Direct coupling procedure for the synthesis of N-acyl-2-oxazolidinones derived from α,β-unsaturated carboxylic acids

Article abstract of DOI:10.1080/00397919608003613

An efficient direct coupling procedure for the synthesis of N-acyl-2-oxazolidinones derived from α,β-unsaturated carboxylic acids is described in which 2-chloro-1-methylpyridinium iodide is employed as the dehydrating agent.

Full text of DOI:10.1080/00397919608003613

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Synthetic Communications:
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Synthetic Organic Chemistry
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Direct Coupling Procedure
for the Synthesis of N-Acyl-2-
oxazolidinones Derived from
α,β-Unsaturated Carboxylic
Acids
a
a
Joop Knol & Ben L. Feringa
a
Department of Organic and Molecular Inorganic
Chemistry, Groningen Centre for Catalysis and
Synthesis , University of Groningen , Nijenborgh
4, 9747, AG Groningen, The Netherlands
Published online: 21 Aug 2006.
To cite this article: Joop Knol & Ben L. Feringa (1996) Direct Coupling Procedure
for the Synthesis of N-Acyl-2-oxazolidinones Derived from α,β-Unsaturated
Carboxylic Acids, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 26:2, 261-268, DOI:
10.1080/00397919608003613
To link to this article: http://dx.doi.org/10.1080/00397919608003613
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