A review of enantioselective dual transition metal/photoredox catalysis

被引:138
|
作者
Zhang, Hong-Hao [1 ]
Chen, Hui [1 ]
Zhu, Chengjian [1 ]
Yu, Shouyun [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Jiangsu Key Lab Adv Organ Mat, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
transition metal catalysis; photoredox catalysis; dual catalysis; asymmetric catalysis; SINGLE-ELECTRON TRANSMETALATION; C-H BONDS; PHOTOREDOX CATALYSIS; COOPERATIVE PHOTOREDOX; ASYMMETRIC INDUCTION; COPPER; TRANSFORMATIONS; ALLYLATION; CYANATION; ACIDS;
D O I
10.1007/s11426-019-9701-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal catalysis is one of the most important tools to construct carbon-carbon and carbon-heteroatom bonds in modern organic synthesis. Visible-light photoredox catalysis has recently drawn considerable attention of the scientific community owing to its unique activation modes and significance for the green synthesis. The merger of photoredox catalysis with transition metal catalysts, termed metallaphotoredox catalysis, has become a popular strategy for expanding the synthetic utility of visiblelight photocatalysis. This strategy has led to the discovery of novel asymmetric transformations, which are unfeasible or not easily accessible by a single catalytic system. This contemporary area of organic chemistry holds promise for the development of economical and environmentally friendly methods for the asymmetric synthesis of chiral compounds. In this review, the advances in the enantioselective metallaphotoredox catalysis (EMPC) are summarized.
引用
收藏
页码:637 / 647
页数:11
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