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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2024 Volume 34, Issue 4, Pages 563–565 (Mi mendc188)

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.

Language: English

DOI: 10.1016/j.mencom.2024.06.031



© Steklov Math. Inst. of RAS, 2025