Visible-Light Mediated Nickel-Catalyzed Asymmetric Difunctionalizations of Alkenes

被引:1
作者
Zhao, Han-Tong [1 ,2 ]
Lin, Jia-Ni [1 ,2 ]
Shu, Wei [1 ,2 ,3 ]
机构
[1] Southern Univ Sci & Technol, Guangming Adv Res Inst, Shenzhen Grubbs Inst, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Guangdong, Peoples R China
[3] Sichuan Univ Sci & Engn, Coll Chem & Environm Engn, Zigong 643000, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkenes; Difunctionalization reaction; Visible light; Nickel catalysis; Asymmetric catalysis; TRANSITION-METAL; MERGER; PHOTOREDOX; ARYLATION; ENABLES;
D O I
10.1002/chem.202402712
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Difunctionalizations of alkenes represent one of the most straightforward protocols to build molecular complexity due to the simultaneous construction of two vicinal bonds cross pi-bond of alkenes. It is extremely attractive yet challenging to control the stereochemistry outcome of this event. Over the past years, visible-light and Ni-catalyzed asymmetric difunctionalizations of alkenes provide an environmental benign and promising solution for the construction of saturated carbon centers with the control of regio- and enantioselectivity. In this Concept, the initiative and progress of regio- and enantioselective difunctionalizations of alkenes enabled by visible-light and nickel catalysis has been summarized. Moreover, further efforts and directions for the development of visible-light mediated Ni-catalyzed asymmetric difunctionalizations of alkenes has been discussed.
引用
收藏
页数:8
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