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By Direct Oxidation of the Corresponding Hexoses

Yields of osones obtained by the oxidation of sugars by Fenton s reagent are low, and the osones are invariably contaminated both with starting material and with the products of further oxidation in consequence, the method has had only limited application.44 [Pg.49]

Nicoll, Strause and Waring46 oxidized D-glucose and D-fructose in aqueous solution with excess cupric acetate at 50° for the purpose of ascertaining whether the general principles underlying the mechanism of carbohydrate oxidation in alkaline solutions are sufficient to explain the course of such oxidations in acid solutions. D-Glucosone was claimed to be one of the first products of oxidation the osone was not isolated, and, [Pg.49]

They showed that osone formation is accompanied by the production of formic acid, thought to arise from the oxidation of hydroxymethylene formed by rupture of IV. [Pg.50]

Weidenhagen48 further investigated this reaction he found that osone formation could become the main reaction if ethanol or methanol was used as a solvent, the cupric acetate was not in excess, and the reaction time was limited. Oxidation of D-glucose or D-fructose was reported to give a 40% yield of D-glucosone.14-46 [Pg.50]

The oxidation of D-glucose with potassium persulfate occurs very slowly at room temperature the optimum temperature is 40°, but the yield of osone is very small.38 [Pg.50]


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