Crystallography Open Database

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7245794 CIFC16 H16 O SP 1 21/n 16.0752; 9.8777; 22.1887
90; 91.536; 90
1331.04Zhu, Can-Ming; Liang, Rong-Bin; Xiao, Yonghong; Zhou, Wei; Tong, Qing-Xiao; Zhong, Jian-Ji
Metal-free and site-selective α-C–H functionalization of tetrahydrofuran enabled by the photocatalytic generation of bromine radicals
Green Chemistry, 2023, 25, 960-965
7245933 CIFC4 H6.22 B0.22 F0.89 N0.89 Rh0.22I 41/a c d :215.9403; 15.9403; 31.662
90; 90; 90
8045.1Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245934 CIFC13.5 H17 B0.5 Cl F2 N2 Rh0.5P 1 21/n 113.617; 17.292; 13.8897
90; 116.871; 90
2917.4Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245935 CIFC127 H147 B2 Cl9 F8 N8 Rh2P 1 21/c 115.1914; 15.8408; 55.703
90; 93.157; 90
13384.2Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao
Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins
Green Chemistry, 2023, 25, 1368-1379
7245956 CIFC38 H29 N OP 1 21/n 19.7566; 23.006; 13.329
90; 109.053; 90
2827.9Zhuang, Hongfeng; Hou, Qin; Han, Feng; Lv, Haotian; Miao, Chengxia
Heteropolyacid catalyzed O-alkylation of oximes with alcohols via a carbocation in dimethyl carbonate and mechanism insight
Green Chemistry, 2023, 25, 310-317
7245973 CIFC22 H13 N O2 SP n a 2111.7823; 17.2564; 8.5563
90; 90; 90
1739.7Chen, Shiliu; Yan, Qinqin; Fan, Jie; Guo, Changyou; Li, Lijun; Liu, Zhong-Quan; Li, Zejiang
Photo-induced spirocyclization of biaryl ynones with ammonium thiocyanate: access to thiocyanate-featured spiro[5,5]trienones
Green Chemistry, 2023, 25, 153-160
7245974 CIFC26 H22 F3 N3P 1 21/n 19.705; 16.0805; 13.7744
90; 93.165; 90
2146.4Sharma, Himanshi; Kumar, Manoj; Sethi, Aaftaab; Poonam,; Rathi, Brijesh
Metal-free construction of aminated isoquinoline frameworks from 2-(2-oxo-2-arylethyl) benzonitrile in an aqueous medium
Green Chemistry, 2023, 25, 167-171
7246014 CIFC20 H19 I O6 SP 16.8727; 7.4757; 10.7012
75.161; 88.164; 77.878
519.48Peng, Chuxiong; Gu, Fengyan; Lin, Xiaofeng; Ding, Ning; Zhan, Qichen; Cao, Peng; Cao, Tao
Highly selective catalyst- and additive-free iodosulfonylation of cyclopropenes in water
Green Chemistry, 2023, 25, 671-677
7246049 CIFC13 H25 N O7 SP 21 21 217.9459; 13.5525; 15.5352
90; 90; 90
1672.9Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.
Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene
Green Chemistry, 2023, 25, 606-613
7246050 CIFC13 H19 N O5 SP 21 21 216.1009; 12.5179; 19.3009
90; 90; 90
1474.02Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.
Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene
Green Chemistry, 2023, 25, 606-613
7246051 CIFC23 H16 Fe O2P -16.7731; 10.9956; 12.2301
72.319; 75.206; 77.254
828.85Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian
Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2
Green Chemistry, 2023, 25, 554-559
7246052 CIFC18 H14 Fe O3P -110.4854; 11.7036; 12.3518
72.325; 79.087; 75.017
1384.97Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian
Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2
Green Chemistry, 2023, 25, 554-559
7246055 CIFC10.8 H8.8 Cl0.4 N0.4 O0.8 S0.4 Se0.4P 1 21/n 111.9543; 8.3309; 24.4205
90; 102.103; 90
2377.98Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay
100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen
Green Chemistry, 2023, 25, 779-788
7246056 CIFC21 H14 I N S2I 1 2/a 117.9022; 6.0537; 34.1626
90; 91.27; 90
3701.45Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay
100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen
Green Chemistry, 2023, 25, 779-788
7246068 CIFC17 H16 Cl N3P -16.7166; 9.3699; 12.656
68.667; 79.026; 72.896
706Liu, Qingqing; Ci, Chenggang; Zhao, He; Xie, Rong; Jiang, HuanFeng; Zhang, Min
Direct access to functional phenazines via oxidative annulation of anilines and o-phenylenediamines with a reusable cobalt catalyst
Green Chemistry, 2023, 25, 678-683
7246122 CIFC13 H15 N O6C 1 2/c 125.911; 4.6748; 23.299
90; 104.436; 90
2733.1Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László
Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant
Green Chemistry, 2023, 25, 746-754
7246123 CIFC13 H12 O4P -16.5868; 8.2313; 11.126
106.015; 97.159; 95.387
570.1Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László
Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant
Green Chemistry, 2023, 25, 746-754
7246138 CIFC24 H20 F5 O4P -18.3761; 8.4007; 16.0336
98.767; 99.704; 91.221
1097.79Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar
Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes
Green Chemistry, 2023, 25, 1014-1022
7246139 CIFC18 H22 O4P 1 21/n 17.0243; 20.574; 11.0931
90; 91.591; 90
1602.5Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar
Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes
Green Chemistry, 2023, 25, 1014-1022
7246144 CIFC18 H18 O9P 1 21/c 118.6508; 5.8796; 14.7464
90; 94.7151; 90
1611.61Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246145 CIFC37 H30 O10P -110.361; 13.355; 13.4649
62.271; 70.487; 70.729
1520.04Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246146 CIFC21 H24 O11P 1 21/n 110.5648; 16.247; 12.4776
90; 110.308; 90
2008.6Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246147 CIFC39 H35 N O10P 1 21/c 19.1956; 33.6799; 10.508
90; 97.813; 90
3224.19Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.
Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions
Green Chemistry, 2023, 25, 1045-1055
7246166 CIFC19 H19 N O3P b c a18.0732; 8.28431; 20.8875
90; 90; 90
3127.36Wei, Wan-Jie; Zhan, Lei; Jiang, Cai-Na; Tang, Hai-Tao; Pan, Ying-Ming; Ma, Xian-Li; Mo, Zu-Yu
Electrochemical oxidative cascade cyclization of olefinic amides and alcohols leading to the synthesis of alkoxylated 4H-3,1-benzoxazines and indolines
Green Chemistry, 2023, 25, 928-933
7246185 CIFC27 H27 N OP 21 21 217.7837; 31.1021; 8.6447
90; 90; 90
2092.79Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang
Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane
Green Chemistry, 2023, 25, 1120-1127
7246186 CIFC25 H29 N OP 1 21 111.2; 7.8745; 11.8582
90; 103.292; 90
1017.81Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang
Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane
Green Chemistry, 2023, 25, 1120-1127
7246229 CIFC9 H5 N3 OP 1 21/n 13.7252; 11.5014; 18.9837
90; 91.706; 90
813Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander
Amenamevir by Ugi-4CR
Green Chemistry, 2023, 25, 1322-1325
7246230 CIFC24 H26 N4 O5 SI 1 2/a 119.6089; 13.7807; 17.823
90; 101.936; 90
4712.08Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander
Amenamevir by Ugi-4CR
Green Chemistry, 2023, 25, 1322-1325
7246286 CIFC24 H16 F5 O2 PP 1 21/c 118.8874; 6.1813; 17.2323
90; 91.402; 90
2011.2Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang
Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans
Green Chemistry, 2023, 25, 2000-2010
7246287 CIFC36 H25 F5 O3 P2P -111.345; 12.0953; 14.1162
89.245; 77.498; 62.787
1673.55Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang
Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans
Green Chemistry, 2023, 25, 2000-2010
7246321 CIFC10.33 H7.33 N1.33 O1.33 S0.67P -110.3322; 10.7423; 14.3583
97.245; 100.734; 116.704
1358.21Zhang, Zhicheng; Wen, Linzi; Xu, Shihai; Tang, Yu; Cao, Xiaohui; Feng, Pengju
Consecutive cross-dehydrogenative C–O and C–N construction for the synthesis of polyarene with AIE properties under electrochemical condition involving oxygen radical species
Green Chemistry, 2023, 25, 2287-2292
7246353 CIFC25 H30 Fe K N2 O8P -19.877; 12.1262; 12.1406
66.668; 83.456; 83.448
1322.68Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.
