Efficient
one-pot synthesis of N-imidoyl-(1H)-indoles has been described, which is achieved by the
palladium-catalyzed oxidative insertion of 2-(phenylethynyl)aniline,
arylboronic acid, and isonitrile. This method provides a new way to
synthesize N-imidoyl-(1H)-indoles,
which has a wide substrate scope, good functional group tolerance,
and mild reaction condition.