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- W2952113485 abstract "The synthesis of the core ring system of the sclerophytin diterpenes is described. The key tetrahydrofuran-containing intermediate is assembled via a Lewis acid-promoted [4+3] annulation reaction between a mixed dimethyl acetal and a bis-TES dienol ether. The resulting β-keto ester was homologated, cyclized, and ring expanded to afford the sclerophytin ring system." @default.
- W2952113485 created "2019-06-27" @default.
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- W2952113485 date "2010-05-22" @default.
- W2952113485 modified "2023-09-24" @default.
- W2952113485 title "ChemInform Abstract: Synthesis of the Core Ring System of the Sclerophytin Diterpenes Utilizing a Lewis Acid Promoted [4 + 3] Annulation Strategy." @default.
- W2952113485 cites W2083040599 @default.
- W2952113485 doi "https://doi.org/10.1002/chin.200215193" @default.
- W2952113485 hasPublicationYear "2010" @default.
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