Issue 9, 2021

Recent advances in the chemistry of ketyl radicals

Abstract

Ketyl radicals are valuable reactive intermediates for synthesis and are used extensively to construct complex, functionalized products from carbonyl substrates. Single electron transfer (SET) reduction of the C[double bond, length as m-dash]O bond of aldehydes and ketones is the classical approach for the formation of ketyl radicals and metal reductants are the archetypal reagents employed. The past decade has, however, witnessed significant advances in the generation and harnessing of ketyl radicals. This tutorial review highlights recent, exciting developments in the chemistry of ketyl radicals by comparing the varied contemporary – for example, using photoredox catalysts – and more classical approaches for the generation and use of ketyl radicals. The review will focus on different strategies for ketyl radical generation, their creative use in new synthetic protocols, strategies for the control of enantioselectivity, and detailed mechanisms where appropriate.

Graphical abstract: Recent advances in the chemistry of ketyl radicals

Article information

Article type
Tutorial Review
Submitted
13 Apr 2020
First published
23 Mar 2021
This article is Open Access
Creative Commons BY license

Chem. Soc. Rev., 2021,50, 5349-5365

Recent advances in the chemistry of ketyl radicals

Á. Péter, S. Agasti, O. Knowles, E. Pye and D. J. Procter, Chem. Soc. Rev., 2021, 50, 5349 DOI: 10.1039/D0CS00358A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements