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铃木-宫浦(杂)芳基交叉偶联反应:最新研究成果与建议

Suzuki-Miyaura (hetero-)aryl cross-coupling: recent findings and recommendations.

作者信息

Meringdal Jonas W, Menche Dirk

机构信息

Kekulé-Institut für Organische Chemie und Biochemie, University Bonn, 53121 Bonn, Germany.

出版信息

Chem Soc Rev. 2025 Jun 16;54(12):5746-5765. doi: 10.1039/d4cs01108b.

Abstract

The Suzuki-Miyaura cross-coupling is a powerful method for carbon-carbon bond formation, widely applied with various substrates, catalysts, reagents and solvents. However, numerous reported protocols make finding optimal conditions for a specific substrate time-consuming. This tutorial review provides a comprehensive overview on recent developments in Suzuki-Miyaura reactions, focusing on optimizing the most common application: palladium and nickel phosphine catalyzed (hetero-)aryl bond formation. Key mechanistic insights into ligand selection, base and boron reagent choice as well as potential additives, and their effects on the reaction outcome are discussed in detail. Based on a systematic analysis, these parameters will be grouped together. Recommended conditions for each group will then be provided to accelerate the optimization process and enhance the application of this pivotal bond forming reaction.

摘要

铃木-宫浦交叉偶联反应是一种用于形成碳-碳键的强大方法,广泛应用于各种底物、催化剂、试剂和溶剂。然而,众多已报道的方案使得为特定底物寻找最佳条件非常耗时。本教程综述全面概述了铃木-宫浦反应的最新进展,重点是优化最常见的应用:钯和镍膦催化的(杂)芳基键形成。详细讨论了配体选择、碱和硼试剂选择以及潜在添加剂的关键机理见解,以及它们对反应结果的影响。基于系统分析,将对这些参数进行分组。然后将为每组提供推荐条件,以加速优化过程并增强这一关键键形成反应的应用。

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