Synthesis of the bicyclic dienone core of the antitumor agent ottelione B.
The intramolecular Diels-Alder adduct 12 was converted via dimesylate 20 into dienone 7, which represents the unusual, and apparently quite stable, core of the antitumor agent ottelione B (1).
| Main Authors: | , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2002
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