Department of Chemistry, Indian Institute of Science Education and Research, Bhopal, Bhopal Bypass Road, Bhauri, Bhopal, 462066, India.
Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai-400076, India.
Chem Soc Rev. 2022 Aug 30;51(17):7358-7426. doi: 10.1039/d1cs00923k.
Transition metal catalysis has contributed immensely to C-C bond formation reactions over the last few decades, and alkylation is no exception. The superiority of such methodologies over traditional alkylation is evident from minimal reaction steps, shorter reaction times, and atom economy while also allowing control over regio- and stereo-selectivity. In particular, hydrocarbonation of alkenes has grabbed increased attention due its fundamental ability to effectively and selectively synthesise a wide range of industrially and pharmaceutically relevant moieties. This review attempts to provide a scientific viewpoint and a systematic analysis of the recent developments in transition-metal-catalyzed alkylation of various C-H bonds using simple and activated olefins. The key features and mechanistic studies involved in these transformations are described briefly.
过渡金属催化在过去几十年中极大地促进了 C-C 键形成反应,烷基化反应也不例外。与传统烷基化相比,这些方法的优越性在于反应步骤更少、反应时间更短、原子经济性更高,同时还能控制区域和立体选择性。特别是,烯烃的加氢甲酰化由于其有效和选择性合成广泛的工业和药物相关部分的基本能力而引起了越来越多的关注。本综述试图提供一个科学的观点和对使用简单和活化的烯烃进行各种 C-H 键的过渡金属催化烷基化反应的最新发展的系统分析。这些转化中涉及的关键特征和机理研究被简要描述。