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- W2034676106 abstract "2-Pyridineseleninic anhydride, prepared in situ by oxidation of the corresponding diselenide with iodoxybenzene, is an efficient reagent for the conversion of olefins to unsaturated ketones with retention of the original position of the double bond. This reagent is, therefore, much more reactive towards olefins than benzeneseleninic anhydride. An explanation has been offered." @default.
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- W2034676106 title "Oxidation of olefins with 2-pyridineseleninic anhydride" @default.
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- W2034676106 doi "https://doi.org/10.1016/s0040-4020(01)97207-2" @default.
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