Abstract:
A facile route towards the synthesis of cyclopentene fused chromene derivatives from strained phenol
substituted fulvene derived bicyclic hydrazines is described. The reaction is proceeding through base catalyzed sequential intramolecular ring opening and ring closure of azabicyclic olefins. The transition metal
free method provides an easy access to biologically relevant fused chromene ring system under relatively
mild reaction conditions.