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Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction

A mechanistic study into the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction, incorporating sulfur dioxide, is described. Utilising spectroscopic and computational techniques, an exploration into the individual components of the competing catalytic cycles is delineated, including identific...

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Detalles Bibliográficos
Autores principales: Hall, Callum G. J., Sneddon, Helen F., Pogány, Peter, Lindsay, David M., Kerr, William J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284122/
https://www.ncbi.nlm.nih.gov/pubmed/37350817
http://dx.doi.org/10.1039/d3sc01337e
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author Hall, Callum G. J.
Sneddon, Helen F.
Pogány, Peter
Lindsay, David M.
Kerr, William J.
author_facet Hall, Callum G. J.
Sneddon, Helen F.
Pogány, Peter
Lindsay, David M.
Kerr, William J.
author_sort Hall, Callum G. J.
collection PubMed
description A mechanistic study into the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction, incorporating sulfur dioxide, is described. Utilising spectroscopic and computational techniques, an exploration into the individual components of the competing catalytic cycles is delineated, including identification of the resting state catalyst, transmetalation of arylboronic acid onto copper(i), the sulfur dioxide insertion process, and the oxidative addition of aryl halide to Cu(I). Studies also investigated prominent side-reactions which were uncovered, including a competing copper(ii)-catalysed mechanism. This led to an additional proposed and connected Cu(I)/Cu(II)/Cu(III) catalytic cycle to account for by-product formation.
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spelling pubmed-102841222023-06-22 Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction Hall, Callum G. J. Sneddon, Helen F. Pogány, Peter Lindsay, David M. Kerr, William J. Chem Sci Chemistry A mechanistic study into the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction, incorporating sulfur dioxide, is described. Utilising spectroscopic and computational techniques, an exploration into the individual components of the competing catalytic cycles is delineated, including identification of the resting state catalyst, transmetalation of arylboronic acid onto copper(i), the sulfur dioxide insertion process, and the oxidative addition of aryl halide to Cu(I). Studies also investigated prominent side-reactions which were uncovered, including a competing copper(ii)-catalysed mechanism. This led to an additional proposed and connected Cu(I)/Cu(II)/Cu(III) catalytic cycle to account for by-product formation. The Royal Society of Chemistry 2023-05-31 /pmc/articles/PMC10284122/ /pubmed/37350817 http://dx.doi.org/10.1039/d3sc01337e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Hall, Callum G. J.
Sneddon, Helen F.
Pogány, Peter
Lindsay, David M.
Kerr, William J.
Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title_full Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title_fullStr Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title_full_unstemmed Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title_short Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki–Miyaura reaction
title_sort experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative suzuki–miyaura reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284122/
https://www.ncbi.nlm.nih.gov/pubmed/37350817
http://dx.doi.org/10.1039/d3sc01337e
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