3-aryl-5-furylpyrazolines and their biological activities

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dc.contributor.authorCetin, A
dc.contributor.authorCansiz, A
dc.contributor.authorDigrak, M
dc.date.accessioned2026-08-12T17:10:46Z
dc.date.issued2003
dc.departmentFırat Üniversitesi
dc.description.abstractAryl-furyl substituted pyrazolines 2a-c and 4a-c were prepared by the reaction of alpha,beta-unsaturated carbonyl compounds with hydrazine or phenyl hydrazine. N-chloroacetyl derivatives 3a-c were obtained by the N-acetylation of 2a-c. The antibacterial activities of synthesized pyrazolines were examined by employing the disk-diffusion technique. All synthesized compounds showed antibacterial effects in 1200 mug concentration. (C) 2003 Wiley Periodicals, Inc.
dc.identifier.doi10.1002/hc.10159
dc.identifier.endpage347
dc.identifier.issn1042-7163
dc.identifier.issn1098-1071
dc.identifier.issue4
dc.identifier.orcid0000-0002-3692-6740
dc.identifier.scopus2-s2.0-0038510066
dc.identifier.scopusqualityQ3
dc.identifier.startpage345
dc.identifier.urihttps://doi.org/10.1002/hc.10159
dc.identifier.urihttps://hdl.handle.net/11508/50860
dc.identifier.volume14
dc.identifier.wosWOS:000183236300011
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofHeteroatom Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.title3-aryl-5-furylpyrazolines and their biological activities
dc.typeArticle

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