Completely unprotected peptides carrying chemoselectively addressable groups react under very mild conditions with free reducing sugars or lipidic aldehydes to form glycopeptides or lipopeptides (for example the somatostatin analogue 1) of any desired structural complexity.
No takes yet. Share an insight, caveat, or question.
Cervigni et al. (1996) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: