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Mendeleev Communications, 2024, Volume 34, Issue 4, Pages 563–565
DOI: https://doi.org/10.1016/j.mencom.2024.06.031
(Mi mendc188)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Synthesis of new functionalized thiazolidin-4-ones by the condensation of thioureas with dialkyl acetylenedicarboxylates

A. A. Streltsov, A. N. Izmest’ev, Yu. A. Strelenko, A. N. Kravchenko, G. A. Gazieva

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Thiazolidin-4-ones functionalized at the position 5 and their heterocycle-annulated analogues were obtained based on the reaction of thioureas with dialkyl acetylenedicarboxylates. In most cases the reaction proceeds with high selectivity to form 2-iminothiazolidin-4-one-type products.
Keywords: thiazolidin-4-ones, acetylenedicarboxylates, Michael addition, cyclocondensation, thioureas, thiosemicarbazides.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (4.0 Mb)


Citation: A. A. Streltsov, A. N. Izmest’ev, Yu. A. Strelenko, A. N. Kravchenko, G. A. Gazieva, “Synthesis of new functionalized thiazolidin-4-ones by the condensation of thioureas with dialkyl acetylenedicarboxylates”, Mendeleev Commun., 34:4 (2024), 563–565
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  • https://www.mathnet.ru/eng/mendc/v34/i4/p563
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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