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- W1965921036 endingPage "2028" @default.
- W1965921036 startingPage "2020" @default.
- W1965921036 abstract "A highly efficient dearomatization reaction of α-substituted β-naphthols with excellent chemoselectivity and regioselectivity has been developed. Mechanistic studies demonstrated that the dearomatized alkylation product is the thermodynamically more stable compound. The etherification product could be further transformed to the dearomatization product." @default.
- W1965921036 created "2016-06-24" @default.
- W1965921036 creator A5015636416 @default.
- W1965921036 creator A5019588728 @default.
- W1965921036 date "2014-05-07" @default.
- W1965921036 modified "2023-10-17" @default.
- W1965921036 title "Palladium-Catalyzed Intermolecular Allylic Dearomatization Reaction of α-Substituted β-Naphthol Derivatives: Scope and Mechanistic Investigation" @default.
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- W1965921036 doi "https://doi.org/10.1002/adsc.201400154" @default.
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