Abstract
AbstractAnhand der Cyclisierung der silylsubstituierten Divinylketone (I) zu den cis‐Hexahydroind‐2‐en‐1‐onen (II) und (III) (ca 3:1) werden der Einfluß der Substituenten R1‐R4 auf den Ringbildungsprozeß, die Natur der Zwischenprodukte und die Gründe für die einzigartige Fähigkeit von Fe‐trichlorid, diese Cyclisierung zu induzieren, diskutiert.
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