Practical Synthesis of the Disaccharide Epitope, D-Galactopyranosyl-α-1,3-D- galactopyranose, by using 1,2;5,6-Di-O-cyclohexylidene-α-D-galactofuranose as the Glycosyl Acceptor

Abstract

D-Galactosyl-α-1,3-D-galactopyranose (1) was chemically prepared in a good yield by coupling phenyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-galactopyranoside (5) or 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl bromide (8) with 1,2:5,6-di-O-cyclohexylidene-α-D-galactofuranose (3) with subsequent de-O-benzylation and de-O-cyclohexylidenation of the resulting protected α-1,3-disaccharide.

• 1,2:5,6-di-O-cyclohexylidene-α-D-galactofuranose
• D-galactopyranosyl-α-1,3-D-galactopyranose
• xenotransplantation
• α-glycosydation