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• W2321189762 abstract "Lucidene and alboatrin are complex benzopyran derived natural products. A key step in their biogenesis may involve a hetero Diels–Alder cycloaddition between an o-quinone methide intermediate with a simple, or activated tri-substituted olefin. Experimental evidence is provided to support this hypothesis, with the biomimetic synthesis of both (±)-lucidene and (±)-alboatrin successfully achieved using a new and efficient method for o-quinone methide generation." @default.
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• W2321189762 date "2005-01-01" @default.
• W2321189762 modified "2023-09-26" @default.
• W2321189762 title "A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of the benzopyran derived natural products (±)-lucidene and (±)-alboatrin" @default.
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• W2321189762 doi "https://doi.org/10.1039/b508972g" @default.
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