121280-53-3

Upstream product

• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 48149-74-2 allyl D-glucopyranoside 
• 2595-07-5 allyl β-D-glucopyranoside 
• 10343-15-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-allyloxy-tetrahydro-pyran-4-yl ester 
• 2280-44-6 D-Glucose 

Downstream Products

• 121280-54-4 allyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-β-D-glucopyranoside 
• 1105543-73-4 C₃₃H₃₈O₉ 
• 212192-95-5 allyl 2,3-di-O-benzyl-6-O-(4-methoxybenzyl)-β-D-glucopyranoside 

Relevant academic research and scientific papers

Sulfonated sugar compounds, pharmaceutical compositions which contain the same, and methods of treating tumors with the same

Sulfoquinovosylacyl propanediol compounds represented by formula (I): wherein R1 is an acyl residue of a fatty acid, Y is a number of 1, 2 or 3, and M represents a cation having a positive charge equal to Y and pharmaceutically acceptable salts

Synthesis of a di- and a trisaccharide related to the antigen from Klebsiella type 43

Starting from D-galactose, D-mannose and D-glucose methyl α-D- galactopyranosyl-(1→3)-α-D-mannopyranosyl-(1→2)-α-D-mannopyranoside and allyl β-D-mannopyranosyl-(1→4)-β-D-glucopyranosyl uronate were synthesised in a highly stereoselective manner.

Synthetic studies on ciguatoxin [2]; synthesis of the A,B,C-ring system

The synthesis of the A,B,C-ring system having all the natural substituents of ciguatoxin was achieved from D-glucose.