REACTIONS OF 1,3,5-TRIAZINYLNITROFORMALDOXIMES. 2. THE REACTION OF 1,3,5-TRIAZINYLNITROFORMALDOXIMES WITH MONOSUBSTITUTED ACETYLENES

Authors

  • В. В. Бахарев Samara State Technical University, Samara 443100
  • А. А. Гидаспов Samara State Technical University, Samara 443100
  • Е. В. Переседова Samara State Technical University, Samara 443100
  • Д. Б. Криволапов A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center of the Russian Academy of Sciences, Kazan 420088, Tatarstan Republic
  • Е. В. Миронова A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center of the Russian Academy of Sciences, Kazan 420088, Tatarstan Republic
  • И. А. Литвинов A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center of the Russian Academy of Sciences, Kazan 420088, Tatarstan Republic

DOI:

https://doi.org/10.1007/6584

Keywords:

3, 5-disubstituted isoxazoles, acetylene derivatives, 1, 5-triazinylnitrile oxides, 5-triazinylnitroformaldoximes

Abstract

1,3,5-Triazinylnitrile oxides were prepared in situ  from 2-R-4-R'-1,3,5-triazin-6-ylnitroformaldoximes and were treated with substituted acetylenes to give 3,5-disubstituted isoxazoles. The X-ray data obtained for 5-hydroxymethyl-3-(4'-dimethylamino-2'-methoxy-1,3,5-triazin-6'-yl)isoxazole is discussed.

How to Cite
Bakharev, V. V.; Gidaspov, A. A.; Peresedova, E. V.; Krivolapov, D. B.; Mironova, E. V.; Litvinov, I. A.  Chem. Heterocycl. Compd. 2009, 45, 1075. [Khim. Geterotsikl. Soedin. 2009, 1345.]

For this article in the English edition see DOI 10.1007/s10593-009-0382-8

 

Published

2022-02-14

Issue

Section

Original Papers