Regioselective and Stereospecific Dehydrogenative Annulation Utilizing Silylium Ion-Activated Alkenes

Treatment of dialkylbenzylsilanes (1) with trityl tetrakis(pentafluorophenyOborate (TPFPB) afforded the corresponding silylium ions in equilibrium with their intra-or intermolecular 2r-complexes, which underwent dehydrogenative annulation with various alkenes to form 1,2,3,4tetrahydro-2-silanaphthalenes (4) in up to 82% isolated yield. Sterically bulkier substituents on the silicon atom tended to increase the yield of cyclic products 4. The annulation products retained the stereochemistry in cases of the reactions using internal alkenes. The use of diisopropyl(1-naphthyl)silane (2) instead of 1 also resulted in annulation to obtain the 2,3-dihydro-1-sila-1H-phenalene derivatives 6. Electrophilic aromatic substitution at the 8position was predominant, despite the two potentially reactive positions on the naphthyl group. The steric hindrance of the naphthyl group prevented addition of the cis-alkene to the silylium ion, which would considerably decrease yields of the desired products from 2 compared to those from 1.