Reissert‐Type Acylation with Acylzirconocene Chloride Complexes

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<jats:title>Abstract</jats:title><jats:p>In the presence of ClCO<jats:sub>2</jats:sub>Et, the use of CuI in MeNO<jats:sub>2</jats:sub> efficiently catalyzed the Reissert‐type acylation of isoquinoline derivatives with acylzirconocene chlorides. In the reaction of quinolines with acylzirconocene chlorides, the choice of catalyst and solvent was crucial to the regioselective formation of adducts. The cationic Rh<jats:sup>I</jats:sup>‐catalyzed reaction in MeNO<jats:sub>2</jats:sub> preferentially afforded 1,2 adducts. On the other hand, the Cu<jats:sup>I</jats:sup>‐catalyzed reaction in CH<jats:sub>2</jats:sub>Cl<jats:sub>2</jats:sub> preferentially afforded 1,4 adducts.</jats:p>

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