Long-acting contraceptive agents: Cyclopropyl and cyclobutyl esters of norethisterone

Several esters of norethisterone (17α-ethynyl-17β-hydroxyestr-4-en-3-one) with carboxylic acids containing a cyclopropyl or cyclobutyl ring have been synthesized and the stereochemistries of the side-chains determined.

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Bibliographische Detailangaben
Veröffentlicht in:	Steroids 1983-03, Vol.41 (3), p.291-307
Hauptverfasser:	Shafiee, A., Vossoghi, M., Savabi, F., Vlahov, R., Tarpanov, V., Boshkova-Ljapova, M., Milenkov, B., Stoilova, V., Vlahov, J., Snatzke, G.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alicyclic compounds, terpenoids, prostaglandins, steroids Chemistry Delayed-Action Preparations Esters Exact sciences and technology Indicators and Reagents Magnetic Resonance Spectroscopy Norethindrone - analogs & derivatives Norethindrone - chemical synthesis Organic chemistry Preparations and properties Spectrophotometry Steroids Structure-Activity Relationship
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Beschreibung
Zusammenfassung:	Several esters of norethisterone (17α-ethynyl-17β-hydroxyestr-4-en-3-one) with carboxylic acids containing a cyclopropyl or cyclobutyl ring have been synthesized and the stereochemistries of the side-chains determined.
ISSN:	0039-128X 1878-5867
DOI:	10.1016/0039-128X(83)90100-9