Nitrosylsulfuric acid as an oxidant in the synthesis of 3,5-diarylisoxazoles
- Авторы: Bondarenko O.B.1, Komarov A.I.1, Kuznetsova L.I.1, Nikolaeva S.N.1, Gavrilova A.Y.1, Zyk N.V.1,2
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Учреждения:
- Department of Chemistry, M. V. Lomonosov Moscow State University
- Institute of Physiologically Active Compounds, Russian Academy of Sciences
- Выпуск: Том 67, № 3 (2018)
- Страницы: 517-520
- Раздел: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/242344
- DOI: https://doi.org/10.1007/s11172-018-2103-x
- ID: 242344
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Аннотация
By six examples, it was demonstrated that nitrosylsulfuric acid can be successfully used for oxidation of 3,5-diaryl-4,5-dihydroisoxazoles to the corresponding 3,5-diarylisoxazoles. If the starting isoxazolines contain the aromatic substituents activated towards electrophilic substitution, nitration of both newly formed isoxazole and substituted benzene rings occurred.
Об авторах
O. Bondarenko
Department of Chemistry, M. V. Lomonosov Moscow State University
Автор, ответственный за переписку.
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992
A. Komarov
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992
L. Kuznetsova
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992
S. Nikolaeva
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992
A. Gavrilova
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992
N. Zyk
Department of Chemistry, M. V. Lomonosov Moscow State University; Institute of Physiologically Active Compounds, Russian Academy of Sciences
Email: k527.5msu@gmail.com
Россия, 1 Leninskie Gory, Moscow, 119992; 1 Severnyi proezd, Chernogolovka, Moscow Region, 142432
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