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耦合光催化与取代化学以扩展和归一化氧化还原活性卤化物。

Coupling Photocatalysis and Substitution Chemistry to Expand and Normalize Redox-Active Halides.

作者信息

Rathnayake Manjula D, Weaver Jimmie D

机构信息

Department of Chemistry, Oklahoma State University, 107 Physical Sciences, Stillwater, Oklahoma 74078, United States.

出版信息

Org Lett. 2021 Mar 19;23(6):2036-2041. doi: 10.1021/acs.orglett.1c00173. Epub 2021 Feb 26.

Abstract

Photocatalysis can generate radicals in a controlled fashion and has become an important synthetic strategy. However, limitations due to the reducibility of alkyl halides prevent their broader implementation. Herein we explore the use of nucleophiles that can substitute the halide and serve as an electron capture motif that normalize the variable redox potentials across substrates. When used with photocatalysis, bench-stable, commercially available collidinium salts prove to be excellent radical precursors with a broad scope.

摘要

光催化能够以可控的方式产生自由基,已成为一种重要的合成策略。然而,由于卤代烃的还原性导致的局限性阻碍了它们的更广泛应用。在此,我们探索使用能够取代卤化物并作为电子捕获基序的亲核试剂,以归一化不同底物间可变的氧化还原电位。当与光催化一起使用时,实验室稳定、市售的可力丁盐被证明是具有广泛适用范围的优异自由基前体。

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