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Abstract | Cited by

Flavones were directly alkylated at the C-3 position in moderate yields using a xanthate-based oxidative radical addition procedure. This methodology is a suitable synthetic tool for the direct substitution of the vinylic and unactivated C–H bond of the C ring of the flavone by an alkyl functionality under neutral conditions.

Graphical abstract: Microwave-assisted C-3 selective oxidative radical alkylation of flavones

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