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Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans

A transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols was developed for the facile synthesis of 2-substituted benzo[b]furans. Various 2-aryl and 2-alkyl substituted benzo[b]furans can be obtained with good to excellent yields using readily available Cs(2)CO(3) as the cat...

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Detalles Bibliográficos
Autores principales: Liu, Yong, Lu, Tao, Tang, Wei-Fang, Gao, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084342/
https://www.ncbi.nlm.nih.gov/pubmed/35542491
http://dx.doi.org/10.1039/c8ra03882a
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author Liu, Yong
Lu, Tao
Tang, Wei-Fang
Gao, Jian
author_facet Liu, Yong
Lu, Tao
Tang, Wei-Fang
Gao, Jian
author_sort Liu, Yong
collection PubMed
description A transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols was developed for the facile synthesis of 2-substituted benzo[b]furans. Various 2-aryl and 2-alkyl substituted benzo[b]furans can be obtained with good to excellent yields using readily available Cs(2)CO(3) as the catalyst under mild reaction conditions. The broad substrates scope and the typical maintenance of vigorous efficiency on gram scale make this protocol a potentially practical method to synthesize 2-substituted benzo[b]furans derivatives.
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spelling pubmed-90843422022-05-09 Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans Liu, Yong Lu, Tao Tang, Wei-Fang Gao, Jian RSC Adv Chemistry A transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols was developed for the facile synthesis of 2-substituted benzo[b]furans. Various 2-aryl and 2-alkyl substituted benzo[b]furans can be obtained with good to excellent yields using readily available Cs(2)CO(3) as the catalyst under mild reaction conditions. The broad substrates scope and the typical maintenance of vigorous efficiency on gram scale make this protocol a potentially practical method to synthesize 2-substituted benzo[b]furans derivatives. The Royal Society of Chemistry 2018-08-10 /pmc/articles/PMC9084342/ /pubmed/35542491 http://dx.doi.org/10.1039/c8ra03882a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Yong
Lu, Tao
Tang, Wei-Fang
Gao, Jian
Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title_full Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title_fullStr Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title_full_unstemmed Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title_short Transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
title_sort transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols for efficient and facile synthesis of 2-substituted benzo[b]furans
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084342/
https://www.ncbi.nlm.nih.gov/pubmed/35542491
http://dx.doi.org/10.1039/c8ra03882a
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