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Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry

We report an efficient and sustainable electrochemical synthesis of copper(i) acetylides using simultaneous copper oxidation and Hofmann elimination of quaternary ammonium salts. The electrochemically-generated base was also regenerated electrochemically, making it catalytic. A ‘Click test’ (CuAAC r...

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Detalles Bibliográficos
Autores principales: Seavill, Peter W., Holt, Katherine B., Wilden, Jonathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071997/
https://www.ncbi.nlm.nih.gov/pubmed/35528428
http://dx.doi.org/10.1039/c9ra06782e
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author Seavill, Peter W.
Holt, Katherine B.
Wilden, Jonathan D.
author_facet Seavill, Peter W.
Holt, Katherine B.
Wilden, Jonathan D.
author_sort Seavill, Peter W.
collection PubMed
description We report an efficient and sustainable electrochemical synthesis of copper(i) acetylides using simultaneous copper oxidation and Hofmann elimination of quaternary ammonium salts. The electrochemically-generated base was also regenerated electrochemically, making it catalytic. A ‘Click test’ (CuAAC reaction) was performed to assess product purity and an electrochemically-promoted, one-pot CuAAC reaction was performed, which serves as a promising initial demonstration of this approach in a pharmaceutically-relevant reaction.
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spelling pubmed-90719972022-05-06 Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry Seavill, Peter W. Holt, Katherine B. Wilden, Jonathan D. RSC Adv Chemistry We report an efficient and sustainable electrochemical synthesis of copper(i) acetylides using simultaneous copper oxidation and Hofmann elimination of quaternary ammonium salts. The electrochemically-generated base was also regenerated electrochemically, making it catalytic. A ‘Click test’ (CuAAC reaction) was performed to assess product purity and an electrochemically-promoted, one-pot CuAAC reaction was performed, which serves as a promising initial demonstration of this approach in a pharmaceutically-relevant reaction. The Royal Society of Chemistry 2019-09-17 /pmc/articles/PMC9071997/ /pubmed/35528428 http://dx.doi.org/10.1039/c9ra06782e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Seavill, Peter W.
Holt, Katherine B.
Wilden, Jonathan D.
Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title_full Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title_fullStr Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title_full_unstemmed Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title_short Electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
title_sort electrochemical synthesis of copper(i) acetylides via simultaneous copper ion and catalytic base electrogeneration for use in click chemistry
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071997/
https://www.ncbi.nlm.nih.gov/pubmed/35528428
http://dx.doi.org/10.1039/c9ra06782e
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