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Recent advances in the chemistry of ketyl radicals

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...

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Autores principales: Péter, Áron, Agasti, Soumitra, Knowles, Oliver, Pye, Emma, Procter, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111543/
https://www.ncbi.nlm.nih.gov/pubmed/33972956
http://dx.doi.org/10.1039/d0cs00358a
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author Péter, Áron
Agasti, Soumitra
Knowles, Oliver
Pye, Emma
Procter, David J.
author_facet Péter, Áron
Agasti, Soumitra
Knowles, Oliver
Pye, Emma
Procter, David J.
author_sort Péter, Áron
collection PubMed
description 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.
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spelling pubmed-81115432021-06-02 Recent advances in the chemistry of ketyl radicals Péter, Áron Agasti, Soumitra Knowles, Oliver Pye, Emma Procter, David J. Chem Soc Rev Chemistry 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. The Royal Society of Chemistry 2021-03-23 /pmc/articles/PMC8111543/ /pubmed/33972956 http://dx.doi.org/10.1039/d0cs00358a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Péter, Áron
Agasti, Soumitra
Knowles, Oliver
Pye, Emma
Procter, David J.
Recent advances in the chemistry of ketyl radicals
title Recent advances in the chemistry of ketyl radicals
title_full Recent advances in the chemistry of ketyl radicals
title_fullStr Recent advances in the chemistry of ketyl radicals
title_full_unstemmed Recent advances in the chemistry of ketyl radicals
title_short Recent advances in the chemistry of ketyl radicals
title_sort recent advances in the chemistry of ketyl radicals
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111543/
https://www.ncbi.nlm.nih.gov/pubmed/33972956
http://dx.doi.org/10.1039/d0cs00358a
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