121556-97-6Relevant articles and documents
TAUTOMERISM AND CONFIGURATIONAL ISOMERISM IN DIOXIMES OF β-DICARBONYL COMPOUNDS
Ershov, A. Yu.,Yakimovich, S. I.,Zelenin, K. N.,Zerova, I. V.
, p. 2062 - 2070 (2007/10/02)
According to the data from 1H and 13C NMR spectroscopy, the dioximes of β-carbonyl compounds exist in solutions in the dioxime form, represented by a series of configurational isomers, or as a mixture of the dioxime and the cyclic isoxazoline forms.The conditions for the appearance of the ring-chain equilibrium in the dioximes of β-dicarbonyl compounds were determined, and the dependence of the tautomeric and configurational composition on the structure of the β-dicarbonyl component and the nature of the solvent was studied.