Large-Scale Synthesis of a Lewis b Tetrasaccharide Derivative, its Acrylamide Copolymer, and Related DI- and Trisaccharides for Use in Adhesion Inhibition Studies withHelicobacter Pylori.
作者:
K. Eklind,
R. Gustafsson1,
A.K. Tidén,
T. Norberg,
P.M. Åberg2,
期刊:
Journal of Carbohydrate Chemistry
(Taylor Available online 1996)
卷期:
Volume 15,
issue 9
页码: 1161-1178
ISSN:0732-8303
年代: 1996
DOI:10.1080/07328309608006504
出版商: Taylor & Francis Group
数据来源: Taylor
摘要:
The 2-aminoethyl glycoside ofO-α-L-fucopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-[O-α-L-fucopyranosyl-(1→4)]-2-acetamido-2-deoxy-β-D-glucopyranose (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 withHelicobacter pylori. Also synthesized were the corresponding derivatives ofO-α-L-fucopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranose andO-β-L-fucopyranosyl-(1→2)-β-D-galactopyranose.
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