Some electrophilic reactivity studies of di-(2-indolyl)dibenzofurans and di-(2-indolyl)carbazoles

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dc.authorid0000-0001-9386-4892
dc.authorid0000-0002-7347-2223
dc.authorid0000-0002-0951-9621
dc.authorscopusid55308985300
dc.authorscopusid24504085000
dc.authorscopusid55326408200
dc.authorscopusid16833488100
dc.authorscopusid35516284500
dc.authorwosidSengul, Ibrahim Fazil/AAG-4368-2019
dc.authorwosidk, h/ABA-1339-2020
dc.contributor.authorŞengül, İbrahim Fazıl
dc.contributor.authorSomphol, Kittiya
dc.contributor.authorKandemir, Hakan
dc.contributor.authorKumar, Naresh
dc.contributor.authorBlack, David StC.
dc.date.accessioned2022-05-11T14:29:55Z
dc.date.available2022-05-11T14:29:55Z
dc.date.issued2014
dc.departmentFakülteler, Fen Edebiyat Fakültesi, Kimya Bölümü
dc.description.abstract3,6-Bis-(2-indolyl)dibenzofurans 1,2, and carbazoles 3-6 underwent a range of electrophilic substitution reactions to produce formyl indoles 7-12, biindolyls 24-28 and 33-34, glyoxylamides 40-42, and amides 48. (C) 2014 Elsevier Ltd. All rights reserved.
dc.description.sponsorshipUniversity of New South Wales; Turkish GovernmentTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK)
dc.description.sponsorshipWe thank the University of New South Wales and the Turkish Government for their financial support.
dc.identifier.doi10.1016/j.tet.2014.11.014
dc.identifier.endpage9614
dc.identifier.issn0040-4020
dc.identifier.issue51en_US
dc.identifier.scopus2-s2.0-84911869349
dc.identifier.scopusqualityQ2
dc.identifier.startpage9601
dc.identifier.urihttps://doi.org/10.1016/j.tet.2014.11.014
dc.identifier.urihttps://hdl.handle.net/20.500.11776/7176
dc.identifier.volume70
dc.identifier.wosWOS:000347127900004
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthorKandemir, Hakan
dc.language.isoen
dc.publisherPergamon-Elsevier Science Ltd
dc.relation.ispartofTetrahedron
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBis-indoles
dc.subjectBiindolyls
dc.subjectDibenzofurans
dc.subjectCarbazoles
dc.subjectIndole synthesis
dc.subjectFormylation
dc.subjectGlyoxylic amides
dc.subjectElectrophilic substitution
dc.subjectSolid-State Structures
dc.subjectMacrocyclic Amide
dc.subjectComplexes
dc.subject4,6-Dimethoxyindoles
dc.subjectBiindolyls
dc.subjectChloride
dc.subjectIndoles
dc.titleSome electrophilic reactivity studies of di-(2-indolyl)dibenzofurans and di-(2-indolyl)carbazoles
dc.typeArticle

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