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Li, Lingchun, Wang, Fei, Ni, Chuanfa, Hu, Jinbo (2013) Synthesis ofgem-Difluorocyclopropa(e)nes and O-, S-, N-, and P-Difluoromethylated Compounds with TMSCF2Br. Angewandte Chemie, 125 (47). 12616-12620 doi:10.1002/ange.201306703

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis ofgem-Difluorocyclopropa(e)nes and O-, S-, N-, and P-Difluoromethylated Compounds with TMSCF2Br
JournalAngewandte Chemie
AuthorsLi, LingchunAuthor
Wang, FeiAuthor
Ni, ChuanfaAuthor
Hu, JinboAuthor
Year2013 (November 18)Volume125
Issue47
PublisherWiley
DOIdoi:10.1002/ange.201306703Search in ResearchGate
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Mindat Ref. ID7323518Long-form Identifiermindat:1:5:7323518:1
GUID0
Full ReferenceLi, Lingchun, Wang, Fei, Ni, Chuanfa, Hu, Jinbo (2013) Synthesis ofgem-Difluorocyclopropa(e)nes and O-, S-, N-, and P-Difluoromethylated Compounds with TMSCF2Br. Angewandte Chemie, 125 (47). 12616-12620 doi:10.1002/ange.201306703
Plain TextLi, Lingchun, Wang, Fei, Ni, Chuanfa, Hu, Jinbo (2013) Synthesis ofgem-Difluorocyclopropa(e)nes and O-, S-, N-, and P-Difluoromethylated Compounds with TMSCF2Br. Angewandte Chemie, 125 (47). 12616-12620 doi:10.1002/ange.201306703
In(2013, November) Angewandte Chemie Vol. 125 (47) Wiley

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Li, Lingchun, Wang, Fei, Ni, Chuanfa, Hu, Jinbo (2013) Synthesis ofgem-Difluorocyclopropa(e)nes and O-, S-, N-, and P-Difluoromethylated Compounds with TMSCF2Br. Angewandte Chemie International Edition, 52 (47). 12390-12394 doi:10.1002/anie.201306703
Xie, Qiqiang, Ni, Chuanfa, Zhang, Rongyi, Li, Lingchun, Rong, Jian, Hu, Jinbo (2017) Efficient Difluoromethylation of Alcohols Using TMSCF2Br as a Unique and Practical Difluorocarbene Reagent under Mild Conditions. Angewandte Chemie, 129 (12). 3254-3258 doi:10.1002/ange.201611823
Li, Lingchun, Ni, Chuanfa, Xie, Qiqiang, Hu, Mingyou, Wang, Fei, Hu, Jinbo (2017) TMSCF 3 as a Convenient Source of CF 2 =CF 2 for Pentafluoroethylation, (Aryloxy)tetrafluoroethylation, and Tetrafluoroethylation. Angewandte Chemie, 129 (33). 10103-10107 doi:10.1002/ange.201705734
Xie, Qiqiang, Ni, Chuanfa, Zhang, Rongyi, Li, Lingchun, Rong, Jian, Hu, Jinbo (2017) Efficient Difluoromethylation of Alcohols Using TMSCF2Br as a Unique and Practical Difluorocarbene Reagent under Mild Conditions. Angewandte Chemie International Edition, 56 (12). 3206-3210 doi:10.1002/anie.201611823
Li, Lingchun, Ni, Chuanfa, Wang, Fei, Hu, Jinbo (2016) Deoxyfluorination of alcohols with 3,3-difluoro-1,2-diarylcyclopropenes. Nature Communications, 7. doi:10.1038/ncomms13320
Pan, Shitao, Xie, Qiqiang, Wang, Xiu, Huang, Rumin, Lu, Yuhao, Ni, Chuanfa, Hu, Jinbo (2024) Controllable Double Difluoromethylene Insertions into S−Cu Bonds: (Arylthio)tetrafluoroethylation of Aryl Iodides with TMSCF2Br. Angewandte Chemie, 136 (14) doi:10.1002/ange.202400839
Xie, Qiqiang, Zhu, Ziyue, Li, Lingchun, Ni, Chuanfa, Hu, Jinbo (2019) A General Protocol for C−H Difluoromethylation of Carbon Acids with TMSCF 2 Br. Angewandte Chemie, 131 (19). 6471-6476 doi:10.1002/ange.201900763
Li, Lingchun, Ni, Chuanfa, Xie, Qiqiang, Hu, Mingyou, Wang, Fei, Hu, Jinbo (2017) TMSCF 3 as a Convenient Source of CF 2 =CF 2 for Pentafluoroethylation, (Aryloxy)tetrafluoroethylation, and Tetrafluoroethylation. Angewandte Chemie International Edition, 56 (33). 9971-9975 doi:10.1002/anie.201705734
Hu, Mingyou, Ni, Chuanfa, Li, Lingchun, Han, Yongxin, Hu, Jinbo (2015) gem-Difluoroolefination of Diazo Compounds with TMSCF3 or TMSCF2Br: Transition-Metal-Free Cross-Coupling of Two Carbene Precursors. Journal Of The American Chemical Society, 137 (45) 14496-14501 doi:10.1021/jacs.5b09888
Xie, Qiqiang, Li, Lingchun, Zhu, Ziyue, Zhang, Rongyi, Ni, Chuanfa, Hu, Jinbo (2018) From C 1 to C 2 : TMSCF 3 as a Precursor for Pentafluoroethylation. Angewandte Chemie, 130 (40). 13395-13399 doi:10.1002/ange.201807873
Ni, Chuanfa, Liu, Jun, Zhang, Laijun, Hu, Jinbo (2007) A Remarkably Efficient Fluoroalkylation of Cyclic Sulfates and Sulfamidates with PhSO2CF2H: Facile Entry into β-Difluoromethylated or β-Difluoromethylenated Alcohols and Amines. Angewandte Chemie, 119 (5). 800-803 doi:10.1002/ange.200603983
 
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