Şenol Z.Zaim Ö.Balci M.2024-06-122024-06-1220051300-0527https://hdl.handle.net/20.500.14551/17347The reaction of ?-pinene and dibromocarbene produced a fairly unstable product, 2,7,7-trimethyl3,3-dibromotricyclo[4.1.1.02,4] octane, from which 3-bromo-7,7-dimethyl-2-methylenebicyclo[4,1,1]oct-3-ene and 3-bromo-2,7,7-trimethylbicyclo [4,1,1]octa-2,4-diene were obtained in chloroform at room temperature and in various other media and conditions. Two new compounds, 3-bromo-2,7,7-trimethylbicyclo [4.1.1]oct-3-en-2-ol and 2-(4-bromo-5-methylcyclohepta-3,5-dien-1-yl) propan-2-ol, were observed in aqueous acetone in addition to the previous two. The stability and formation mechanism of the formed products are discussed. © TÜBİTAK.eninfo:eu-repo/semantics/closedAccess[Abstarct Not Available]A new approach to the ring opening reactions of 2,7,7-trimethyl-3,3- dibromotricyclo[4.1.1.02,4]octaneArticle2955315382-s2.0-32644441115Q3