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Russian Chemical Bulletin

, Volume 60, Issue 5, pp 1016–1018 | Cite as

Reactions of malonodithioamides with acetylenedicarboxylic esters

  • K. L. Obydennov
  • M. F. Kosterina
  • E. L. Klimareva
  • V. A. Bakulev
  • Yu. Yu. Morzherin
Brief Communications

Abstract

Reactions of malonothioamides with acetylenedicarboxylates proceed as an addition of the sulfur atom at the triple bond with subsequent intramolecular reaction between the ester group and the nitrogen atom, that leads to substituted thiazolidines. Unsubstituted malonodithioamide and N-cyclohexylmalonodithioamide give adducts involving both thioamide fragments, whereas N,N′-bis(4-methoxyphenyl)malonodithioamide forms the 1: 1 adducts.

Key words

thiazolidinones malonodithioamides acetylenedicarboxylates heterocyclization 

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Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • K. L. Obydennov
    • 1
  • M. F. Kosterina
    • 1
  • E. L. Klimareva
    • 1
  • V. A. Bakulev
    • 1
  • Yu. Yu. Morzherin
    • 1
  1. 1.Ural Federal University named after the First President of Russia B. N. El’tsynEkaterinburgRussian Federation

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