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Keto–enol tautomerism of some ortho-substituted α-methylthio-α-diethoxyphosphorylacetophenones

✍ Scribed by Paulo R. Olivato; A. Rodrigues; R. Rittner


Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
201 KB
Volume
705
Category
Article
ISSN
0022-2860

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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