Palladium catalyzed cross-coupling of 3-methylthiophene-2-carbonyl chloride with aryl/het-aryl boronic acids: a convenient method for synthesis of thienyl ketones

dc.contributor.authorRizwan, Kainat F.
dc.contributor.authorKarakaya, Idris
dc.contributor.authorZubair, Muhammad Waqas
dc.contributor.authorRasool, Nasir
dc.date.accessioned2025-10-29T12:08:03Z
dc.date.issued2022
dc.departmentGebze Teknik Üniversitesi
dc.description.abstractBi-aryl ketones are important motifs in large number of pharmaceutical compounds and natural products. A protocol for the synthesis of thienyl ketones has been developed via Pd (0) catalyzed cross-coupling reaction. The desired thienyl ketones (3a-x) were synthesized by cross coupling of 3-methylthiophene-2-carbonyl chloride with variety of aryl/heteroaryl-boronic acids in good to excellent yields (46–91%) under mild conditions (1.5 eq Cs<inf>2</inf>CO<inf>3</inf> at 50 °C). Different functional groups were well tolerated under the developed reaction conditions. © 2024 Elsevier B.V., All rights reserved.
dc.identifier.doi10.1080/17415993.2022.2079379
dc.identifier.endpage506
dc.identifier.issn1741-5993
dc.identifier.issn1741-6000
dc.identifier.issue5
dc.identifier.scopus2-s2.0-85131352755
dc.identifier.scopusqualityQ2
dc.identifier.startpage494
dc.identifier.urihttps://doi.org/10.1080/17415993.2022.2079379
dc.identifier.urihttps://hdl.handle.net/20.500.14854/14285
dc.identifier.volume43
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofJournal of Sulfur Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_Scopus_20251020
dc.subjectarylboronic acid
dc.subjectCoupling
dc.subjectpalladium
dc.subjectsynthesis
dc.subjectthienyl ketone
dc.titlePalladium catalyzed cross-coupling of 3-methylthiophene-2-carbonyl chloride with aryl/het-aryl boronic acids: a convenient method for synthesis of thienyl ketones
dc.typeArticle

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