Non-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2

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dc.contributor.authorUnver, Halil
dc.contributor.authorBiyikoglu, Mutluhan
dc.contributor.authorBulut, Adnan
dc.date.accessioned2020-06-25T18:06:59Z
dc.date.available2020-06-25T18:06:59Z
dc.date.issued2013
dc.departmentKırıkkale Üniversitesi
dc.description.abstractSince alkyl Lewis acids are Bronsted bases, they give a non-acidic reaction media. In this context, acylation of thiophene is investigated in the presence of EtAlCl2 and non-acidic media. Besides 8 examples of thiophene, one example for pyrrole is synthesized in moderate to high yields (up to 99 %).en_US
dc.identifier.citationUnver, H., Biyikoglu, M., & Bulut, A. (2013). Non-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2. Asian Journal of Chemistry, 25(15), 8772–8774.en_US
dc.identifier.doi10.14233/ajchem.2013.15607
dc.identifier.endpage8774en_US
dc.identifier.issn0970-7077
dc.identifier.issn0975-427X
dc.identifier.issue15en_US
dc.identifier.scopus2-s2.0-84886621689
dc.identifier.scopusqualityQ4
dc.identifier.startpage8772en_US
dc.identifier.urihttps://doi.org/10.14233/ajchem.2013.15607
dc.identifier.urihttps://hdl.handle.net/20.500.12587/5432
dc.identifier.volume25en_US
dc.identifier.wosWOS:000325204200122
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherAsian Journal Of Chemistryen_US
dc.relation.ispartofAsian Journal Of Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectThiopheneen_US
dc.subjectAcylationen_US
dc.subjectAlkyl Lewis aciden_US
dc.subjectElectrophilic aromatic substitutionen_US
dc.titleNon-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2en_US
dc.typeArticle

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