15776-99-5Relevant articles and documents
Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis
Gao, Guo-Lin,Yang, Chao,Xia, Wujiong
, p. 1041 - 1044 (2017)
The protocol presented here is a new strategy for visible light induced C-H trifluoromethylation at C4 of benzimidazoles using Togni's reagent in the presence of fac-Ir(ppy)3. Its advantages are its operational simplicity, mild reaction conditions, low catalyst loading and wide substrate scope in which electron-withdrawing, electron-donating groups and different protecting groups are tolerated.
Cu-Catalyzed Regioselective C-H Alkylation of Benzimidazoles with Aromatic Alkenes
He, Yu-Ting,Mao, Yang-Jie,Hao, Hong-Yan,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian
supporting information, p. 8250 - 8255 (2020/11/18)
Herein we report a novel Cu-catalyzed regioselective C2-H alkylation of benzimidazoles with aromatic alkenes. The reaction features exclusive regioselectivity and broad substrate scope in the intermolecular alkylation of benzimidazoles with terminal and i
SYNTHESIS OF ONCOLYTIC ANALOGS OF 1,2-DIMETHYL-4,5-DIAMINOBENZENE.
WOOLLEY,STEWART
, p. 599 - 601 (2007/10/09)
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