Related Experiment Video
Updated: Nov 6, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Recent advances in the chemistry of ketyl radicals
Áron Péter1, Soumitra Agasti, Oliver Knowles
1Department of Chemistry, The University of Manchester, Oxford Road, Manchester, UK. david.j.procter@manchester.ac.uk.
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.
Related Concept Videos
Radical Reactivity: Overview
Radical Reactivity: Electrophilic Radicals
Radical Reactivity: Steric Effects
Along with electronic...
Radical Formation: Addition
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview
Radical Reactivity: Nucleophilic Radicals

