A novel approach has been found and the first total synthesis of (±)-Salvirecognine was accomplished by using it. In which intramolecular cyclization and Friedel-Crafts alkylation took place simultaneously to afford key intermediates for synthesis of aro A novel approach has been found and the first total synthesis of (±) -Salvirecognine was accomplished by using it. In which intramolecular cyclization and Friedel-Crafts alkylation took place in to afford key intermediates for synthesis of aro