Chen Xiao, Engle Keary M, Wang Dong-Hui, Yu Jin-Quan
Chemical Development Department, Albany Molecular Research, Inc., 21 Corporate Circle, Albany, NY 12203, USA.
Angew Chem Int Ed Engl. 2009;48(28):5094-115. doi: 10.1002/anie.200806273.
In the past decade, palladium-catalyzed C-H activation/C-C bond-forming reactions have emerged as promising new catalytic transformations; however, development in this field is still at an early stage compared to the state of the art in cross-coupling reactions using aryl and alkyl halides. This Review begins with a brief introduction of four extensively investigated modes of catalysis for forming C-C bonds from C-H bonds: Pd(II)/Pd(0), Pd(II)/Pd(IV), Pd(0)/Pd(II)/Pd(IV), and Pd(0)/Pd(II) catalysis. A more detailed discussion is then directed towards the recent development of palladium(II)-catalyzed coupling of C-H bonds with organometallic reagents through a Pd(II)/Pd(0) catalytic cycle. Despite the progress made to date, improving the versatility and practicality of this new reaction remains a tremendous challenge.
在过去十年中,钯催化的C-H活化/C-C键形成反应已成为有前景的新型催化转化反应;然而,与使用芳基和烷基卤化物的交叉偶联反应的现有技术水平相比,该领域的发展仍处于早期阶段。本综述首先简要介绍了四种广泛研究的由C-H键形成C-C键的催化模式:Pd(II)/Pd(0)、Pd(II)/Pd(IV)、Pd(0)/Pd(II)/Pd(IV)和Pd(0)/Pd(II)催化。然后更详细地讨论了通过Pd(II)/Pd(0)催化循环,钯(II)催化C-H键与有机金属试剂偶联的最新进展。尽管迄今已取得进展,但提高这种新反应的通用性和实用性仍然是一项巨大挑战。