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Pd 催化的通过 C-H 活化的有机金属试剂的氧化偶联。

Pd-catalyzed oxidative coupling with organometallic reagents via C-H activation.

机构信息

Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Peking University, Beijing, China.

出版信息

Chem Commun (Camb). 2010 Feb 7;46(5):677-85. doi: 10.1039/b908581e. Epub 2010 Jan 5.

Abstract

Direct selective palladium catalyzed C-H functionalization has become a highly attractive strategy in organic synthesis and represents a highly desirable goal. Compared with cross-coupling reactions of C-H bonds with aryl or alkyl halides/pseudohalides, the strategy of cross-coupling reactions of C-H bonds with organometallic reagents is of great significance and obvious advantages. This feature article provides a comprehensive summary of recent advances and an intensive analysis on Pd-catalyzed C-H activation and oxidative coupling with various organometallic reagents.

摘要

直接选择性钯催化的 C-H 功能化已成为有机合成中极具吸引力的策略,代表了一个非常理想的目标。与 C-H 键与芳基或烷基卤化物/拟卤化物的交叉偶联反应相比,C-H 键与有机金属试剂的交叉偶联反应策略具有重要意义和明显优势。本文综述了近年来钯催化的 C-H 活化和与各种有机金属试剂的氧化偶联反应的最新进展,并进行了深入分析。

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