Acylated benzothiazinesulfoneamides: Synthesis and molecular structure
- Authors: Tevs O.A.1, Veremeichik Y.V.1, Shurpik D.N.2, Lodochnikova O.A.3, Plemenkov V.V.1
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Affiliations:
- Kant Baltic Federal University
- Kazan (Volga Region) Federal University
- Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Centre
- Issue: Vol 86, No 8 (2016)
- Pages: 1850-1853
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/215930
- DOI: https://doi.org/10.1134/S1070363216080120
- ID: 215930
Cite item
Abstract
1,2,3,4,4a,10b-Hexahydro-1,4-methano-6H-dibenzo[c,e]-5,6-thiazine-5,5-dioxide has been converted into the corresponding N-acyl derivatives via the reaction with acid chlorides and anhydrides. X-Ray diffraction data have revealed the presence of an intramolecular С–H···O=S hydrogen bond in the molecules of the obtained compounds.
About the authors
O. A. Tevs
Kant Baltic Federal University
Email: plem-kant@yandex.ru
Russian Federation, ul. Universitetskaya 2, Kaliningrad, 236040
Ya. V. Veremeichik
Kant Baltic Federal University
Email: plem-kant@yandex.ru
Russian Federation, ul. Universitetskaya 2, Kaliningrad, 236040
D. N. Shurpik
Kazan (Volga Region) Federal University
Email: plem-kant@yandex.ru
Russian Federation, Kazan, Tatarstan
O. A. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Centre
Email: plem-kant@yandex.ru
Russian Federation, Kazan, Tatarstan
V. V. Plemenkov
Kant Baltic Federal University
Author for correspondence.
Email: plem-kant@yandex.ru
Russian Federation, ul. Universitetskaya 2, Kaliningrad, 236040