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- W2949841608 abstract "A convenient four step procedure is developed for the synthesis of tetrahydropyranones (IV) based on the conversion of unsaturated aldehydes (I) into corresponding nitrile oxides, 1,3-dipolar cycloaddition, SmI2-mediated reductive ring-opening of resulting isoxazolines (III), and Amberlyst-15 promoted 6-endo-trig oxa-Michael cyclization of intermediate β-hydroxyenones." @default.
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- W2949841608 date "2013-04-25" @default.
- W2949841608 modified "2023-09-27" @default.
- W2949841608 title "ChemInform Abstract: A Short and Flexible Route to Tetrahydropyran-4-ones via Conjugated Nitrile Oxides Cycloaddition and Oxa-Michael Cyclization: A Concise Diastereoselective Total Synthesis of (.+-.)-Diospongin A." @default.
- W2949841608 cites W2165212758 @default.
- W2949841608 doi "https://doi.org/10.1002/chin.201320153" @default.
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