A strategy for the palladium-catalyzed intermolecular synthesis of polysubstituted cyclopentenones is reported. The three-component reaction utilizes vinyl iodides and internal alkynes to form the carbon framework of the cyclopentenone with Cr(CO) serving as an easy to handle, solid CO surrogate, and a hydrosilane as a hydride source. We demonstrate the scope of the reaction which includes a wide range of functional groups.
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