Dehydrogenative Photocyclization of 3-Styryl Indoles to Fused Indole Systems

Abstract

The synthesis of 5-aryl-or 5,6-diaryl-11H-benzo-[a]carbazoles has been achieved from 3-styryl indoles through catalyst-free photoinitiated dehydrogenative cyclization transformation, providing a range of structurally diverse products in excellent yields under mild conditions. The protocol is also applicable to furan and thiophene samples. This Mallory-type reaction takes place in an argon atmosphere without external oxidants. Finally, detailed mechanistic studies were performed, and kinetic isotope effect experiments indicate that dehydrogenative annulation reaction involves photoinduced 6π-electrocyclic ringclosing and hydrogen evolution cascade processes.