 CIFC22 H19 Cl F N4 O2 SP 1 21/n 17.17026; 21.7971; 13.6848
90; 98.637; 90		2114.55Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei
Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions
Green Chemistry, 2021, 23, 9571-9576
7243894 CIFC23 H20 Cl N O4 SP 1 21/c 112.7213; 10.0584; 17.2909
90; 106.273; 90		2123.84Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei
Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions
Green Chemistry, 2021, 23, 9571-9576
7243895 CIFC25 H25 N O4 SI 1 2/a 119.8661; 9.09317; 25.7813
90; 109.671; 90		4385.48Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei
Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions
Green Chemistry, 2021, 23, 9571-9576
7243896 CIFC23 H22 N4 O2 SP b c a8.65981; 17.7339; 27.7046
90; 90; 90		4254.66Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei
Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions
Green Chemistry, 2021, 23, 9571-9576
7243979 CIFC16 H19 Cl N2 OP 21 21 217.78804; 10.18953; 19.93923
90; 90; 90		1582.31Fauziev, Ruslan V.; Ivanov, Roman E.; Kuchurov, Ilya V.; Zlotin, Sergei G.
A carbon dioxide-promoted three-component Strecker reaction
Green Chemistry, 2021, 23, 10137-10144
7244045 CIFC18 H13 N3C 1 2/c 110.9525; 12.9657; 20.7069
90; 103.542; 90		2858.77Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie
Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings
Green Chemistry, 2022, 24, 837-845
7244046 CIFC19 H15 Br N2 O2P -18.5331; 9.1322; 11.9513
77.749; 79.907; 65.413		823.62Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie
Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings
Green Chemistry, 2022, 24, 837-845
7244047 CIFC19 H15 N3 OP -17.5372; 7.833; 13.1572
81.704; 86.697; 83.076		762.41Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie
Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings
Green Chemistry, 2022, 24, 837-845
7244048 CIFC12 H14 O3P 1 21/c 117.7291; 7.5614; 8.1518
90; 102.867; 90		1065.36Hu, Deqing; Jiang, Xuefeng
Stepwise benzylic oxygenation via uranyl-photocatalysis
Green Chemistry, 2022, 24, 124-129
7244160 CIFC15 H12 Br N3 O2 SP 21 21 214.8673; 11.348; 27.751
90; 90; 90		1532.8Prasanth, Thumpati; Chakraborti, Gargi; Mandal, Tirtha; Ravichandiran, Velayutham; Dash, Jyotirmayee
Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles
Green Chemistry, 2022, 24, 911-915
7244161 CIFC11 H14 N4 O3 SP 21 21 215.3437; 14.4207; 16.6141
90; 90; 90		1280.3Prasanth, Thumpati; Chakraborti, Gargi; Mandal, Tirtha; Ravichandiran, Velayutham; Dash, Jyotirmayee
Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles
Green Chemistry, 2022, 24, 911-915
7244265 CIFC12 H32 N2 O4 SP 1 21/n 18.7824; 8.8235; 22.0837
90; 95.202; 90		1704.25Turek, Marika; Biczak, Robert; Pawłowska, Barbara; Różycka-Sokołowska, Ewa; Owsianik, Krzysztof; Marciniak, Bernard; Bałczewski, Piotr
The need to change the approach to the safe use of herbicides by developing chiral and environmentally friendly formulations: a series of enantioselective (R)- and (S)-phenylethylammonium chloroacetates
Green Chemistry, 2022, 24, 1693-1703
7244297 CIFC23 H26 O3P 1 21/n 111.353; 13.367; 12.835
90; 100.25; 90		1917Sharapov, Ainur D.; Fatykhov, Ramil F.; Khalymbadzha, Igor A.; Sharutin, Vladimir V.; Santra, Sougata; Zyryanov, Grigory V.; Chupakhin, Oleg N.; Ranu, Brindaban C.
Mechanochemical synthesis of coumarins via Pechmann condensation under solvent-free conditions: an easy access to coumarins and annulated pyrano[2,3-f] and [3,2-f]indoles
Green Chemistry, 2022, 24, 2429-2437
7244371 CIFC26 H32 O4P 1 21/c 110.5639; 21.9239; 10.4796
90; 111.989; 90		2250.54Zhao, Quan-Qing; Rehbein, Julia; Reiser, Oliver
Thermoneutral synthesis of spiro-1,4-cyclohexadienes by visible-light-driven dearomatization of benzylmalonates
Green Chemistry, 2022, 24, 2772-2776
7244381 CIFC13 H17 N O2P n a 2110.1132; 5.7769; 20.392
90; 90; 90		1191.4Liu, Xiao-Dong; Wang, Qiu-An; Zhu, Yan-Ping; Peng, Zhi-Hong; Li, Jin-Heng
Copper-catalyzed aerobic hydroxyamination of alkenes of unsaturated keto oximes in EtOH toward cyclic nitrones
Green Chemistry, 2022, 24, 2476-2482
7244382 CIFC17 H12 N2 OP 1 21/c 112.0038; 12.5724; 8.96
90; 100.273; 90		1330.54Li, Jianxiao; He, Dan; Lin, Zidong; Cen, Liying; Wu, Wanqing; Jiang, Huanfeng
NHC–palladium-catalyzed ionic liquid-accelerated regioselective oxyarylation of alkynes with diaryl ethers
Green Chemistry, 2022, 24, 1983-1988
7244383 CIFC46 H39 N O P2 RuP 1 21/n 112.7847; 19.6339; 14.688
90; 91.112; 90		3686.19Kar, Sayan; Luo, Jie; Rauch, Michael; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Dehydrogenative ester synthesis from enol ethers and water with a ruthenium complex catalyzing two reactions in synergy
Green Chemistry, 2022, 24, 1481-1487
7244424 CIFC336 H312 Cl16 Cu8 N32 O68 S16I 1 2/a 121.1362; 11.2833; 38.192
90; 104.463; 90		8819.6Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha
Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions
Green Chemistry, 2022, 24, 2542-2556
7244425 CIFC21 H22 Cl2 Cu N2 SP 1 21/c 117.0171; 9.2223; 13.3042
90; 96.124; 90		2076Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha
Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions
Green Chemistry, 2022, 24, 2542-2556
7244426 CIFC21 H20 Cl2 Cu N2 SP -18.7543; 8.91433; 14.2328
92.973; 97.234; 113.73		1002.26Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha
Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions
Green Chemistry, 2022, 24, 2542-2556
7244427 CIFC22 H23 Cl5 Cu N2 SP b c a19.10688; 9.75754; 26.37158
90; 90; 90		4916.62Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha
Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions
Green Chemistry, 2022, 24, 2542-2556
7244428 CIFC43 H48 Cl2 Cu N4 O9 S2P 1 21/c 115.4634; 16.5496; 18.8584
90; 111.195; 90		4499.65Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha
Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions
Green Chemistry, 2022, 24, 2542-2556
7244481 CIFC14 H10 O6P 1 21/c 113.5207; 11.759; 7.7352
90; 97.6; 90		1219.02Gan, Shaoyan; Yin, Jingru; Yu, Zhiyou; Song, Lijuan; Shi, Lei
A one-pot and two-stage Baeyer–Villiger reaction using 2,2′-diperoxyphenic acid under biomolecule-compatible conditions
Green Chemistry, 2022, 24, 2232-2239
7244482 CIFC20 H19 N O2 SC 1 2/c 126.979; 9.2286; 14.3392
90; 102.602; 90		3484.1He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao
Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations
Green Chemistry, 2022, 24, 2483-2491
7244483 CIFC30 H31 N O3P 21 21 218.224; 14.043; 21.164
90; 90; 90		2444He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao
Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations
Green Chemistry, 2022, 24, 2483-2491
7244484 CIFC26 H29 N O3P 1 21 18.0026; 15.666; 8.8626
90; 93.268; 90		1109.3He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao
Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations
Green Chemistry, 2022, 24, 2483-2491
7244523 CIFC26 H25 N3 O6P b c a12.6825; 14.325; 26.5675
90; 90; 90		4826.7Maiti, Debajit; Das, Ranajit; Prabakar, Tejas; Sen, Subhabrata
Blue LED induced solvent-free multicomponent reactions among aryl diazoacetates, pyridine derivatives and maleimides: direct eco-friendly synthesis of densely functionalized itaconimides
Green Chemistry, 2022, 24, 3001-3008
7244542 CIFC15 H20 O4P b c a16.3085; 7.9252; 21.384
90; 90; 90		2763.84Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.
Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2
Green Chemistry, 2022, 24, 2535-2541
7244543 CIFC16 H20 O5 SP 1 21/n 113.9329; 6.1434; 19.2618
90; 96.736; 90		1637.34Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.
Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2
Green Chemistry, 2022, 24, 2535-2541
7244544 CIFC16 H20 O6P 1 21 110.8206; 6.2424; 12.0066
90; 109.921; 90		762.48Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.
Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2
Green Chemistry, 2022, 24, 2535-2541
7244545 CIFC15 H20 O3 SP c a 2121.6035; 7.9904; 16.8357
90; 90; 90		2906.19Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.
Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2
Green Chemistry, 2022, 24, 2535-2541
7244580 CIFC15 H12 N2 OP 1 21/n 116.392; 7.1332; 20.1084
90; 95.662; 90		2339.75Ren, Jie; Pi, Chao; Cui, Xiuling; Wu, Yangjie
Divergent C(sp2)–H arylation of heterocycles via organic photoredox catalysis
Green Chemistry, 2022, 24, 3017-3022
7244581 CIFC15 H12 O3P 1 21/c 18.9535; 14.0575; 9.4542
90; 90.799; 90		1189.83Zhou, Bei; He, Yu-Juan; Tao, Yun-Feng; Liu, Lan-Xiang; Hu, Min; Chang, Zu-Hui; Lei, Hong; Lin, Jun; Lin, Tong; Du, Guan-Ben
Electrocatalytic synthesis of α,α-gem-dihalide ketones from α-mono-halide ketones and unexpected dimer condensation
Green Chemistry, 2022, 24, 2859-2870
7244591 CIFC19 H19 N O2P -17.9813; 11.4019; 17.8408
92.73; 90.852; 108.525		1536.9Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong
Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone
Green Chemistry, 2022, 24, 2919-2926
7244592 CIFC18 H17 N O2P -18.21; 9.4039; 10.1909
111.938; 99.562; 97.455		703.68Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong
Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone
Green Chemistry, 2022, 24, 2919-2926
7244593 CIFC18 H17 N O2P 1 21/n 111.7113; 9.8511; 25.285
90; 97.144; 90		2894.5Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong
Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone
Green Chemistry, 2022, 24, 2919-2926
7244594 CIFC19 H19 N O2P 1 21/n 112.6474; 7.3679; 17.5437
90; 110.655; 90		1529.7Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong
Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone
Green Chemistry, 2022, 24, 2919-2926
7244625 CIFC42 H36 N4 O2 S2P -111.9441; 12.2012; 13.45
76.259; 72.322; 79.906		1802.8Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang
Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions
Green Chemistry, 2022, 24, 3250-3256
7244626 CIFC87 H71 Cl8 N8 O4 S4P 1 21/c 124.764; 12.538; 13.43
90; 91.148; 90		4169.1Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang
Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions
Green Chemistry, 2022, 24, 3250-3256
7244644 CIFC24 H16 O5P 1 21/c 14.998; 19.0007; 18.7257
90; 96.275; 90		1767.6Karmakar, Indrajit; Brahmachari, Goutam
Electrochemical and mechanochemical synthesis of dihydrofuro[3,2-c]chromenones via intramolecular Csp3–H cross-dehydrogenative oxygenation within warfarin frameworks: an efficient and straightforward dual approach
Green Chemistry, 2022, 24, 2825-2838
7244664 CIFC29 H24 O5P -19.1359; 10.8744; 12.1839
83.076; 88.393; 84.055		1195Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang
Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides
Green Chemistry, 2022, 24, 3623-3628
7244665 CIFC23 H20 O6P c c n12.0593; 16.1161; 20.7106
90; 90; 90		4025.1Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang
Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides
Green Chemistry, 2022, 24, 3623-3628
7244666 CIFC28 H24 O5P b c a16.277; 14.959; 19.366
90; 90; 90		4715.4Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang
Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides
Green Chemistry, 2022, 24, 3623-3628
7244667 CIFC28 H24 O5P n a 2120.333; 6.4811; 35.365
90; 90; 90		4660.4Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang
Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides
Green Chemistry, 2022, 24, 3623-3628
7244670 CIFC16 H14 Br N OP 1 21/m 16.3843; 7.1053; 15.724
90; 100.963; 90		700.3Goh, Jeffrey; Ong, Seng Kheong; Tan, Yan Sheng; Loh, Teck-Peng
Catalyst-free C–N bond formation under biocompatible reaction conditions
Green Chemistry, 2022, 24, 3321-3325
7244678 CIFC17 H22 N2 O6C 1 2 120.3983; 8.668; 14.0946
90; 125.998; 90		2016.2Yuan, Zhenbo; Lu, Liushen; Liu, Meiling; Liu, Xuanzhong; Liu, Changmei; Yin, Dejing; Zhang, Yan; Rao, Yijian
Natural product cercosporin as a bioinspired photocatalyst for the synthesis of peptides containing kynurenine via an energy transfer mechanism
Green Chemistry, 2022, 24, 3277-3283
7244714 CIFC15 H13 N O5 SP 1 21/n 16.5529; 7.7286; 27.9324
90; 93.449; 90		1412.07Chikunova, Elena I.; Kukushkin, Vadim Yu.; Dubovtsev, Alexey Yu.
Atom-economic synthesis of β-ketosulfones based on gold-catalyzed highly regioselective hydration of alkynylsulfones
Green Chemistry, 2022, 24, 3314-3320
7244715 CIFC17 H18 Br N O3 SP 1 21/n 111.1683; 9.4026; 16.7625
90; 95.079; 90		1753.34Guo, Sheng-Qiang; Yang, Hui-Qing; Jiang, Yu-Zhen; Wang, Ai-Lian; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Zheng, Haixue; Xu, Peng-Fei
Organophotoredox catalytic four-component radical-polar crossover cascade reactions for the stereoselective synthesis of β-amido sulfones
Green Chemistry, 2022, 24, 3120-3124
7244749 CIFC27 H25 N O3P n a 2124.355; 6.4076; 13.2555
90; 90; 90		2068.6Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian
Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles
Green Chemistry, 2022, 24, 3772-3777
7244750 CIFC25 H20 N2 OP 1 21/n 19.2685; 18.7779; 10.9806
90; 101.311; 90		1874Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian
Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles
Green Chemistry, 2022, 24, 3772-3777
7244751 CIFC23 H17 N O3C 1 2/c 111.9483; 17.9325; 16.013
90; 90.01; 90		3431Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian
Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles
Green Chemistry, 2022, 24, 3772-3777
7244752 CIFC32 H44 O6C 1 2 123.861; 6.1612; 10.0136
90; 95.846; 90		1464.47Freese, Thomas; Fridrich, Bálint; Crespi, Stefano; Lubbe, Anouk S.; Barta, Katalin; Feringa, Ben L.
A molecular motor from lignocellulose
Green Chemistry, 2022, 24, 3689-3696
7244753 CIFC16 H20 O4P -111.0534; 11.594; 12.4153
75.979; 86.095; 73.276		1478.4Freese, Thomas; Fridrich, Bálint; Crespi, Stefano; Lubbe, Anouk S.; Barta, Katalin; Feringa, Ben L.
A molecular motor from lignocellulose
Green Chemistry, 2022, 24, 3689-3696
7244843 CIFC19 H25 N O4P 1 21/c 120.4311; 10.9478; 17.313
90; 109.488; 90		3650.6Tao, Ji-Yu; Wang, Ying-Xue; Zhang, Qing-Hong; Ni, Kun; Zhu, Tong-Hao; Zhao, Kai
Transition-metal-free regioselective and stereoselective C(sp2)–C(sp3) coupling of enamides with ethers or alkanes via photoredox-catalyzed cross-dehydrogenative coupling reactions
Green Chemistry, 2022, 24, 4004-4011
7244844 CIFC24 H17 F3 O3P 1 21/c 112.313; 13.516; 15.514
90; 129.048; 90		2005.1Zhang, Yan; Ma, Chanchan; Cai, Zhenzhi; Struwe, Julia; Chen, Shengjie; Xu, Jinming; Li, Shiyin; Zeng, Wangyu; Ackermann, Lutz
Electrooxidative tricyclic 6–7–6 fused-system domino assembly to allocolchicines by a removable radical strategy
Green Chemistry, 2022, 24, 3697-3703
7244845 CIFC31 H26 O6 SC 1 2/c 134.743; 7.6413; 19.9522
90; 100.316; 90		5211.3Zhang, Yan; Ma, Chanchan; Cai, Zhenzhi; Struwe, Julia; Chen, Shengjie; Xu, Jinming; Li, Shiyin; Zeng, Wangyu; Ackermann, Lutz
Electrooxidative tricyclic 6–7–6 fused-system domino assembly to allocolchicines by a removable radical strategy
Green Chemistry, 2022, 24, 3697-3703
7244855 CIFC17 H19 N OP 21 21 219.7488; 9.7803; 14.7582
90; 90; 90		1407.14Lu, Hui-Rong; Geng, Hui; Ding, Guan-Tian; Huang, Pei-Qiang
Catalyst- and solvent-free aminolysis of the asymmetric derivatives of Evans’ chiral N-acyloxazolidinones: enantioselective synthesis of chiral amides and its applications
Green Chemistry, 2022, 24, 4405-4413
7244869 CIFC16 H14 N2 O2P b c a12.403; 7.2153; 29.2429
90; 90; 90		2616.99Yang, Xinjie; Wang, Hao; Zhang, Yanhua; Su, Weike; Yu, Jingbo
Generation of aryl radicals from in situ activated homolytic scission: driving radical reactions by ball milling
Green Chemistry, 2022, 24, 4557-4565
7244879 CIFC23 H15 N OP 1 21 15.6; 14.98; 9.85
90; 105.15; 90		798Bae, Jaehan; Iqbal, Naeem; Hwang, Ho Seong; Cho, Eun Jin
Sustainable preparation of photoactive indole-fused tetracyclic molecules: a new class of organophotocatalysts
Green Chemistry, 2022, 24, 3985-3992
7244947 CIFC22 H15 F2 N O2 SP 1 21/c 112.72729; 5.5688; 25.1187
90; 92.836; 90		1778.13Ma, Qiang; Li, Ming; Chen, Zhuo; Ni, Shao-Fei; Wright, James S.; Wen, Li-Rong; Zhang, Lin-Bao
An approach for the synthesis of 2-aryl-3-sulfonyl substituted quinolines through an electrochemical cascade annulation pathway
Green Chemistry, 2022, 24, 4425-4431
7244948 CIFC22 H17 N O2 SP 1 21/c 112.5262; 5.4497; 25.0014
90; 93.991; 90		1702.56Ma, Qiang; Li, Ming; Chen, Zhuo; Ni, Shao-Fei; Wright, James S.; Wen, Li-Rong; Zhang, Lin-Bao
An approach for the synthesis of 2-aryl-3-sulfonyl substituted quinolines through an electrochemical cascade annulation pathway
Green Chemistry, 2022, 24, 4425-4431
7244962 CIFC19 H13 F3 N2 O SP 1 21/c 18.5655; 25.6875; 7.7171
90; 99.014; 90		1677Chen, Shiliu; Yan, Qinqin; Fan, Jie; Gao, Yongjun; Yang, Xiulong; Li, Lijun; Liu, Zhongquan; Li, Zejiang
Photoinduced cascade cyclization of alkynes with NH4SCN: access to SCN-containing dibenzazepines or dioxodibenzothiazepines
Green Chemistry, 2022, 24, 4742-4747
7244963 CIFC17 H20 O2 SP b c a5.64; 23.42; 24.97
90; 90; 90		3298Sharma, Deepak; Hussain, Yaseen; Sharma, Manisha; Chauhan, Pankaj
Electrochemical cascade synthesis of α-thio-substituted masked aldehydes
Green Chemistry, 2022, 24, 4783-4788
7244969 CIFC18 H18 O2P -18.858; 9.5201; 9.7104
101.608; 109.911; 92.242		749Zhou, Chunlin; Wang, Xinchao; Yang, Lei; Fu, Lei; Li, Gang
Visible-light-driven regioselective carbocarboxylation of 1,3-dienes with organic halides and CO2
Green Chemistry, 2022, 24, 6100-6107
