The main conversions of c~-ketol fatty acids (18:2 and 18:3), accompanying their redox interactions with 2,6dichlorophenolindophenol (DCPIP) and copper(II) acetate, were studied. The highest rates of oxidation with DCPIP were observed in the alkaline water solutions. In the acidic aqueous media or i
✦ LIBER ✦
Hydriodic Acid Reduction of α-Ketol and α-Diketo Fatty Acids
✍ Scribed by Osman, S. M. ;Ahmad, M.
- Publisher
- John Wiley and Sons
- Year
- 1970
- Weight
- 339 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0931-5985
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✦ Synopsis
Abstract
The hydriodic acid reduction of α‐ketol and α‐diketo derivatives of three monoethenoid fatty acids, oleic, petroselinic and erucic acids, has been studied. The formation of an isomeric mixture of monoketo acids in each has been established by characterization of monocarboxylic or dicarboxylic acids, the hydrolysed fragments of Beckmann rearrangement of the corresponding oximes of monoketo acids, by thin‐layer chromatography (TLC). Hydriodic acid has been found to be a satisfactory reagent for the synthesis of monoketo acids from the α‐ketol and α‐diketo acids.
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