Issue 87, 2013

An efficient synthesis of trisubstituted oxazoles via chemoselective O-acylations and intramolecular Wittig reactions

Abstract

Preparation of new types of trisubstituted oxazoles is realized via chemoselective O-acylations and intramolecular Wittig reactions with ester functionalities using in situ formed phosphorus ylides as key intermediates. A plausible reaction mechanism for this undiscovered chemistry is also proposed based on the existence of expected and rearranged isomeric oxazoles.

Graphical abstract: An efficient synthesis of trisubstituted oxazoles via chemoselective O-acylations and intramolecular Wittig reactions

Supplementary files

Article information

Article type
Communication
Submitted
01 Aug 2013
Accepted
06 Sep 2013
First published
06 Sep 2013

Chem. Commun., 2013,49, 10266-10268

An efficient synthesis of trisubstituted oxazoles via chemoselective O-acylations and intramolecular Wittig reactions

Y. Tsai, Y. Fan, C. Lee, C. Huang, U. Das and W. Lin, Chem. Commun., 2013, 49, 10266 DOI: 10.1039/C3CC45883K

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