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Issue 44, 2014
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Access to 6H-naphtho[2,3-c]chromenes by a palladium-catalyzed reaction of 2-haloaryl allene with 2-alkynylphenol

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Abstract

A palladium-catalyzed reaction of 2-haloaryl allene with 2-alkynylphenol is described, leading to 6H-naphtho[2,3-c]chromenes in good to excellent yields. This transformation proceeds efficiently with excellent chemoselectivity and regioselectivity.

Graphical abstract: Access to 6H-naphtho[2,3-c]chromenes by a palladium-catalyzed reaction of 2-haloaryl allene with 2-alkynylphenol

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Publication details

The article was received on 16 Jan 2014, accepted on 06 Mar 2014 and first published on 07 Mar 2014


Article type: Communication
DOI: 10.1039/C4CC00374H
Citation: Chem. Commun., 2014,50, 5891-5894
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    Access to 6H-naphtho[2,3-c]chromenes by a palladium-catalyzed reaction of 2-haloaryl allene with 2-alkynylphenol

    X. Pan, M. Chen, L. Yao and J. Wu, Chem. Commun., 2014, 50, 5891
    DOI: 10.1039/C4CC00374H

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