Selective O- and N-nitration of steroids fused to the pyrazole ring
- Авторы: Shakhnes A.K.1, Dalinger I.L.1, Shashkov A.S.1, Chernoburova E.I.1, Shchetinina M.A.1, Zavarzin I.V.1
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Учреждения:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Выпуск: Том 67, № 10 (2018)
- Страницы: 1920-1926
- Раздел: Article
- URL: https://journal-vniispk.ru/1066-5285/article/view/243129
- DOI: https://doi.org/10.1007/s11172-018-2308-z
- ID: 243129
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Аннотация
Chemoselective methods for O- and N-nitration of steroids fused to the pyrazole ring were developed. The nitrating agents were acetyl, propionyl, and trifluoroacetyl nitrates generated from carboxylic acid anhydrides and either copper nitrate or nitric acid. Depending on the reaction conditions, the developed methods allow both selective nitration at the pyrazole nitrogen atom leaving intact the hydroxy group of steroid framework and dinitration giving rise to the corresponding nitrates of steroidal nitropyrazoles.
Об авторах
A. Shakhnes
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
I. Dalinger
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
A. Shashkov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
E. Chernoburova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
M. Shchetinina
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
I. Zavarzin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Автор, ответственный за переписку.
Email: zavi@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
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