Preparation of 3β‐Acetoxy‐17a‐Oxo‐Androst‐5‐Ene‐7,17‐Dione, a Biologically Active Impurity Isolated from the Production of 3β‐Acetoxyandrost‐5‐Ene‐7,17‐Dione-Reference-Cited by-同舟云学术

Preparation of 3β‐Acetoxy‐17a‐Oxo‐Androst‐5‐Ene‐7,17‐Dione, a Biologically Active Impurity Isolated from the Production of 3β‐Acetoxyandrost‐5‐Ene‐7,17‐Dione

Published:2005-04-01 Issue:7 Volume:35 Page:979-985
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Coutts Lisa D.¹,DeOrazio Russell J.¹,Meckler Harold¹

Affiliation:

1. a Albany Molecular Research Inc., Chemical Development and Medicinal Chemistry Departments , Albany, New York, USA

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-200051712

Reference8 articles.

1. Foricher , J. Fürbringer , C. and Pfoertner , K. Process for the catalytic oxidation of isoprenoids having allylic groups. US Patent 5,030,739. July 9, 1991.

2. Novel Catalysis by N-Hydroxyphthalimide in the Oxidation of Organic Substrates by Molecular Oxygen

3. Ergosteroids II: Biologically Active Metabolites and Synthetic Derivatives of Dehydroepiandrosterone 11This work was supported by Humanetics Corp., St. Louis Park, Minnesota.

4. Ergosteroids III. syntheses and biological activity of seco-steroids related to dehydroepiandrosterone

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