113409-92-0

Upstream product

• 67831-42-9 benzyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 931-59-9 benzenesulfenyl chloride 

Downstream Products

• 114079-17-3 benzyl O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 114079-16-2 benzyl O-(4-O-acetyl-2,3,6-tri-O-benzyl-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 71672-07-6 benzyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 62746-92-3 benzyl O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

SULFENATE ESTERS AS GLYCOSYL ACCEPTORS: A NOVEL APPROACH TO O-GLYCOSIDES FROM THIOGLYCOSIDES AND SULFENATE ESTERS

The reactions of thioglycosides and sulfenate esters were effected in the presence of Lewis acid to give corresponding O-glycosides.The stereoselectivity was highly dependent on the solvent.

SULFENATE ESTERS AS GLYCOSYL ACCEPTORS: A NOVEL APPROACH TO THE SYNTHESIS OF 2-DEOXYGLYCOSIDES

An approach to the synthesis of 2-deoxyglycosides from glycals was developed by use of Lewis acid mediated activation of benzenesulfenate esters.