期刊
ORGANIC LETTERS
卷 21, 期 10, 页码 3600-3605出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01015
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资金
- JSPS KAKENHI [JP15H05802, JP17H03049, JP18H06097]
The photocatalyst-free C-H gamma,gamma,gamma-trifluoroalkylation of quinolines under visible light irradiation is reported. By the combination of readily available alkenes and Umemoto's reagent II, a variety of gamma,gamma,gamma-trifluoroalkyl groups were installed into quinolines via chemoselective sequential radical processes. This transformation provides rapid access to a variety of quinoline derivatives with scarcely explored fluoroalkyl groups, affording a novel library of N-heteroaromatic compounds and versatile building blocks for applications in medicinal chemistry.
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