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Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides

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Abstract

Monothiooxamides were synthesized by the reaction of chloroacetamides with elemental sulfur and cyclic amines in the presence of triethylamine. The compounds were tested for fungicidal and aphicidal activity.

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Authors and Affiliations

  1. Institute of Organic Synthesis and Coal Fuel Chemistry of Republic of Kazakhstan, Limited Liability Company, Karaganda, Kazakhstan

    O. V. Bakbardina, N. Zh. Rakhimzhanova, M. A. Gazalieva, S. D. Fazylov & E. Zh. Baimagambetov

  2. Research Institute of Plant Protection, Almaty, Kazakhstan

    O. V. Bakbardina, N. Zh. Rakhimzhanova, M. A. Gazalieva, S. D. Fazylov & E. Zh. Baimagambetov

Authors
  1. O. V. Bakbardina
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  2. N. Zh. Rakhimzhanova
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  3. M. A. Gazalieva
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  4. S. D. Fazylov
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  5. E. Zh. Baimagambetov
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Additional information

Original Russian Text © O.V. Bakbardina, N.Zh. Rakhimzhanova, M.A. Gazalieva, S.D. Fazylov, E.Zh. Baimagambetov, 2006, published in Zhurnal Prikladnoi Khimii, 2006, Vol. 79, No. 3, pp. 513–514.

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Bakbardina, O.V., Rakhimzhanova, N.Z., Gazalieva, M.A. et al. Synthesis and biological activity of anabasine and cytisine derivatives of monothiooxamides. Russ J Appl Chem 79, 504–505 (2006). https://doi.org/10.1134/S1070427206030384

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  • DOI: https://doi.org/10.1134/S1070427206030384

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