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1-Acyl-5-hydrazinopyrazolidines and their ring-chain tautomerism
Authors:Zelenin  K. N.  Golubeva  G. A.  Afanas'eva  S. V.  Sviridova  L. A.  Bezhan  I. P.  Malov  M. Yu.  Bundel'   Yu. G.
Affiliation:(1) M. V. Lomonosov Moscow State University, 117234 Moscow;(2) S. M. Kirov Military Medical Academy, 195009 Leningrad
Abstract:1-Acetyl-5-hydroxyl-2-isopropyl(phenyl)pyrazolidines, as well as 1-hydroxyperhydropyrazolo[1,2-a]-4H-pyridazine-5,8-dione, react readily with alkyl-, aryl-, and acylhydrazines and hydroxylamine to give the corresponding products of substitution of the OH group, which, depending on the nature of the hydrazine, exist in the linear beta-hydrazidohydrazone (oxime) form or in the form of a cyclic tautomer, viz., the corresponding 1-acetyl-5-hydrazinopyrazolidine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1238–1241, September, 1985.
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