Email this article Halocyclization of products of allyl isothiocyanate addition to acyclic methylene active compounds
- Authors: Litvinchuk M.B.1, Bentya A.V.2, Slyvka N.Y.1, Vovk M.V.2
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Affiliations:
- Lesya Ukrainka Eastern-European National University
- Institute of Organic Chemistry
- Issue: Vol 53, No 5 (2017)
- Pages: 709-716
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/216196
- DOI: https://doi.org/10.1134/S1070428017050104
- ID: 216196
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Abstract
Products of allyl isothiocyanate addition to methylene active compounds, salt-like N-allyl-N,S-ketenacetals or N-allylthioamides, react with iodine, bromine or N-bromosuccinimide with the formation of derivatives of 2-ylidene-5-halomethylthiazolidines. A dependence was found of isomeric composition of obtained thiazolidines on the solvent nature.
About the authors
M. B. Litvinchuk
Lesya Ukrainka Eastern-European National University
Author for correspondence.
Email: mariia.litvinchuk@gmail.com
Ukraine, pr. Voli 13, Lutsk, 43025
A. V. Bentya
Institute of Organic Chemistry
Email: mariia.litvinchuk@gmail.com
Ukraine, Kiev
N. Yu. Slyvka
Lesya Ukrainka Eastern-European National University
Email: mariia.litvinchuk@gmail.com
Ukraine, pr. Voli 13, Lutsk, 43025
M. V. Vovk
Institute of Organic Chemistry
Email: mariia.litvinchuk@gmail.com
Ukraine, Kiev
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