1133159-10-0

Upstream product

• 1133159-40-6 p-tolyl 2,3-anhydro-1-thio-α-D-rhamnopyranoside 
• 98-88-4 benzoyl chloride 

Downstream Products

• 1133161-70-2 benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside 
• 1133160-69-6 methyl 4-O-benzoyl-2,6-dideoxy-2-p-(tolylthio)-β-D-glucopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 1133160-52-7 n-octyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranoside 
• 1133162-86-3 benzyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranosyl-(1->3)-4-O-benzoyl-2,6-dideoxy-β-D-arabino-hexopyranoside 
• 1133160-75-4 methyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranosyl-(1->4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1133160-47-0 benzyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranoside 
• 1133160-63-0 tert-butyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranoside 
• 1133160-57-2 cyclohexyl 4-O-benzoyl-2,6-dideoxy-2-(p-tolylthio)-β-D-glucopyranoside 

Relevant academic research and scientific papers

2,3-Anhydrosugars in glycoside bond synthesis. Application to 2,6-dideoxypyranosides

We describe here the first use of 2,3-anhydrosugars as glycosylating agents for the preparation of 2-deoxypyranosides. In particular, the methodology was used to assemble 2,6-dideoxysugar glycosides. Glycosylation of a panel of alcohols with one of two 6-