Approach to the synthesis of the repeating units of immunodeterminant bacterial polysaccharides: synthesis and13C n.m.r. analysis of β-D-galactopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-L-rhamnopyranose
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1979/C3/C39790000828
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthetic oligorhamnans related to the most common O-chain backbone from phytopathogenic bacteria;Tetrahedron;2006-09
2. Glycosylation Using Hemiacetal Sugar Derivatives: Synthesis ofO-α-D-Rhamnosyl-(1→3)-O-α-D-rhamnosyl-(1→2)-d-rhamnose andO-α-D-Tyvelosyl-(1→3)-O-α-D-mannosyl-(1→4)-L-rhamnose;Bulletin of the Chemical Society of Japan;2003-07
3. Oligomerization of a rhamnanic trisaccharide repeating unit of O-chain polysaccharides from phytopathogenic bacteria;Tetrahedron Letters;2002-12
4. Structural studies on O-specific polysaccharides of lipopolysaccharides from Yersinia enterocolitica serovars O:5 and O:5,27;European Journal of Biochemistry;1986-04
5. Somatic antigens of Pseudomonas aeruginosa. The structure of the O-specific polysaccharide chains of lipopolysaccharides of P. aeruginosa serogroup O4 (Lanyi) and related serotype O6 (Habs) and immunotype 1 (Fisher);European Journal of Biochemistry;1985-08
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