Syntheses of specifically deoxygenated methyl α-isomaltotriosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference18 articles.
1. Seven structurally different murine monoclonal galactan-specific antibodies show identity in their galactosyl-binding subsite arrangements
2. Mapping of subsites of monoclonal, anti-carbohydrate antibodies using deoxy and deoxyfluoro sugars
3. Binding characteristics of IgA 16.4.12E, a monoclonal antibody with specificity for the nonreducing terminal epitope of alpha-(1—-6)-dextrans. Comparisons between IgA hybridoma 16.4.12E and myeloma W3129
4. Systematic chemical synthesis and n.m.r. spectra of methyl α-glycosides of isomalto-oligosaccharides and related compounds
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1. Functionalised Saccharides;Organic Synthesis with Carbohydrates;2008-01-28
2. Acetal−Vinyl Sulfide Cyclization on Sugar Substrates: Effect of Structure and Substituent;The Journal of Organic Chemistry;2002-12-13
3. Solution- and solid-phase oligosaccharide synthesis using glucosyl iodides: a comparative study;Carbohydrate Research;2002-11
4. Anomerization of Methyl Glycosides by Acid-Catalysed Methanolysis: Trapping of Intermediates;Journal of Carbohydrate Chemistry;1999-01-01
5. Synthesis of the methyl α-glycosides of some isomalto-oligosaccharides specifically deoxygenated at position C-3;Carbohydrate Research;1996-04
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