Výsledky vyhledávání

Septanose Carbohydrates. III. Oxidation-Reduction Products From 1,2-3,4-Di-O-isopropylidene-α-D-glucoseptanose: Preparation of L-Idose Derivatives

Autor: JD Stevens, GE Driver

Publikováno v: Australian Journal of Chemistry. 43:2063

Oxidation of 1,2:3,4-di-O-isopropylidene-α-D-glucoseptanose (1a) with dimethyl sulfoxide and acetic anhydride has yielded methylthiomethyl ether (1b), ketone (2), and a novel product (3). Reduction of (2) gave (1a) and its L-ido isomer (4a) which yi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f770c605dfa732b1cdfda397d4f5f361
https://doi.org/10.1071/ch9902063

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Akademický článek

Preparation of 1,2-O-isopropylidene derivatives of alpha-D-galactoseptanose, beta-L-altroseptanose, and 3-O-methyl-alpha-D-guloseptanose.

Autor: Driver GE; School of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia., Stevens JD

Publikováno v: Carbohydrate research [Carbohydr Res] 2001 Aug 23; Vol. 334 (2), pp. 81-9.

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