This is the authors' abstract. We don't add key points for this paper.
A method is disclosed for the convergent synthesis of multiply glycosylated peptides. The approach centers on a convergent technique for generating masked, complex glycopeptide-containing C-terminal acyl donors. Activation of the latent donor in situ and use directly in segment coupling with a second peptide bearing a complex carbohydrate produces a completely unprotected, bifunctional glycopeptide. The system demonstrates a minimum level of hydrolysis and epimerization at the C-terminal amino acid residue of the acyl donor during fully convergent segment coupling and is therefore a powerful tool for the synthesis of glycoproteins.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Warren et al. (2004) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: