Abstract:Die Umsetzung des 3a‐Acetoxy‐16a, 17a‐epoxy‐5β‐pregnan‐l 1,20‐dions (I) mit Fluorwasserstoff in Tetrahydrofuran/Chloroform (5 Stunden bei Zimmertemperatur) ergibt die löß‐Fluor‐(II) und 17a‐Fluor‐Verbindungen (III), die Umlagerungsprodukte Δ12‐(IV), Δ13‐(V) und Δ8(14)‐18‐Nor‐17a‐pregnan‐Derivate (VI) sowie das fluorierte Umlagerungsprodukt (VII).
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