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基于非共价相互作用的过渡金属催化区域选择性 C-H 转化的最新进展。

Recent progress of transition metal-catalysed regioselective C-H transformations based on noncovalent interactions.

机构信息

Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasugakoen, Kasuga-shi, Fukuoka 816-8580, Japan.

出版信息

Org Biomol Chem. 2020 Jun 10;18(22):4126-4134. doi: 10.1039/d0ob00703j.

Abstract

Transition metal-catalysed C-H transformations are powerful methods to obtain functionalised organic molecules from simple starting materials. Controlling regioselectivity is one of the most important issues in C-H transformations. Since the remarkable work by Murai and co-workers in 1993, many groups have reported ortho-selective C(sp2)-H transformations using directing group methods, in which interactions exist between substrates and catalytically active metal centres. In this review, new methodologies to achieve regioselective C-H transformations are described. In these methhodologies, noncovalent interactions between substrates and reagents or ligands of catalysts play important roles. In these cases, selective functionalization of remote C-H bonds, such as meta- and para-C-H bonds, can also be realized.

摘要

过渡金属催化的 C-H 转化是从简单起始原料获得官能化有机分子的有力方法。控制区域选择性是 C-H 转化中最重要的问题之一。自 1993 年 Murai 及其同事的出色工作以来,许多小组已经报道了使用导向基团方法的邻选择性 C(sp2)-H 转化,其中底物与催化活性金属中心之间存在相互作用。在本综述中,描述了实现区域选择性 C-H 转化的新方法。在这些方法中,底物和催化剂的试剂或配体之间的非共价相互作用起着重要作用。在这些情况下,也可以实现远程 C-H 键的选择性官能化,例如间位和对位 C-H 键。

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