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α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions

We herein report α-arylsulfonyloxyacrylates as a kind of useful and attractive O-centered electrophiles for Suzuki cross-coupling reactions. A range of α-(hetero)aryl substituted acrylates has been prepared via the palladium-catalysed C–C cross-coupling reactions between potassium (hetero)aryltriflu...

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Detalles Bibliográficos
Autores principales: Zhang, Zhongya, Zhang, Li, Huai, Linge, Wang, Zhentao, Fang, Yewen
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/PMC10026373/
https://www.ncbi.nlm.nih.gov/pubmed/36950707
http://dx.doi.org/10.1039/d3ra00401e
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author Zhang, Zhongya
Zhang, Li
Huai, Linge
Wang, Zhentao
Fang, Yewen
author_facet Zhang, Zhongya
Zhang, Li
Huai, Linge
Wang, Zhentao
Fang, Yewen
author_sort Zhang, Zhongya
collection PubMed
description We herein report α-arylsulfonyloxyacrylates as a kind of useful and attractive O-centered electrophiles for Suzuki cross-coupling reactions. A range of α-(hetero)aryl substituted acrylates has been prepared via the palladium-catalysed C–C cross-coupling reactions between potassium (hetero)aryltrifluoroborates and α-arylsulfonyloxyacrylates. Moreover, α-arylsulfonyloxyacrylate could also react with B-alkyl-9-BBN to produce α-alkyl substituted acrylates. The synthetic application of this new method was demonstrated by the preparation of the intermediate for synthesis of retinoid X receptors-selective retinoids. These Suzuki reaction-based protocols feature broad substrate scope, generality, and mild reaction conditions.
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spelling pubmed-100263732023-03-21 α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions Zhang, Zhongya Zhang, Li Huai, Linge Wang, Zhentao Fang, Yewen RSC Adv Chemistry We herein report α-arylsulfonyloxyacrylates as a kind of useful and attractive O-centered electrophiles for Suzuki cross-coupling reactions. A range of α-(hetero)aryl substituted acrylates has been prepared via the palladium-catalysed C–C cross-coupling reactions between potassium (hetero)aryltrifluoroborates and α-arylsulfonyloxyacrylates. Moreover, α-arylsulfonyloxyacrylate could also react with B-alkyl-9-BBN to produce α-alkyl substituted acrylates. The synthetic application of this new method was demonstrated by the preparation of the intermediate for synthesis of retinoid X receptors-selective retinoids. These Suzuki reaction-based protocols feature broad substrate scope, generality, and mild reaction conditions. The Royal Society of Chemistry 2023-03-20 /pmc/articles/PMC10026373/ /pubmed/36950707 http://dx.doi.org/10.1039/d3ra00401e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Zhang, Zhongya
Zhang, Li
Huai, Linge
Wang, Zhentao
Fang, Yewen
α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title_full α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title_fullStr α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title_full_unstemmed α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title_short α-Arylsulfonyloxyacrylates: attractive O-centered electrophiles for synthesis of α-substituted acrylates via Pd-catalysed Suzuki reactions
title_sort α-arylsulfonyloxyacrylates: attractive o-centered electrophiles for synthesis of α-substituted acrylates via pd-catalysed suzuki reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026373/
https://www.ncbi.nlm.nih.gov/pubmed/36950707
http://dx.doi.org/10.1039/d3ra00401e
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