The Δ14‐16‐oxo‐androstene derivative VIII has been prepared in a fully stereospecific way from the tricyclic ketone I by di‐methallylation, ozonisation of the methallyl double bonds, condensation of the 2β‐acetonyl residue with the 4 β‐hydroxyl group with formation of the cyclic enol ether V, and cyclisation.
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Wieland et al. (1958) studied this question.
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