| Literature DB >> 21928148 |
Goutam Guchhait1, Anup Kumar Misra.
Abstract
A convergent synthesis of the tetrasaccharide repeating unit of the O-antigen of the verotoxin producing E. coli O176 has been achieved in excellent yield adopting a [2+2] block glycosylation strategy. The β-D-mannosidic moiety of the tetrasaccharide was prepared from β-D-glucoside and α-D-galactosamine moiety was derived from D-galactal. The tetrasaccharide was synthesized as its 2-trimethylsilylethyl glycoside in excellent yield. All intermediate steps are high yielding. © Springer Science+Business Media, LLC 2011Entities:
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Year: 2011 PMID: 21928148 DOI: 10.1007/s10719-011-9351-4
Source DB: PubMed Journal: Glycoconj J ISSN: 0282-0080 Impact factor: 2.916