Vicinal diols are abundant among natural and synthetic molecules, and also represent valuable intermediates throughout organic synthesis. Olefin dihydroxylation is an effective strategy to access these derivatives owing to the broad range and availability of alkene feedstocks. OsO4 is among the most used reagents to achieve this transformation, yet its high toxicity and cost remain concerning. Herein, we present a mechanistically distinct strategy for olefin dihydroxylation using nitroarenes as photoresponsive oxidants. Upon purple LEDs irradiation, these species undergo a [3+2]-photocycloaddition with a wide range of olefins to give stable 1,3,2-dioxazolidine intermediates. These species can be accumulated in solution and then reduced in situ to the desired diols, utilising readily accessible and easy to handle solid reagents as H2 surrogates.
Keywords: Dihydroxylation; Nitroarenes; Olefin Functionalization; Oxidation; Photochemistry.
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