Journal
CARBOHYDRATE RESEARCH
Volume 345, Issue 14, Pages 2067-2073Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.carres.2010.07.023
Keywords
L-Rhamnose; 6-Deoxy-alpha-L-talose; Oligosaccharide; Mesorhizobium huakuii
Funding
- Chinese Universities Scientific Fund [2009-1-43]
- National Basic Research Program of China [2010CB126105]
- NSFC [20902108]
- China and the Key Program of Zhejiang Province [2008C11043]
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The synthesis of a trisaccharide and a hexasaccharide, the monomer and dimer of the repeating unit of O-antigen polysaccharide from Mesorhizobium huakuii IFO15243, has been accomplished through suitable protecting group manipulations and stereoselective glycosylation reactions starting from commercially available L-rhamnose. The target oligosaccharides in the form of their p-methoxyphenyl glycosides are suitable for further glycoconjugate formation via selective cleavage of this group. (C) 2010 Elsevier Ltd. All rights reserved.
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