Abstract:
A metal-free, TBHP-promoted economical route is developed via the sp2 C–H bond functionalization
strategy for the synthesis of indenoquinolinones, 4-azafluorenones and fluorenones. Reactions provided
excellent yield of the products under mild conditions. We have successfully synthesized 11H-indeno
[1,2-b]quinolin-11-one, an antibacterial agent, in excellent yields.