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

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Chemistry of Heterocyclic Compounds Aims and scope

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.

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Additional information

For Communication 2, see [1].

I. Franko Lvov State University, Lvov 290602, Ukraine. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 555–559, April, 1998.

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Obushak, N.D., Matiichuk, V.S., Ganushchak, N.I. et al. Synthesis of heterocycles from products of the anion arylation of unsaturated compounds. 3. 2-arylimino-5-arylmethyl-4-thiazolidones. Chem Heterocycl Compd 34, 492–496 (1998). https://doi.org/10.1007/BF02290893

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  • DOI: https://doi.org/10.1007/BF02290893

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