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dc.contributor.authorÖzenç, Köseceli Ayşen
dc.contributor.authorÇelik, İlhami
dc.contributor.authorKökten, Şule
dc.date.accessioned2019-10-20T14:27:52Z
dc.date.available2019-10-20T14:27:52Z
dc.date.issued2017
dc.identifier.issn1300-0527
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TWpRME16QXpNdz09
dc.identifier.urihttps://hdl.handle.net/11421/17893
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 K2 CO3 as a base catalyst. The targeted N -substituted azole acrylates were efficiently obtained in good yields (39%–89%).en_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 K2 CO3 as a base catalyst. The targeted N -substituted azole acrylates were efficiently obtained in good yields (39%–89%).en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMühendisliken_US
dc.subjectKimyaen_US
dc.titleStereoselective and regioselective synthesis of NN-substituted methyl 2-((azolyl)methyl)-3-arylacrylates from Baylis-Hillman acetatesen_US
dc.typeotheren_US
dc.relation.journalTurkish Journal of Chemistryen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Kimya Bölümüen_US
dc.identifier.volume41en_US
dc.identifier.issue3en_US
dc.identifier.startpage323en_US
dc.identifier.endpage334en_US
dc.relation.publicationcategoryDiğeren_US]
dc.contributor.institutionauthorÇelik, İlhami


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