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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8111543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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