1693-80-7

Upstream product

• 4539-78-0 2,3,4-tri-O-benzyl-D-glucopyranosideuronic acid benzyl ester 
• 75336-65-1 methyl 2,3,4-tris-O-(phenylmethyl)-α-D-glucopyranuorate 
• 536-11-8 D-melibiose 
• 512-69-6 D-raffinose 
• 70792-91-5 D-raffinose aldehyde 
• 104880-42-4 β-fructofuranosyl O-(α-D-galactopyranosyl uronic acid)-(1-6)-O-α-D-glucopyranoside 
• 13100-46-4 1,2,3,4-tetra-O-acetyl-β-D-glucopyranose 
• 78172-72-2 1,2,3,4-tetra-O-acetyl-6-O-(benzyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-β-D-glucopyranose 
• 4356-85-8 benzyl (2,3,4-tri-O-benzyl-D-glucopyranosyl chloride)uronate 
• 185380-18-1 (2S,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-(2-methoxy-ethoxy)-tetrahydro-pyran-2-carboxylic acid benzyl ester 
• 185380-13-6 (2S,3S,4S,5R,6R)-6-Allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-carboxylic acid benzyl ester 
• 185380-12-5 methyl (allyl 2,3,4-tri-O-benzyl-β-D-glucopyranosid)uronate 
• 114663-53-5 methyl (allyl 2,3,4-tri-O-acetyl-β-D-glucopyranosid)uronate 
• 141520-78-7 methyl (allyl β-D-glucopyranosid)uronate 

Downstream Products

• 6556-12-3 D-glucuronic acid 

Relevant academic research and scientific papers

Formation of Uronic Acid by Galactose Oxidase

The C-6 hydroxymethyl group of methyl D-galactopyranoside and oligosaccharides containing D-galactopyranosyl residues were found to be oxidized with oxygen by galactose oxidase to the corresponding carboxyl group via an aldehyde intermediate.

Stereoselective Syntheses of α-Glucuronides Using Dehydrative Glycosylation

Methyl and benzyl 2,3,4-tri-O-benzyl-D-glucopyranuronates, prepared from D-glucurono-6,3-lactone, afforded selectively the corresponding α-glucopyranosiduronates by the aid of the condensing reagent system composed of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and triethylamine. Using this method, O-α-D-glucopyranuronosyl-(1→3)-O-α-L-arabinofuranosyl- (1→3)-D-xylopyranose, one of the minimal component units in the structure of plantago-mucilage A from the seeds of Plantago asiatica Linne constituting a Chinese medicine : chegianzi [HU~P].

PREPARATION AND CHARACTERIZATION OF β-D-FRUCTOFURANOSYL O-(α-D-GALACTOPYRANOSYL URONIC ACID)-(1->6)-O-α-D-GLUCOPYRANOSIDE AND O-(α-D-GALACTOPYRANOSYL URONIC ACID)-(1->6)-D-GLUCOSE

β-D-Fructofuranosyl O-(α-D-galactopyranosyl uronic acid)-(1->6)-O-α-D-glucopyranoside (3) was prepared by treating raffinose with D-galactose oxidase, followed by hypoiodite oxidation of the resulting aldehyde.Mild acid hydrolysis of 3 gave O-(α-D-galactopyranosyl uronic acid)-(1->6)-D-glucose.

SYNTHESIS OF PART OF THE ANTIGENIC REPEATING-UNIT OF Streptococcus pneumoniae TYPE II

Condensation of methyl 4-O-acetyl-3-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside with 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl chloride gave a mixture of methyl O--(12)-O-(2,3,