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Department of Chemistry, University of Wisconsin – Madison, 1101 University Ave, Madison, USA
E-mail: stahl@chem.wisc.edu
; Fax: +1 608 262 6143
; Tel: +1 608 265 6288
Org. Biomol. Chem., 2012,10, 3866-3870
DOI:
10.1039/C2OB25310K
Received
11 Feb 2012,
Accepted
22 Mar 2012
First published online
23 Mar 2012
The copper(II)-mediated oxidative cyclization of enamides to oxazoles is reported. A range of 2,5-disubstituted oxazoles were prepared in moderate to good yields in two steps from simple amide and alkyne precursors.