Synthesis of benzothiazine sulfonamides via heteroatomic Diels–Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
- Autores: Veremeichik Y.1, Shurpik D.2, Lodochnikova O.3, Plemenkov V.1
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Afiliações:
- Immanuel Kant Baltic Federal University
- Kazan (Volga) Federal University
- Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
- Edição: Volume 86, Nº 2 (2016)
- Páginas: 296-299
- Seção: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/213732
- DOI: https://doi.org/10.1134/S1070363216020158
- ID: 213732
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Resumo
Reaction of 4-fluoro-N-sulfinylaniline with norbornene and norbornadiene has afforded the Diels–Alder adducts of benzothiazine structure that have been oxidized into the corresponding benzothiazine sulfonamides. Structure of the obtained compounds and stereochemistry of the diene addition and epoxidation of norbornene olefin bonds have established by means of X-ray diffraction method.
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Sobre autores
Ya. Veremeichik
Immanuel Kant Baltic Federal University
Autor responsável pela correspondência
Email: olga@iopc.ru
Rússia, Kaliningrad
D. Shurpik
Kazan (Volga) Federal University
Email: olga@iopc.ru
Rússia, Kazan, Tatarstan
O. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: olga@iopc.ru
Rússia, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
V. Plemenkov
Immanuel Kant Baltic Federal University
Email: olga@iopc.ru
Rússia, Kaliningrad