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Ring transformations in the reactions of 1,4-dinitropyrazole with N-nucleophiles

Journal article published in 2007 by R. Jedrysiak ORCID, M. Sawicki, P. Wagner, J. Suwinski
This paper is available in a repository.
This paper is available in a repository.

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Abstract

The reactions of 1,4-dinitropyrazole with primary amines, hydrazines, hydroxylamine and amidines were studied. 1,4-Dinitropyrazole in these reactions served as the synthetic equivalent of nitromalonaldehyde. The reaction of dinitropyrazole with primary arylhydrazines proved to be a convenient approach to the synthesis of 1-aryl-4-nitropyrazoles.