Solid-phase N-glycopeptide synthesis using allyl side-chain protected Fmoc-amino acids

Abstract:

A method for the preparation of glycopeptides using a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/allyl) with selective allyl removal and direct coupling of glycosylamines to the carboxyl function while the peptide is attached to the resin is described. © 1994.

Año de publicación:

1994

Keywords:

• glycopeptides
• solid-phase synthesis
• allyl esters
• Orthogonal protection

Fuente:

scopus