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Russian Chemical Bulletin

, Volume 54, Issue 7, pp 1667–1671 | Cite as

Acylimines of hexafluoroacetone and methyl trifluoropyruvate in cyclocondensation with 2-aminothiazolines

  • V. B. Sokolov
  • A. Yu. Aksinenko
  • T. A. Epishina
  • T. V. Goreva
  • A. N. Pushin
  • I. V. Martynov
Article

Abstract

Reactions of acylimines of hexafluoroacetone and methyl trifluoropyruvate with 2-aminothiazolines afforded fluorine-containing heterocycles of two structural types: 6,7-dihydro-2H-thiazolo[3,2-a][1,3,5]triazines and 2,3,5,6-tetrahydroimidazo[2,1-b]thiazoles.

Key words

acylimines hexafluoroacetone methyl trifluoropyruvate 2-aminothiazolines 6,7-dihydro-2H-[1,3]thiazolo[3,2-a][1,3,5]triazines 2,3,5,6-tetrahydroimidazo[2,1-b]thiazoles cyclocondensation 

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Copyright information

© Springer Science+Business Media, Inc. 2005

Authors and Affiliations

  • V. B. Sokolov
    • 1
  • A. Yu. Aksinenko
    • 1
  • T. A. Epishina
    • 1
  • T. V. Goreva
    • 1
  • A. N. Pushin
    • 1
  • I. V. Martynov
    • 1
  1. 1.Institute of Physiologically Active SubstancesRussian Academy of SciencesChernogolovka, Moscow RegionRussian Federation

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