A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations
Green Chemistry, 2023, 25, 2262-2267
7246354 CIFC23 H27 Fe N2 O6P 1 21/c 19.0238; 12.9234; 19.4802
90; 96.797; 90
2255.78Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.
A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations
Green Chemistry, 2023, 25, 2262-2267
7246413 CIFC15 H10 I N OP 1 21/c 113.0551; 7.4021; 13.9932
90; 101.381; 90
1325.65Wu, Jianglong; Ma, Yinfeng; Wang, Yan; Wang, Chenyu; Luo, Hui; Li, Dianjun; Yang, Jinhui
Copper-catalyzed direct synthesis of 3-methylene-2-arylisoindolin-1-ones with calcium carbide as a surrogate of gaseous acetylene
Green Chemistry, 2023, 25, 3425-3430
7246418 CIFC20 H19 N O2P 439.58017; 9.58017; 33.7964
90; 90; 90
3101.82Feng, Tian; Zhu, Zile; Zhang, Dongmei; Wang, Siyi; Li, Ruopu; Zhu, Zhaolin; Zhang, Xinxing; Qiu, Youai
Electrochemical dual α,β-C(sp3)–H functionalization of cyclic N-aryl amines
Green Chemistry, 2023, 25, 2681-2689
7246419 CIFC16 H19 N O3 S2P 1 21/c 111.6432; 16.4149; 9.6857
90; 113.866; 90
1692.87Wang, Qian; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming; Duan, Wen-Gui; He, Mu-Xue
Electrochemically driven α-thiocarbamylation via a dehydrocoupling strategy of β-ketoesters with amines and CS2
Green Chemistry, 2023, 25, 2572-2576
7246425 CIFC20 H19 N OP 1 21/c 125.949; 10.787; 11.392
90; 101.972; 90
3119.4Wei, Minghui; Liu, Chengkou; Wang, Chang-Sheng; Li, Yuguang; Qiu, Peng; Dong, Quanxiao; Yang, Zhao; Fang, Zheng; Guo, Kai
Synthesis of pyrido[1,2-a]indol-6(7H)-ones via a visible light-photocatalyzed formal (4 + 2) cycloaddition of indole-derived bromides and alkenes or alkynes
Green Chemistry, 2023, 25, 2453-2457
7246452 CIFC13 H19 Cl2 NP 21 21 214.9594; 10.7311; 27.2017
90; 90; 90
1447.67Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246453 CIFC13 H18 Br Cl F NP 1 21 14.8988; 10.7881; 13.7759
90; 98.02; 90
720.92Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246454 CIFC14 H21 Br Cl NP 21 21 214.9604; 10.8195; 29.3754
90; 90; 90
1576.55Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246455 CIFC14 H21 Br Cl NP 1 21 19.5543; 6.5919; 12.4634
90; 98.424; 90
776.49Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246456 CIFC13 H18 Br Cl F NP 21 21 217.6197; 14.1232; 27.1001
90; 90; 90
2916.36Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246457 CIFC13 H18 Br Cl F NP 1 21 14.8335; 26.095; 11.3444
90; 90.954; 90
1430.67Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246458 CIFC13 H18 Br Cl F NP 21 21 214.7559; 10.6799; 28.6366
90; 90; 90
1454.53Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming
Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization
Green Chemistry, 2023, 25, 4667-4673
7246493 CIFC14 H13 N O2P b c a8.6581; 12.1447; 22.107
90; 90; 90
2324.6Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246494 CIFC14 H12 Cl N O2P 1 21/c 113.6538; 9.0781; 10.6852
90; 108.522; 90
1255.83Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246495 CIFC14 H11 N OP 1 21/n 15.9303; 7.6388; 23.149
90; 94.506; 90
1045.4Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246496 CIFC14 H12 Br N O2P 21 21 215.4795; 11.4206; 19.3592
90; 90; 90
1211.48Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song
Synthesis of renewable isoindolines from bio-based furfurals
Green Chemistry, 2023, 25, 3297-3305
7246497 CIFC14 H12 Cl N3 O SP 1 21 110.7651; 4.8762; 13.0778
90; 106.91; 90
656.81Hommelsheim, Renè; Bausch, Sandra; van Nahl, Robin; Ward, Jas S.; Rissanen, Kari; Bolm, Carsten
