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- W2951760232 endingPage "2285" @default.
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- W2951760232 abstract "A variety of olefins is shown to be cleaved oxidatively to the corresponding acids with oxone as the reagent. The simple methodology that works well for a range of alkenes, i.e., styrenes, nitrostyrenes, stilbenes, cinnamic acids, chalcones, etc., involves heating of the reactant with oxone in acetonitrile–water mixture (1:1, v/v) at reflux. The oxidation cascade involves initial dihydroxylation followed by oxidative cleavage and oxidation of the resultant aldehydes to acids." @default.
- W2951760232 created "2019-06-27" @default.
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- W2951760232 date "2014-04-01" @default.
- W2951760232 modified "2023-10-16" @default.
- W2951760232 title "Oxidation cascade with oxone: cleavage of olefins to carboxylic acids" @default.
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- W2951760232 doi "https://doi.org/10.1016/j.tet.2014.01.042" @default.
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