A convenient strategy has been developed for the synthesis of a branched pentasaccharide
containing a rare sugar, 4-acetamido-4-deoxy-β-d-quinovose, corresponding to the cell wall O-antigen of Acinetobacter baumannii strain 9 in very good yield. The desired pentasaccharide has been achieved as a fully
deprotected form enabling the scope for the conjugation with an appropriate aglycone
or protein. The constructions of 1,2-cis glycosyl linkages between the d-galactosamine and d-glucose moieties in the molecule were achieved using thioglycosides as glycosyl donors
under iodonium ion–promoted glycosylation conditions in an ether-based solvent.
Keywords
Carbohydrates - Glycosylation - Glycosides - Oligosaccharides - Total synthesis -
Acinetobacter baumannii
