402913-30-8

Upstream product

• 255894-68-9 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranosyl 2,2,2-trichloroacetamidate 
• 135129-67-8 methyl 3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 64650-81-3 allyl α-L-rhamnopyranoside 
• 113893-72-4 2,3,4-tri-O-acetyl-L-rhamnopyranosyl trichloroacetimidate 
• 135129-66-7 methyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 1053351-01-1 allyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl(1->3)-α-L-rhamnopyranoside 
• 242473-77-4 allyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of an L-rhamnose tetrasaccharide, the common and major structure of the repeating unit of the O-antigenic polysaccharide of a strain of Klebsiella pneumoniae and Pseudomonas holci

A tetrasaccharide, α-L-Rhap-(1 → 3)-α-L-Rhap-(1 → 2)-α-L-Rhap-(1 → 2)-L-Rhap, the common and major structure of the repeating unit of the O-antigenic polysaccharide of a strain of Klebsiella pneumoniae and Pseudomonas holci was synthesized as its methyl and octyl glycosides. Selective 3-O-glycosylation of allyl α-L-rhamnopyranoside with 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl trichloroacetimidate gave allyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1 → 3)-α-L-rhamnopyranoside (3). Benzoylation, deallylation, and trichloroacetimidation afforded 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1 → 3)-2,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate (6). Self condensation of 3,4-di-O-benzoyl-β-L-rhamnopyranose 1,2-methyl orthoester or 1,2-octyl orthoester gave methyl or octyl 2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1 → 2)-3,4-di-O-benzoyl-α-L-rhamnopyranoside (16 or 17), and subsequent selective deacetylation gave the disaccharide acceptor (18 or 19). Coupling of 6 with 18 (or 19), followed by deacylation in ammonia-saturated methanol, produced the target tetrasacharide.