Discovery of Oxygen Induced Chemoselectivity in Pd-Catalyzed C–H Functionalization: Cross-Dehydrogenative Coupling vs C–H Amination
Sheba Ann Babu, Sunil Varughese, Jomon Mathew, Jubi John
Abstract
We have come across a substrate namely, 5-benzoyl-pyrrolo[2,1- a ]isoquinoline in which three different functionalizable C–H bonds were identified that could be judiciously transformed site selectively for the generation of complex polyring fused N -heterocycles. A Pd-catalyzed cross-dehydrogenative coupling of 5-benzoyl-pyrrolo[2,1- a ]isoquinoline afforded 8 H -indeno-pyrrolo[2,1- a ]isoquinolinone and an oxygen induced palladium catalyzed selective C–H amination in the same substrate provided a pentacene viz., 9 H -indolo-pyrrolo[2,1- a ]isoquinoline. We also observed the formation of a multiring fused benzazepine scaffold by the site selective C–H amination in 5-(4-nitro benzoyl)-pyrrolo[2,1- a ]isoquinoline.