8-epipuupehedione has been researched along with drimenol* in 1 studies
1 other study(ies) available for 8-epipuupehedione and drimenol
Article | Year |
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An efficient stereoselective synthesis of cytotoxic 8-epipuupehedione.
An efficient and highly stereoselective synthesis of cytotoxic 8-epipuupehedione (1b) was achieved starting from natural (-)-drimenol (6). The key step to obtain stereoselectivity was the simultaneous demethylation and oxidation of the dihydrobenzopyran methoxy derivatives 10a and 10b. Topics: Animals; Antineoplastic Agents; Cyclization; Drug Screening Assays, Antitumor; Molecular Structure; Oxidation-Reduction; Polycyclic Sesquiterpenes; Porifera; Stereoisomerism; Terpenes; Tumor Cells, Cultured | 2003 |