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Russian Chemical Reviews, 1998, Volume 67, Issue 8, Pages 633–648
DOI: https://doi.org/10.1070/RC1998v067n08ABEH000437
(Mi rcr1420)
 

This article is cited in 29 scientific papers (total in 29 papers)

1,2,4-Triazine N-oxides and their annelated derivatives

D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin

Ural State Technical University, Ekaterinburg
Abstract: This review deals with the synthesis and properties of 1,2,4-triazine N-oxides and their annelated derivatives. Methods for the incorporation of the N-oxide group in the 1,2,4-triazine ring by direct oxidation and cyclisation involving nitro, nitroso, and isonitroso groups are discussed. Reactions of 1,2,4-triazine N-oxides with electrophiles, nucleophiles, and dienophiles are considered. The effect of the N-oxide group on the chemical shifts in the 1H, 13C, and 14N NMR spectra and the specific features of decomposition of 1,2,4-triazine N-oxides under electron impact are analysed. The bibliography includes 107 references.
Received: 15.12.1997
Bibliographic databases:
Document Type: Article
UDC: 547.853
Language: English
Original paper language: Russian


Citation: D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin, “1,2,4-Triazine N-oxides and their annelated derivatives”, Usp. Khim., 67:8 (1998), 707–722; Russian Chem. Reviews, 67:8 (1998), 633–648
Linking options:
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  • https://doi.org/10.1070/RC1998v067n08ABEH000437
  • https://www.mathnet.ru/eng/rcr/v67/i8/p707
  • This publication is cited in the following 29 articles:
    1. Jiarong Zhang, Huan Huo, Lianjie Zhai, Fuqiang Bi, Bozhou Wang, FirePhysChem, 2024  crossref
    2. Alexander N. Larin, Elena K. Avakyan, Oleg P. Demidov, Anastasia A. Borovleva, Alexander A. Zubenko, Diana Yu. Pobedinskaya, Artem P. Ermolenko, Stepan E. Kolosov, Ivan V. Borovlev, Eur J Org Chem, 2024  crossref
    3. Anastasia A. Borovleva, Elena K. Avakyan, Gulminat A. Amangasieva, Oleg P. Demidov, Diana Yu. Pobedinskaya, Artem P. Ermolenko, Alexander N. Larin, Ivan V. Borovlev, Chem Heterocycl Comp, 58:4-5 (2022), 235  crossref
    4. A. Rammohan, A. P. Krinochkin, D. S. Kopchuk, Ya. K. Shtaitz, I. S. Kovalev, M. I. Savchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, Russ J Org Chem, 58:2 (2022), 175  crossref
    5. Taniya O.S., Kopchuk D.S., Khasanov A.F., Kovalev I.S., Santra S., Zyryanov V G., Majee A., Charushin V.N., Chupakhin O.N., Coord. Chem. Rev., 442 (2021), 213980  crossref  isi
    6. Savchuk I M., Kopchuk D.S., Egorov I.N., Khasanov A.F., Rybakova S.S., Zyryanov V G., Rusinov V.L., Chupakhin O.N., Russ. J. Gen. Chem., 91:5 (2021), 779–784  crossref  isi
    7. Kopchuk D.S., Nikonov I.L., Khasanov A.F., Giri K., Santra S., Kovalev I.S., Nosova E.V., Gundala S., Venkatapuram P., Zyryanov G.V., Majee A., Chupakhin O.N., Org. Biomol. Chem., 16:28 (2018)  crossref  isi  scopus
    8. Piercey D.G., Chavez D.E., Scott B.L., Imler G.H., Parrish D.A., Angew. Chem.-Int. Edit., 55:49 (2016), 15315–15318  crossref  isi  scopus
    9. Davin G. Piercey, David E. Chavez, Brian L. Scott, Greg H. Imler, Damon A. Parrish, Angewandte Chemie, 128:49 (2016), 15541  crossref
    10. Valery N. Charushin, Oleg N. Chupakhin, Topics in Heterocyclic Chemistry, 37, Metal Free C-H Functionalization of Aromatics, 2014, 1  crossref
    11. Nahir Dib, Luciana Fernández, Mercedes Gonzalez, Hugo Cerecetto, Edgardo Durantini, Luis Otero, Marisa Santo, J Incl Phenom Macrocycl Chem, 79:1-2 (2014), 65  crossref
    12. R. E. Trifonov, V. A. Ostrovskii, V. L. Rusinov, O. N. Chupakhin, Russ J Org Chem, 49:3 (2013), 450  crossref
    13. Cristina Gómez de la Oliva, Pilar Goya Laza, Carmen Ochoa de Ocariz, Modern Heterocyclic Chemistry, 2011, 1777  crossref
    14. Levinson F.S. Varganov R.V. Zakiev M.M. Shakirova I.M. Sheremetev A.B. Dmitriev D.E. Krivolapov D.B. Litvinov I.A. Sharafutdinova D.R. Efremov Yu.Ya., Mendeleev Commun., 18:6 (2008), 329–331  crossref  isi  elib  scopus
    15. V. Charushin, V. Rusinov, O. Chupakhin, Comprehensive Heterocyclic Chemistry III, 2008, 95  crossref
    16. Charushin V.N. Chupakhin O.N., Mendeleev Commun., 17:5 (2007), 249–254  crossref  isi  elib  scopus
    17. Matern A.I. Charushin V.N. Chupakhin O.N., Uspekhi Khimii, 76:1 (2007), 27–45  mathnet  isi
    18. A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov, A. I. Matern, M. M. Nikitin, O. N. Chupakhin, I. L. Eremenko, G. G. Aleksandrov, Russ J Org Chem, 41:11 (2005), 1702  crossref
    19. Makosza M., Wojciechowski K., Chem. Rev., 104:5 (2004), 2631–2666  crossref  isi  scopus
    20. Régis Goumont, Emmanuel Jan, Mieczyslaw Makosza, Francois Terrier, Org. Biomol. Chem., 1:12 (2003), 2192  crossref
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