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Vier auf einen Streich: Einige Coralloidolide, Mitglieder eines mediterranen Zweigs der Furanocembranoid‐Familie von Diterpenen, wurden synthetisiert. Die Totalsynthesen umfassen biomimetische Transformationen, die oft hoch chemoselektiv verlaufen und außerdem die Anwendung von Schutzgruppen vermeiden. Die faszinierende Reaktivität von 2,5‐Dien‐1,4‐dionen wurde im Detail untersucht.
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