Syntheses of triglycosyl tetrapeptides and a hexaglycosyl tetrapeptide

Article abstract of DOI:10.1016/0008-6215(96)00004-3

A stereo-controlled synthesis of the model compound for the phytoalexin elicitor-active glycoprotein is described. Glycosylation of the trisaccharide, 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1 → 6)-2,3,4-tri-O-acetyl-α-D-mannopyranosyl-(1 → 6)-2,3,4-tri-O-acetyl-α-D-mannopyranosyl trichloroacetimidate (12), with N-(9-fluorenylmethoxycarbonyl)-L-seryl-L-proline benzyl ester (3) or N-(carbobenzoxy)-L-seryl-L-proline methyl ester (4) by use of BE₃ · OEt₂ gave the triglycosyl-seryl-proline derivatives. The N- as well as C-terminus of these triglycosyl dipeptides could be deblocked selectively to give compounds 14 and 16, which are versatile intermediates for the completion of model compound synthesis of glycopeptide. Triglycosyl tetrapeptides (18, 21) and hexaglycosyl tetrapeptide (23) have been prepared by the convergent block synthesis.