88331-98-0

Upstream product

• 88337-87-5 methyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 88331-96-8 methyl 2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 14917-55-6 methyl 6-deoxy-α-L-mannopyranoside 
• 98-88-4 benzoyl chloride 

Downstream Products

• 88337-88-6 8-(methoxycarbonyl)octyl O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1->3)-O-(2,4-di-O-benzoyl-α-L-rhamnopyranosyl)-(1->3)-O-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 89202-38-0 2,3,4-Tri-O-acetyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranose 

Relevant academic research and scientific papers

ARTIFICIAL CARBOHYDRATE ANTIGENS: A BLOCK SYNTHESIS OF A LINEAR, TETRASACCHARIDE REPEATING-UNIT OF THE Shigella flexneri VARIANT Y POLYSACCHARIDE

Glycosylation of methyl 2,4-di-O-benzoyl-α-L-rhamnopyranoside with 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide gave methyl 2,4-di-O-benzoyl-3-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside (4) in 93percent yield.Conversion of 4 into th