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自由基C(sp3)-H官能团化及交叉偶联反应

Radical C(sp3)-H functionalization and cross-coupling reactions.

作者信息

Golden Dung L, Suh Sung-Eun, Stahl Shannon S

机构信息

Department of Chemistry, University of Wisconsin-Madison, WI, USA.

These authors contributed equally: Dung L. Golden, Sung-Eun Suh.

出版信息

Nat Rev Chem. 2022 Jun;6(6):405-427. doi: 10.1038/s41570-022-00388-4. Epub 2022 May 17.

Abstract

C─H functionalization reactions are playing an increasing role in the preparation and modification of complex organic molecules, including pharmaceuticals, agrochemicals, and polymer precursors. Radical C─H functionalization reactions, initiated by hydrogen-atom transfer (HAT) and proceeding via open-shell radical intermediates, have been expanding rapidly in recent years. These methods introduce strategic opportunities to functionalize C(sp)─H bonds. Examples include synthetically useful advances in radical-chain reactivity and biomimetic radical-rebound reactions. A growing number of reactions, however, proceed via "radical relay" whereby HAT generates a diffusible radical that is functionalized by a separate reagent or catalyst. The latter methods provide the basis for versatile C─H cross-coupling methods with diverse partners. In the present review, highlights of recent radical-chain and radical-rebound methods provide context for a survey of emerging radical-relay methods, which greatly expand the scope and utility of intermolecular C(sp)─H functionalization and cross coupling.

摘要

碳-氢键官能团化反应在复杂有机分子(包括药物、农用化学品和聚合物前体)的制备和修饰中发挥着越来越重要的作用。由氢原子转移(HAT)引发并通过开壳层自由基中间体进行的自由基碳-氢键官能团化反应近年来发展迅速。这些方法为碳(sp)-氢键的官能团化带来了策略性机遇。实例包括自由基链反应活性和仿生自由基反弹反应在合成方面的有用进展。然而,越来越多的反应是通过“自由基接力”进行的,即氢原子转移产生一个可扩散的自由基,该自由基被另一种试剂或催化剂官能团化。后一种方法为与多种反应伙伴进行通用的碳-氢键交叉偶联方法提供了基础。在本综述中,近期自由基链反应和自由基反弹方法的亮点为新兴自由基接力方法的综述提供了背景,这些新兴方法极大地扩展了分子间碳(sp)-氢键官能团化和交叉偶联的范围及实用性。

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