Aishwarya Shelke, Kartikey Singh, Suvarn S. Kulkarni
We report the first total synthesis of conjugation-ready trisaccharide repeating units from Acinetobacter baumannii clinical isolates MG1 and strain 24, both featuring the same trisaccharide framework. A key synthetic challenge addressed here is the stereoselective installation of a 1,2- cis glycosidic linkage with a poorly nucleophilic axially oriented C4-OH of the d -GalNAcA acceptor, which was efficiently achieved by conformational switching of the pyranose ring from 4 C 1 to 1 C 4 leading to enhanced reactivity.