1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29963
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dc.contributor.authorKoz, Gamze-
dc.contributor.authorKoz, Ömer-
dc.date.accessioned2022-12-19T13:17:27Z-
dc.date.available2022-12-19T13:17:27Z-
dc.date.issued2016-04-22-
dc.identifier.citationKoz, G. vd. (2016). "Enantioselective synthesis of 2-amino-4-(nitromethyl)-4H-chromene-3-carbonitriles from 2-iminochromenes". Synthetic Communications, 46(10), 909-915.en_US
dc.identifier.issn0039-7911-
dc.identifier.issn1532-2432-
dc.identifier.urihttps://doi.org/10.1080/00397911.2016.1177728-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/00397911.2016.1177728-
dc.identifier.urihttp://hdl.handle.net/11452/29963-
dc.description.abstractA series of medicinally important 2-amino-4-(nitromethyl)-4H-chromene-3-carbonitriles were synthesized using enantioselective conjugate addition of nitromethane to 2-iminochromenes. The reactions were performed using L8-Cu (II) catalytic system and moderate to good enantioselectivities (62-88%) and yields (66-96%) were obtained.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectAmino alcohol catalysten_US
dc.subjectEnantioselective conjugate additionen_US
dc.subject2-iminochromeneen_US
dc.subjectNitromethaneen_US
dc.subjectAsymmetric conjugate additionen_US
dc.subjectMichael additionen_US
dc.subjectPrivileged structuresen_US
dc.subjectEfficienten_US
dc.subjectDerivativesen_US
dc.subjectNitroalkanesen_US
dc.subjectApoptosisen_US
dc.subjectChromeneen_US
dc.subjectSalicylaldehydesen_US
dc.subjectMalononitrileen_US
dc.titleEnantioselective synthesis of 2-amino-4-(nitromethyl)-4H-chromene-3-carbonitriles from 2-iminochromenesen_US
dc.typeArticleen_US
dc.identifier.wos000378147800007tr_TR
dc.identifier.scopus2-s2.0-84973129536tr_TR
dc.relation.tubitakBIDEB 2218en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage909tr_TR
dc.identifier.endpage915tr_TR
dc.identifier.volume46tr_TR
dc.identifier.issue10tr_TR
dc.relation.journalSynthetic Communicationsen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.researcheridB-1200-2012tr_TR
dc.relation.collaborationYurt içitr_TR
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.wosICen_US
dc.indexed.wosCCREen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid7004177880tr_TR
dc.subject.scopusDihydropyrano(2,3-C)Pyrazole; Catalyst; Benzopyransen_US
dc.subject.emtreeAmineen_US
dc.subject.emtreeChromene derivativeen_US
dc.subject.emtreeCopperen_US
dc.subject.emtreeCyanideen_US
dc.subject.emtreeImineen_US
dc.subject.emtreeNitro derivativeen_US
dc.subject.emtreeNitromethaneen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCatalysisen_US
dc.subject.emtreeCatalysten_US
dc.subject.emtreeConjugationen_US
dc.subject.emtreeEnantioselectivityen_US
dc.subject.emtreeQuantum yielden_US
dc.subject.emtreeReaction analysisen_US
dc.subject.emtreeSynthesisen_US
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