224622-46-2

Upstream product

• 224622-28-0 allyl 2,3,6-tri-O-benzoyl-α-D-mannopyranoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 98-88-4 benzoyl chloride 
• 41308-76-3 allyl α-D-mannopyranoside 

Downstream Products

• 224622-57-5 3'',4''-di-O-acetyl-α-L-xylopyranose 1'',2''--2'-yl orthoacetate 
• 224622-58-6 allyl 4-O-<2-O-(2,3,4-tri-O-acetyl-β-L-xylopyranosyl)-3,4-di-O-benzoyl-α-L-rhamnopyranosyl>-2,3,6-tri-O-benzoyl-α-D-mannopyranoside 
• 224622-52-0 allyl 4-O-(2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside 
• 224622-50-8 3,4-di-O-benzoyl-β-L-rhamnopyranose 1,2-(allyl 2,3,6-tri-O-benzoyl-α-D-mannopyranosid-4-yl orthoacetate) 
• 224622-54-2 allyl 4-O-(3,4-di-O-benzoyl-α-L-rhamnopyranosyl)-2,3,6-tri-O-benzoyl-α-D-mannopyranoside 
• 224622-49-5 (3aR,5S,6R,7R,7aR)-2-((2R,3S,4R,5S,6S)-6-Allyloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy)-2,5-dimethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 

Relevant academic research and scientific papers

Facile synthesis of a branched trisaccharide - The repeating unit of antigen O2 polymer using orthoester formation - rearrangement strategy

The synthesis of a branched trisaccharide, the repeating unit of the antigen O2 polymer containing L-rhamnose, D-mannose, and L-xylose, was achieved using orthoester formation - rearrangement strategy.