7244970 CIFC28 H32 O2P 1 21/c 19.5909; 23.7105; 10.2921
90; 106.352; 90		2245.8Zhou, Chunlin; Wang, Xinchao; Yang, Lei; Fu, Lei; Li, Gang
Visible-light-driven regioselective carbocarboxylation of 1,3-dienes with organic halides and CO2
Green Chemistry, 2022, 24, 6100-6107
7244984 CIFC27 H21 N3 O2 SP -19.8859; 9.9067; 23.766
89.459; 81.983; 73.84		2212.7Meng, Xiangtai; Xu, Hehua; Liu, Rui; Zheng, Yu; Huang, Shenlin
Electrochemical triamination of alkynes: controllable synthesis of functionalized indolines and indoles
Green Chemistry, 2022, 24, 4754-4760
7244985 CIFC25 H26 N2 O4 SP -18.5563; 11.6457; 12.4602
75.907; 77.454; 74.029		1142.6Meng, Xiangtai; Xu, Hehua; Liu, Rui; Zheng, Yu; Huang, Shenlin
Electrochemical triamination of alkynes: controllable synthesis of functionalized indolines and indoles
Green Chemistry, 2022, 24, 4754-4760
7245027 CIFC23 H18 N2 OP -18.1325; 9.3708; 11.6459
74.368; 81.158; 83.467		842.08Guan, Wenjing; Ying, Ke; Yuan, Chengcheng; Hang, Jinlin; Liu, Chengkou; Huang, Xiangxing; Fang, Zheng; Guo, Kai
Catalyst- and oxidant-free electrooxidative site-selective [3/4 + 2] annulation to fused polycyclic heteroaromatics
Green Chemistry, 2022, 24, 5191-5196
7245081 CIFC44 H46 N6 O6P 1 21/n 112.921; 22.128; 14.966
90; 113.873; 90		3912.9Sarkar, Rajib; Dam, Binoyargha; Kyndiah, Lenida; Sarkar, Fillip Kumar; Gajurel, Sushmita; Pal, Amarta Kumar
Graphite oxide catalyzed one-pot synthesis of highly functionalized spirodibenzo[1,4]diazepine derivatives in aqueous ethanol medium
Green Chemistry, 2022, 24, 5579-5591
7245085 CIFC12 H13 F N2 O3 SP 1 21/c 18.0016; 9.3863; 18.181
90; 97.48; 90		1353.9Guo, Haijin; Liu, Yunyun; Wen, Chengping; Wan, Jie-Ping
Electrochemical enaminone C–H thiolation/C–N amination cascade for thiazole synthesis and its diastereoselective dearomatization
Green Chemistry, 2022, 24, 5058-5063
7245136 CIFC72 H48 Cl3 F18 N18 P3P 1 21/n 115.627; 21.005; 21.972
90; 78.05; 90		7056Rao, Cai-Hui; Ma, Shuai; Cui, Jing-Wang; Jia, Meng-Ze; Yao, Xin-Rong; Zhang, Jie
A bifunctional small molecular photocatalyst with a redox center and a Lewis acid site for one-pot tandem oxidation–acetalization
Green Chemistry, 2022, 24, 5862-5868
7245189 CIFC18 H19 N O2P b c a8.8424; 12.5877; 26.417
90; 90; 90		2940.4Qu, Zhonghua; Tian, Tong; Tan, Yongbo; Ji, Xiaochen; Deng, Guo-Jun; Huang, Huawen
Redox-neutral ketyl radical coupling/cyclization of carbonyls with N-aryl acrylamides through consecutive photoinduced electron transfer
Green Chemistry, 2022, 24, 7403-7409
7245190 CIFC18 H19 N O2P -17.8246; 9.2051; 10.7849
94.614; 101.272; 99.213		746.96Qu, Zhonghua; Tian, Tong; Tan, Yongbo; Ji, Xiaochen; Deng, Guo-Jun; Huang, Huawen
Redox-neutral ketyl radical coupling/cyclization of carbonyls with N-aryl acrylamides through consecutive photoinduced electron transfer
Green Chemistry, 2022, 24, 7403-7409
7245191 CIFC10 H13 Br O4 SP -16.7194; 7.7474; 12.013
88.533; 79.948; 87.813		615.21Liu, Jiang; Xu, Jingcheng; Mei, Haibo; Han, Jianlin
Electrochemical multi-component reaction of potassium metabisulfite with alkenes and alcohols enabling synthesis of sulfonate esters
Green Chemistry, 2022, 24, 6113-6118
7245192 CIFC29 H21 N3 OP -19.3505; 10.5661; 11.8126
79.178; 74.762; 80.249		1097.1Jalani, Hitesh B.; Sivaraman, Aneesh; Min, Kyoung ho; Lee, Hwa Young; Oh, Na Kyoung; Kang, Hyeseul; Keum, Gyochang; Choi, Yongseok; Lee, Kyeong
Metal/catalyst-free sequential C–N bond forming cascades at room temperature: environment-friendly one-pot synthesis of 5-aminoimidazoles from aryl glyoxals, anilines, and amidines
Green Chemistry, 2022, 24, 6501-6510
7245193 CIFC19 H17 F3 N2 O SP 1 21/n 18.7917; 10.247; 19.1126
90; 98.05; 90		1704.86Lan, Jianyong; Lin, Kejun; Zhang, Xing; Zhu, Tingshun
Stereoselective migratory heteroaryltrifluoromethylation of allylic amines via electrosynthesis
Green Chemistry, 2022, 24, 6138-6144
7245194 CIFC14 H16 N2 O3P 1 21/c 115.1633; 5.1388; 17.4106
90; 101.494; 90		1329.45Lei, Xiaofang; Angeli, Giasemi K.; Neochoritis, Constantinos G.; Dömling, Alexander
Sustainable multicomponent indole synthesis with broad scope
Green Chemistry, 2022, 24, 6168-6171
7245195 CIFC17 H15 Cl N2 OP -19.4666; 9.9691; 16.311
100.153; 104.072; 92.751		1463.08Lei, Xiaofang; Angeli, Giasemi K.; Neochoritis, Constantinos G.; Dömling, Alexander
Sustainable multicomponent indole synthesis with broad scope
Green Chemistry, 2022, 24, 6168-6171
7245196 CIFC23 H27 O6 PP 41 21 29.4927; 9.4927; 47.965
90; 90; 90		4322.2Li, Hai; Yu, Kai-Cheng; Su, Jia-Kun; Ouyang, Wei; Fan, Nai-Li; Hu, Xiang-Guo
Photo-mediated synthesis of 1,2-dideoxy-2-phosphinylated carbohydrates from glycals: the reduction of glycosyl radicals to glycosyl anions
Green Chemistry, 2022, 24, 8280-8291
7245197 CIFC24 H27 O8 PP 21 21 2111.9882; 12.7368; 16.1339
90; 90; 90		2463.5Li, Hai; Yu, Kai-Cheng; Su, Jia-Kun; Ouyang, Wei; Fan, Nai-Li; Hu, Xiang-Guo
Photo-mediated synthesis of 1,2-dideoxy-2-phosphinylated carbohydrates from glycals: the reduction of glycosyl radicals to glycosyl anions
Green Chemistry, 2022, 24, 8280-8291
7245256 CIFC24 H28 F2 N2 OP b c a10.1227; 19.823; 21.73
90; 90; 90		4360.4Rodríguez, Ricardo I.; Sicignano, Marina; García, Montaña J.; Enríquez, Rodrigo G.; Cabrera, Silvia; Alemán, José
Taming photocatalysis in flow: easy and speedy preparation of α-aminoamide derivatives
Green Chemistry, 2022, 24, 6613-6618
7245271 CIFC22 H24 N2 O2P 1 21/c 114.6248; 11.859; 11.3672
90; 107.271; 90		1882.58Guan, Ting; Guo, Jing-Yu; Zhang, Qing-Hong; Xu, Xin-Wen; Yu, Xiao-Yu; Zhang, Yu; Zhao, Kai
Photoredox-catalyzed regio- & stereoselective C(sp2)–H cyanoalkylation of enamides with cycloketone oximes via selective C–C bond cleavage/radical addition cascade
Green Chemistry, 2022, 24, 6524-6530
7245278 CIFC28 H30 N2 O3 SP 21 21 2110.6469; 15.8266; 28.9384
90; 90; 90		4876.2SCHLIMPEN, Fabian; AST, Tun; Benneteau, Valerie; Pale, Patrick; Chassaing, Stefan
From A3/KA2 to AYA/KYA Multicomponent Coupling Reactions with Terminal Ynamides as Alkyne Surrogates - A Direct, Green Route to γ-Amino-Ynamides
Green Chemistry, 2022
7245304 CIFC29 H24 SeP -19.9628; 10.1107; 12.9334
71.458; 73.161; 63.999		1092.75Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay
Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics
Green Chemistry, 2022, 24, 7029-7038
7245305 CIFC26 H17 Cl SeP 1 21/c 115.3921; 10.1833; 13.1358
90; 107.775; 90		1960.65Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay
Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics
Green Chemistry, 2022, 24, 7029-7038
7245306 CIFC27 H20 SeP 1 21/c 111.2182; 10.3531; 17.3831
90; 100.258; 90		1986.66Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay
Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics
Green Chemistry, 2022, 24, 7029-7038
7245307 CIFC17 H11 Br N2 O SP 1 21/n 112.839; 9.1349; 13.4055
90; 99.269; 90		1551.7Gu, Qingyun; Cheng, Zhenfeng; Xiong, Xing; Xiong, Biao; Zhao, Yu; Xu, Hua-Dong; Zhang, Yanan; Qiu, Xiaodong; Zeng, Xiaobao
Electrochemical oxidative regio- and stereo-selective thio(seleno)cyanation of enamides and mechanistic insights
Green Chemistry, 2022, 24, 6556-6561
7245329 CIFC17 H16 Br N O3 SP -18.2932; 8.8298; 12.4718
95.863; 90.752; 116.824		808.94Wu, Ying-Ai; Wang, Rui-An; Jiang, Shu-Yun; Jiang, Tai-Bai; Song, Jun-Rong; Shi, Jun; Wu, Wei; Pan, Wei-Dong; Ren, Hai
Water enables the tunable electrochemical synthesis of heterocyclic 3a- or 5a-bromoindolines
Green Chemistry, 2022, 24, 6720-6726
7245347 CIFC20 H33 B N2 SP 1 21/n 17.8039; 17.1774; 14.8916
90; 91.57; 90		1995.48Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian
A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator
Green Chemistry, 2022, 24, 7113-7121
7245348 CIFC15 H20 B N3 OP 21 21 216.2427; 7.8871; 29.178
90; 90; 90		1436.63Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian
A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator
Green Chemistry, 2022, 24, 7113-7121
7245349 CIFC16 H21 B N2 O2P -19.0836; 9.1558; 11.0863
114.228; 106.84; 93.503		787.46Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian
A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator
Green Chemistry, 2022, 24, 7113-7121
7245350 CIFC15 H9 Cl2 N O SP 1 21/n 116.3755; 7.2951; 23.9248
90; 103.152; 90		2783.1Fu, Yuanyuan; Zhu, Shengzhen; Zhao, Xueyan; Huang, Shenlin
Photoredox-catalyzed coupling of acyl oxime acetates with thiophenols to give arylthioesters in water at room temperature
Green Chemistry, 2022, 24, 6849-6853
7245376 CIFC27 H28 Cl N3 O3P -18.293; 8.812; 19.773
88.368; 87.164; 67.4		1332.3Zhang, Aijiang; Chen, Changjuan; Zuo, Chunshan; Xu, Xiaobo; Cai, Tao; Li, Xiaotao; Yuan, Ying; Yang, Huanhuan; Meng, Gege
Imidazolium-based ionic liquids containing multipoint hydrogen bond donors as bifunctional organocatalysts for efficient cooperative conversion of CO2 to cyclic carbonates
Green Chemistry, 2022, 24, 7194-7207
7245393 CIFC17 H15 N O2P 1 c 16.9187; 12.6378; 14.994
90; 96.541; 90		1302.5Meng, Haifang; Xu, Huiying; Zhou, Zhi; Tang, Zhenhao; Li, Yidi; Zhou, Yu; Yi, Wei; Wu, Xiaowei
Recyclable rhodium-catalyzed C–H activation/[4 + 2] annulation with unconventional regioselectivity at ambient temperature: experimental development and mechanistic insight
Green Chemistry, 2022, 24, 7012-7021
7245396 CIFC15 H13 F O3 SP -15.6822; 9.1526; 14.0751
108.654; 100.575; 91.47		678.97Dam, Binoyargha; Sahoo, Ashish Kumar; Patel, Bhisma K.
