104731-82-0

Upstream product

• 53270-14-7 benzyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 104731-78-4 benzyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 104731-75-1 benzyl O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1<*>4)-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Sulfide-mediated dehydrative glycosylation

The development of a new method for glycosylation with 1-hydroxy glycosyl donors employing dialkyl sulfonium reagents is described. The process employs the reagent combination of a dialkyl sulfide and triflic anhydride to effect anomeric bond construction

CHEMICAL SYNTHESIS OF DISACCHARIDES OF THE SPECIFIC PHENOLIC GLYCOLIPID ANTIGENS FROM MYCOBACTERIUM LEPRAE AND OF RELATED SUGARS

O-(3,6-Di-O-methyl-β-D-glucopyranosyl)-(14)-2,3-di-O-methyl-L-rhamnopyranose, which is the nonreducing disaccharide of the haptenic trisaccharide of the Mycobacterium leprae-specific, phenolic glycolipid I, O-(6-O-methyl-β-D-glucopyranosyl)-(14)-2,3