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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.


ABSTRACT: 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 Cs2CO3 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.

SUBMITTER: Liu Y 

PROVIDER: S-EPMC9084342 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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

Liu Yong Y   Lu Tao T   Tang Wei-Fang WF   Gao Jian J  

RSC advances 20180810 50


A transition-metal-free base catalyzed intramolecular cyclization of 2-ynylphenols was developed for the facile synthesis of 2-substituted benzo[<i>b</i>]furans. Various 2-aryl and 2-alkyl substituted benzo[<i>b</i>]furans can be obtained with good to excellent yields using readily available Cs<sub>2</sub>CO<sub>3</sub> 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 pract  ...[more]

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