Highly regioselective synthesis of 2,4,5-(hetero)aryl substituted oxazoles by intermolecular [3+2]-cycloaddition of unsymmetrical internal alkynes
Research output: Contribution to journal › Article
Colleges, School and Institutes
A robust N-nucleophilic 1,3-N,O-dipole equivalent reacts with unsymmetrical internal alkynes under gold catalysis. Conjugation from a remote nitrogen lone pair enables and controls this convergent and highly regioselective process. This journal is © 2013 The Royal Society of Chemistry.
|Number of pages||3|
|Publication status||Published - 7 Oct 2013|