Selective O- and N-nitration of steroids fused to the pyrazole ring
- Авторлар: 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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Мекемелер:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Шығарылым: Том 67, № 10 (2018)
- Беттер: 1920-1926
- Бөлім: Article
- URL: https://journal-vniispk.ru/1066-5285/article/view/243129
- DOI: https://doi.org/10.1007/s11172-018-2308-z
- ID: 243129
Дәйексөз келтіру
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.
Авторлар туралы
A. Shakhnes
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
I. Dalinger
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
A. Shashkov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
E. Chernoburova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
M. Shchetinina
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
I. Zavarzin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: zavi@ioc.ac.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
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