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Royal Society of Chemistry, Organic and Biomolecular Chemistry, 5(10), p. 941-944, 2012

DOI: 10.1039/c1ob06699d

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Stereoselective synthesis of N-aryl proline amides by biotransformation-Ugi-Smiles sequence

This paper is available in a repository.
This paper is available in a repository.

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Abstract

An efficient combination of MAO-N-catalyzed desymmetrization of cyclic meso-amines with Ugi-Smiles multicomponent chemistry produced optically pure N-aryl proline amides. This method represents the first report of a fully asymmetric Ugi-Smiles process.