Synthesis of the 2-deoxy analogue of the methyl α-glycoside of the monosaccharide repeating unit of the O-polysaccharide of Vibrio cholerae O:1
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference16 articles.
1. Synthesis and crystal structure of methyl 4,6-dideoxy-4-(3-deoxy-l-glycero-tetronamido) - 2-O-methyl-α-d-mannopyranoside, the methyl α-glycoside of the terminal unit, and presumed antigenic determinant, of the O-specific polysaccharide of Vibrio cholerae O:1, serotype Ogawa
2. Occurrence of 2-O-Methyl-N-(3-Deoxy-L-glycero-tetronyl)-D-perosamine (4-amino-4,6-dideoxy-D-manno-pyranose) in Lipopolysaccharide from Ogawa but Not from Inaba O Forms of O1 Vibrio cholerae
3. Structural studies of the Vibrio cholerae o-antigen
4. Identification of a novel sugar, 4-amino-4,6-dideoxy-2-O-methylmannose in the lipopolysaccharide of Vibrio cholerae O1 serotype Ogawa
5. Synthesis of specifically deoxygenated ligands related to (1→6)-β-d-galacto-oligosaccharides, and studies on their binding to monoclonal antigalactan antibodies
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1. ChemInform Abstract: Synthesis of Ligands Related to the Vibrio cholerae O-Specific Antigen. Part 6. Synthesis of the 2-Deoxy Analogue of the Methyl α- Glycoside of the Monosaccharide Repeating Unit of the O-Polysaccharide of Vibrio cholerae O:1.;ChemInform;2010-08-12
2. Functionalised Saccharides;Organic Synthesis with Carbohydrates;2008-01-28
3. Synthesis of 2-Deoxy Glycosides;Comprehensive Glycoscience;2007
4. Phosphoramidites and solid supports based on N-substituted 2,4-dihydroxybutyramides: universal reagents for synthesis of modified oligonucleotides;Tetrahedron;2006-07
5. Formation of Ethyl 1-Thiomannopyranosides from 2-O-Chloroacetylated and 2-O-Levulinoylated Synthons;European Journal of Organic Chemistry;2006-06
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