Recent Advances in the Synthesis of Fluoroalkylated Alkenes and Alkynes via Fluoroalkyl Radical Substitution Reactions

被引:11
作者
Yamamoto, Yoshihiko [1 ]
机构
[1] Nagoya Univ, Grad Sch Pharmaceut Sci, Dept Basic Med Sci, Chikusa Ku, Nagoya 4648601, Japan
关键词
Alkenes; Alkynes; Fluoroalkylation; Radical reaction; Substitution; ALPHA; BETA-UNSATURATED CARBOXYLIC-ACIDS; CATALYZED DECARBOXYLATIVE DIFLUOROALKYLATION; DENITRATIVE TRIFLUOROMETHYLATION; SELECTIVE DIFLUOROALKYLATION; C-VINYL-CF3; COMPOUNDS; COPPER; PHOTOREDOX; FLUORINE; ARYL; DIFLUOROMETHYLATION;
D O I
10.1002/adsc.202300928
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Trifluoromethylated alkenes and alkynes are versatile building blocks for organofluorine synthesis. In addition, (trifluoromethyl)alkene motifs are found in biofunctional molecules. Hence, their synthesis is an important research objective. Although trifluoromethylated alkenes and alkynes have been prepared using transition-metal-mediated coupling reactions, more environmentally benign processes that obviate the use of precious metal catalysts and/or harsh reaction conditions should be developed. This review outlines recent advances in the synthesis of fluoroalkylated alkenes and alkynes via fluoroalkyl radical substitution reactions.
引用
收藏
页码:3572 / 3585
页数:14
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