Jump to main content
Jump to site search

Issue 44, 2014
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

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
  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements