Synthesis of benzothiazine sulfonamides via heteroatomic Diels–Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
- Авторы: Veremeichik Y.1, Shurpik D.2, Lodochnikova O.3, Plemenkov V.1
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Учреждения:
- Immanuel Kant Baltic Federal University
- Kazan (Volga) Federal University
- Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
- Выпуск: Том 86, № 2 (2016)
- Страницы: 296-299
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/213732
- DOI: https://doi.org/10.1134/S1070363216020158
- ID: 213732
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Аннотация
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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Об авторах
Ya. Veremeichik
Immanuel Kant Baltic Federal University
Автор, ответственный за переписку.
Email: olga@iopc.ru
Россия, Kaliningrad
D. Shurpik
Kazan (Volga) Federal University
Email: olga@iopc.ru
Россия, Kazan, Tatarstan
O. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: olga@iopc.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
V. Plemenkov
Immanuel Kant Baltic Federal University
Email: olga@iopc.ru
Россия, Kaliningrad