50767-75-4

Upstream product

• 3067-56-9 D-glucurono-3,6-lactone acetonide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 50767-75-4 methyl 3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranuronate 
• 2671-19-4 1,2-O-isopropylidene-α-D-glucofuranuronic acid 

Downstream Products

• 84283-88-5 methyl 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-<5-(2)H>idofuranuronate 
• 84283-83-0 3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranuronamide 
• 50767-75-4 methyl 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-idofuranuronate 
• 328379-59-5 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-idofuranose 
• 84283-83-0 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-idofuranuronamide 
• 55094-54-7 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-idofuranuronic acid 
• 20513-98-8 1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone 
• 84283-85-2 3,5-O-benzylidene-1,2-O-isopropylidene-β-L-idofuranurononitrile 
• 84283-85-2 3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranurononitrile 

Relevant academic research and scientific papers

SYNTHESIS OF L-IDURONIC ACID DERIVATIVES BY EPIMERISATION OF ANANCOMERIC D-GLUCURONIC ACID ANALOGUES

Derivatives of L-iduronic acid were prepared by epimerisation of D-glucuronic acid derivatives that were constrained to adopt a conformation having C-6 in an axial position, so that the L-iduronic acid derivatives would be thermodynamically more stable.Me