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dc.contributor.authorUludağ, Nesimi
dc.contributor.authorYılmaz, Recep
dc.contributor.authorAsutay, Oktay
dc.contributor.authorÇolak, Naki
dc.date.accessioned2019-05-10T09:38:49Z
dc.date.available2019-05-10T09:38:49Z
dc.date.issued2016
dc.identifier.citationUludag, N., Yılmaz, R.K., Asutay, O., Çolak, N. (2016). Facile synthesis of the azocino[4,3-b]indole framework of strychnopivotine and other Strychnos alkaloids. Chemistry of Heterocyclic Compounds, 52(3), 196-199.en_US
dc.identifier.issn0009-3122
dc.identifier.urihttps://doi.org/10.1007/s10593-016-1860-4
dc.identifier.urihttps://hdl.handle.net/11491/492
dc.description.abstract[Figure not available: see fulltext.]A new synthetic route to the 1,5-methanoazocino[4,3-b]indole is described. The aim of the present study is to provide a tetracyclic skeleton for the synthesis of pentacyclic Strychnos alkaloids (tubifolidine and strychnopivotine). Starting from a carbazole derivative, the ring closure was achieved by an intramolecular aldol reaction. The final product was obtained in 45% in the overall yield over 7 steps. © 2016, Springer Science+Business Media New York.en_US
dc.language.isoeng
dc.publisherSpringer New York LLCen_US
dc.relation.isversionof10.1007/s10593-016-1860-4en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1,5-methanoazocino[4,3-b]indoleen_US
dc.subjectStrychnos Alkaloidsen_US
dc.titleFacile synthesis of the azocino[4,3-b]indole framework of strychnopivotine and other Strychnos alkaloidsen_US
dc.typearticleen_US
dc.relation.journalChemistry of Heterocyclic Compoundsen_US
dc.departmentHitit Üniversitesi, Fen Edebiyat Fakültesi, Kimya Bölümüen_US
dc.authorid0000-0001-7181-9556en_US
dc.identifier.volume52en_US
dc.identifier.issue3en_US
dc.identifier.startpage196en_US
dc.identifier.endpage199en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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