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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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.
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container_end_page 307
container_issue 3
container_start_page 291
container_title Steroids
container_volume 41
creator Shafiee, A.
Vossoghi, M.
Savabi, F.
Vlahov, R.
Tarpanov, V.
Boshkova-Ljapova, M.
Milenkov, B.
Stoilova, V.
Vlahov, J.
Snatzke, G.
description 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.
doi_str_mv 10.1016/0039-128X(83)90100-9
format Article
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source MEDLINE; Elsevier ScienceDirect Journals
subjects 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
title Long-acting contraceptive agents: Cyclopropyl and cyclobutyl esters of norethisterone
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