Abstract:
Non-traceless modified Staudinger reaction was utilized as a safe method in this work to synthesize novel synthons of UDP-N-acetyl-L-fucosamine as potential inhibitors of or substrates for bacterial glycosyltransfares, responsible for the biosynthesis of the capsular polysaccharide of Staphyloccous aureus. Carbon-13 and proton spectral techniques were used in the characterization of formed products.