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Glycosyl donors and acceptors may be covalently linked to aspartic acid residues via OH-6 esters. Peptide elaboration allows glycosylation reactions to be performed between donors and acceptors linked to this peptide template. These reactions display increased regio- and stereoselectivities, which are dependent on the nature of the peptide. Simple molecular modelling is used to rationalise the differing product distributions obtained by variation of the linking amino acid sequence. Copyright (C) 2000 Elsevier Science Ltd.

Original publication

DOI

10.1016/S0957-4166(99)00494-2

Type

Journal article

Journal

Tetrahedron Asymmetry

Publication Date

28/01/2000

Volume

11

Pages

231 - 243