1150587-91-9Relevant academic research and scientific papers
Visible-light-induced direct C(sp3)-H difluromethylation of tetrahydroisoquinolines with the in situ generated difluoroenolates
Li, Weipeng,Zhu, Xuebin,Mao, Haibin,Tang, Zhongkai,Cheng, Yixiang,Zhu, Chengjian
supporting information, p. 7521 - 7523 (2014/07/07)
An effective approach to C1-difluoromethylated tetrahydroisoquinoline derivatives has been developed through C-H functionalization of tertiary amines by visible-light photoredox catalysis. This method uses stable, easily obtained α,α-difluorinated gem-dio
CuBr-catalyzed oxidative difluoromethylation of tertiary amines with difluoroenol silyl ethers
Chu, Lingling,Zhang, Xingang,Qing, Feng-Ling
supporting information; experimental part, p. 2197 - 2200 (2009/09/28)
CuBr-catalyzed oxidative difluoromethylation of readily available tertiary amines with difluoroenol silyl ethers was performed under mild conditions to afford β-amine-a,a-difluoro ketones.
