A new approach to the ring opening reactions of 2,7,7-trimethyl-3,3- dibromotricyclo[4.1.1.02,4]octane
dc.authorscopusid | 12243965500 | |
dc.authorscopusid | 56024061700 | |
dc.authorscopusid | 7006382595 | |
dc.contributor.author | Şenol Z. | |
dc.contributor.author | Zaim Ö. | |
dc.contributor.author | Balci M. | |
dc.date.accessioned | 2024-06-12T10:28:38Z | |
dc.date.available | 2024-06-12T10:28:38Z | |
dc.date.issued | 2005 | |
dc.description.abstract | The 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. | en_US |
dc.identifier.endpage | 538 | en_US |
dc.identifier.issn | 1300-0527 | |
dc.identifier.issue | 5 | en_US |
dc.identifier.scopus | 2-s2.0-32644441115 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 531 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.14551/17347 | |
dc.identifier.volume | 29 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Turkish Journal of Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | [Abstarct Not Available] | en_US |
dc.title | A new approach to the ring opening reactions of 2,7,7-trimethyl-3,3- dibromotricyclo[4.1.1.02,4]octane | en_US |
dc.type | Article | en_US |