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Mendeleev Communications, 2003, Volume 13, Issue 5, Pages 226–228
DOI: https://doi.org/10.1070/MC2003v013n05ABEH001754 (Mi mendc4034) 		 
This article is cited in 3 scientific papers (total in 3 papers)

Noncyclic intermediate in the synthesis of pyrazolidinylpyrazoles

I. V. Dlinnykh, G. A. Golubeva, P. B. Terentiev, L. A. Sviridova

Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
Full-text PDF (83 kB) Citations (3)
DOI: https://doi.org/10.1070/MC2003v013n05ABEH001754
Abstract: Hydroxypyrazolidine 1 reacts with 5-aminopyrazoles 2 to form selectively the products of substitution to 4 or 5-aminogroup positions; the isolated intermediate of interaction of noncyclic tautomer 1 with two molecules of aminopyrazole carried out the cyclization into 4-pyrazolidinyl-5-aminopyrazole eliminating one molecule of aminopyrazole
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Document Type: Article
Language: English


Citation: I. V. Dlinnykh, G. A. Golubeva, P. B. Terentiev, L. A. Sviridova, “Noncyclic intermediate in the synthesis of pyrazolidinylpyrazoles”, Mendeleev Commun., 13:5 (2003), 226–228
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  • https://www.mathnet.ru/eng/mendc/v13/i5/p226
    • This publication is cited in the following 3 articles:
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