Nitrodeiodination of 4-iodo-1-methylpyrazoles

E. V. Tret'yakov, S. F. Vasilevsky

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

4-Iodo-1-methylpyrazoles react with a nitrating mixture at 55°C to give the corresponding 4-nitro-1-methylpyrazoles. The qualitative dependence of the nitrodeiodination rate on the structure of the heterocycles and the reaction conditions was considered.

Original languageEnglish
Pages (from-to)2581-2584
Number of pages4
JournalRussian Chemical Bulletin
Volume45
Issue number11
DOIs
Publication statusPublished - 1 Jan 1996
Externally publishedYes

Keywords

  • Iodo-N-alkylpyrazoles
  • Nitro-N-alkylpyrazoles
  • Nitrodehalogenation
  • Oxidative iodination

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Nitrodeiodination of 4-iodo-1-methylpyrazoles. / Tret'yakov, E. V.; Vasilevsky, S. F.

In: Russian Chemical Bulletin, Vol. 45, No. 11, 01.01.1996, p. 2581-2584.

Research output: Contribution to journalArticle

Tret'yakov, E. V. ; Vasilevsky, S. F. / Nitrodeiodination of 4-iodo-1-methylpyrazoles. In: Russian Chemical Bulletin. 1996 ; Vol. 45, No. 11. pp. 2581-2584.
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