Frontiers in Radical Fluoromethylation by Visible-Light Organic Photocatalysis

被引:39
|
作者
Koike, Takashi [1 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Midori Ku, R1-27,4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
关键词
organocatalyst; radical reaction; sustainable chemistry; fluorine; photocatalysis; TRANSITION-METAL-FREE; TRIFLUOROMETHYLATION REACTIONS; FLUOROALKYLATION REACTIONS; PHOTOREDOX CATALYSIS; ALKENES; PERFLUOROALKYLATION; HETEROARENES; EFFICIENT; TRIFLUOROMETHANESULFINATE; FUNCTIONALIZATION;
D O I
10.1002/ajoc.202000058
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Fluoromethyl groups, including tri-, di-, and mono-fluoromethyl (CF3, CF2H, and CH2F, respectively) groups, are important structural motifs in medicinal chemistry. Radical fluoromethylation has attracted significant interest for the late-stage functionalization of complex bioactive molecules. Recently, light energy has been used for radical reactions in synthesis of various valuable products. Strategies using organic photocatalysts (OPCs) are beneficial for synthetic radical chemistry and various aspects of "sustainable development goals (SDGs)". Particularly, over the past several years, considerable progress has been made in the field of photoinduced radical fluoromethylation by OPCs. In this minireview, the concepts of representative reaction systems for fluoromethyl radical generation will be discussed.
引用
收藏
页码:529 / 537
页数:9
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