Organocatalysis in Inert C-H Bond Functionalization

被引:652
作者
Qin, Yan [1 ,2 ]
Zhu, Lihui [1 ,2 ]
Luo, Sanzhong [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; HYPERVALENT IODINE REAGENTS; LIGHT PHOTOREDOX CATALYSIS; TRANSITION-METAL CATALYSIS; CHIRAL PHOSPHORIC-ACID; ASYMMETRIC BINARY-ACID; N-HETEROCYCLIC CARBENE; TERT-BUTYL NITRITE; PALLADIUM(II)-CATALYZED DIRECT CONVERSION; DEHYDROGENATIVE COUPLING REACTIONS;
D O I
10.1021/acs.chemrev.6b00657
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As two coexisting and fast-growing research fields in modern synthetic chemistry, the merging of organocatalysis and C-H bond functionalization is well foreseeable, and the joint force along this line has been demonstrated to be a powerful approach in making inert C-H bond functionafization more viable, predictable, and selective. In this review, we provide a comprehensive summary of organocatalysis in inert C-H bond functionalization over the past two decades. The review is arranged by types of inert C-H bonds including alkane C-H, arene C-H, and vinyl C-H as well as those activated benzylic allylic C-H, and C-H bonds alpha to the heteroatom such as nitrogen and oxygen. In each section, the discussion is classified by the explicit organocatalytic mode involved.
引用
收藏
页码:9433 / 9520
页数:88
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