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• W2952177750 abstract "Abstract The homoallylic alcohol tethered with a benzylic hydroxyl group, that is, ( E )-4-(2-(hydroxymethyl)phenyl)but-3-en-1-ol undergoes smooth Prins bicyclization with various aldehydes in the presence of 20 mol % Sc(OTf) 3 and 4 A MS at 80 °C to afford a novel series of 1-(tetrahydrofuran-3-yl)-1,3-dihydroisobenzofuran derivatives in good yields with high diastereoselectivity." @default.
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• W2952177750 date "2013-03-01" @default.
• W2952177750 modified "2023-09-24" @default.
• W2952177750 title "Diastereoselective synthesis of 1-(tetrahydrofuran-3-yl)-1,3-dihydroisobenzofuran derivatives via Prins bicyclization" @default.
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• W2952177750 doi "https://doi.org/10.1016/j.tetlet.2013.01.006" @default.
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