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Russian Journal of General Chemistry

, Volume 88, Issue 10, pp 2227–2229 | Cite as

New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium

  • S. N. Adamovich
  • Е. N. Oborina
  • I. А. Ushakov
  • А. N. Mirskova
Letters to the Editor
  • 13 Downloads

Abstract

Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolamine hydrochloride by one-pot method in quantitative yield (up to 99.8%).

Keywords

het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium triethanolamine hydrochloride crezacine 

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References

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Copyright information

© Pleiades Publishing, Ltd. 2018

Authors and Affiliations

  • S. N. Adamovich
    • 1
  • Е. N. Oborina
    • 1
  • I. А. Ushakov
    • 2
  • А. N. Mirskova
    • 1
  1. 1.A.E. Favorskii Irkutsk Institute of Chemistry, Siberian BranchRussian Academy of SciencesIrkutskRussia
  2. 2.Irkutsk National Research Technical UniversityIrkutskRussia

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