Abstract
A tetrasaccharide repeating unit corresponding to the cell-wall lipopolysaccharide of E. coli O40 was synthesized by using a convergent block glycosylation strategy. A disaccharide donor was coupled to a disaccharide acceptor by a stereoselective glycosylation. A 2-aminoethyl linker was chosen as the anomeric protecting group at the reducing end of the tetrasaccharide. All glycosylation steps are significantly high yielding and stereoselective.
Original language | English |
---|---|
Pages (from-to) | 2053-2059 |
Number of pages | 7 |
Journal | Beilstein Journal of Organic Chemistry |
Volume | 8 |
DOIs | |
Publication status | Published - 22 Nov 2012 |
Keywords
- Escherichia coli
- Glycosylation
- Lipopolysaccharide
- O-antigen; tetrasaccharide