Straightforward access to novel indolo[2,3-<i>b</i>]indoles <i>via</i> aerobic copper-catalyzed [3+2] annulation of diarylamines and indoles
Taoyuan Liang, Lingzhen Gong, He Zhao, Huanfeng Jiang, Min Zhang
Abstract
Herein, we report an unprecedented aerobic copper-catalyzed [3+2] annulation reaction of diarylamines with indoles, which allows direct access to novel 2-diarylaminoindolo[2,3-b]indoles, a class of potential photoelectric device molecules. The developed transformation proceeds with broad substrate scope, good functional group tolerance, high chemo-selectivity, and no need for pre-preparation of specific agents, which offers a practical route for diverse and atom-economic synthesis of the desired products that are difficult to prepare with the conventional approaches.
Topics & Concepts
AnnulationChemistryCatalysisCopperCombinatorial chemistryOrganic chemistryMedicinal chemistryCatalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and Catalysis