FeCl3-Catalyzed Combinatorial Synthesis of Functionalized Spiro[Indolo-3,10′-indeno [1,2-b]quinolin]-trione Derivatives

An efficient, inexpensive, environmentally friendly and high yield one-pot roil-le to new spiro[indolo-3,10'-indeno [1,2-b] quinolin]-trione derivatives has been developed, involving three-component reaction of enaminones, N-substituted isatins and Indane-1,3-dione catalyzed by FeCl3. The approach to this spiro-heterocycle is noteworthy because it results in the formation of three new sigma (two C-C and one C-N) bonds in a single operation, leading to the construction of novel Spiro skeleton. This method works on a large scale in excellent yields.