| Literature DB >> 17892864 |
Chunjuan Liu1, Fredrik Skogman, Ye Cai, Todd L Lowary.
Abstract
Described is the synthesis of the trisaccharide alpha-D-Manp-(1-->3)-alpha-D-Manp-(1-->3)-beta-D-GlcpNAcO(CH2)8N3, the glycan portion of which corresponds to the 'adaptor-primer' moiety linking the O-chain and core oligosaccharide in the lipopolysaccharide of several Escherichia coli and Klebsiella pneumoniae serotypes. This report represents the first synthesis of this trisaccharide motif, and in the route involved, a key step is a [2+1] coupling of a protected Manp-(1-->3)-alpha-D-Manp glycosyl donor with a GlcpNAc acceptor. The azido group was included in the target to facilitate future preparation of neoglycoconjugates.Entities:
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Year: 2007 PMID: 17892864 DOI: 10.1016/j.carres.2007.08.020
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104