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Solid-phase synthesis of thioether-linked glycopeptide mimics for application to glycoprotein semisynthesis
Derek Macmillan1, Alison M Daines, Monika Bayrhuber
1Department of Chemistry, University of Edinburgh, Kings Buildings, West Mains Road, Edinburgh EH9 3JJ, Scotland. derek.macmillan@ed.ac.uk
Organic Letters
|April 27, 2002
Abstract:
[reaction: see text]. Glycoproteins are particularly suited to protein semisynthesis since homogeneous samples for biological analyses are not readily available using traditional recombinant techniques. Here we apply glycosyl iodoacetamides, normally used for the modification of bacterially derived proteins, to solid-phase glycopeptide synthesis. This provides access to glycopeptide alpha-thioesters, which may lend themselves to the semisynthesis of homogeneous N-linked glycoprotein mimics and novel glycopeptide libraries.