Nitrosylsulfuric acid as an oxidant in the synthesis of 3,5-diarylisoxazoles
- Autores: 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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Afiliações:
- Department of Chemistry, M. V. Lomonosov Moscow State University
- Institute of Physiologically Active Compounds, Russian Academy of Sciences
- Edição: Volume 67, Nº 3 (2018)
- Páginas: 517-520
- Seção: Full Articles
- URL: https://journal-vniispk.ru/1066-5285/article/view/242344
- DOI: https://doi.org/10.1007/s11172-018-2103-x
- ID: 242344
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Resumo
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.
Sobre autores
O. Bondarenko
Department of Chemistry, M. V. Lomonosov Moscow State University
Autor responsável pela correspondência
Email: k527.5msu@gmail.com
Rússia, 1 Leninskie Gory, Moscow, 119992
A. Komarov
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Rússia, 1 Leninskie Gory, Moscow, 119992
L. Kuznetsova
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Rússia, 1 Leninskie Gory, Moscow, 119992
S. Nikolaeva
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Rússia, 1 Leninskie Gory, Moscow, 119992
A. Gavrilova
Department of Chemistry, M. V. Lomonosov Moscow State University
Email: k527.5msu@gmail.com
Rússia, 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
Rússia, 1 Leninskie Gory, Moscow, 119992; 1 Severnyi proezd, Chernogolovka, Moscow Region, 142432
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