737766-91-5

Upstream product

• 737766-90-4 allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 161007-95-0 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyltrichloroacetimidate 
• 432519-15-8 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 518975-31-0 allyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside 

Downstream Products

• 737766-92-6 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 3)-2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate 

Relevant academic research and scientific papers

Synthesis of a hexasaccharide fragment of group E streptococci polysaccharide and the tetrasaccharide repeating unit of E. coli O7:K98:H6

Syntheses of a hexasaccharide, the dimer of the repeating unit of the group E streptococci polysaccharide, and a tetrasaccharide, the repeating unit of the E. coli O7:K98:H6, were achieved by constructing alternate α-L-(1→2) - and α-L-(1→3)-linked L-rhamnopyranose backbones and substituting with β-linked D-glucopyranose side chains for the former, and a D-glucopyranosyluronate branch for the latter, respectively, at O-2 of the L-rhamnose ring.