Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding Δ4-3-ketosteroids-Reference-Cited by-同舟云学术

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Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding Δ4-3-ketosteroids

Published:2006-02 Issue:2 Volume:71 Page:116-119
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Gioia Maria L. Di,Leggio Antonella,Pera Adolfo Le,Perri Francesca,Pitrelli Andrea F.,Liguori Angelo

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference5 articles.

1. Ring expansion by tandem double Tebbe–Claisen technology;Paquette;Can J Chem,1992

2. Oxidation of testosterone acetate with per acids;Gorodetsky;J Org Chem,1967

3. Peroxide oxidation of Δ4-3-ketosteroids;Holland;Can J Chem,1982

4. Baeyer–Villiger oxidation of 19-substituted steroidal ketones: structure of rearranged products involving participation of the 19-substituent;Hrycko;J Chem Soc Perkin Trans,1989

5. Epoxidation and Baeyer–Villiger oxidation of γ-hydroxy-α,β-unsaturated ketones on exposure to m-chloroperbenzoic acid;Mendelovici;J Chem Soc, Perkin Trans,1992

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1. Polyhydroxylated sesquiterpenes and ergostane glycosides produced by the endophytic fungus Xylaria sp. from Azadirachta indica;Phytochemistry;2022-07

2. Steroids: partial synthesis in medicinal chemistry;Natural Product Reports;2007

3. D-homoannulation of 17α,21-dihydroxy-20-keto steroids (corticosteroids);Steroids;2006-12

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