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

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

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2024, Volume: 34, Number: 4, Pages: 563-565 Pages count : 3 DOI: 10.1016/j.mencom.2024.06.031

Authors

Streltsov Andrey A. ¹ , Izmest’ev Alexei N. ¹ , Strelenko Yurii A. ¹ , Kravchenko Angelina N. ¹ , Gazieva Galina A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

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.

Streltsov A.A. , Izmest’ev A.N. , Strelenko Y.A. , Kravchenko A.N. , Gazieva G.A.
Synthesis of new functionalized thiazolidin-4-ones by the condensation of thioureas with dialkyl acetylenedicarboxylates
Mendeleev Communications. 2024. V.34. N4. P.563-565. DOI: 10.1016/j.mencom.2024.06.031 WOS Scopus OpenAlex

≡ Web of science:	WOS:001294246400001
≡ Scopus:	2-s2.0-85200798389
≡ OpenAlex:	W4401451337