A new approach to the ring opening reactions of 2,7,7-trimethyl-3,3-dibromotricyclo[4.1.1.$0^{2,4}$] octane
dc.contributor.author | Balcı, Metin | |
dc.contributor.author | Şenol, Zekir | |
dc.contributor.author | Zaim, Ömer | |
dc.date.accessioned | 2024-06-12T10:18:21Z | |
dc.date.available | 2024-06-12T10:18:21Z | |
dc.date.issued | 2005 | |
dc.department | Trakya Üniversitesi | en_US |
dc.description.abstract | The reaction of $alpha$−pinene and dibromocarbene produced a fairly unstable product, 2,7,7-trimethyl-3,3-dibromotricyclo[4.1.1.$0^{2,4}$]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. | en_US |
dc.identifier.endpage | 538 | en_US |
dc.identifier.issn | 1300-0527 | |
dc.identifier.issn | 1303-6130 | |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 531 | en_US |
dc.identifier.trdizinid | 49056 | en_US] |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/49056 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14551/15482 | |
dc.identifier.volume | 29 | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Turkish Journal of Chemistry | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | A new approach to the ring opening reactions of 2,7,7-trimethyl-3,3-dibromotricyclo[4.1.1.$0^{2,4}$] octane | en_US |
dc.type | Article | en_US |