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- W2059068785 abstract "The lithium salts, derived from position 3 of phthalides by treatment with hindered bases, participate in Michael addition reactions with a variety of conjugated olefins. For singly-activated olefins the conjugate anion reacts intramolecularly with the lactone group to produce 4-hydroxytetralones in moderate to good yield. Dehydration of these hydroxytetralones, by brief treatment with acid, produces the corresponding α-naphthol. Substituted phthalides react similarly making the method a general one for the production of substituted α-naphthols." @default.
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- W2059068785 date "1981-01-01" @default.
- W2059068785 modified "2023-10-02" @default.
- W2059068785 title "A new route to 4-hydroxytetralones and 1-naphthols" @default.
- W2059068785 doi "https://doi.org/10.1039/p19810000465" @default.
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