Large Scale Synthesis of A Derivative of An α-Galactosyl Trisaccharide Epitope Involved in the Hyperacute Rejection of Xenotransplantation
摘要:
A derivative of an alpha-galactosyl trisaccharide xenoactive antigen, (2,3,4,6-tetra-O-benzyl-alpha-D-galactopyranosyl)-(1-->3)-(2,4,6-tri-O-acetyl-beta-D-galactopyranosyl)-(1-->4)-2,3,6-tri-O-acetyl-beta-D-glucopyranosyl azide (5), was synthesized on a large scale (50 gram). The synthesis involved a high yielding and highly stereoselective (alpha \beta>20:1) glycosylation reaction utilizing a thiogalactoside as the donor and a selectively protected lactose azide as the acceptor. This derivative serves as a versatile intermediate that can be transformed into a variety of alpha-Gal containing glycoconjugates highly desired in xenotransplantation research and pharmaceutical development.
Large Scale Synthesis of A Derivative of An α-Galactosyl Trisaccharide Epitope Involved in the Hyperacute Rejection of Xenotransplantation
摘要:
A derivative of an alpha-galactosyl trisaccharide xenoactive antigen, (2,3,4,6-tetra-O-benzyl-alpha-D-galactopyranosyl)-(1-->3)-(2,4,6-tri-O-acetyl-beta-D-galactopyranosyl)-(1-->4)-2,3,6-tri-O-acetyl-beta-D-glucopyranosyl azide (5), was synthesized on a large scale (50 gram). The synthesis involved a high yielding and highly stereoselective (alpha \beta>20:1) glycosylation reaction utilizing a thiogalactoside as the donor and a selectively protected lactose azide as the acceptor. This derivative serves as a versatile intermediate that can be transformed into a variety of alpha-Gal containing glycoconjugates highly desired in xenotransplantation research and pharmaceutical development.