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Nitropyrazoles 21. Selective nucleophilic substitution of the nitro group in 1-amino-3,4-dinitropyrazole Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2012, Volume: 61, Number: 2, Pages: 467-468 Pages count : 2 DOI: 10.1007/s11172-012-0066-x
Authors Shkineva T.K. 1 , Dalinger I.L. 1 , Vatsadze I.A. 1 , Kormanov A.V. 1 , Shevelev S.A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Abstract: Nucleophilic substitution of the nitro group in a model representative of N-aminopyrazoles, 1-amino-3,4-dinitropyrazole, has been studied for the first time. The compound was shown to undergo nucleophilic substitution with S-nucleophiles. The reaction was effected with regioselective substitution of the nitro group at position 3 and in good yields.
Cite: Shkineva T.K. , Dalinger I.L. , Vatsadze I.A. , Kormanov A.V. , Shevelev S.A.
Nitropyrazoles 21. Selective nucleophilic substitution of the nitro group in 1-amino-3,4-dinitropyrazole
Russian Chemical Bulletin. 2012. V.61. N2. P.467-468. DOI: 10.1007/s11172-012-0066-x WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000312068000035
≡ Scopus: 2-s2.0-84877081284
≡ OpenAlex: W1969571078
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