keto-enol tautomerism

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keto-enol tautomerism

(ˈkiːtəʊˈiːnɒl)
n
(Chemistry) chem tautomerism in which the tautomers are an enol and a keto form. The change occurs by transfer of a hydrogen atom within the molecule
References in periodicals archive ?
The observed results were quantified using NMR spectroscopy with an internal standard leading to a general process that could potentially negate the need for the traditional three step process of oxidation, enolization, and 0-alkylation.
1] due to vNH and vC=O groups respectively, which disappears in the corresponding complexes suggesting the enolization of the -C=O of the aroyl keto group giving rise to the -C=N-N=C moiety [15 ] and consequent deprotonation upon coordination.
The absence of these signals in the spectra of the complexes indicate coordination through the phenolic oxygen and enolization of the -C=O of the aroyl keto group and consequent deprotonation.
Our interest in enolizable ketones resulted in a recent paper reporting on the syntheses and enolization of 4-alkyl-2-(2-pyridyl) cyclohexanones (Sund et al.
It has been reported in the literature that in alkaline medium sugar will form enediol with the hydroxyl group and also that the rate of enolization is the same as the rate of oxidation [14] However, in the present study, the double reciprocal plots of the pseudo-first-order rate constants against the sugar concentrations were linear (fig.
The formation of possible kinetic enolization products (4-oxygenated products) was not observed.