Declas, NinaWaser, Jerome2020-08-272020-08-272020-08-272020-06-1610.1002/anie.202006707https://infoscience.epfl.ch/handle/20.500.14299/171144WOS:000558873900001We report an Umpolung strategy of enol ethers to generate oxy-allyl cation equivalents based on the use of hypervalent iodine reagents. Under mild basic conditions, the addition of nucleophiles to aryloxy-substituted vinylbenziodoxolone (VBX) reagents, easily available in two steps from silyl alkynes, resulted in the stereoselective formation of substituted aryl enol ethers. The reaction was most efficient with phenols as nucleophiles, but preliminary results were also achieved for C- and N- nucleophiles. In absence of external nucleophiles, the 2-iodobenzoate group of the reagent was transferred. The obtained aryl enol ethers could then be transformed into alpha-difunctionalized ketones by oxidation. The described "allyl cation"-like reactivity contrast with the well-established "vinyl-cation" behavior of alkenyl iodonium salts.Chemistry, MultidisciplinaryChemistryallyl cationsenol ethershypervalent iodine reagentsumpolungvinylbenziodoxolonescycloadditionarylationconstructionreactivityepoxyethermechanismenamidesaryltext::journal::journal article::research article