Here we report the chemical synthesis of conjugation-ready trisaccharides, representing biological repeating units of Pseudomonas aeruginosa serotype 10 and 19 O-antigens. The α-D-QuiN 3 glycosidic bond was stereoselectively synthesized through TMSI�Ph 3 P�O mediated 1,2-cis glycosylation. Selective oxidation of the C6−OH group at the disaccharide stage allowed for benzylidene-promoted construction of the α-L-GalN 3 glycosidic bond and simplification of the postglycosylation process at the trisaccharide stage. The low reaction temperature and neighboring electron-donating effect facilitated the efficient synthesis of the trisaccharide.