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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2024, том 34, выпуск 4, страницы 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


Аннотация: 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.

Ключевые слова: thiazolidin-4-ones, acetylenedicarboxylates, Michael addition, cyclocondensation, thioureas, thiosemicarbazides.

Язык публикации: английский

DOI: 10.1016/j.mencom.2024.06.031



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