Efficient Synthesis of 21-Acetoxypregna-1,4,9(11),16-Tetraene-3,20-Dione, a Key Intermediate in the Synthesis of Highly Active Fluorinated Corticosteroids from 9α-Hydroxyandrostenedione

V. A. Andryushina; T. S. Stytsenko; N. V. Karpova; V. V. Yaderets; V. V. Dzhavakhiya

doi:10.1007/s11094-018-1898-y

Efficient Synthesis of 21-Acetoxypregna-1,4,9(11),16-Tetraene-3,20-Dione, a Key Intermediate in the Synthesis of Highly Active Fluorinated Corticosteroids from 9α-Hydroxyandrostenedione

作者: Andryushina V.A.¹, Stytsenko T.S.¹, Karpova N.V.¹, Yaderets V.V.¹, Dzhavakhiya V.V.¹
隶属关系:
1. Federal Research Center Fundamentals of Biotechnology, Russian Academy of Sciences
期: 卷 52, 编号 9 (2018)
页面: 776-780
栏目: Drug Synthesis Methods and Manufacturing Technology
URL: https://ogarev-online.ru/0091-150X/article/view/245460
DOI: https://doi.org/10.1007/s11094-018-1898-y
ID: 245460

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An efficient synthesis of 21-acetoxypregna-1,4,9(11),16-tetraene-3,20-dione, a key intermediate in the synthesis of highly active fluorinated corticosteroids from phytosterols, was developed. The method consisted of an original sequence of chemical and microbiological reactions and could be used to synthesize betamethasone, sinaflan, triamcinolone, and other fluorinated corticoids.