The effect of the double bond pyramidalization on the mode of the bromination reaction: Bromination of benzobicyclononadiene

dc.authorid0000-0002-9577-2251en_US
dc.authorid0000-0002-5098-1842en_US
dc.contributor.authorBalcı, Metin
dc.contributor.authorGüney, Murat
dc.contributor.authorDaştan, Arif
dc.contributor.authorAzizoğlu, Akın
dc.date.accessioned2019-10-17T10:37:45Z
dc.date.available2019-10-17T10:37:45Z
dc.date.issued2007en_US
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.descriptionAzizoğlu, Akın (Balikesir Author)en_US
dc.description.abstractThe bromination of 6,7,8,9-tetrahydro-5H-5,9-ethenobenzo[a][7]annulene yielded regio- and stereospecifically formed dibromides arising from the alkyl shift where the bromine exclusively attacks the double bond from the endo face of the double bond. DFT calculations on model compounds showed that the pyramidalization of the double bond and steric repulsion caused by the methylene protons are responsible for the stereo- and regioselective addition of bromine.en_US
dc.identifier.doi10.1021/jo070253b
dc.identifier.endpage4762en_US
dc.identifier.issn0022-3263
dc.identifier.issue13en_US
dc.identifier.scopus2-s2.0-34250817421
dc.identifier.scopusqualityQ2
dc.identifier.startpage4756en_US
dc.identifier.urihttps://doi.org/10.1021/jo070253b
dc.identifier.urihttps://hdl.handle.net/20.500.12462/8191
dc.identifier.volume72en_US
dc.identifier.wosWOS:000247246100019
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherAmer Chemical Socen_US
dc.relation.ispartofJournal of Organic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.titleThe effect of the double bond pyramidalization on the mode of the bromination reaction: Bromination of benzobicyclononadieneen_US
dc.typeArticleen_US

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