Selective O- and N-nitration of steroids fused to the pyrazole ring


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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.

作者简介

A. Shakhnes

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

I. Dalinger

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

A. Shashkov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

E. Chernoburova

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

M. Shchetinina

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

I. Zavarzin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: zavi@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

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