LARGE-SCALE SYNTHESIS OF A LEWIS-B TETRASACCHARIDE DERIVATIVE, ITS ACRYLAMIDE COPOLYMER, AND RELATED DISACCHARIDES AND TRISACCHARIDES FOR USE IN ADHESION INHIBITION STUDIES WITH HELICOBACTER-PYLORI
K. Eklind et al., LARGE-SCALE SYNTHESIS OF A LEWIS-B TETRASACCHARIDE DERIVATIVE, ITS ACRYLAMIDE COPOLYMER, AND RELATED DISACCHARIDES AND TRISACCHARIDES FOR USE IN ADHESION INHIBITION STUDIES WITH HELICOBACTER-PYLORI, Journal of carbohydrate chemistry, 15(9), 1996, pp. 1161-1178
The 2-aminoethyl glycoside of -(1-->4)]-2-acetamido-2-deoxy-beta-D-glu
copyranose (Lewis B tetrasaccharide) was synthesized on a large scale
and acryloylated with acryloyl chloride. The obtained oligosaccharide
2-acrylamidoethyl glycoside was then copolymerized with acrylamide to
form a water-soluble, high molecular weight polymer, suitable for use
in adhesion inhibition studies with Helicobacter pylori. Also synthesi
zed were the corresponding derivatives of l-(1-->3)-2-acetamido-2-deox
y-beta-D-glucopyranose and ha-L-fucopyranosyl-(1-->2)-beta-D-galactopy
ranose.