An easy access to tetralin and indane skeletons has been developed using a diastereoselective intramolecular Friedel鈥揅rafts alkylation. Treatment of diastereomeric mixtures of benzyl carbinols with a catalytic amount of Ca(NTf2)2/Bu4NPF6 yields the respective tetralin or indane in good yields with high levels of regio- and diastereoselectivity.