Studies on the synthesis of the azocino[4,3-b]indole framework and related compounds

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dc.authoriduludag, Nesimi -- 0000-0002-2819-3612en_US
dc.contributor.authorUludag, Nesimi
dc.contributor.authorPatir, Suleyman
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:16:00Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:16:00Z
dc.date.issued2007
dc.departmentHacettepe Univ, Fac Educ, Dept Sci, TR-06800 Ankara, Turkey -- Cumhuriyet Univ, Fac Educ, Dept Chem, TR-58140 Sivas, Turkeyen_US
dc.description.abstractAn efficient method for the synthesis of C-4 position alkylated azocino[4,3-b]indole 13 and 18 is described. Reduction of compounds 5, 6, 7 and 8 yielded the corresponding alcohols. Compounds 5, 6, 7 and 8 were synthesized through several steps starting from 1. The resulting alcohols underwent acid catalyzed ring closure to give tetracyclic azocino[4,3-b]indole 9, 10, 11 and 12. Finally, compounds 9 and 17 were alkylated at C-4 position to the corresponding products 13 and 18. The structure of the compounds 13 and 18 has been confirmed by X-ray single crystal analysis.en_US
dc.identifier.doi10.1002/jhet.5570440613en_US
dc.identifier.endpage1322en_US
dc.identifier.issn0022-152X
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-38949165218en_US
dc.identifier.scopusqualityQ3
dc.identifier.startpage1317en_US
dc.identifier.urihttps://dx.doi.org/10.1002/jhet.5570440613
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10510
dc.identifier.volume44en_US
dc.identifier.wosWOS:000250794200013en_US
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherHETERO CORPORATIONen_US
dc.relation.ispartofJOURNAL OF HETEROCYCLIC CHEMISTRYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleStudies on the synthesis of the azocino[4,3-b]indole framework and related compoundsen_US
dc.typeArticleen_US

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