Abstract
AbstractA catalytic annulation cascade is achieved that affords an efficient access to phthalides from readily available benzoic acids and saturated ketones. The reaction is catalyzed by a bimetallic Ir/Cu system and proceeds via the combination of Cu‐catalyzed dehydrogenation of ketones and Ir‐catalyzed direct C−H functionalization under the assistance of the weakly coordinating carboxyl followed by the β−H elimination and intramolecular Michael addition. This method shows a broad scope of substrates and good functional group tolerance. The protocol furnishes an alternative strategy for the construction of diverse 3‐substituted phthalides.
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