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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).
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Guoyong Song
Beijing Forestry University
Fen Wang
Henan Forestry Vocational College
Xingwei Li
California Institute of Technology
Chemical Society Reviews
Chinese Academy of Sciences
Dalian Institute of Chemical Physics
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Song et al. (Sun,) studied this question.
synapsesocial.com/papers/69dae14300ab073a278394a9 — DOI: https://doi.org/10.1039/c2cs15281a