Frisch Anja C, Beller Matthias
Leibniz-Institut für Organische Katalyse, Universität Rostock e.V. Buchbinderstrasse 5-6, 18055 Rostock, Germany.
Angew Chem Int Ed Engl. 2005 Jan 21;44(5):674-88. doi: 10.1002/anie.200461432.
Despite the problems inherent to metal-catalyzed cross-coupling reactions with alkyl halides, these reactions have become increasingly important during the last few years. Detailed mechanistic investigations have led to a variety of novel procedures for the selective cross-coupling of non-activated alkyl halides bearing beta hydrogen atoms with a variety of organometallic nucleophiles under mild reaction conditions. This Minireview highlights selected examples of metal-catalyzed coupling methods and is intended to encourage chemists to exploit the potential of these approaches in organic synthesis.
尽管金属催化的与卤代烷的交叉偶联反应存在固有问题,但在过去几年中这些反应变得越来越重要。详细的机理研究已产生了多种新颖的方法,可在温和的反应条件下,使带有β氢原子的未活化卤代烷与各种有机金属亲核试剂进行选择性交叉偶联。本综述突出介绍了金属催化偶联方法的一些选定实例,旨在鼓励化学家在有机合成中利用这些方法的潜力。