Structure de Bases de Schiff Derivees de 4‐Acylpyrazoline‐5‐Ones et 5‐Thiones

Abstract
The structure of 21 1‐phenyl‐3‐R‐4,1′‐alkyl (aryl)aminoalkyl(aryl)idenepyrazolin‐5‐ones or 5‐thiones is examined.Whereas the chelated NH exo Z form exists always in the pyrazolin‐5‐thiones compounds, this type of tautomer is only observed, for the pyrazolinones derivatives, when one or two steric interactions between substituents (R3‐R1′, and/or R1′‐R2′,) occur.

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