Synthesis of 3-amino-substituted benzothiadiazine oxides by a palladium-catalysed cascade reaction
Green Chemistry, 2023, 25, 3021-3026
7246540 CIFC15 H20 Br N O2P -17.079; 9.363; 11.864
93.881; 97.142; 100.629
763.5Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei
Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes
Green Chemistry, 2023, 25, 3543-3548
7246541 CIFC16 H23 N O3P 1 21/n 16.676; 23.1; 9.948
90; 94.562; 90
1529.3Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei
Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes
Green Chemistry, 2023, 25, 3543-3548
7246546 CIFC14 H10 O2P 32 2 18.415; 8.415; 13.689
90; 90; 120
839.48Bhukta, Swadhapriya; Chatterjee, Rana; Dandela, Rambabu
Metal-free, 2-MeTHF mediated C(sp)–H functionalization of alkynes with anilines to access diaryl 1,2-diketones bearing lower E-factors
Green Chemistry, 2023, 25, 3034-3039
7246554 CIFC20 H18 N2P 1 21/n 112.54957; 5.45668; 21.5051
90; 100.046; 90
1450.07Everaert, Jonas; Leus, Karen; Rijckaert, Hannes; Debruyne, Maarten; Van Hecke, Kristof; Morent, Rino; De Geyter, Nathalie; Van Speybroeck, Veronique; Van Der Voort, Pascal; Stevens, Christian V.
A recyclable rhodium catalyst anchored onto a bipyridine covalent triazine framework for transfer hydrogenation of N-heteroarenes in water
Green Chemistry, 2023, 25, 3267-3277
7246560 CIFC30 H28 O3P -19.7371; 10.1536; 12.7652
102.012; 94.177; 110.29
1143.27Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan
Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2
Green Chemistry, 2023, 25, 3633-3643
7246561 CIFC22 H18 O3P -18.998; 11.5521; 18.5351
79.764; 84.293; 67.467
1750.2Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan
Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2
Green Chemistry, 2023, 25, 3633-3643
7246605 CIFC18 H16 N2P 21 21 216.607; 10.064; 21.6
90; 90; 90
1436.2Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246606 CIFC18 H14 Cl2 N2I 1 c 17.817; 18.49; 11.24
90; 96.61; 90
1614Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246607 CIFC18 H14 Br2 N2C 1 c 112.96; 18.557; 7.814
90; 120.687; 90
1616.1Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.
Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst
Green Chemistry, 2023, 25, 3443-3448
7246608 CIFC19 H19 N O3 S SeP 1 21/c 114.852; 8.3709; 15.745
90; 111.498; 90
1821.3Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246609 CIFC19 H19 N O4 SeP 1 21/n 16.042; 7.1534; 41.598
90; 91.97; 90
1796.8Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246610 CIFC23 H18 Br N O3 S SeP b c a9.9532; 24.647; 17.5152
90; 90; 90
4296.8Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang
Versatile electrooxidative amino- and oxyselenation of alkenes
Green Chemistry, 2023, 25, 3925-3930
7246637 CIFC26 H30 Br2 O6P 1 21 16.1791; 15.1836; 14.4771
90; 95.557; 90
1351.87Qiu, Huixin; Ren, Jiayi; Zhang, Long; Song, Ran; Si, Wen; Yang, Daoshan; Wen, Lirong; Lv, Jian
Enantioselective Meerwein–Ponndorf–Verley reduction of β,γ-unsaturated α-keto esters by asymmetric binary-acid catalysis in the green solvent iPrOH
Green Chemistry, 2023, 25, 3948-3955
7246659 CIFC20 H14 F5 N O3P 1 21/c 117.1352; 7.89497; 14.2824
90; 110.302; 90
1812.12Huang, Panyi; Yan, Zhiyang; Ling, Jiaxin; Li, Peixuan; Wang, Jiayang; Li, Jianjun; Sun, Bin; Jin, Can
Catalyst-free intramolecular radical cyclization cascades initiated by the direct homolysis of Csp3–Br under visible light
Green Chemistry, 2023, 25, 3989-3994
7246660 CIFC16 H25 B O4P 1 21 16.4643; 21.3155; 11.9798
90; 91.899; 90
1649.79Huninik, Paweł; Szyling, Jakub; Czapik, Agnieszka; Walkowiak, Jędrzej
