Synthesis and investigation of isomeric mono- and dinitro derivatives of 3-methyl-4-(pyrazol-3-yl)furazan
DOI:
https://doi.org/10.1007/2450Keywords:
furazan, nitropyrazole, heteronuclear NMR, nitration, X-ray structural analysisAbstract
The regioselective introduction of nitro groups in pyrazoles, containing a furazanyl substituent at position 3(5) was investigated. All synthetically accessible isomeric mono- and dinitropyrazole derivatives were obtained. X-ray structural investigation was performed for all mononitroisomers and a dinitro derivative.
How to Cite
Dalinger, I. L.; Vatsadze, I. A.; Shkineva, T. K.; Komarov, A. V.; Kozeev, A. M.; Avrekiev, B. B.; Dalinger, A. I.; Beklemishev, M. K.; Sheremetev, A. B. Chem. Heterocycl. Compd. 2015, 51, 545. [Khim. Geterotsikl. Soedin. 2015, 51, 545.]
For this article in the English edition see DOI 10.1007/s10593-015-1739-9