Applications of Organosilanes in Visible Light-induced Catalytic Asymmetric Reactions

被引:5
|
作者
Hou, Liuzhen [1 ]
Cao, Weidi [1 ]
Feng, Xiaoming [1 ]
机构
[1] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
Asymmetric catalysis; Organosilanes; Photoredox catalysis; Radical reactions; NUCLEOPHILE-ASSISTED CLEAVAGE; SINGLE-ELECTRON-TRANSFER; TRANSITION-METAL; PHOTOREDOX CATALYSIS; CONJUGATE ADDITIONS; ORGANIC-SYNTHESIS; SILICON-COMPOUNDS; ALLYLSILANES; ALKYLATION; OXIDATION;
D O I
10.1002/cctc.202400385
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Over the past decades, visible light-mediated photocatalysis has found a mainstream of applications in synthetic chemistry. Organosilanes have been proven to be a useful class of electron donors to generate the highly active radical species via photoinduced single electron transfer oxidation/fragmentation sequence, which may undergo follow-up radical coupling or addition process. This minireview highlights the comprehensive advances of organosilanes in photoredox catalyzed asymmetric organic synthesis, with particular emphasis placed on reaction mechanisms. We hope that this review will inspire further design and development of new reactions with such class of readily accessible reagents. This review provides the overview of comprehensive advances in the chemistry of organosilanes in asymmetric photoredox catalyzed organic synthesis, which are introduced from the mechanism perspective including C-Si bond cleavage and C-H bond cleavage of organosilanes. It is hopeful to provide guidance and assistance for the development of this field in future. image
引用
收藏
页数:12
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