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Lipopolysaccharides oligosaccharide synthesis

N. K. Kochetkov, in L. Anderson and F. M. Unger (Eds.), Synthesis of O-antigenic polysaccharides. Pathways for the polymerization of oligosaccharide repeating units, Bacterial Lipopolysaccharides Structure, Synthesis and Biological Activities, ACS Symp. Ser., Vol. 231, Amer. Chem. Soc., New York, 1983, pp. 65-81. [Pg.17]

Jack bean a-mannosidase has also been able to catalyze the transglycosylation of rhamnose residue. It has been used in the synthesis of a disaccharide Rhaal,2RhaaSEt in 32.1% yield from RhaapNP and ethyl 1-thio-a-D-rhamnopyranoside. The disaccharide product is a derivative of the common oligosaccharide unit of antigenic lipopolysaccharides from Pseudomonas (33). [Pg.405]

In the area of glycolipids reviews have been published on the synthesis of bacterial lipopolysaccharides, glycolipid oligosaccharides and Sia Le and sulfated analogues as selectin receptors, and glycosphingolipids containing poly-iV-acetylactosamine and polyglycosylceramides. ... [Pg.63]

See other pages where Lipopolysaccharides oligosaccharide synthesis is mentioned: [Pg.17]    [Pg.593]    [Pg.308]    [Pg.166]    [Pg.317]    [Pg.342]    [Pg.1]    [Pg.144]    [Pg.98]    [Pg.191]    [Pg.207]    [Pg.233]    [Pg.206]    [Pg.123]    [Pg.257]    [Pg.660]    [Pg.171]    [Pg.626]    [Pg.297]    [Pg.288]    [Pg.123]    [Pg.143]    [Pg.238]    [Pg.239]    [Pg.604]    [Pg.193]    [Pg.49]    [Pg.78]    [Pg.54]    [Pg.1162]    [Pg.37]   
See also in sourсe #XX -- [ Pg.203 ]



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