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Mendeleev Communications, 2010, Volume 20, Issue 5, Pages 253–254
DOI: https://doi.org/10.1016/j.mencom.2010.09.003 (Mi mendc3055) 		 
This article is cited in 52 scientific papers (total in 52 papers)

The specific reactivity of 3,4,5-trinitro-1H-pyrazole

I. L. Dalinger, I. A. Vatsadze, T. K. Shkineva, G. P. Popova, S. A. Shevelev

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (228 kB) Citations (52) Supplementary materials
DOI: https://doi.org/10.1016/j.mencom.2010.09.003
Abstract: Nitration of 3,5-dinitropyrazole with HNO3–H2SO4 mixture gives 3,4,5-trinitro-1H-pyrazole, which in reaction with ammonia, amines or thiols under mild conditions undergoes regioselective nucleophilic substitution of the 4-positioned nitro group.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (68.3 Kb)


Citation: I. L. Dalinger, I. A. Vatsadze, T. K. Shkineva, G. P. Popova, S. A. Shevelev, “The specific reactivity of 3,4,5-trinitro-1H-pyrazole”, Mendeleev Commun., 20:5 (2010), 253–254
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  • https://www.mathnet.ru/eng/mendc/v20/i5/p253
    • This publication is cited in the following 52 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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