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Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives
Alcohols and their derivatives are ubiquitous and versatile motifs in organic synthesis. Deoxygenative transformations of these compounds are often challenging due to the thermodynamic penalty associated with the cleavage of the C−O bond. However, electrochemically driven redox events have been show...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107720/ https://www.ncbi.nlm.nih.gov/pubmed/36278406 http://dx.doi.org/10.1002/anie.202211952 |
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author | Villo, Piret Shatskiy, Andrey Kärkäs, Markus D. Lundberg, Helena |
author_facet | Villo, Piret Shatskiy, Andrey Kärkäs, Markus D. Lundberg, Helena |
author_sort | Villo, Piret |
collection | PubMed |
description | Alcohols and their derivatives are ubiquitous and versatile motifs in organic synthesis. Deoxygenative transformations of these compounds are often challenging due to the thermodynamic penalty associated with the cleavage of the C−O bond. However, electrochemically driven redox events have been shown to facilitate the C−O bond cleavage in alcohols and their derivatives either through direct electron transfer or through the use of electron transfer mediators and electroactive catalysts. Herein, a comprehensive overview of preparative electrochemically mediated protocols for C−O bond activation and functionalization is detailed, including direct and indirect electrosynthetic methods, as well as photoelectrochemical strategies. |
format | Online Article Text |
id | pubmed-10107720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101077202023-04-18 Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives Villo, Piret Shatskiy, Andrey Kärkäs, Markus D. Lundberg, Helena Angew Chem Int Ed Engl Reviews Alcohols and their derivatives are ubiquitous and versatile motifs in organic synthesis. Deoxygenative transformations of these compounds are often challenging due to the thermodynamic penalty associated with the cleavage of the C−O bond. However, electrochemically driven redox events have been shown to facilitate the C−O bond cleavage in alcohols and their derivatives either through direct electron transfer or through the use of electron transfer mediators and electroactive catalysts. Herein, a comprehensive overview of preparative electrochemically mediated protocols for C−O bond activation and functionalization is detailed, including direct and indirect electrosynthetic methods, as well as photoelectrochemical strategies. John Wiley and Sons Inc. 2022-12-05 2023-01-23 /pmc/articles/PMC10107720/ /pubmed/36278406 http://dx.doi.org/10.1002/anie.202211952 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Villo, Piret Shatskiy, Andrey Kärkäs, Markus D. Lundberg, Helena Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title | Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title_full | Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title_fullStr | Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title_full_unstemmed | Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title_short | Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives |
title_sort | electrosynthetic c−o bond activation in alcohols and alcohol derivatives |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107720/ https://www.ncbi.nlm.nih.gov/pubmed/36278406 http://dx.doi.org/10.1002/anie.202211952 |
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