C-C, C-O and C-N bond formation via rhodium(III)-catalyzed oxidative C-H activation

被引:2085
作者
Song, Guoyong [1 ]
Wang, Fen [1 ]
Li, Xingwei [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
关键词
INTRAMOLECULAR ALKANE ARYLATION; INTERNAL ALKYNES; BENZOIC-ACIDS; COUPLING REACTIONS; RHODIUM; RH; OLEFINATION; DERIVATIVES; CLEAVAGE; FUNCTIONALIZATION;
D O I
10.1039/c2cs15281a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rhodium(III)-catalyzed direct functionalization of C-H bonds under oxidative conditions leading to C-C, C-N, and C-O bond formation is reviewed. Various arene substrates bearing nitrogen and oxygen directing groups are covered in their coupling with unsaturated partners such as alkenes and alkynes. The facile construction of C-E (E = C, N, S, or O) bonds makes Rh(III) catalysis an attractive step-economic approach to value-added molecules from readily available starting materials. Comparisons and contrasts between rhodium(III) and palladium(II)-catalyzed oxidative coupling are made. The remarkable diversity of structures accessible is demonstrated with various recent examples, with a proposed mechanism for each transformation being briefly summarized (critical review, 138 references).
引用
收藏
页码:3651 / 3678
页数:28
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