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- W2023526069 abstract "Topologically mobile difluorinated cyclooctenones undergo rapid, high-yielding, and completely stereoselective epoxidations with methyl(trifluoromethyl)dioxirane. The epoxides resist conventional hydrolysis but react smoothly in basic media under microwave irradiation to afford unique hemiacetals and hemiaminals in good yield. [reaction: see text]" @default.
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- W2023526069 date "2004-03-25" @default.
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- W2023526069 title "Unexpectedly Selective Formation and Reactions of Epoxycyclooctenones under Microwave-Mediated Conditions" @default.
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- W2023526069 doi "https://doi.org/10.1021/ol0496327" @default.
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