Thiophene-2,5-dicarboxylic acid bis-aryl(alkyl) amides

dc.contributor.authorKoparir, M
dc.contributor.authorCansiz, A
dc.contributor.authorÇetin, A
dc.date.accessioned2026-08-12T17:13:12Z
dc.date.issued2005
dc.departmentFırat Üniversitesi
dc.description.abstractA base-catalyzed condensation of diacetamido sulfides [(RNHCOCH2)(2)S)] with glyoxal affording thiophene-2,5-dicarboxylic acid bis-aryl(alkyl)amides has been accomplished under mild conditions. Excellent results were readily obtained when R was a substituted 3-nitrophenyl, 4-nitrophenyl, 4-chlorophenyl group, but the yield was poor when R was cyclohexyl. Unknown compounds were characterized by elemental analyses, IR, H-1, and C-13 NMR techniques. (c) 2005 Wiley Periodicals, Inc.
dc.identifier.doi10.1002/hc.20153
dc.identifier.endpage506
dc.identifier.issn1042-7163
dc.identifier.issue6
dc.identifier.orcid0000-0002-3692-6740
dc.identifier.orcid0000-0003-1031-783X
dc.identifier.scopus2-s2.0-27744434846
dc.identifier.scopusqualityQ3
dc.identifier.startpage503
dc.identifier.urihttps://doi.org/10.1002/hc.20153
dc.identifier.urihttps://hdl.handle.net/11508/51332
dc.identifier.volume16
dc.identifier.wosWOS:000231987700008
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherJohn Wiley & Sons Inc
dc.relation.ispartofHeteroatom Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectHinsberg-Reaction
dc.subjectFacile Synthesis
dc.subjectDiketo Sulfides
dc.subject2,5-Diacylthiophenes
dc.titleThiophene-2,5-dicarboxylic acid bis-aryl(alkyl) amides
dc.typeArticle

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