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Electrochemical Synthesis of Isoxazolines: Method and Mechanism

An electrochemical method for the green and practical synthesis of a broad range of substituted isoxazoline cores is presented. Both aryl and more challenging alkyl aldoximes are converted to the desired isoxazoline in an electrochemically enabled regio‐ and diastereoselective reaction with electron...

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Autores principales: Holman, Samuel D. L., Wills, Alfie G., Fazakerley, Neal J., Poole, Darren L., Coe, Diane M., Berlouis, Leonard A., Reid, Marc
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/PMC9303936/
https://www.ncbi.nlm.nih.gov/pubmed/35076117
http://dx.doi.org/10.1002/chem.202103728
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author Holman, Samuel D. L.
Wills, Alfie G.
Fazakerley, Neal J.
Poole, Darren L.
Coe, Diane M.
Berlouis, Leonard A.
Reid, Marc
author_facet Holman, Samuel D. L.
Wills, Alfie G.
Fazakerley, Neal J.
Poole, Darren L.
Coe, Diane M.
Berlouis, Leonard A.
Reid, Marc
author_sort Holman, Samuel D. L.
collection PubMed
description An electrochemical method for the green and practical synthesis of a broad range of substituted isoxazoline cores is presented. Both aryl and more challenging alkyl aldoximes are converted to the desired isoxazoline in an electrochemically enabled regio‐ and diastereoselective reaction with electron‐deficient alkenes. Additionally, in‐situ reaction monitoring methods compatible with electrochemistry equipment have been developed in order to probe the reaction pathway. Supporting analyses from kinetic (time‐course) modelling and density functional theory support a stepwise, radical‐mediated mechanism, and discounts hypothesised involvement of closed shell [3+2] cycloaddition pathways.
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spelling pubmed-93039362022-07-28 Electrochemical Synthesis of Isoxazolines: Method and Mechanism Holman, Samuel D. L. Wills, Alfie G. Fazakerley, Neal J. Poole, Darren L. Coe, Diane M. Berlouis, Leonard A. Reid, Marc Chemistry Research Articles An electrochemical method for the green and practical synthesis of a broad range of substituted isoxazoline cores is presented. Both aryl and more challenging alkyl aldoximes are converted to the desired isoxazoline in an electrochemically enabled regio‐ and diastereoselective reaction with electron‐deficient alkenes. Additionally, in‐situ reaction monitoring methods compatible with electrochemistry equipment have been developed in order to probe the reaction pathway. Supporting analyses from kinetic (time‐course) modelling and density functional theory support a stepwise, radical‐mediated mechanism, and discounts hypothesised involvement of closed shell [3+2] cycloaddition pathways. John Wiley and Sons Inc. 2022-02-10 2022-03-01 /pmc/articles/PMC9303936/ /pubmed/35076117 http://dx.doi.org/10.1002/chem.202103728 Text en © 2022 The Authors. Chemistry - A European Journal 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 Research Articles
Holman, Samuel D. L.
Wills, Alfie G.
Fazakerley, Neal J.
Poole, Darren L.
Coe, Diane M.
Berlouis, Leonard A.
Reid, Marc
Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title_full Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title_fullStr Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title_full_unstemmed Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title_short Electrochemical Synthesis of Isoxazolines: Method and Mechanism
title_sort electrochemical synthesis of isoxazolines: method and mechanism
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303936/
https://www.ncbi.nlm.nih.gov/pubmed/35076117
http://dx.doi.org/10.1002/chem.202103728
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