Efficient syntheses
of 3,3-difluorooxindoles and 3-fluorooxindoles
via fluorination of hydrazonoindolin-2-one with Selectfluor are reported.
Under different solvent conditions, this method produced 3,3-difluorooxindoles
and 3-fluorooxindoles selectively. The broad substrate scope and mild
reaction conditions make this transformation a valuable method in
drug discovery and development.