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Tetra-n-butylammonium fluoride:: an efficient base for aza-Michael addition -: synthesis of glycosyl β-amino acid esters

Journal

TETRAHEDRON-ASYMMETRY
Volume 13, Issue 1, Pages 21-24

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0957-4166(02)00047-2

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A mild and efficient route to glycosyl beta-amino acid esters. exploiting the stereoselective Michael addition of benzylamine, in the presence of tetra-n-butylammonium fluoride, to sugar derived gamma-alkoxy alpha,beta-unsaturated esters is described. (C) 2602 Published by Elsevier Science Ltd.

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