Abstract
Podocarpa-8,11,13-trien-12-ol
(2) has been converted by ozonolysis and subsequent transformations into the
lactone (13), a tobacco flavouring agent, and into the bicyclic acetate (11) ,
a compound with a woody odour.
Cited by
16 articles.
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1. Oxidative degradation of benzene rings;Tetrahedron;2003-02
2. A Convenient Synthesis of Chiral, Non-Racemic [4aS,8aR]-5,5,8a-Trimethyl Octahydro-2,2-(1,3-Dioxolane)-Naphthalene;Synthetic Communications;2000-04
3. Oxidations of 12-Deoxy-, 12-Hydroxy-, 12-Methoxy-, and 12-Hydroxy-13-methoxy-podocarpa-8,11,13-triene Derivatives;Australian Journal of Chemistry;1998
4. Utilization of Podocarpic Acid for Nagilactone Synthesis;Australian Journal of Chemistry;1997
5. Synthesis of a Novel Diterpenoid Rearrangement Product;Australian Journal of Chemistry;1995