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镍催化的还原偶联反应。

Nickel-Catalyzed Reductive Couplings.

机构信息

Department of Chemistry, Center for Supramolecular Materials and Catalysis, Shanghai University, 99 Shang-Da Road, Shanghai, 200444, China.

Shanghai Key Lab of Chemical Assessment and Sustainability, Tongji University, 1239 Siping Road, Shanghai, 200092, China.

出版信息

Top Curr Chem (Cham). 2016 Aug;374(4):43. doi: 10.1007/s41061-016-0042-2. Epub 2016 Jun 23.

Abstract

The Ni-catalyzed reductive coupling of alkyl/aryl with other electrophiles has evolved to be an important protocol for the construction of C-C bonds. This chapter first emphasizes the recent progress on the Ni-catalyzed alkylation, arylation/vinylation, and acylation of alkyl electrophiles. A brief overview of CO2 fixation is also addressed. The chemoselectivity between the electrophiles and the reactivity of the alkyl substrates will be detailed on the basis of different Ni-catalyzed conditions and mechanistic perspective. The asymmetric formation of C(sp(3))-C(sp(2)) bonds arising from activated alkyl halides is next depicted followed by allylic carbonylation. Finally, the coupling of aryl halides with other C(sp(2))-electrophiles is detailed at the end of this chapter.

摘要

镍催化的烷基/芳基与其他亲电试剂的还原偶联已发展成为构建 C-C 键的重要方法。本章首先强调了镍催化的烷基亲电试剂的烷基化、芳基化/乙烯基化和酰化的最新进展。还简要介绍了二氧化碳固定。根据不同的镍催化条件和反应机理,将详细讨论亲电试剂和烷基底物的反应性之间的化学选择性。接着描述了由活化的烷基卤化物产生的 C(sp(3))-C(sp(2))键的不对称形成,随后是烯丙基羰基化。最后,在本章的最后详细描述了芳基卤化物与其他 C(sp(2))-亲电试剂的偶联。

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