Abstract
A [Cp*IrCl2]2-catalyzed amidocarbonation of olefins with sulfoxonium ylides has been developed to generate diverse biologically important isoindolin-1-ones in high efficiency under mild reaction conditions. Mechanism studies indicated that this cascade reaction was triggered by amino-iridation of the olefin unit to generate iridacycle, followed by formal migratory insertion with sulfoxonium ylides. This newly developed method features broad substrate scopes and operational simplicity.
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