Issue 3, 2016

Rhodium-catalyzed oxidative coupling of N-acyl anilines with alkynes using an acylamino moiety as the traceless directing group

Abstract

A rhodium-catalyzed oxidative annulation of N-acyl anilines with alkynes was developed by using the acylamino group as a traceless directing group for the first time. Various N-acyl anilines and para- or meta-substituted diphenylacetylenes were well tolerated, and a series of 1,2,3,4-tetrasubstituted naphthalenes were readily synthesized in good to excellent yields. Meanwhile, this method also provides a new strategy for the N-dearylation of N-phenylamides.

Graphical abstract: Rhodium-catalyzed oxidative coupling of N-acyl anilines with alkynes using an acylamino moiety as the traceless directing group

Supplementary files

Article information

Article type
Research Article
Submitted
19 Nov 2015
Accepted
13 Jan 2016
First published
14 Jan 2016

Org. Chem. Front., 2016,3, 349-353

Author version available

Rhodium-catalyzed oxidative coupling of N-acyl anilines with alkynes using an acylamino moiety as the traceless directing group

K. Geng, Z. Fan and A. Zhang, Org. Chem. Front., 2016, 3, 349 DOI: 10.1039/C5QO00387C

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