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HRID392671

反应详情

EQUATION

反应方程式

HRID 392671 的结构方程式

REACTANTS

反应物

3
结构：OO
HCID784

Hydrogen peroxide

H2O2

结构：CC(=O)NC1C(O)OC(CO)C(O)C1O
HCID899

2-Acetamido-2-deoxyhexopyranose

C8H15NO6

结构：O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO
HCID3037556

(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal

C6H12O6

PRODUCTS

生成物

2
结构：CC(=O)N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O
HCID35717

N-[(3R,4R,5R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

C8H15NO6

结构：O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO
HCID3037556

(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal

C6H12O6

PROCEDURE

实验过程

N-Acetylhexosamine dialdose may, for example, be manufactured by oxidation of the 6-position of N-acetylhexosamine either chemically or enzymatically. An example of the chemical oxidation is a Fenton method where oxidation is carried out with hydrogen peroxide in the presence of a ferrous salt while that of the enzymatic oxidation is an oxidation using galactose oxidase [EC 1.1.3.9; Cooper, et al.; The Journal of Biological Chemistry, volume 234, pages 445-448 (1959)]. Oxidation of N-acetyl-D-galactosamine with galactose oxidase gives N-acetylgalactosamine dialdose.