Abstract
The Lewis acidity of 4-ylidene-3,5-dioxopyrazolidines decreases with increasing electron-donor capacity of the substituents in the para position of the 4-benzylidene residue and in the α-position of the exocyclic double bond. An analogous effect is found for the substituents in the 4-benzylidene residue on the NH-acidity of 1-phenyl-4-benzylidene-3,5-dioxopyrazolidines. The observed effect is analogous to their influence on the halfwave potential in the polarographic reduction on a dropping mercury electrode.
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For Communication 26, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 83–85, January, 1989.
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Moldaver, B.L., Aronzon, M.E. & Evstratova, K.I. Studies in pyrazolidine chemistry. Chem Heterocycl Compd 25, 71–73 (1989). https://doi.org/10.1007/BF00472623
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DOI: https://doi.org/10.1007/BF00472623