Abstract
A palladium-catalyzed intermolecular arylcarbonylation of unactivated alkenes has been developed. Unsymmetrical diaryliodonium salts (DAISs) were used as arylation reagents, the bulky aryl group (ArL ) of which was exclusively incorporated into the arylcarbonylated products, which contained the ArL group and a carboxylic ester group at the α- and β-carbon position, respectively, of the original terminal C-C double bond. The reaction features excellent chemo- and regioselectivity, high functional-group tolerance, and very mild reaction conditions.
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