Crystallography Open Database

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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 CIFC40 H35 Cl N3 O5.5F 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 CIFC13 H9 F6 N O2 SeP 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 CIFC27 H26 F2 N2 O6P 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 CIFC11 H12 O5P 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

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