Recent Advances in Photochemical Asymmetric Three-Component Reactions

被引:6
|
作者
Huang, Haichao [1 ]
Lin, Yu-Mei [1 ]
Gong, Lei [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Key Lab Chem Biol Fujian Prov, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen 361005, Fujian, Peoples R China
来源
CHEMICAL RECORD | 2023年 / 23卷 / 12期
基金
中国国家自然科学基金;
关键词
photocatalysis; asymmetric catalysis; three-component reactions; visible light; radical; TRANSFER RADICAL-ADDITION; DUAL PHOTOREDOX; CASCADE; FUNCTIONALIZATION; ARYLATION; LIGHT; ARYL; STEREOCENTERS; REARRANGEMENT; 1,3-DIENES;
D O I
10.1002/tcr.202300275
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the past decades, asymmetric photochemical synthesis has garnered significant attention for its sustainability and unique ability to generate enantio-enriched molecules through distinct reaction pathways. Photochemical asymmetric three-component reactions have demonstrated significant potential for the rapid construction of chiral compounds with molecular diversity and complexity. However, noteworthy challenges persist, including the participation of high-energy intermediates such as radical species, difficulties in precise control of stereoselectivity, and the presence of competing background and side reactions. Recent breakthroughs have led to the development of sophisticated strategies in this field. This review explores the intricate mechanisms, synthetic applications, and limitations of these methods. We anticipate that it will contribute towards advancing asymmetric catalysis, photochemical synthesis, and green chemistry. This review primarily revolves around the photochemical asymmetric three-component transformations facilitated by transition metal catalysis or organocatalysis. The intricate reaction mechanisms, diverse synthetic applications, and inherent limitations of these methods are thoroughly examined and discussed.image
引用
收藏
页数:18
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