14686-84-1

Upstream product

• 98-88-4 benzoyl chloride 
• 53437-43-7 methyl 4-O-acetyl-α-L-rhamnopyranoside 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 14686-86-3 methyl 4-O-acetyl-2,3-di-O-isopropylidene-α-L-rhamnopyranoside 

Downstream Products

• 178318-63-3 1,4-di-O-acetyl-2,3-di-O-benzoyl-α-L-rhamnopyranose 
• 139710-70-6 methyl-2,3-di-O-benzoyl-4-O-(3,4,6-tri-O-acetyl-2-O-benzyl-α-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 178318-69-9 4-O-(4-O-acetyl-2,3-di-O-benzoyl-α-L-rhamnopyranosyl)-1,2-O-[1-(exo-cyano)ethylidene-3,6-di-O-benzoyl]-β-D-mannopyranose 
• 178318-64-4 4-O-acetyl-2,3-di-O-benzoyl-α-L-rhamnopyranosylbromide 
• 14686-83-0 methyl-2,3-di-O-benzoyl-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthetic Cyclic Oligosaccharides - Syntheses and Structural Properties of a Cyclo(1->4)-α-L-rhamnopyranosyl-(1->4)-α-D-mannopyranosyl>trioside and -tetraoside

An efficient polycondensation-cyclization approach to the synthesis of cyclodextrin analogues is demonstrated by the preparation of cyclohexaoside 1 and cyclooctaoside 2.The key intermediate, disaccharide 3, bearing the cyanoethylidene group as a glycosyl