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近期通过直接脱水偶联策略构建 C-C 键的方法。

Recent approaches for C-C bond formation via direct dehydrative coupling strategies.

机构信息

Laboratory for Organic & Microwave-Assisted Chemistry, (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, B-3001, Leuven, Belgium.

出版信息

Chem Soc Rev. 2013 Feb 7;42(3):1121-46. doi: 10.1039/c2cs35397k.

Abstract

In recent years, reaction of inexpensive and abundantly available alcohols (C-OH) with unactivated nucleophilic coupling partners (C-H), leading to the construction of the C-C bond, has emerged as one of the vital strategies since it is an atom-economical and environmentally benign approach with water as the by-product. Various transition metal-catalyzed or metal-free approaches for the direct dehydrative coupling employing the C-OH bond (including in situ activation) have recently been devised. This review article aims to highlight advances in such waste-free C-C bond forming dehydrative strategies.

摘要

近年来,廉价且丰富的醇(C-OH)与非活化亲核偶联试剂(C-H)反应,构建 C-C 键,已成为一种重要策略,因为这是一种原子经济和环境友好的方法,副产物为水。最近已经设计了各种过渡金属催化或无金属的方法,用于直接脱水偶联 C-OH 键(包括原位活化)。本文旨在强调无废物 C-C 键形成脱水策略方面的进展。

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