97589-70-3

Upstream product

• 75414-17-4 2,3,6-tri-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,5-anhydro-D-arabino-hex-1-enitol 
• 87760-36-9 2,3,6-tri-O-benzoyl-4-O-(2,3,4,5-tetra-O-benzoyl-β-D-galactopyranosyl)-1,5-anhydro-D-arabino-hex-1-enitol 
• 61198-91-2 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1→4)-2,3,6-tri-O-benzoyl-α-D-glucopyranosyl bromide 
• 91280-47-6 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranose 
• 4710-82-1 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)-(1,2,3,6-tetra-O-benzoyl)-β-D-glucopyranose 

Downstream Products

• 97523-41-6 3,6-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-1,5-anhydro-D-fructose O-benzoyloxime 
• 97523-40-5 3,6-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-1,5-anhydro-D-fructose monohydrate 
• 97523-57-4 3,6-di-O-benzoyl-2-nitroso-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-1,5-anhydro-D-arabino-hex-1-enitol 
• 97523-66-5 C₅₂H₄₉NO₁₇ 
• 97523-63-2 benzyl hexa-O-benzoyl-N-acetyl-α-D-lactosaminide 
• 97550-79-3 3,6-di-O-benzoyl-2-<(p-cyanobenzoyl)oximino>-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-α-D-arabino-hexopyranosyl bromide 
• 97523-53-0 C₅₀H₄₇NO₁₆ 
• 97550-99-7 C₅₀H₄₇NO₁₆ 
• 97523-48-3 methyl 3,6-di-O-benzoyl-2-oximino-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-arabino-hexopyranoside 
• 97523-58-5 methyl hexa-O-benzoyl-α-D-lactosuloside oxime 
• 97523-52-9 methyl 2-acetamido-3,6-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-2-deoxy-β-D-mannopyranoside 
• 97523-62-1 methyl N-acetylhexa-O-benzoyl-α-D-lactosaminide 

Relevant academic research and scientific papers

Convenient access to 4-O-glycosylated 1,5-anhydro-d-fructoses via disaccharide-derived 2-hydroxyglycal esters

Efficient six-step protocols are described for the conversion of common disaccharides, such as maltose, cellobiose, or lactose, into the corresponding 4-O-glycosyl-1,5-anhydro-d-fructoses. Overall yields of 40-45% are favorably compared to the alternative eleven-step procedure from their monosaccharide components (～15%).

Disaccharide-Derived 2-Oxo- and 2-Oximinoglycosyl Bromides: Novel, Conveniently Accessible Building Blocks for the Expedient Construction of Oligosaccharides with α-D-Glucosamine, β-D-Mannose, and β-D-Mannosamine as Constituent Sugars

A concise, practical, large-scale adaptable approach has been developed for the transformation of bulk disaccharides such as lactose, maltose, and cellobiose into disaccharide building blocks suitably functionalized for direct glycobiosylation, i.e., benz

SELECTIVE DEACYLATION OF ENOL ESTERS WITH HYDROXYLAMINE

An effective procedure for selectively cleaving enol esters in the presence of normal ester functions has been developed, involving hydroxylaminolysis to the oxime of the parent ketone.