An oxy-palladation, formal Wagner–Meerwein rearrangement and fluorination cascade has been established for generating fluorinated oxazolidine-2,4-diones and oxazolidin-2-ones. The reaction has a broad substrate scope in which both aryl and alkyl groups can be utilized as efficient migrating groups. Experimental evidence suggests that the reaction is initiated by anti -oxy-palladation of the olefin, followed by oxidative generation of an alkyl Pd IV intermediate and a concerted migration–fluorination.
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Wu et al. (2016) studied this question.
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