Visible-light-mediated synthesis of β-keto sulfones using g-C3N4 as a recyclable photocatalyst under sustainable conditions
Green Chemistry, 2022, 24, 7122-7130
7245397 CIFC15 H14 O3 SP b c a11.5468; 10.2038; 22.824
90; 90; 90		2689.2Dam, Binoyargha; Sahoo, Ashish Kumar; Patel, Bhisma K.
Visible-light-mediated synthesis of β-keto sulfones using g-C3N4 as a recyclable photocatalyst under sustainable conditions
Green Chemistry, 2022, 24, 7122-7130
7245398 CIFC19 H20 N2 O6P -16.4061; 11.99; 12.381
96.571; 104.937; 105.103		870.1Pereira, Juliana G.; Ravasco, João M. J. M.; Vale, João R.; Queda, Fausto; Gomes, Rafael F. A.
A direct Diels–Alder reaction of chitin derived 3-acetamido-5-acetylfuran
Green Chemistry, 2022, 24, 7131-7136
7245399 CIFC23 H19 N3 O9 SP -17.23789; 12.2345; 13.6811
72.142; 82.584; 80.322		1132.82Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi
Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions
Green Chemistry, 2022, 24, 7162-7170
7245400 CIFC23 H19 N3 O9 SP 1 21/c 115.7934; 6.97062; 20.9252
90; 106.862; 90		2204.61Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi
Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions
Green Chemistry, 2022, 24, 7162-7170
7245401 CIFC54 H63 Fe3 Mn O6P 1 21/n 111.5777; 23.2895; 17.4903
90; 92.923; 90		4709.93Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi
Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions
Green Chemistry, 2022, 24, 7162-7170
7245456 CIFC2.61 H2.17 N0.09 O0.17P -19.206; 10.087; 13.161
99.033; 97.884; 107.657		1127.7Nie, Chang-Rui; Zhao, Hong-Ping; Liang, Wang-Fu; Zhong, Xin-Xian; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang
Base-catalyzed and DMSO-promoted intramolecular hydroalkoxylation to prepare pentacyclic chromeno[4,3-b]indolines
Green Chemistry, 2022, 24, 6854-6859
7245467 CIFC36 H30 Br2 N10 Ni O2I 41/a c d :217.2287; 17.2287; 50.201
90; 90; 90		14901.1Zhang, Chunyan; Liang, Qianqian; Yang, Wei; Zhang, Guohui; Hu, Maolin; Zhang, Guoying
Nickel(i)-catalyzed (de)hydrogenative coupling of amines and alkyl heteroarenes with alcohols
Green Chemistry, 2022, 24, 7368-7375
7245475 CIFC20 H16 OP -15.6133; 11.125; 23.1
91.6; 90.153; 90.094		1442Li, Chao; Ding, Ran; Guo, Heng-Yi; Xia, Shuang; Shu, Lei; Wang, Pei-Long; Li, Hongji
Catalyst-free benzylic C(sp3)–H cross-coupling with organotrifluoroborates enabled by electrochemistry
Green Chemistry, 2022, 24, 7883-7888
7245495 CIFC19 H25 N O3P 1 21/c 121.4567; 11.733; 15.3116
90; 109.708; 90		3628.9Yao, Zhen; Yang, Ji; Luo, Zhenli; Wang, Heyu; Zhang, Xin; Ye, Jianhan; Xu, Lijin; Shi, Qian
Photo-driven metal-free multicomponent reaction between aldehydes, anilines and 4-substituted-DHPs for the synthesis of secondary amines
Green Chemistry, 2022, 24, 7968-7973
7245545 CIFC24 H21 Cl4 N O2P 1 21/c 115.828; 9.9575; 16.1714
90; 116.785; 90		2275.3Chen, Shaomin; Chen, Zhiyan; Zhang, Tianjian; Zhao, Bo; You, Bo; Li, Minghao; Gu, Yanlong
Brønsted acid-catalyzed cascade cyclization: an efficient strategy for divergent synthesis of cyclohepta[b]indole derivatives
Green Chemistry, 2022, 24, 7376-7381
7245546 CIFC16 H17 Cl F3 N O4P -19.1441; 10.1797; 10.2607
114.406; 94.673; 99.133		847.17Yi, Yaping; Fan, Zhengning; Xi, Chanjuan
Photoredox-catalyzed intermolecular dearomative trifluoromethylcarboxylation of indoles and heteroanalogues with CO2 and fluorinated radical precursors
Green Chemistry, 2022, 24, 7894-7899
7245547 CIFC19 H18 N4 O3P 1 21/c 19.5056; 28.8708; 13.6219
90; 114.812; 90		3393.2Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang
Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron
Green Chemistry, 2022, 24, 8088-8099
7245548 CIFC25 H22 N4 O6P 1 c 111.8352; 14.4349; 6.7368
90; 105.77; 90		1107.6Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang
Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron
Green Chemistry, 2022, 24, 8088-8099
7245549 CIFC25 H20 N4 O6P 1 21/n 15.2165; 13.1426; 31.0132
90; 89.95; 90		2126.21Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang
Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron
Green Chemistry, 2022, 24, 8088-8099
7245565 CIFC20 H17 I2 N O2P 1 21/c 17.6126; 23.4046; 11.2824
90; 103.859; 90		1951.66Lu, Yuling; Chen, Chunmei; Zhu, Hucheng; Luo, Zengwei; Zhang, Yonghui
Highly efficient and fast synthesis of di-iodinated succinimide derivatives from 1,6-enyne and I2 under air at room temperature
Green Chemistry, 2022, 24, 8021-8028
7245574 CIFC24 H23 Cl3 N2 O3P -15.819; 9.8242; 20.3104
92.796; 92.658; 95.189		1153.44Liang, Jiazhi; Huang, Jian; Yang, Qin; Fu, Yang; Ding, Qiuping; Peng, Yiyuan
Synthesis of dihydroindazolo[2,3-f]phenanthridin-5(6H)-ones via Rh(iii)-catalyzed C–H activation of 2-aryl indazoles and annulation with iodonium ylides
Green Chemistry, 2022, 24, 8441-8446
7245575 CIFC24 H25 N3 O5P 1 21/c 112.5652; 14.3595; 12.2203
90; 100.202; 90		2170.05González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María
Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts
Green Chemistry, 2022, 24, 7988-7995
7245576 CIFC25 H27 N3 O5P -110.1914; 10.379; 11.8123
73.566; 67.677; 83.029		1108.5González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María
Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts
Green Chemistry, 2022, 24, 7988-7995
7245577 CIFC31 H29 Cl3 F N3 O5P -19.94; 10.793; 16.25
108.53; 96.84; 106.91		1538González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María
Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts
Green Chemistry, 2022, 24, 7988-7995
7245578 CIFC25 H24 N2 O4P -18.9559; 11.0368; 12.1951
90.73; 106.001; 100.401		1137.18González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María
Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts
Green Chemistry, 2022, 24, 7988-7995
7245579 CIFC13 H18 N2 O3P 1 21/n 110.9497; 10.1546; 12.5474
90; 111.425; 90		1298.7González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María
Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts
Green Chemistry, 2022, 24, 7988-7995
7245608 CIFC28 H27 F7 N4 O4P 1 21 19.8007; 19.457; 15.5025
90; 99.565; 90		2915.1Chen, Yu-Lan; Sun, Li-Wen; Chen, Jia-Wei; Zhu, Ming-Quan; Ma, Mengtao; Shen, Zhi-Liang; Chu, Xue-Qiang
Four-component defluorinative reaction of allylic fluorides, amidines, and Cs2CO3 under transition-metal-free conditions
Green Chemistry, 2022, 24, 6816-6822
7245620 CIFC11 H14 N2 O3 SP 1 21/n 18.9547; 8.4131; 16.386
90; 99.853; 90		1216.26Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245621 CIFC13 H10 N2 O3 SP -16.9208; 7.4115; 11.9359
101.965; 90.131; 92.439		598.35Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245622 CIFC11 H12 N2 O3 SP -17.9773; 8.6323; 8.8553
92.357; 103.812; 111.69		544.55Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245623 CIFC11 H12 N2 O3 SP -18.0147; 8.1452; 9.4761
94.6; 107.839; 107.022		553.18Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245624 CIFC15 H14 N2 O3 SP 1 21/c 19.887; 7.8158; 18.9459
90; 101.306; 90		1435.63Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245625 CIFC15 H14 N2 O4 SP 21 21 2111.2705; 12.223; 20.2303
90; 90; 90		2786.91Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming
Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines
Green Chemistry, 2022, 24, 8377-8385
7245630 CIFC22 H22 F3 N3 O2C 1 c 18.6009; 21.017; 11.5416
90; 94.661; 90		2079.4Xuan, Liangming; Du, Ruyang; Lei, Panpan; Zhao, Wei; Tan, Lixiang; Ni, Chuanzhi; Wang, Haifeng; Yan, Qiongjiao; Wang, Wei; Chen, Fener
Remote C(sp3)–H heteroarylation of N-fluorocarboxamides with quinoxalin-2(1H)-ones under visible-light-induced photocatalyst-free conditions
Green Chemistry, 2022, 24, 9475-9481
7245730 CIFC40 H36 N8 Ni O2C 1 2/c 117.601; 11.3637; 24.466
90; 93.413; 90		4884.8Sekar, Pandiaraj; Vasanthakumar, Punitharaj; Shanmugam, Ramasamy; Senthil Kumar, Shanmugam; Agnoli, Stefano; Deepak, Rajasekharan Jayakumari; Murugan, Karthik; Bhuvanesh, Nattamai; Karvembu, Ramasamy
Green synthesis of a redox-active riboflavin-integrated Ni-MOF and its versatile electrocatalytic applications towards oxygen evolution and reduction, and HMF oxidation reactions
Green Chemistry, 2022, 24, 9233-9244
7245762 CIFC19 H17 N3 SP -18.3612; 9.7442; 10.6475
65.818; 86.321; 79.417		777.84Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin
Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines
