Method of manufacturing an aldose or an aldose derivative

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

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536 111, C07K 100, C07K 302

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active

059986085

ABSTRACT:
The invention relates to a method of manufacturing an aldose or an aldose derivative, with n carbon atoms, characterised by the fact than an aqueous solution of a salt of acid derivative of monosaccharide with n+2 carbon atoms containing at least one .alpha.-hydroxy acid unit, with the exception of gluconic acid, is brought into contact with hydrogen peroxide in the presence of at least one salt of a metal chosen from the group consisting of cobalt, nickel and ruthenium.

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Journal of the American Chemical Society (1950), vol. 72, p. 4546 (Fletcher et al.
Yanagihara et al., "Preparation of 2-Hydroxymethylated Aldose by the Stereospecific Rearrangement of Ketose," Bull. Society Chemistry Japan, 68(1), 237-242 (Jan., 1995).
Yano et al., "Reactions of Metal Complexes with Carbohydrates: Synthesis and Characterization of Novel Nickel(II) Complexes Containing Glycoslamines Derived From a Monossaccharide and a Diamine. An X-Ray Crystallographic Study of (Ethylenediamine){N-(2-aminoethyl)-D-fructopyranosylamine}nickel(II) .cndot. Cl.sub.2 .cndot. CH.sub.3 OH," Carbohydrate Research, 142(2), 179-193 (Oct. 15, 1985).
Yamauchi et al., "Epimerization and Isomerization of Various Monosaccharides Using Metal-Diamine Sysems," Carbohdrate Research, 204, 233-239 (Sep. 5, 1990).
Concise Encyclopedia Chemistry, Eagleston (ed.), Walter de Gruyter, New York, NY, 1994, pp. 31, 35 and 1140.

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