Organocatalytic hydroboration of olefins in pyrrolidinium ionic liquids
Green Chemistry, 2023, 25, 3715-3722
7246679 CIFC58 H37.89 Cl0.11 N6 O8 S2P -19.521; 12.027; 12.459
63.128; 82.674; 72.395
1212.9Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246680 CIFC31 H23.91 Cl0.09 N2 O2 SP -19.279; 11.406; 13.046
80.4; 80.8; 69.338
1266.2Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246681 CIFC30 H22 N2 O2 SP -19.907; 11.5183; 11.8511
108.421; 104.16; 99.584
1199.6Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246682 CIFC60 H43.54 Cl0.56 N4 O6 S2P -111.803; 12.782; 17.329
89.118; 81.911; 71.924
2459.5Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli
Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process
Green Chemistry, 2023, 25, 4302-4308
7246708 CIFC21 H19 N2 O3 SP 1 21/n 114.2948; 8.5708; 15.3612
90; 95.345; 90
1873.84Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji
Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles
Green Chemistry, 2023, 25, 3982-3988
7246709 CIFC19 H19 N3 O2 SP 1 21/n 111.349; 10.096; 15.893
90; 97.84; 90
1804Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji
Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles
Green Chemistry, 2023, 25, 3982-3988
7246809 CIFC17 H16 Cl N3 O3 SeP -17.3092; 10.4613; 12.143
72.439; 87.404; 81.976
876.56Liu, Huan; Ye, Zi-Lin; Cai, Zhong-Jian; Ji, Shun-Jun
A multicomponent reaction of isocyanides, selenium powder and 3-aminooxetanes in pure water: green and efficient synthesis of 1,3-selenazolines
Green Chemistry, 2023, 25, 4239-4243
7246811 CIFC8 H20 Au Cl4 NP 1 2/n 19.1149; 7.9249; 10.3451
90; 92.043; 90
746.8Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246812 CIFC8 H20 Au Br4 NP 1 2/n 19.3812; 8.2418; 10.5053
90; 90.562; 90
812.21Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246813 CIFC16 H36 Au Cl4 NP 1 21/n 114.8787; 8.931; 18.277
90; 107.259; 90
2319.32Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246814 CIFC16 H36 Au Br4 NP 4/n :212.1431; 12.1431; 8.5038
90; 90; 90
1253.93Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246815 CIFC19 H42 Au Br4 NP 1 21/c 18.1965; 8.7398; 38.9304
90; 92.271; 90
2786.62Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav
Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts
Green Chemistry, 2023, 25, 5899-5906
7246829 CIFC11 H9 N O2 SP 1 21/c 112.545; 3.9268; 21.018
90; 106.758; 90
991.4Li, Dandan; Chen, Long; Jin, Yang; Wang, Xiaochen; Liu, Long; Li, Yilin; Chen, Gongyuan; Wu, Guanhao; Qin, Yujie; Yang, Leilei; Wang, Mengke; Zhao, Lulu; Xu, Zhihong; Wen, Jiangwei
An electrochemical-enabled cascaded cyclization of enaminones with potassium thiocyanate and alcohols to access 2-alkoxythiazoles
Green Chemistry, 2023, 25, 4656-4661
7246830 CIFC24 H19 N O3P 1 21/c 18.998; 13.804; 14.731
90; 92.647; 90
1827.8Yang, Na; Li, Anni; Gao, Hui; Liao, Li-Mei; Yang, Yu-Ping; Wang, Pei-Long; Li, Hongji
Electrochemical oxidation-induced benzylic C(sp3)–H functionalization towards the atom-economic synthesis of oxazole heterocycles
Green Chemistry, 2023, 25, 5128-5133
7246831 CIFC22 H16 Br N SP 21 21 222.70389; 13.29859; 5.82409
90; 90; 90
1758.47Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246832 CIFC22 H16 Cl N SC 1 2/c 124.9095; 5.8669; 25.8562
90; 111.533; 90
3514.94Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246833 CIFC22 H16 Br N SP 1 21/m 110.2654; 7.0454; 12.4963
90; 92.802; 90
902.7Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246834 CIFC22 H17 Cl N SP 1 21/m 110.1263; 6.9258; 12.6138
