This work demonstrates defluorinative allylation in aromatic ketones using C-H activation, suggesting broad utility.
The first Cp*Co(III)-catalyzed ortho-C-H perfluoroallylation of aromatic ketones via weakly coordinating ketone-directed C-H activation was developed. This method features good functional group tolerance, high efficiency, and broad substrate scope. A variety of aromatic ketones such as propiophenones, diaryl ketones, and bioactive chalcones were compatible with this catalytic system. Furthermore, mechanistic studies reveal that the C-H activation step may not be involved in the turnover-limiting step.
No takes yet. Share an insight, caveat, or question.
Yu et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: