83921-79-3Relevant articles and documents
Simple and mild stereoselective O-glycosidation using 1,2-anhydrosugars under neutral conditions
Somasundaram, Devaraj,Balasubramanain, Kalpattu K.,Shanmugasundaram, Bhagavathy
supporting information, p. 764 - 767 (2019/02/16)
The ring opening of α-D-1,2-anhydrohexapyranoses with phenols proceeded smoothly in ethyl acetate (neutral conditions) in the absence of metal ion catalysts or additives to stereoselectively furnish 1,2-cis-α-aryl glycosides as the major product and 1,2-t
SYNTHETIC OLIGOSACCHARIDES FOR MORAXELLA VACCINE
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, (2011/11/13)
The present invention provides synthetic Moraxella catarrhalis lipooligosaccharide (LOS)-based oligosaccharides and conjugates containing various M. catarrhalis serotype-specific oligosaccharide antigens or various core M. catarrhalis oligosaccharide structures or motifs corresponding to one or more of the three major serotypes and/or members within a given serotype. The oligosaccharides may be synthesized by a chemical assembly methodology relying on a limited number of monosaccharide and disaccharide building blocks. The invention further provides M. catarrhalis LOS-based immunogenic and immunoprotective compositions and antibodies derived therefrom for diagnosing, treating, and preventing infections caused by M. catarrhalis.
Carboxymethylglycoside lactones (CMGLs): structural variations on the carbohydrate moiety
Listkowski, Arkadiusz,Ing, Pisethnaline,Cheaib, Rouba,Chambert, Stephane,Doutheau, Alain,Queneau, Yves
, p. 2201 - 2210 (2008/02/11)
New glucose and galactose based bicyclic lactones, with variations in the anomeric configuration, the protecting groups (acetyl or benzyl) and the furanosyl or pyranosyl rings were synthesized from allyl glycosides and used for the preparation of a series