期刊
ORGANIC LETTERS
卷 19, 期 18, 页码 4738-4741出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02056
关键词
-
资金
- National Basic Research Program of China (973 Program) [2015CB856600]
- National Natural Science Foundation of China [21325206, 21632001]
- National Young Top-notch Talent Support Program
- Peking University Health Science Center [BMU20160541]
A mild and efficient protocol for photoredox-catalyzed azidofluoroalkylation of simple alkenes is described with readily available fluoroalkyl iodides. This method allows for a direct and regioselective formation of C-R-F and C-N-3 bonds from the C=C moiety. A variety of fluoroalkyl groups including the CF3 group can be selectively introduced to olefins to afford a series of,beta-fluoroalkylated azides.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据