929619-11-4

Upstream product

• 100-44-7 benzyl chloride 
• 48149-74-2 allyl D-glucopyranoside 

Downstream Products

• 929619-12-5 allyl 2,3,6-tri-O-benzyl-4-O-(4-methoxybenzyl)-D-glucopyranoside 
• 121280-62-4 2,3,6-tri-O-benzyl-4-O-(4-methoxybenzyl)-D-glucopyranose 
• 929619-16-9 3,2,6-tri-O-benzyl-N-benzyloxycarbonyl-4-O-[5-(adamantan-1-yl-methoxy)-pentyl]-1-deoxynojirimycin 
• 929619-15-8 3,2,6-tri-O-benzyl-N-benzyloxycarbonyl-4-O-p-methoxybenzyl-1-deoxynojirimycin 
• 929619-13-6 3,2,6-tri-O-benzyl-4-O-p-methoxybenzyl-D-glucitol 
• 929619-14-7 3,2,6-tri-O-benzyl-4-O-p-methoxybenzyl-1-deoxynojirimycin 
• 143834-17-7 3,2,6-tri-O-benzyl-N-benzyloxycarbonyl-1-deoxynojirimycin 

Relevant academic research and scientific papers

Synthesis of 1-deoxyhept-2-ulosyl-glycono-1,5-lactone utilizing α-selective O-glycosidation of 2,6-anhydro-1-deoxy-d-hept-1-enitols

A series of 1-deoxy-heptulo-2-pyranosyl-glycono-1,5-lactones were synthesized utilizing completely α-selective O-glycosidation of heptenitols. Anomeric configuration of the products was confirmed by 3JC,H coupling measurement and X-ray crystal structural analysis. The benzyl-protected ketosyl saccharides were partly unstable, and glycosidic linkage was prone to cleave under the usual debenzylation conditions. To prevent this, we surveyed various additives for the Pd-catalyzed hydrogenation reaction and found that basic alumina was the most effective.

Modified α-D-Glcρ-(1-2)-α-D-Glcρ-(1-3)-α-D-Glcρ-analogues

Disclosed is the trisaccharide α-D-Glcp-(1-2)-α-D-Glcp-(1-3)-α-D-Glcp and compounds related thereto as well as pharmaceutical compositions thereof.

Modified kojibiosides analogues

Disclosed are novel analogues of kojibiose and pharmaceutical compositions comprising such analogues.