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.
Образец цитирования:
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