Issue 13, 1982

Zizaene and cedrene sesquiterpenes. Novel synthesis of tricyclic intermediates for their preparation

Abstract

The tricyclic enone (8), conveniently prepared from the diene (5)via the adduct (7), afforded the endo-and exo-alcohols (9) whose toluene-p-sulphonates (10) were readily converted into the tricyclic ketones (11) and (12), thus paving the way for a new total synthesis of racemic zizaene (1) and of racemic cedrene (2) respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 762-763

Zizaene and cedrene sesquiterpenes. Novel synthesis of tricyclic intermediates for their preparation

K. Pramod and G. S. R. S. Rao, J. Chem. Soc., Chem. Commun., 1982, 762 DOI: 10.1039/C39820000762

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