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Palladium nanoparticles as efficient catalyst for C–S bond formation reactions

The development of green, economical and sustainable chemical processes is one of the primary challenges in organic synthesis. Herein, we report an efficient and heterogeneous palladium-catalyzed sulfonylation of vinyl cyclic carbonates with sodium sulfinates via decarboxylative cross-coupling. Both...

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Detalles Bibliográficos
Autores principales: Zhang, Mei-Na, Khan, Shahid, Zhang, Junjie, Khan, Ajmal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056434/
https://www.ncbi.nlm.nih.gov/pubmed/35520647
http://dx.doi.org/10.1039/d0ra05848c
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author Zhang, Mei-Na
Khan, Shahid
Zhang, Junjie
Khan, Ajmal
author_facet Zhang, Mei-Na
Khan, Shahid
Zhang, Junjie
Khan, Ajmal
author_sort Zhang, Mei-Na
collection PubMed
description The development of green, economical and sustainable chemical processes is one of the primary challenges in organic synthesis. Herein, we report an efficient and heterogeneous palladium-catalyzed sulfonylation of vinyl cyclic carbonates with sodium sulfinates via decarboxylative cross-coupling. Both aliphatic and aromatic sulfinate salts react with various vinyl cyclic carbonates to deliver the desired allylic sulfones featuring tri- and even tetrasubstituted olefin scaffolds in high yields with excellent selectivity. The process needs only 2 mol% of Pd(2)(dba)(3) and the in situ formed palladium nano-particles are found to be the active catalyst.
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spelling pubmed-90564342022-05-04 Palladium nanoparticles as efficient catalyst for C–S bond formation reactions Zhang, Mei-Na Khan, Shahid Zhang, Junjie Khan, Ajmal RSC Adv Chemistry The development of green, economical and sustainable chemical processes is one of the primary challenges in organic synthesis. Herein, we report an efficient and heterogeneous palladium-catalyzed sulfonylation of vinyl cyclic carbonates with sodium sulfinates via decarboxylative cross-coupling. Both aliphatic and aromatic sulfinate salts react with various vinyl cyclic carbonates to deliver the desired allylic sulfones featuring tri- and even tetrasubstituted olefin scaffolds in high yields with excellent selectivity. The process needs only 2 mol% of Pd(2)(dba)(3) and the in situ formed palladium nano-particles are found to be the active catalyst. The Royal Society of Chemistry 2020-08-21 /pmc/articles/PMC9056434/ /pubmed/35520647 http://dx.doi.org/10.1039/d0ra05848c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Mei-Na
Khan, Shahid
Zhang, Junjie
Khan, Ajmal
Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title_full Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title_fullStr Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title_full_unstemmed Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title_short Palladium nanoparticles as efficient catalyst for C–S bond formation reactions
title_sort palladium nanoparticles as efficient catalyst for c–s bond formation reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056434/
https://www.ncbi.nlm.nih.gov/pubmed/35520647
http://dx.doi.org/10.1039/d0ra05848c
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AT zhangjunjie palladiumnanoparticlesasefficientcatalystforcsbondformationreactions
AT khanajmal palladiumnanoparticlesasefficientcatalystforcsbondformationreactions