Beilstein J. Org. Chem.2021,17, 2915–2921, doi:10.3762/bjoc.17.199
was then deprotected and N-acetylated to finally afford the desired trisaccharide repeating unit as its α-p-methoxyphenyl glycoside.
Keywords: capsular polysaccharide; carbohydratevaccines; O-antigen; oligosaccharide synthesis; one-pot synthesis; Introduction
O-antigens or O-specific
PDF
Graphical Abstract
Figure 1:
Structure of the repeating unit of the lipopolysaccharide of Providencia stuartii O49 serotype.
Beilstein J. Org. Chem.2012,8, 787–803, doi:10.3762/bjoc.8.89
development not only of new tools for tumor diagnosis and monitoring but also in the design of new anticancer drugs [8]. Attempts have been made to mount an immune response against tumor oligosaccharides by carbohydratevaccines [9] and also to inhibit adhesive processes, such as the interaction between
PDF
Graphical Abstract
Scheme 1:
Synthesis of (4-{[(β-D-galactopyranosyl)oxy]methyl}furan-3-yl)methyl hydrogen sulfate (GSF, 5) and ...