Issue 9, 2013

Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes

Abstract

The first example of copper-mediated oxidative annulation of phenols and unactivated internal alkynes to afford benzofuran derivatives was reported. Various phenols and unactivated internal alkynes were successfully employed. Mechanistic studies disclosed a new strategy on annulations of alkynes with phenols through reversible electrophilic carbocupration of phenol followed by alkyne insertion and cyclization.

Graphical abstract: Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes

Supplementary files

Article information

Article type
Edge Article
Submitted
27 May 2013
Accepted
03 Jun 2013
First published
04 Jun 2013

Chem. Sci., 2013,4, 3706-3711

Benzofuran synthesis via copper-mediated oxidative annulation of phenols and unactivated internal alkynes

R. Zhu, J. Wei and Z. Shi, Chem. Sci., 2013, 4, 3706 DOI: 10.1039/C3SC51489G

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