Green Chemistry, 2022, 24, 9482-9488
7245763 CIFC22 H20 Br N3P 1 21/c 16.3317; 10.0072; 29.5714
90; 92.36; 90		1872.13Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin
Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines
Green Chemistry, 2022, 24, 9482-9488
7245764 CIFC21 H19 N3P -18.365; 10.655; 10.809
115.055; 99.78; 98.016		835.6Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin
Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines
Green Chemistry, 2022, 24, 9482-9488
7245794 CIFC16 H16 O SP 1 21/n 16.0752; 9.8777; 22.1887
90; 91.536; 90		1331.04Zhu, Can-Ming; Liang, Rong-Bin; Xiao, Yonghong; Zhou, Wei; Tong, Qing-Xiao; Zhong, Jian-Ji
Metal-free and site-selective α-C–H functionalization of tetrahydrofuran enabled by the photocatalytic generation of bromine radicals
Green Chemistry, 2023, 25, 960-965
7245915 CIFC23 H26 N2 O6P -18.6271; 11.5365; 12.0186
112.233; 90.786; 95.43		1100.68Qian, Hang; Wang, Cui-Cui; Shen, Zi-Chen; Sun, Ming-Xue; Zhang, Hong-Chao; Fan, Shiming; Feng, Juan; Liu, Shouxin; Zhang, Zhi-Wei
Catalyst- and additive-free [3 + 3] cyclization–aromatization of β,γ-dioxobutanoate with amines for synthesis of p-aminophenols
Green Chemistry, 2022, 24, 9690-9696
7245933 CIFC4 H6.22 B0.22 F0.89 N0.89 Rh0.22I 41/a c d :215.9403; 15.9403; 31.662
90; 90; 90		8045.1Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245934 CIFC13.5 H17 B0.5 Cl F2 N2 Rh0.5P 1 21/n 113.617; 17.292; 13.8897
90; 116.871; 90		2917.4Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245935 CIFC127 H147 B2 Cl9 F8 N8 Rh2P 1 21/c 115.1914; 15.8408; 55.703
90; 93.157; 90		13384.2Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245956 CIFC38 H29 N OP 1 21/n 19.7566; 23.006; 13.329
90; 109.053; 90		2827.9Zhuang, Hongfeng; Hou, Qin; Han, Feng; Lv, Haotian; Miao, Chengxia
Heteropolyacid catalyzed O-alkylation of oximes with alcohols via a carbocation in dimethyl carbonate and mechanism insight
Green Chemistry, 2023, 25, 310-317
7245973 CIFC22 H13 N O2 SP n a 2111.7823; 17.2564; 8.5563
90; 90; 90		1739.7Chen, Shiliu; Yan, Qinqin; Fan, Jie; Guo, Changyou; Li, Lijun; Liu, Zhong-Quan; Li, Zejiang
Photo-induced spirocyclization of biaryl ynones with ammonium thiocyanate: access to thiocyanate-featured spiro[5,5]trienones
Green Chemistry, 2023, 25, 153-160
7245974 CIFC26 H22 F3 N3P 1 21/n 19.705; 16.0805; 13.7744
90; 93.165; 90		2146.4Sharma, Himanshi; Kumar, Manoj; Sethi, Aaftaab; Poonam,; Rathi, Brijesh
Metal-free construction of aminated isoquinoline frameworks from 2-(2-oxo-2-arylethyl) benzonitrile in an aqueous medium
Green Chemistry, 2023, 25, 167-171
7246014 CIFC20 H19 I O6 SP 16.8727; 7.4757; 10.7012
75.161; 88.164; 77.878		519.48Peng, Chuxiong; Gu, Fengyan; Lin, Xiaofeng; Ding, Ning; Zhan, Qichen; Cao, Peng; Cao, Tao
Highly selective catalyst- and additive-free iodosulfonylation of cyclopropenes in water
Green Chemistry, 2023, 25, 671-677
7246049 CIFC13 H25 N O7 SP 21 21 217.9459; 13.5525; 15.5352
90; 90; 90		1672.9Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.
Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene
Green Chemistry, 2023, 25, 606-613
7246050 CIFC13 H19 N O5 SP 21 21 216.1009; 12.5179; 19.3009
90; 90; 90		1474.02Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.
Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene
Green Chemistry, 2023, 25, 606-613
7246051 CIFC23 H16 Fe O2P -16.7731; 10.9956; 12.2301
72.319; 75.206; 77.254		828.85Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian
Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2
Green Chemistry, 2023, 25, 554-559
7246052 CIFC36 H28 Fe2 O6P -110.4854; 11.7036; 12.3518
72.325; 79.087; 75.017		1384.97Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian
Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2
Green Chemistry, 2023, 25, 554-559
7246055 CIFC10.8 H8.8 Cl0.4 N0.4 O0.8 S0.4 Se0.4P 1 21/n 111.9543; 8.3309; 24.4205
90; 102.103; 90		2377.98Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay
100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen
Green Chemistry, 2023, 25, 779-788
7246056 CIFC21 H14 I N S2I 1 2/a 117.9022; 6.0537; 34.1626
90; 91.27; 90		3701.45Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay
100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen
Green Chemistry, 2023, 25, 779-788
7246068 CIFC17 H16 Cl N3P -16.7166; 9.3699; 12.656
68.667; 79.026; 72.896		706Liu, Qingqing; Ci, Chenggang; Zhao, He; Xie, Rong; Jiang, HuanFeng; Zhang, Min
Direct access to functional phenazines via oxidative annulation of anilines and o-phenylenediamines with a reusable cobalt catalyst
Green Chemistry, 2023, 25, 678-683
7246122 CIFC13 H15 N O6C 1 2/c 125.911; 4.6748; 23.299
90; 104.436; 90		2733.1Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László
Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant
Green Chemistry, 2023, 25, 746-754
7246123 CIFC13 H12 O4P -16.5868; 8.2313; 11.126
106.015; 97.159; 95.387		570.1Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László
Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant
Green Chemistry, 2023, 25, 746-754
7246138 CIFC24 H20 F5 O4P -18.3761; 8.4007; 16.0336
98.767; 99.704; 91.221		1097.79Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar
Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes
Green Chemistry, 2023, 25, 1014-1022
7246139 CIFC18 H22 O4P 1 21/n 17.0243; 20.574; 11.0931
90; 91.591; 90		1602.5Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar
Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes
Green Chemistry, 2023, 25, 1014-1022
7246144 CIFC18 H18 O9P 1 21/c 118.6508; 5.8796; 14.7464
90; 94.7151; 90		1611.61Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246145 CIFC37 H30 O10P -110.361; 13.355; 13.4649
62.271; 70.487; 70.729		1520.04Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246146 CIFC21 H24 O11P 1 21/n 110.5648; 16.247; 12.4776
90; 110.308; 90		2008.6Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246147 CIFC39 H35 N O10P 1 21/c 19.1956; 33.6799; 10.508
90; 97.813; 90		3224.19Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246166 CIFC19 H19 N O3P b c a18.0732; 8.28431; 20.8875
90; 90; 90		3127.36Wei, Wan-Jie; Zhan, Lei; Jiang, Cai-Na; Tang, Hai-Tao; Pan, Ying-Ming; Ma, Xian-Li; Mo, Zu-Yu
Electrochemical oxidative cascade cyclization of olefinic amides and alcohols leading to the synthesis of alkoxylated 4H-3,1-benzoxazines and indolines
Green Chemistry, 2023, 25, 928-933
7246185 CIFC27 H27 N OP 21 21 217.7837; 31.1021; 8.6447
90; 90; 90		2092.79Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang
Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane
Green Chemistry, 2023, 25, 1120-1127
7246186 CIFC25 H29 N OP 1 21 111.2; 7.8745; 11.8582
90; 103.292; 90		1017.81Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang
Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane
Green Chemistry, 2023, 25, 1120-1127
7246229 CIFC9 H5 N3 OP 1 21/n 13.7252; 11.5014; 18.9837
90; 91.706; 90		813Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander
Amenamevir by Ugi-4CR
Green Chemistry, 2023, 25, 1322-1325
7246230 CIFC24 H26 N4 O5 SI 1 2/a 119.6089; 13.7807; 17.823
90; 101.936; 90		4712.08Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander
Amenamevir by Ugi-4CR
Green Chemistry, 2023, 25, 1322-1325
7246286 CIFC24 H16 F5 O2 PP 1 21/c 118.8874; 6.1813; 17.2323
90; 91.402; 90		2011.2Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang
Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans
Green Chemistry, 2023, 25, 2000-2010
7246287 CIFC36 H25 F5 O3 P2P -111.345; 12.0953; 14.1162
89.245; 77.498; 62.787		1673.55Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang
Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans
Green Chemistry, 2023, 25, 2000-2010
7246321 CIFC10.33 H7.33 N1.33 O1.33 S0.67P -110.3322; 10.7423; 14.3583
97.245; 100.734; 116.704		1358.21Zhang, Zhicheng; Wen, Linzi; Xu, Shihai; Tang, Yu; Cao, Xiaohui; Feng, Pengju
Consecutive cross-dehydrogenative C–O and C–N construction for the synthesis of polyarene with AIE properties under electrochemical condition involving oxygen radical species
Green Chemistry, 2023, 25, 2287-2292
7246353 CIFC25 H30 Fe K N2 O8P -19.877; 12.1262; 12.1406
66.668; 83.456; 83.448		1322.68Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.
