The reaction of 3-azolyl-6-R-1,2,4,5-tetrazines with guanidine afforded a series of new 3-guanidino-6-R-1,2,4,5-tetrazines. When treated with hydrogen peroxide, these compounds can undergo oxidative transformation of the tetrazine ring to form 2,5-disubstituted 1,3,4-oxadiazoles. The reaction of the new tetrazines with concentrated nitric acid leads to the nitration of functional groups in the tetrazine ring.
Original languageEnglish
Pages (from-to)2965-2973
Number of pages9
JournalRussian Chemical Bulletin
Issue number12
Publication statusPublished - 1 Dec 2023

    Level of Research Output

  • VAK List

    ASJC Scopus subject areas

  • General Chemistry

    WoS ResearchAreas Categories

  • Chemistry, Multidisciplinary

ID: 52298692