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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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