Issue 10, 2012
From the journal:

Chemical Communications

Palladium-catalyzed hydroacyloxylation of ynamides†‡

Donna L. Smith,a   William R. F. Goundryb  and  Hon Wai Lam*a  

* Corresponding authors

a EaStCHEM, School of Chemistry, University of Edinburgh, Joseph Black Building, The King's Buildings, West Mains Road, Edinburgh, United Kingdom
E-mail: h.lam@ed.ac.uk
Tel: +44-131-650-4831

b AstraZeneca Process Research and Development, Charter Way, Silk Road Business Park, Macclesfield, Cheshire, United Kingdom

Abstract

In the presence of substoichiometric Pd(OAc)2, carboxylic acids undergo highly regio- and stereoselective additions to ynamides to provide α-acyloxyenamides.

Graphical abstract: Palladium-catalyzed hydroacyloxylation of ynamides

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1CC13595C
Article type
Communication
Submitted
16 Jun 2011
Accepted
01 Aug 2011
First published
22 Aug 2011

Chem. Commun., 2012,48, 1505-1507

Permissions

Request permissions

Palladium-catalyzed hydroacyloxylation of ynamides

D. L. Smith, W. R. F. Goundry and H. W. Lam, Chem. Commun., 2012, 48, 1505 DOI: 10.1039/C1CC13595C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements