Synthesis of the bicyclic dienone core of the antitumor agent ottelione B
Chemical Communications Pub Date: 2002-07-31 DOI: 10.1039/B205753K
Abstract
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).
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Journal Name：Chemical Communications
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CAS no.: 89640-58-4
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