A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations
Green Chemistry, 2023, 25, 2262-2267
7246354 CIFC23 H27 Fe N2 O6P 1 21/c 19.0238; 12.9234; 19.4802
90; 96.797; 90		2255.78Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.
A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations
Green Chemistry, 2023, 25, 2262-2267
7246413 CIFC15 H10 I N OP 1 21/c 113.0551; 7.4021; 13.9932
90; 101.381; 90		1325.65Wu, Jianglong; Ma, Yinfeng; Wang, Yan; Wang, Chenyu; Luo, Hui; Li, Dianjun; Yang, Jinhui
Copper-catalyzed direct synthesis of 3-methylene-2-arylisoindolin-1-ones with calcium carbide as a surrogate of gaseous acetylene
Green Chemistry, 2023, 25, 3425-3430
7246418 CIFC20 H19 N O2P 439.58017; 9.58017; 33.7964
90; 90; 90		3101.82Feng, Tian; Zhu, Zile; Zhang, Dongmei; Wang, Siyi; Li, Ruopu; Zhu, Zhaolin; Zhang, Xinxing; Qiu, Youai
Electrochemical dual α,β-C(sp3)–H functionalization of cyclic N-aryl amines
Green Chemistry, 2023, 25, 2681-2689
7246419 CIFC16 H19 N O3 S2P 1 21/c 111.6432; 16.4149; 9.6857
90; 113.866; 90		1692.87Wang, Qian; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming; Duan, Wen-Gui; He, Mu-Xue
Electrochemically driven α-thiocarbamylation via a dehydrocoupling strategy of β-ketoesters with amines and CS2
Green Chemistry, 2023, 25, 2572-2576
7246425 CIFC20 H19 N OP 1 21/c 125.949; 10.787; 11.392
90; 101.972; 90		3119.4Wei, Minghui; Liu, Chengkou; Wang, Chang-Sheng; Li, Yuguang; Qiu, Peng; Dong, Quanxiao; Yang, Zhao; Fang, Zheng; Guo, Kai
Synthesis of pyrido[1,2-a]indol-6(7H)-ones via a visible light-photocatalyzed formal (4 + 2) cycloaddition of indole-derived bromides and alkenes or alkynes
Green Chemistry, 2023, 25, 2453-2457
7246452 CIFC13 H19 Cl2 NP 21 21 214.9594; 10.7311; 27.2017
90; 90; 90		1447.67Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246453 CIFC13 H18 Br Cl F NP 1 21 14.8988; 10.7881; 13.7759
90; 98.02; 90		720.92Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246454 CIFC14 H21 Br Cl NP 21 21 214.9604; 10.8195; 29.3754
90; 90; 90		1576.55Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246455 CIFC14 H21 Br Cl NP 1 21 19.5543; 6.5919; 12.4634
90; 98.424; 90		776.49Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246456 CIFC13 H18 Br Cl F NP 21 21 217.6197; 14.1232; 27.1001
90; 90; 90		2916.36Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246457 CIFC13 H18 Br Cl F NP 1 21 14.8335; 26.095; 11.3444
90; 90.954; 90		1430.67Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246458 CIFC13 H18 Br Cl F NP 21 21 214.7559; 10.6799; 28.6366
90; 90; 90		1454.53Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246493 CIFC14 H13 N O2P b c a8.6581; 12.1447; 22.107
90; 90; 90		2324.6Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246494 CIFC14 H12 Cl N O2P 1 21/c 113.6538; 9.0781; 10.6852
90; 108.522; 90		1255.83Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246495 CIFC14 H11 N OP 1 21/n 15.9303; 7.6388; 23.149
90; 94.506; 90		1045.4Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246496 CIFC14 H12 Br N O2P 21 21 215.4795; 11.4206; 19.3592
90; 90; 90		1211.48Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246497 CIFC14 H12 Cl N3 O SP 1 21 110.7651; 4.8762; 13.0778
90; 106.91; 90		656.81Hommelsheim, Renè; Bausch, Sandra; van Nahl, Robin; Ward, Jas S.; Rissanen, Kari; Bolm, Carsten
Synthesis of 3-amino-substituted benzothiadiazine oxides by a palladium-catalysed cascade reaction
Green Chemistry, 2023, 25, 3021-3026
7246540 CIFC15 H20 Br N O2P -17.079; 9.363; 11.864
93.881; 97.142; 100.629		763.5Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei
Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes
Green Chemistry, 2023, 25, 3543-3548
7246541 CIFC16 H23 N O3P 1 21/n 16.676; 23.1; 9.948
90; 94.562; 90		1529.3Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei
Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes
Green Chemistry, 2023, 25, 3543-3548
7246546 CIFC14 H10 O2P 32 2 18.415; 8.415; 13.689
90; 90; 120		839.48Bhukta, Swadhapriya; Chatterjee, Rana; Dandela, Rambabu
Metal-free, 2-MeTHF mediated C(sp)–H functionalization of alkynes with anilines to access diaryl 1,2-diketones bearing lower E-factors
Green Chemistry, 2023, 25, 3034-3039
7246554 CIFC20 H18 N2P 1 21/n 112.54957; 5.45668; 21.5051
90; 100.046; 90		1450.07Everaert, Jonas; Leus, Karen; Rijckaert, Hannes; Debruyne, Maarten; Van Hecke, Kristof; Morent, Rino; De Geyter, Nathalie; Van Speybroeck, Veronique; Van Der Voort, Pascal; Stevens, Christian V.
A recyclable rhodium catalyst anchored onto a bipyridine covalent triazine framework for transfer hydrogenation of N-heteroarenes in water
Green Chemistry, 2023, 25, 3267-3277
7246560 CIFC30 H28 O3P -19.7371; 10.1536; 12.7652
102.012; 94.177; 110.29		1143.27Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan
Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2
Green Chemistry, 2023, 25, 3633-3643
7246561 CIFC44 H36 O6P -18.998; 11.5521; 18.5351
79.764; 84.293; 67.467		1750.2Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan
Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2
Green Chemistry, 2023, 25, 3633-3643
7246605 CIFC18 H16 N2P 21 21 216.607; 10.064; 21.6
90; 90; 90		1436.2Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246606 CIFC18 H14 Cl2 N2I 1 c 17.817; 18.49; 11.24
90; 96.61; 90		1614Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246607 CIFC18 H14 Br2 N2C 1 c 112.96; 18.557; 7.814
90; 120.687; 90		1616.1Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246608 CIFC19 H19 N O3 S SeP 1 21/c 114.852; 8.3709; 15.745
90; 111.498; 90		1821.3Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246609 CIFC19 H19 N O4 SeP 1 21/n 16.042; 7.1534; 41.598
90; 91.97; 90		1796.8Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246610 CIFC23 H18 Br N O3 S SeP b c a9.9532; 24.647; 17.5152
90; 90; 90		4296.8Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246637 CIFC26 H30 Br2 O6P 1 21 16.1791; 15.1836; 14.4771
90; 95.557; 90		1351.87Qiu, Huixin; Ren, Jiayi; Zhang, Long; Song, Ran; Si, Wen; Yang, Daoshan; Wen, Lirong; Lv, Jian
Enantioselective Meerwein–Ponndorf–Verley reduction of β,γ-unsaturated α-keto esters by asymmetric binary-acid catalysis in the green solvent iPrOH
Green Chemistry, 2023, 25, 3948-3955
7246659 CIFC20 H14 F5 N O3P 1 21/c 117.1352; 7.89497; 14.2824
90; 110.302; 90		1812.12Huang, Panyi; Yan, Zhiyang; Ling, Jiaxin; Li, Peixuan; Wang, Jiayang; Li, Jianjun; Sun, Bin; Jin, Can
Catalyst-free intramolecular radical cyclization cascades initiated by the direct homolysis of Csp3–Br under visible light
Green Chemistry, 2023, 25, 3989-3994
7246660 CIFC16 H25 B O4P 1 21 16.4643; 21.3155; 11.9798
90; 91.899; 90		1649.79Huninik, Paweł; Szyling, Jakub; Czapik, Agnieszka; Walkowiak, Jędrzej
Organocatalytic hydroboration of olefins in pyrrolidinium ionic liquids
Green Chemistry, 2023, 25, 3715-3722
7246679 CIFC58 H37.89 Cl0.11 N6 O8 S2P -19.521; 12.027; 12.459
63.128; 82.674; 72.395		1212.9Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246680 CIFC31 H23.91 Cl0.09 N2 O2 SP -19.279; 11.406; 13.046
80.4; 80.8; 69.338		1266.2Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246681 CIFC30 H22 N2 O2 SP -19.907; 11.5183; 11.8511
108.421; 104.16; 99.584		1199.6Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246682 CIFC60 H43.54 Cl0.56 N4 O6 S2P -111.803; 12.782; 17.329
89.118; 81.911; 71.924		2459.5Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246708 CIFC21 H19 N2 O3 SP 1 21/n 114.2948; 8.5708; 15.3612
90; 95.345; 90		1873.84Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji
Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles
Green Chemistry, 2023, 25, 3982-3988
7246709 CIFC19 H19 N3 O2 SP 1 21/n 111.349; 10.096; 15.893
90; 97.84; 90		1804Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji
Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles
Green Chemistry, 2023, 25, 3982-3988
7246809 CIFC17 H16 Cl N3 O3 SeP -17.3092; 10.4613; 12.143
72.439; 87.404; 81.976		876.56Liu, Huan; Ye, Zi-Lin; Cai, Zhong-Jian; Ji, Shun-Jun
A multicomponent reaction of isocyanides, selenium powder and 3-aminooxetanes in pure water: green and efficient synthesis of 1,3-selenazolines
Green Chemistry, 2023, 25, 4239-4243
7246811 CIFC8 H20 Au Cl4 NP 1 2/n 19.1149; 7.9249; 10.3451
90; 92.043; 90		746.8Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246812 CIFC8 H20 Au Br4 NP 1 2/n 19.3812; 8.2418; 10.5053
90; 90.562; 90		812.21Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246813 CIFC16 H36 Au Cl4 NP 1 21/n 114.8787; 8.931; 18.277
90; 107.259; 90		2319.32Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246814 CIFC16 H36 Au Br4 NP 4/n :212.1431; 12.1431; 8.5038
90; 90; 90		1253.93Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246815 CIFC19 H42 Au Br4 NP 1 21/c 18.1965; 8.7398; 38.9304
90; 92.271; 90		2786.62Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246829 CIFC11 H9 N O2 SP 1 21/c 112.545; 3.9268; 21.018
90; 106.758; 90		991.4Li, Dandan; Chen, Long; Jin, Yang; Wang, Xiaochen; Liu, Long; Li, Yilin; Chen, Gongyuan; Wu, Guanhao; Qin, Yujie; Yang, Leilei; Wang, Mengke; Zhao, Lulu; Xu, Zhihong; Wen, Jiangwei
An electrochemical-enabled cascaded cyclization of enaminones with potassium thiocyanate and alcohols to access 2-alkoxythiazoles
Green Chemistry, 2023, 25, 4656-4661
7246830 CIFC24 H19 N O3P 1 21/c 18.998; 13.804; 14.731
90; 92.647; 90		1827.8Yang, Na; Li, Anni; Gao, Hui; Liao, Li-Mei; Yang, Yu-Ping; Wang, Pei-Long; Li, Hongji
Electrochemical oxidation-induced benzylic C(sp3)–H functionalization towards the atom-economic synthesis of oxazole heterocycles
Green Chemistry, 2023, 25, 5128-5133
7246831 CIFC22 H16 Br N SP 21 21 222.70389; 13.29859; 5.82409
90; 90; 90		1758.47Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246832 CIFC22 H16 Cl N SC 1 2/c 124.9095; 5.8669; 25.8562
90; 111.533; 90		3514.94Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246833 CIFC22 H16 Br N SP 1 21/m 110.2654; 7.0454; 12.4963
90; 92.802; 90		902.7Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246834 CIFC22 H17 Cl N SP 1 21/m 110.1263; 6.9258; 12.6138
90; 92.516; 90		883.79Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246835 CIFC26 H25 N SP -111.3822; 12.2394; 16.8294
74.05; 80.114; 67.955		2083.27Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246851 CIFC17 H14 F3 N O2 SP 1 21/c 19.3303; 17.815; 10.836
90; 112.207; 90		1667.6Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246852 CIFC18 H16 F3 N O2 SP 1 21/n 19.8704; 16.865; 11.3723
90; 115.314; 90		1711.3Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246853 CIFC18 H16 F3 N O2 SP -18.9764; 9.7004; 10.5392
102.617; 92.927; 99.557		879.46Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246854 CIFC16 H11 F3 O2 SP 1 21/c 18.8998; 16.2836; 10.5436
90; 107.423; 90		1457.88Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246876 CIFC24 H21 NP 21 21 217.6105; 12.1722; 19.257
90; 90; 90		1783.9Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.
Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters
Green Chemistry, 2023, 25, 5601-5612
7246877 CIFC23 H23 NP 1 21/c 115.447; 5.6795; 21.658
90; 108.34; 90		1803.6Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.
Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters
Green Chemistry, 2023, 25, 5601-5612
7246939 CIFC11 H12 F N O2P 1 21/c 15.2503; 16.2082; 12.1305
90; 99.976; 90		1016.7Hu, Fangzhi; Sun, Zhipeng; Pan, Mengzhe; Wang, Liang; Xu, Lubin; Liu, Xiong-Li; Li, Shuai-Shuai
Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions
Green Chemistry, 2023, 25, 5134-5141
7246940 CIFC26 H25 N O8P 21 21 217.6044; 9.6671; 31.908
90; 90; 90		2345.6Fu, Yun-Dong; Gao, Xiang; Jia, Shi-Kun; Xiao, Xiao; Wang, Min-Can; Huang, Lihua; Mei, Guang-Jian
Catalyst-free racemic and H2O/CPA-catalyzed asymmetric regio-reversed domino processes of triketone enones with azlactones
Green Chemistry, 2023, 25, 5692-5697
7246941 CIFC81 H161.5 Mn Mo6 N9.5 O30P 1 21 124.16; 14.7868; 33.2539
90; 103.708; 90		11541.5Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge
A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles
Green Chemistry, 2023, 25, 6263-6269
7246942 CIFC46 H106 Mn Mo7.5 N4 O44 S14P 21 21 233.5555; 30.4959; 9.33799
90; 90; 90		9555.61Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge
A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles
Green Chemistry, 2023, 25, 6263-6269
7246950 CIFC23 H16 F N OP n a 2112.4459; 27.609; 4.7734
90; 90; 90		1640.23Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246951 CIFC23 H17 N OP 1 21/c 14.8075; 27.2149; 12.4496
90; 92.523; 90		1627.27Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246952 CIFC20 H16 OP -16.3822; 10.211; 11.3886
84.533; 89.069; 74.931		713.37Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246953 CIFC23 H23 N O3P 1 21/c 112.0444; 5.6218; 27.7622
90; 99.864; 90		1852Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246954 CIFC19 H15 N OP 1 21/c 113.198; 5.6188; 18.6771
90; 97.268; 90		1373.91Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246955 CIFC24 H18 F N OP 1 21/n 15.6809; 13.8095; 21.8999
90; 91.229; 90		1717.66Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246956 CIFC22 H21 N O3P 1 21/c 119.3497; 7.1784; 12.8947
90; 103.665; 90		1740.37Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246957 CIFC21 H18 O2P 1 21/c 17.6458; 6.1433; 66.279
90; 91.529; 90		3112.05Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246958 CIFC23 H23 N O4P 21 21 215.4064; 9.6437; 36.2282
90; 90; 90		1888.86Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246994 CIFC8 H6 N4 Ni O2P 4/m b m13.4433; 13.4433; 7.1126
90; 90; 90		1285.4Huang, Hengcong; Gu, Yifan; Wang, Luyao; Jia, Tao; Kitagawa, Susumu; Li, Fengting
A scalable stable porous coordination polymer synthesized from low-cost precursors for efficient C2H2/C2H4 separation
Green Chemistry, 2023, 25, 8040-8046
7247074 CIFC16 H17 N3 O3 SP 1 21/c 116.316; 5.3605; 17.8044
90; 102.726; 90		1519Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.
Ni(ii)-catalyzed oxidative deamination of benzyl amines with water
Green Chemistry, 2023, 25, 6212-6217
7247075 CIFC18 H20 N3 Ni O4 SC 1 2/c 110.662; 22.8698; 14.5817
90; 95.618; 90		3538.5Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.
Ni(ii)-catalyzed oxidative deamination of benzyl amines with water
Green Chemistry, 2023, 25, 6212-6217
7247076 CIFC21 H20 Br Cl2 N3 NiP 1 21/c 110.0731; 20.1087; 10.8313
90; 105.39; 90		2115.28Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.
Ni(ii)-catalyzed oxidative deamination of benzyl amines with water
Green Chemistry, 2023, 25, 6212-6217
7247077 CIFC31 H28 Br2 Cl2 N6 NiP -113.746; 16.148; 16.995
65.764; 69.468; 74.898		3191.2Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.
Ni(ii)-catalyzed oxidative deamination of benzyl amines with water
Green Chemistry, 2023, 25, 6212-6217
7247092 CIFC28 H21 F2 O2 PP -16.1385; 11.76; 17.0258
104.208; 96.087; 103.597		1140.46Chu, Xue-Qiang; Sun, Li-Wen; Ma, Cheng; Chen, Jia-Wei; Chen, Yu-Lan; Ni, Shao-Fei; Zhu, Ming-Quan; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang
“On-water” defluorophosphorylation of trifluoromethylated enones with phosphine oxides
Green Chemistry, 2023, 25, 6489-6497
7247093 CIFC36 H26 F2 N3 O4 PP 1 21/n 113.606; 16.1758; 14.0833
90; 98.198; 90		3067.89Chu, Xue-Qiang; Sun, Li-Wen; Ma, Cheng; Chen, Jia-Wei; Chen, Yu-Lan; Ni, Shao-Fei; Zhu, Ming-Quan; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang
“On-water” defluorophosphorylation of trifluoromethylated enones with phosphine oxides
Green Chemistry, 2023, 25, 6489-6497
7247094 CIFC27 H39 B2 N3 O4P -111.5388; 15.217; 31.3898
88.955; 88.529; 76.813		5364.1Tao, Sheng; Wang, Yang; Pan, Qianxiu; Zhao, Jixing; Bu, Qingqing; Chen, Fei; Liu, Jichang; Dai, Bin; Wei, Donghui; Liu, Ning
Aqueous hydroboration of alkynes via nonclassical generation of N-heterocyclic carbenes
Green Chemistry, 2023, 25, 6704-6716
7247095 CIFC20 H15 N3 OP b c a19.9852; 7.5581; 20.2911
90; 90; 90		3064.97Titenkova, Kseniia; Shuvaev, Alexander D.; Teslenko, Fedor E.; Zhilin, Egor S.; Fershtat, Leonid L.
