1693-80-7Relevant academic research and scientific papers
Formation of Uronic Acid by Galactose Oxidase
Matsumura, Shuichi,Kuroda, Akihiro,Higaki, Norihiko,Hiruta, Yukari,Yoshikawa, Sadao
, p. 1747 - 1750 (1988)
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
Koto, Shinkiti,Miura, Teruhisa,Hirooka, Motoko,Tomaru, Aya,Iida, Mika,Kanemitsu, Masanori,Takenaka, Kazuhiro,Masuzawa, Shinichi,Miyaji, Saeko,Kuroyanagi, Naoko,Yagishita, Miki,Zen, Shonosuke,Yago, Kazuo,Tomonaga, Fumiya
, p. 3247 - 3259 (2007/10/03)
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
Kelleher, Frances M.,Bhavanandan, Veerasingham P.
, p. 89 - 98 (2007/10/02)
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
Schwarzenbach, Dominique,Jeanloz, Roger W.
, p. 193 - 202 (2007/10/02)
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,
