Recent advances in nickel-catalyzed reductive hydroalkylation and hydroarylation of electronically unbiased alkenes

被引:142
作者
Wang, Xiao-Xu [1 ]
Lu, Xi [1 ]
Li, Yan [1 ]
Wang, Jia-Wang [1 ]
Fu, Yao [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Urban Pollutant Convers, Anhui Prov Key Lab Biomass Clean Energy,iChEM, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
nickel; electronically unbiased alkenes; C-C bond formation; reductive hydroalkylation; reductive hydroarylation; CROSS-COUPLING REACTIONS; ASYMMETRIC-SYNTHESIS; UNACTIVATED ALKENES; NEGISHI ARYLATIONS; INTERNAL OLEFINS; ALKYL; HYDROAMINATION; SECONDARY; ACIDS; FUNCTIONALIZATION;
D O I
10.1007/s11426-020-9838-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of simple and easily available feedstock to quickly and efficiently obtain compounds with complex molecular structures through the transition-metal-catalyzed construction of C(sp(3))-C bonds has important significance. As traditional C(sp(3))-C coupling reagents, alkylmetallic reagents often have limitations such as air and moisture sensitivity and difficulties in storage. Nickel-catalyzed reductive olefin hydrocarbonation reactions use alkenes to replace organometallic reagents, reduce the synthesis steps, improve the functional group compatibility, and expand the substrate scope This minireview discusses important progress in the hydroalkylation and hydroarylation of electronically unbiased alkenes in recent years and describes the key mechanism and applications.
引用
收藏
页码:1586 / 1600
页数:15
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