Synthesis of benzothiazine sulfonamides via heteroatomic Diels–Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes
- 作者: Veremeichik Y.1, Shurpik D.2, Lodochnikova O.3, Plemenkov V.1
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隶属关系:
- Immanuel Kant Baltic Federal University
- Kazan (Volga) Federal University
- Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
- 期: 卷 86, 编号 2 (2016)
- 页面: 296-299
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/213732
- DOI: https://doi.org/10.1134/S1070363216020158
- ID: 213732
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详细
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.
作者简介
Ya. Veremeichik
Immanuel Kant Baltic Federal University
编辑信件的主要联系方式.
Email: olga@iopc.ru
俄罗斯联邦, Kaliningrad
D. Shurpik
Kazan (Volga) Federal University
Email: olga@iopc.ru
俄罗斯联邦, Kazan, Tatarstan
O. Lodochnikova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: olga@iopc.ru
俄罗斯联邦, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
V. Plemenkov
Immanuel Kant Baltic Federal University
Email: olga@iopc.ru
俄罗斯联邦, Kaliningrad