Issue 8, 2016

A zinc-catalyzed oxidative reaction of ynamides with phenols and thiophenols: highly site-selective synthesis of versatile α-aryloxy amides and α-arylthio amides

Abstract

A zinc-catalyzed oxidative reaction of ynamides with phenols and thiophenols under mild reaction conditions has been developed, which provides various α-aryloxy amides and α-arylthio amides in moderate to good yields, respectively. Importantly, high chemoselectivity is achieved by such a non-noble metal-catalyzed alkyne oxidation.

Graphical abstract: A zinc-catalyzed oxidative reaction of ynamides with phenols and thiophenols: highly site-selective synthesis of versatile α-aryloxy amides and α-arylthio amides

Supplementary files

Article information

Article type
Research Article
Submitted
21 Apr 2016
Accepted
21 Jun 2016
First published
22 Jun 2016

Org. Chem. Front., 2016,3, 989-993

A zinc-catalyzed oxidative reaction of ynamides with phenols and thiophenols: highly site-selective synthesis of versatile α-aryloxy amides and α-arylthio amides

P. Ruan, C. Shen, L. Li, C. Liu and L. Ye, Org. Chem. Front., 2016, 3, 989 DOI: 10.1039/C6QO00169F

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