Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, PR China.
Chem Soc Rev. 2012 May 7;41(9):3651-78. doi: 10.1039/c2cs15281a. Epub 2012 Feb 29.
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).
铑(III)催化的 C-H 键在氧化条件下的直接功能化反应,导致 C-C、C-N 和 C-O 键的形成,这一过程得到了综述。各种带有氮和氧导向基团的芳基底物与不饱和化合物如烯烃和炔烃进行偶联反应,涵盖其中。C-E(E=C、N、S 或 O)键的易于构建使得铑(III)催化成为一种有吸引力的从易得的起始原料构建增值分子的经济方法。比较了铑(III)和钯(II)催化的氧化偶联之间的差异。通过各种最近的例子展示了所获得的结构的显著多样性,并简要总结了每个转化的提出的反应机理(综述,138 篇参考文献)。