122713-76-2

Upstream product

• 122713-75-1 methyl 2-O-allyl-α-L-fucopyranoside 
• 824-94-2 p-methoxybenzyl chloride 
• 122713-73-9 methyl 2-O-allyl-3,4-O-isopropylidene-α-L-fucopyranoside 
• 14687-15-1 methyl L-fucopyranoside 
• 24577-96-6 methyl 3,4-di-O-isopropylidene-α-L-fucopyranoside 

Downstream Products

• 122713-77-3 methyl 2-O-allyl-4-O-benzyl-3-O-(4-methoxybenzyl)-α-L-fucopyranoside 
• 122713-79-5 methyl 2-O-allyl-3-O-(4-methoxybenzyl)-4-O-<(methylthio)thiocarbonyl>-α-L-fucopyranoside 
• 122713-81-9 methyl 4,6-dideoxy-3-O-(4-methoxybenzyl)-α-L-xylo-hexopyranoside 
• 122713-80-8 methyl 2-O-allyl-4,6-dideoxy-3-O-(4-methoxybenzyl)-α-L-xylo-hexopyranoside 
• 122731-36-6 methyl 4-O-benzyl-3-O-(4-methoxybenzyl)-α-L-fucopyranoside 
• 122713-82-0 methyl 4,6-dideoxy-3-O-(4-methoxybenzyl)-2-O-(trifluoromethylsulfonyl)-α-L-xylo-hexopyranoside 
• 122713-78-4 methyl 4-O-benzyl-3-O-(4-methoxybenzyl)-2-O-(trifluoromethylsulfonyl)-α-L-fucopyranoside 

Relevant academic research and scientific papers

A facile formation of 2,5-anhydro sugars by ring contraction in methyl hexopyranoside 2-triflates under conditions of nucleophilic displacement

Reaction of methyl 3,4-O-isopropylidene-2-O-(trifluoromethylsulfonyl)-α-L-fucopyranoside and its β anomer with a variety of nucleophilic reagents under mild conditions led to displacement of the triflic ester group, with migration of the ring-oxygen atom