75275-66-0Relevant articles and documents
A novel biomimetic synthesis of (S)-(-)-zearalenone: Via macrocyclization and transannular aromatization
Miyatake-Ondozabal, Hideki,Barrett, Anthony G.M.
experimental part, p. 6331 - 6334 (2010/10/19)
On heating, a hydroxy-keto-dioxinone underwent retro-Diels-Alder fragmentation and the resultant α,γ-diketo-ketene was efficiently trapped intramolecularly by a secondary alcohol to provide a macrocyclic triketo-lactone. Following ketal hydrolysis, transannular aromatization gave the resorcylate natural product, (S)-(-)-zearalenone.