Metal-catalyzed C-H functionalization involving isocyanides

被引:297
|
作者
Song, Bingrui [1 ,2 ]
Xu, Bin [1 ,3 ]
机构
[1] Shanghai Univ, Dept Chem, Innovat Drug Res Ctr, Shanghai 200444, Peoples R China
[2] Clariant Chem China LTD, Grp Innovat & Technol, Res Ctr China, Shanghai, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
MU-ETHYNEDIYL COMPLEXES; INTERMOLECULAR OXIDATIVE CYCLIZATION; MICROWAVE-ASSISTED SYNTHESIS; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; VINYL ISOCYANIDES; CASCADE REACTIONS; ISONITRILE INSERTION; SYNTHETIC REACTIONS; RADICAL TRIFLUOROMETHYLATION;
D O I
10.1039/c6cs00384b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isocyanides have a broad range of applications in multicomponent reactions such as Passerini and Ugi processes. Recent advances in metal catalysis have tremendously increased the versatility of isocyanides in organic chemistry. Suitable metal catalysts could selectively activate various C-H bonds to allow direct functionalization under mild conditions, which represents a chemical process with broad synthetic potential. The synergy from the combination of isocyanide insertion and C-H bond activation offers an efficient and powerful tool to establish complicated reactions and to construct useful substances, from which the high potential of such strategy has been convincingly demonstrated in drug discovery, organic synthesis, and materials science. The present review highlights the most recent advances of isocyanide chemistry in metal-catalyzed C-H bond functionalization.
引用
收藏
页码:1103 / 1123
页数:21
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