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dc.contributor.authorÖzenç, Köseceli Ayşen
dc.contributor.authorÇelik, İlhami
dc.contributor.authorKökten, Şule
dc.date.accessioned2019-10-20T09:13:42Z
dc.date.available2019-10-20T09:13:42Z
dc.date.issued2017
dc.identifier.issn1300-0527
dc.identifier.urihttps://dx.doi.org/10.3906/kim-1607-35
dc.identifier.urihttps://hdl.handle.net/11421/17024
dc.descriptionWOS: 000403692800002en_US
dc.description.abstractN-Substituted methyl 2-((azolyl)methyl)-3-arylacrylates were synthesized stereo- and regioselectively with one-pot reaction between Baylis-Hillman acetates and a suitable acylazole in the presence of K2CO3 as a base catalyst. The targeted N-substituted azole acrylates were efficiently obtained in good yields (39%-89%).en_US
dc.description.sponsorshipAnadolu University [1110F163]en_US
dc.description.sponsorshipIt is gratefully acknowledged that this work was supported financially by Anadolu University (Project No: 1110F163).en_US
dc.language.isoengen_US
dc.publisherScientific Technical Research Council Turkey-Tubitaken_US
dc.relation.isversionof10.3906/kim-1607-35en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectImidazoleen_US
dc.subjectBenzimidazoleen_US
dc.subjectBenzotriazoleen_US
dc.subjectBaylis Hillman Acetatesen_US
dc.subjectN-Substituted Azole Acrylatesen_US
dc.titleStereoselective and regioselective synthesis of N-substituted methyl 2-((azolyl)methyl)-3-arylacrylates from Baylis-Hillman acetatesen_US
dc.typearticleen_US
dc.relation.journalTurkish Journal of Chemistryen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.volume41en_US
dc.identifier.issue3en_US
dc.identifier.startpage323en_US
dc.identifier.endpage334en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorÇelik, İlhami


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