90; 92.516; 90
883.79Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246835 CIFC26 H25 N SP -111.3822; 12.2394; 16.8294
74.05; 80.114; 67.955
2083.27Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen
Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions
Green Chemistry, 2023, 25, 5206-5212
7246851 CIFC17 H14 F3 N O2 SP 1 21/c 19.3303; 17.815; 10.836
90; 112.207; 90
1667.6Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246852 CIFC18 H16 F3 N O2 SP 1 21/n 19.8704; 16.865; 11.3723
90; 115.314; 90
1711.3Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246853 CIFC18 H16 F3 N O2 SP -18.9764; 9.7004; 10.5392
102.617; 92.927; 99.557
879.46Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246854 CIFC16 H11 F3 O2 SP 1 21/c 18.8998; 16.2836; 10.5436
90; 107.423; 90
1457.88Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang
Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water
Green Chemistry, 2023, 25, 5233-5239
7246876 CIFC24 H21 NP 21 21 217.6105; 12.1722; 19.257
90; 90; 90
1783.9Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.
Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters
Green Chemistry, 2023, 25, 5601-5612
7246877 CIFC23 H23 NP 1 21/c 115.447; 5.6795; 21.658
90; 108.34; 90
1803.6Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.
Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters
Green Chemistry, 2023, 25, 5601-5612
7246939 CIFC11 H12 F N O2P 1 21/c 15.2503; 16.2082; 12.1305
90; 99.976; 90
1016.7Hu, Fangzhi; Sun, Zhipeng; Pan, Mengzhe; Wang, Liang; Xu, Lubin; Liu, Xiong-Li; Li, Shuai-Shuai
Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions
Green Chemistry, 2023, 25, 5134-5141
7246940 CIFC26 H25 N O8P 21 21 217.6044; 9.6671; 31.908
90; 90; 90
2345.6Fu, Yun-Dong; Gao, Xiang; Jia, Shi-Kun; Xiao, Xiao; Wang, Min-Can; Huang, Lihua; Mei, Guang-Jian
Catalyst-free racemic and H2O/CPA-catalyzed asymmetric regio-reversed domino processes of triketone enones with azlactones
Green Chemistry, 2023, 25, 5692-5697
7246941 CIFC81 H161.5 Mn Mo6 N9.5 O30P 1 21 124.16; 14.7868; 33.2539
90; 103.708; 90
11541.5Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge
A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles
Green Chemistry, 2023, 25, 6263-6269
7246942 CIFC46 H106 Mn Mo7.5 N4 O44 S14P 21 21 233.5555; 30.4959; 9.33799
90; 90; 90
9555.61Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge
A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles
Green Chemistry, 2023, 25, 6263-6269
7246950 CIFC23 H16 F N OP n a 2112.4459; 27.609; 4.7734
90; 90; 90
1640.23Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246951 CIFC23 H17 N OP 1 21/c 14.8075; 27.2149; 12.4496
90; 92.523; 90
1627.27Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246952 CIFC20 H16 OP -16.3822; 10.211; 11.3886
84.533; 89.069; 74.931
713.37Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246953 CIFC23 H23 N O3P 1 21/c 112.0444; 5.6218; 27.7622
90; 99.864; 90
1852Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246954 CIFC19 H15 N OP 1 21/c 113.198; 5.6188; 18.6771
90; 97.268; 90
1373.91Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246955 CIFC24 H18 F N OP 1 21/n 15.6809; 13.8095; 21.8999
90; 91.229; 90
1717.66Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660
7246956 CIFC22 H21 N O3P 1 21/c 119.3497; 7.1784; 12.8947
90; 103.665; 90
1740.37Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.
A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes
Green Chemistry, 2023, 25, 5654-5660

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