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Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions

A simple and efficient protocol developed for one pot three-component synthesis of 2,4,6-triarylpyridines from aromatic aldehydes, substituted acetophenones and ammonium acetate using the versatile super Brønsted acid triflimide (HNTf(2)) as an effective catalyst is described. The reactions proceed...

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Detalles Bibliográficos
Autores principales: Wang, Hongshe, Zhao, Weixing, Du, Juan, Wei, Fenyan, Chen, Qi, Wang, Xiaomei
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/PMC9060662/
https://www.ncbi.nlm.nih.gov/pubmed/35514631
http://dx.doi.org/10.1039/c9ra00653b
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author Wang, Hongshe
Zhao, Weixing
Du, Juan
Wei, Fenyan
Chen, Qi
Wang, Xiaomei
author_facet Wang, Hongshe
Zhao, Weixing
Du, Juan
Wei, Fenyan
Chen, Qi
Wang, Xiaomei
author_sort Wang, Hongshe
collection PubMed
description A simple and efficient protocol developed for one pot three-component synthesis of 2,4,6-triarylpyridines from aromatic aldehydes, substituted acetophenones and ammonium acetate using the versatile super Brønsted acid triflimide (HNTf(2)) as an effective catalyst is described. The reactions proceed well in the presence of 1 mol% of HNTf(2) at 80 °C under solvent-free conditions and provide the corresponding triarylpyridines in good to excellent yields. The method reported has several advantages such as a metal-free and commercially available catalyst, mild reaction conditions and lower loading of catalyst.
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spelling pubmed-90606622022-05-04 Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions Wang, Hongshe Zhao, Weixing Du, Juan Wei, Fenyan Chen, Qi Wang, Xiaomei RSC Adv Chemistry A simple and efficient protocol developed for one pot three-component synthesis of 2,4,6-triarylpyridines from aromatic aldehydes, substituted acetophenones and ammonium acetate using the versatile super Brønsted acid triflimide (HNTf(2)) as an effective catalyst is described. The reactions proceed well in the presence of 1 mol% of HNTf(2) at 80 °C under solvent-free conditions and provide the corresponding triarylpyridines in good to excellent yields. The method reported has several advantages such as a metal-free and commercially available catalyst, mild reaction conditions and lower loading of catalyst. The Royal Society of Chemistry 2019-02-12 /pmc/articles/PMC9060662/ /pubmed/35514631 http://dx.doi.org/10.1039/c9ra00653b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Wang, Hongshe
Zhao, Weixing
Du, Juan
Wei, Fenyan
Chen, Qi
Wang, Xiaomei
Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title_full Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title_fullStr Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title_full_unstemmed Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title_short Retracted Article: An efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
title_sort retracted article: an efficient one pot three-component synthesis of 2,4,6-triarylpyridines using triflimide as a metal-free catalyst under solvent-free conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060662/
https://www.ncbi.nlm.nih.gov/pubmed/35514631
http://dx.doi.org/10.1039/c9ra00653b
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