73223-28-6

Upstream product

• 100-44-7 benzyl chloride 
• 69558-10-7 benzyl 2-O-allyl-4-O-benzyl-α-L-rhamnopyranoside 
• 62774-10-1 benzyl 3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 

Downstream Products

• 78161-36-1 benzyl 3,4-di-O-benzyl-2-O-α-L-rhamnopyranosyl-α-L-rhamnopyranoside 
• 105165-93-3 benzyl 3,4-di-O-benzyl-2-O-<4-O-<2,3-di-O-acetyl-4-O-(2,4-di-O-acetyl-3-O-methyl-β-L-xylopyranosyl)-α-L-rhamnopyrnosyl>-2,3-O-isopropylidene-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 105165-84-2 benzyl 3,4-di-O-benzyl-2-O-<2,3-O-isopropylidene-4-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 105165-83-1 benzyl 3,4-di-O-benzyl-2-O-(2,3-O-isopropylidene-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of the tetrasaccharide repeating-unit of the lipopolysaccharide isolated from Pseudomonas maltophilia.

The title tetrasaccharide having the structure 3-O-Me-beta-L-Xylp-(1----4)- alpha-L-Rhap-(1----4)-alpha-L-Rhap-(1----2)-L-Rhap was obtained by reaction of the alpha-acetobromo derivative of 4-O-(3-O-methyl-beta-L-xylopyranosyl)-L-rhamnopyranose and benzyl

SYNTHESIS, AND CARBON-13 N.M.R. STUDY, OF O-α-L-RHAMNOPYRANOSYL-(13)-O-α-L-RAHMNOPYRANOSYL-(12)-L-RHAMNOPYRANOSE AND O-α-L-RHAMNOPYRANOSYL-(13)-O-α-L-RHAMNOPYRANOSYL-(13)-L-RHAMNOPYRANOSE, CONSTITUENTS OF BACTERIAL, CELLWALL POLYSACCHARIDES

O-α-L-Rhamnopyranosyl-(13)-L-rhamnopyranose (19) and O-α-L-rhamnopyranosyl-(12)-L-rhamnopyranose were obtained by reaction of benzyl 2,4- (7) and 3,4-di-O-benzyl-α-L-rhamnopyranoside (8) with 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide, followed