Synthesis, microwave-promoted catalytic activity in Suzuki-Miyaura cross-coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl group

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dc.authoridTahir, Muhammad Nawaz/0000-0002-6815-9806
dc.authoridYılmaz, Ülkü/0000-0002-2806-4781
dc.authoridGünal, Selami/0000-0002-4752-5176
dc.authoridKUCUKBAY, HASAN/0000-0002-7180-9486
dc.authoridDURMAZ, RIZA/0000-0001-6561-778X
dc.authorwosidDURMAZ, Rıza/HJH-4918-2023
dc.authorwosidTahir, Muhammad Nawaz/F-2900-2015
dc.authorwosidTahir, Muhammad Nawaz/HPB-5726-2023
dc.authorwosidYılmaz, Ülkü/AAA-7545-2020
dc.authorwosidGünal, Selami/AAA-7246-2021
dc.authorwosidKUCUKBAY, HASAN/A-5050-2019
dc.contributor.authorYilmaz, Ulku
dc.contributor.authorKucukbay, Hasan
dc.contributor.authorSireci, Nihat
dc.contributor.authorAkkurt, Mehmet
dc.contributor.authorGunal, Selami
dc.contributor.authorDurmaz, Riza
dc.contributor.authorTahir, M. Nawaz
dc.date.accessioned2024-08-04T20:32:49Z
dc.date.available2024-08-04T20:32:49Z
dc.date.issued2011
dc.departmentİnönü Üniversitesien_US
dc.description.abstractA mixture of benzimidazole salts (2-7), Pd(OAc)(2) and K2CO3 in DMF-H2O catalyzes the Suzuki-Miyaura cross-coupling reactions promoted by microwave irradiation resulting in high yield within a short time. In particular, the yield of the Suzuki-Miyaura reactions with aryl bromides was found to be nearly quantitative. The synthesized benzimidazole salts (2-7) were identified by H-1-C-13, NMR, IR spectroscopic methods and microanalysis. The molecular structure of 1 was determined by X-ray crystallography. The antibacterial and antifungal activities of the novel benzimidazole derivatives (1-7) were also tested against standard strains. Copyright (C) 2011 John Wiley & Sons, Ltd.en_US
dc.description.sponsorshipInonu University [BAPB-2010/124]en_US
dc.description.sponsorshipWe thank Dr Holger Ott (Bruker AXS GmbH, Karlsruhe, Germany) for the data collection. We wish to thank. Inonu University Research Fund (BAPB-2010/124) for financial support of this study.en_US
dc.identifier.doi10.1002/aoc.1772
dc.identifier.endpage373en_US
dc.identifier.issn0268-2605
dc.identifier.issn1099-0739
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-79955047652en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage366en_US
dc.identifier.urihttps://doi.org/10.1002/aoc.1772
dc.identifier.urihttps://hdl.handle.net/11616/95306
dc.identifier.volume25en_US
dc.identifier.wosWOS:000289515300007en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofApplied Organometallic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectbenzimidazole salten_US
dc.subjectcarbeneen_US
dc.subjectpalladium catalysisen_US
dc.subjectcoupling reactionen_US
dc.subjectSuzuki-Miyaura couplingen_US
dc.subjectmicrowaveen_US
dc.subjectantimicrobial activityen_US
dc.titleSynthesis, microwave-promoted catalytic activity in Suzuki-Miyaura cross-coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl groupen_US
dc.typeArticleen_US

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