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

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Russian Chemical Bulletin Aims and scope

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.

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Authors and Affiliations

  1. Institute of Physiologically Active Substances, Russian Academy of Sciences, 142432, Chernogolovka, Moscow Region, Russian Federation

    V. B. Sokolov, A. Yu. Aksinenko, T. A. Epishina, T. V. Goreva, A. N. Pushin & I. V. Martynov

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  1. V. B. Sokolov
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  2. A. Yu. Aksinenko
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  3. T. A. Epishina
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  4. T. V. Goreva
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  5. A. N. Pushin
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  6. I. V. Martynov
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1619–1622, July, 2005.

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Sokolov, V.B., Aksinenko, A.Y., Epishina, T.A. et al. Acylimines of hexafluoroacetone and methyl trifluoropyruvate in cyclocondensation with 2-aminothiazolines. Russ Chem Bull 54, 1667–1671 (2005). https://doi.org/10.1007/s11172-006-0019-3

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  • DOI: https://doi.org/10.1007/s11172-006-0019-3

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