Synthesis of oligosaccharide repeat subunits of O-polysaccharide LPS from Danish Helicobacter pylori

CARB 95

Dinanath Baburao Fulse, dinanathreddy@gmail.com and Kwan Soo Kim, kwan@yonsei.ac.kr. Center for Bioactive Molecular Hybrids, Department of Chemistry, Yonsei University, Seoul, 120-749, South Korea

 

 

 

The synthesis of tri, hexa and nonasaccharide of O-polysacchardie of lipopolysaccharide (LPS) from Danish Helicobacter pylori has been accomplished. The key synthetic strategies are that the axial methyl group in the branched sugar was elaborated after the coupling of building blocks B and C and the branched sugar was introduced in between two rhamonoses of the trisaccharide repeat unit. Coupling of three monosaccharide building blocks and the dimerization and trimerization of the resulting trisaccharide repeat unit was achived by employing CB glycoside method.

 

General Posters
6:00 PM-8:00 PM, Tuesday, August 21, 2007 BCEC -- Exhibit Hall - B2, Poster

Division of Carbohydrate Chemistry

The 234th ACS National Meeting, Boston, MA, August 19-23, 2007