A Facile Approach to Access Multi-Substituted Indenes via Nazarov Cyclisation of Aryl, Vinyl, and Alkyl/Aryl Carbinols

A divergent approach to highly substituted functionalized indenes has been developed. The two-step reaction involving nucleophilic addition reaction of aryl vinyl ketone, an ideal intermediate with aryl or alkyl nucleophilic reagent, followed by electrocyclic reaction (Nazarov cyclization) in the presence of Lewis acid catalyst afforded indene derivatives in good to excellent yield.

Automated summary

A novel method has been developed for the preparation of highly substituted functionalized indenes through a two-step reaction, resulting in good to excellent yields.