Synthesis of the Staphylococcus aureus Strain M Capsular Polysaccharide Repeating Unit.

ABSTRACT: The synthesis of the Staphylococcus aureus strain M capsular polysaccharide repeating unit is reported. A postglycosylation oxidation strategy was utilized for the construction of the α-galactosaminuronic acid linkages, relying on a stereoselective 2-azido-4,6-O-di-tert-butylsilylidene galactopyranoside donor, for which the selectivity was assessed by model glycosylations. The α-fucosamine linkage was installed stereoselectively, using a reactive 2-azidofucosyl donor. An unexpected glycosidic bond cleavage during the TEMPO/PhI(OAc)₂-mediated oxidation of a disaccharide intermediate was circumvented by a TEMPO/PhI(OAc)₂-Pinnick oxidation protocol.

SUBMITTER: Hagen B 

PROVIDER: S-EPMC5442609 | biostudies-literature |

REPOSITORIES: biostudies-literature