Abstract
The reactivity of iodine(III) reagents towards nucleophiles is often associated with umpolung and cationic mechanisms. Herein, we report a general process converting a range of ketone derivatives into α-cyclopropanated ketones by oxidative umpolung. Mechanistic investigation and careful characterization of side products revealed that the reaction follows an unexpected pathway and suggests the intermediacy of non-classical carbocations.
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Bauer, A., Di Mauro, G., Li, J., & Maulide, N. (2020). An α-Cyclopropanation of Carbonyl Derivatives by Oxidative Umpolung. Angewandte Chemie - International Edition, 59(41), 18208–18212. https://doi.org/10.1002/anie.202007439
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