A new synthesis of L-ascorbic acid (vitamin C) from protected derivatives of D-glucitol

Article abstract of DOI:10.1080/00397919108021034

Indirect, anodic oxidation of 1,3,2,4-diacetals of D-glucitol, leads to the 3,5,4,6-diacetals of 2-keto-L-gulonic acid. Hydrolysis of which provides L-xylo-2-hexulosonic acid and hence L-ascorbic acid by lactonization.

Full text of DOI:10.1080/00397919108021034

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Synthetic Communications: An
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A New Synthesis of L-
Ascorbic Acid (Vitamin C) from
Protected Derivatives of D-
Glucitol
P. A. García a , R. Velasco a & F. Barba b
a Department of Organic Chemistry , University of
Murcia , Murcia, Spain
b Department of Organic Chemistry , University of
Alcalá de Henares , Madrid, Spain
Published online: 16 Feb 2007.
To cite this article: P. A. García , R. Velasco & F. Barba (1991) A New Synthesis of
L-Ascorbic Acid (Vitamin C) from Protected Derivatives of D-Glucitol, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:10-11, 1153-1161, DOI: 10.1080/00397919108021034
To link to this article: http://dx.doi.org/10.1080/00397919108021034
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