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Structure of products of addition of thiosemicarbazides and thiosemicarbazones to acetylenedicarboxylic acid and its dimethyl ester

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Addition of 1, 1-di-, 1, 4-di-, and 1, 1, 4-trisubstituted thiosemicarbazides to acetylenedicarboxylic acid and its dimethyl ester affords 2-hydrazono-4-oxo-1, 3-thiazolidine-δ5,α-acetic acids, while 4-monosubstituted thiosemicarbazides give 2-imino-3-amino-1, 3-thiazolidin-4-ones.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, 226006, Riga

    V. Ya. Kauss, É. É. Liepin'sh, I. Ya. Kalvin'sh & É. Lukevits

Authors
  1. V. Ya. Kauss
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  2. É. É. Liepin'sh
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  3. I. Ya. Kalvin'sh
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  4. É. Lukevits
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 120–125, January, 1990.

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Kauss, V.Y., Liepin'sh, É.É., Kalvin'sh, I.Y. et al. Structure of products of addition of thiosemicarbazides and thiosemicarbazones to acetylenedicarboxylic acid and its dimethyl ester. Chem Heterocycl Compd 26, 103–107 (1990). https://doi.org/10.1007/BF00506859

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  • DOI: https://doi.org/10.1007/BF00506859

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