Nickel‐Catalyzed Sequential Synthesis of Alkylated Quinolines and Their Photophysical Studies

Abstract

An efficient nickel‐catalyzed sequential one‐pot strategy for the synthesis of coumarin‐appended quinolines and bis‐quinolines has been developed under mild reaction conditions in moderate to good yields (up to 84%) via dehydrogenative Friedlander annulation followed by C(sp3)‐H functionalization. The utilization of cheap and readily available starting materials, environmentally friendly solvents, and simple operating procedures are the attractive attributes of this method. Additionally, the photophysical properties of the synthesized derivatives were explored utilizing UV‐vis absorption and fluorescence emission studies. Furthermore, the large‐scale synthesis and the synthetic utility of the derivatives highlight the potential applicability of this strategy in synthetic organic chemistry. Moreover, A plausible reaction mechanism is supported by the control experiments and reaction monitoring by 1H NMR analysis.