Metal-Catalyzed Substrate-Directed Enantioselective Functionalization of Unactivated Alkenes

被引:52
作者
Wang, Zi-Xuan [1 ]
Bai, Xiao-Yan [1 ]
Li, Bi-Jie [1 ]
机构
[1] Tsinghua Univ, Dept Chem, CBMS, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
TERTIARY BORONIC ESTERS; ASYMMETRIC HYDROBORATION; HYDROAMINATION; HYDROGENATION; HYDROCARBOFUNCTIONALIZATION; HYDROFUNCTIONALIZATION;
D O I
10.1002/cjoc.201900308
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alkenes are versatile compounds that are available on large scales in industry or through chemical synthesis. Selective functionalization of unactivated alkenes in a chemo-, regio-, diastereo- and enantioselective fashion is a highly sought-after goal in organic synthesis. Substrate-directed enantioselective functionalization of unactivated alkenes provides an important strategy to achieve this goal. Using a functional group on the alkene substrate as a native coordinating group, a two-point binding mode of the substrate to the metal center enables effective control of regio-, diastereo- and enantioselectivities. Through this strategy, a variety of enantioselective functionalization methods have been developed recently. The recent advances in this area are highlighted here.
引用
收藏
页码:1174 / 1180
页数:7
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