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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...

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Autores principales: Villo, Piret, Shatskiy, Andrey, Kärkäs, Markus D., Lundberg, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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