Empowering strategies of electrochemical N–N bond forming reactions: direct access to previously neglected 1,2,3-triazole 1-oxides
Green Chemistry, 2023, 25, 6686-6693
7247129 CIFC16 H16 O2P 1 21 111.9068; 4.8812; 22.718
90; 94.231; 90		1316.8Su, Yu; Wang, Chengyi; Chen, Qipeng; Zhu, Yuanli; Deng, Shaomin; Yang, Shoujin; Jin, Ronghua; Liu, Guohua
Harmonization of an incompatible aqueous aldol condensation/oxa-Michael addition/reduction cascade process over a core–shell-structured thermoresponsive catalyst
Green Chemistry, 2023, 25, 6859-6868
7247197 CIFC24 H27 N O4 SP 1 21/n 15.4248; 30.6105; 12.8838
90; 94.772; 90		2132.01Gao, Yuzhen; Liu, Siqing; Su, Weiping
CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis
Green Chemistry, 2023, 25, 7335-7343
7247198 CIFC30 H23 N O3 SP -18.3269; 11.8421; 13.6257
69.743; 74.537; 81.231		1212.2Gao, Yuzhen; Liu, Siqing; Su, Weiping
CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis
Green Chemistry, 2023, 25, 7335-7343
7247199 CIFC19 H22 O4C 1 2/c 123.0076; 7.7676; 18.0741
90; 99.883; 90		3182.16Gao, Yuzhen; Liu, Siqing; Su, Weiping
CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis
Green Chemistry, 2023, 25, 7335-7343
7247212 CIFC23 H19 N O2P -17.804; 10.261; 11.611
100.605; 102.623; 94.906		884Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul
Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution
Green Chemistry, 2023, 25, 7642-7652
7247213 CIFC23 H17 NP 1 21/c 114.183; 12.855; 8.8411
90; 98.111; 90		1595.8Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul
Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution
Green Chemistry, 2023, 25, 7642-7652
7247214 CIFC17 H15 N O2P 1 21/c 110.699; 24.611; 11.444
90; 112.405; 90		2786Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul
Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution
Green Chemistry, 2023, 25, 7642-7652
7247248 CIFC10 H9 N3 O SP 1 c 18.2596; 11.1219; 11.4922
90; 110.896; 90		986.27Maity, Rajib; Bankura, Abhijit; Das, Indrajit
Electrochemical cascade sequences for remote C7–H bond thiocyanation of quinoxalin-2(1H)-ones with ammonium thiocyanate
Green Chemistry, 2023, 25, 7774-7781
7247249 CIFC12 H11 N3 O SP -13.9964; 8.0048; 17.9743
90.426; 90.934; 98.213		569Maity, Rajib; Bankura, Abhijit; Das, Indrajit
Electrochemical cascade sequences for remote C7–H bond thiocyanation of quinoxalin-2(1H)-ones with ammonium thiocyanate
Green Chemistry, 2023, 25, 7774-7781
7247250 CIFC20 H22 B PP 1 21/c 16.7604; 16.4043; 15.8328
90; 95.946; 90		1746.41Shi, Wei; Zhong, Ping-Fu; Qi, Xu-Kuan; Yang, Chao; Guo, Lin; Xia, Wujiong
Photoinduced ligand-to-iron charge transfer enabled C(sp3)–H phosphorylation of hydrocarbons
Green Chemistry, 2023, 25, 7817-7824
7247251 CIFC19 H24 B PP 1 21/c 16.6016; 17.7257; 14.5686
90; 101.613; 90		1669.89Shi, Wei; Zhong, Ping-Fu; Qi, Xu-Kuan; Yang, Chao; Guo, Lin; Xia, Wujiong
Photoinduced ligand-to-iron charge transfer enabled C(sp3)–H phosphorylation of hydrocarbons
Green Chemistry, 2023, 25, 7817-7824
7247297 CIFC40 H33 N O5P 1 21/c 113.552; 10.2862; 23.234
90; 95.963; 90		3221.3Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin
Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones
Green Chemistry, 2023, 25, 8057-8067
7247298 CIFC35 H30 Cl N O6P 1 21/c 110.4332; 10.0121; 27.9684
90; 98.05; 90		2892.7Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin
Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones
Green Chemistry, 2023, 25, 8057-8067
7247299 CIFC36 H27 N OP -110.3653; 11.5399; 12.1483
86.936; 75.711; 69.063		1314.21Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin
Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones
Green Chemistry, 2023, 25, 8057-8067
7247300 CIFC23 H21 N OP -15.8318; 11.6046; 26.5835
86.525; 87.942; 87.181		1792.6Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin
Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones
Green Chemistry, 2023, 25, 8057-8067
7247301 CIFC29 H27 N O5P -111.0361; 14.2348; 16.7656
79.529; 88.302; 75.05		2501.88Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin
Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones
Green Chemistry, 2023, 25, 8057-8067
7247337 CIFC36 H29 N O3 SP 1 21/c 18.791; 18.1795; 17.9329
90; 95.505; 90		2852.7Mutra, Mohana Reddy; Chandana, T. L.; Wang, Yun-Jou; Wang, Jeh-Jeng
Green and rapid acid-catalyzed ynamide skeletal rearrangement and stereospecific functionalization with anisole derivatives
Green Chemistry, 2023, 25, 8124-8133
7247338 CIFC15 H10 O2C 1 2/c 118.4742; 5.9923; 19.2732
90; 98.981; 90		2107.44Ragupathi, Ayyakkannu; Charpe, Vaibhav Pramod; Hwu, Jih Ru; Hwang, Kuo Chu
Oxidative destruction of chlorinated persistent organic pollutants by hydroxyl radicals via ozone and UV light irradiation
Green Chemistry, 2023, 25, 9695-9704
7247352 CIFC30 H26 N2 O3P 1 21/n 110.2545; 11.784; 18.9397
90; 91.018; 90		2288.29Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247353 CIFC33 H28 N2 OP 1 21/c 116.0365; 8.141; 19.083
90; 93.993; 90		2485.3Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247354 CIFC58 H52 N4 O4I 1 2/a 118.5654; 11.0141; 23.246
90; 104.797; 90		4595.73Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247355 CIFC29 H27 Br N2 O2P 1 21/c 118.9264; 10.15909; 12.951
90; 100.384; 90		2449.37Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247356 CIFC35 H32 N2 OP 1 21/n 111.9969; 12.1767; 18.3724
90; 103.405; 90		2610.8Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247357 CIFC29 H26 N2 O2P 1 21/n 110.605; 11.8204; 17.9554
90; 92.512; 90		2248.64Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247358 CIFC11.76 H8.47 N0.94 O0.94P c a 219.1217; 17.3684; 23.9176
90; 90; 90		3789.25Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247359 CIFC58 H52 N4 O2C 1 2/c 124.6112; 10.2554; 36.0411
90; 99.385; 90		8974.9Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng
Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light
Green Chemistry, 2023, 25, 8074-8081
7247377 CIFC14 H13 N O4P 1 21/n 111.3019; 6.9207; 16.2735
90; 101.713; 90		1246.36Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.
Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones
Green Chemistry, 2024, 26, 771-784
7247378 CIFC18 H22 O3P n a 218.6941; 17.9069; 10.1924
90; 90; 90		1586.8Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.
Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones
Green Chemistry, 2024, 26, 771-784
7247379 CIFC16 H18 O3P 1 21 17.97; 11.1812; 7.9888
90; 110.788; 90		665.57Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.
Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones
Green Chemistry, 2024, 26, 771-784
7247380 CIFC14 H15 N O4P 1 21/c 116.4952; 5.821; 14.2222
90; 112.011; 90		1266.06Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.
Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones
Green Chemistry, 2024, 26, 771-784
7247381 CIFC18 H20 O2P 21 21 217.3138; 12.607; 15.9123
90; 90; 90		1467.19Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.
Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones
Green Chemistry, 2024, 26, 771-784
7247383 CIFC23 H19 N O3 SP -18.9531; 9.9751; 11.6032
81.655; 89.531; 72.972		979.7Xia, Wen; Yang, Yawen; Zhang, Xiaohui; Hu, Liangzhen; Xiong, Yan
Electrochemical synthesis of γ-keto sulfones containing a β-quaternary carbon center via 1,2-migration
Green Chemistry, 2023, 25, 8273-8279
7247384 CIFC25 H24 O3 SP 1 21/c 114.1955; 11.0133; 13.4688
90; 99.284; 90		2078.1Xia, Wen; Yang, Yawen; Zhang, Xiaohui; Hu, Liangzhen; Xiong, Yan
Electrochemical synthesis of γ-keto sulfones containing a β-quaternary carbon center via 1,2-migration
Green Chemistry, 2023, 25, 8273-8279
7247432 CIFC17 H18 SP 21 21 219.4617; 11.8672; 13.219
90; 90; 90		1484.28Mukherjee, Nilanjana; Chatterjee, Tanmay
Recyclable iodine-catalyzed oxidative C–H chalcogenation of 1,1-diarylethenes in water: green synthesis of trisubstituted vinyl sulfides and selenides
Green Chemistry, 2023, 25, 8798-8807
7247433 CIFC16 H16 O3 SP -18.19; 10.9737; 16.0251
92.841; 98.85; 91.328		1420.66Mei, Lan; Shu, Xiao-Rong; Liu, Fa-Liang; Li, Jiao-Zhe; Zhang, Jian-Feng; Tang, Keqi; Wei, Wen-Ting
Multicomponent hydrosulfonylation of alkynes for the synthesis of vinyl sulfones
Green Chemistry, 2023, 25, 8820-8825
7247437 CIFC29 H31 Cl2 Co I O3 P SP 1 21 110.7008; 13.6759; 11.2342
90; 113.51; 90		1507.58Ma, Shuang-Shuang; Sun, Rui; Zhang, Zi-Heng; Guan, Peng-Xin; Lin, Jin-Qing; Li, Chun-Shan; Xu, Bao-Hua
Co(dppbsa)-catalyzed reductive N,N-dimethylation of nitroaromatics with CO2 and hydrosilane
Green Chemistry, 2023, 25, 8625-8632
7247479 CIFC20 H23 N5 O4P 1 21/n 111.4448; 8.3202; 20.9237
90; 104.738; 90		1926.87Liu, Mengjia; He, Ying; Wojtas, Lukasz; Shi, Xiaodong
Design and synthesis of covalently tethered “isoG-star” as a recyclable host for selective cesium separation
Green Chemistry, 2023, 25, 8494-8499
7247480 CIFC32.05 H47.58 N5 O8.68 SiC 1 2 144.243; 19.9018; 17.7791
90; 110.985; 90		14616.5Liu, Mengjia; He, Ying; Wojtas, Lukasz; Shi, Xiaodong
Design and synthesis of covalently tethered “isoG-star” as a recyclable host for selective cesium separation
Green Chemistry, 2023, 25, 8494-8499
7247486 CIFC H F O SP 1 21/c 115.093; 8.0955; 20.7666
90; 105.204; 90		2448.56Li, Jiayu; Guo, Zipeng; Zhang, Xiaofeng; Meng, Xiaoli; Dai, Zhenyang; Gao, Meiyun; Guo, Shuo; Tang, Pingping
Light-induced aryldifluoromethyl-sulfonylation/thioetherification of alkenes using arenethiolates as a photoreductant and sulfur source
Green Chemistry, 2023, 25, 9292-9300
7247510 CIFC18 H21 N O5P 1 21/n 15.78002; 18.6163; 15.854
90; 95.564; 90		1697.89Zhao, Tian-Tian; Zhang, Xu-Gang; He, Wen-Bo; Xu, Peng-Fei
A novel approach for synthesizing α-amino acids via formate mediated hydrogen transfer using a carbon source
Green Chemistry, 2023, 25, 8539-8543
7247511 CIFC21 H18 Cl N O2P 1 21/n 110.4508; 12.4654; 14.1577
90; 99.135; 90		1820.98Zhao, Tian-Tian; Zhang, Xu-Gang; He, Wen-Bo; Xu, Peng-Fei
A novel approach for synthesizing α-amino acids via formate mediated hydrogen transfer using a carbon source
Green Chemistry, 2023, 25, 8539-8543

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