Synthesis of heterocycles from products of the anion arylation of unsaturated compounds. 3. 2-arylimino-5-arylmethyl-4-thiazolidones

Authors

  • Н. Д. Обушак I. Franko Lvov State University, Lvov 290602
  • В. C. Матийчук I. Franko Lvov State University, Lvov 290602
  • Н. И. Ганущак I. Franko Lvov State University, Lvov 290602
  • Ю. Э. Бурлак I. Franko Lvov State University, Lvov 290602

Abstract

The reaction of esters of 3-aryl-2-bromopropionic acids with N-arylthioureas gives 2-arylimino-5-arylmethyl-4-thiazolidones, which exist in solution as (E) and (Z) isomers of the imino form.

How to Cite
Obushak, N. D.; Matiichuk, V. S.; Ganushchak, N. I.; Burlak, Yu. E. Chem. Heterocycl. Compd. 1998, 34, 492. [Khim. Geterotsikl. Soedin. 1998, 34, 555.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290893

Downloads

Published

1998-04-25

Issue

No. 4 (1998)

Section

Original Papers