844699-62-3

Upstream product

• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 191276-09-2 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl trichloroacetimidate 
• 149707-75-5 2,3,4,6-tetra-O-benzoyl-1-O-trichloroacetimidoyl-α-D-galactopyranose 

Downstream Products

• 1272617-08-9 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranose-(1->3)-β-D-xylose 
• 1272617-06-7 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranose-(1->3)-1,2-O-isopropylidene-β-D-xylose 
• 1272617-04-5 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranose-(1->3)-5-aldehyde-1,2-O-isopropylidene-α-D-glucofuranose 
• 1272617-10-3 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranose-(1->3)-2,4-di-O-benzoyl-β-D-xylopyranosyl trichloroacetimidate 

Relevant academic research and scientific papers

Synthesis and anti-fungal activity of seven oleanolic acid glycosides

In order to develop potential anti-fungal agents, seven glycoconjugates composed of α-L-rhamnose, 6-deoxy-α-L-talose, β-D-galactose, a-D-mannose, β-D-xylose- (1→4)-6-deoxy-α-L-talose, β-D-galactose-(1→4)-α-L-rhamnose, β-D-galactose-(1→3)- β- D-xylose-(1→4

Synthesis of analogues of (1 → 6)-branched (1 → 3)-glucohexaose

β-D-Galp-(1 → 3)-[β-D-Galp-(1 → 6)-]α-D-Glcp-(1 → 3)-β-D-Glcp-(1 → 3)-[α-D-Manp-(1 → 6)-]D-Glcp 16 and β-D-Galp-(1 → 3)-[β-D-Glcp-(1 → 6)-]α-D-Glcp-(1 → 3)-β-D-Glcp-(1 → 3)-[α-D-Manp-(1 → 6)-]D-Glcp 18 were synthesized as the analogues of the immunomodula