Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21794
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dc.date.accessioned2021-09-08T12:54:08Z-
dc.date.available2021-09-08T12:54:08Z-
dc.date.issued1997-
dc.identifier.citationCoşkun, N. ve Tirli, F. (1997). "Reactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamides". Synthetic Communications, 27(1), 1-9.tr_TR
dc.identifier.issn0039-7911-
dc.identifier.urihttps://doi.org/10.1080/00397919708004799-
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/00397919708004799-
dc.identifier.urihttp://hdl.handle.net/11452/21794-
dc.description.abstractTertian amines reacted with acid chlorides to give corresponding benzyl chlorides and N-phenacylamides Counterion in species attacked preferentially the benzylic methylene. Effect of substituents in the benzyl group on the reactivity. of acylammonium chlorides was investigated.tr_TR
dc.language.isoentr_TR
dc.publisherTaylor & Francistr_TR
dc.rightsinfo:eu-repo/semantics/closedAccesstr_TR
dc.subjectChemistrytr_TR
dc.subjectIonstr_TR
dc.titleReactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamidestr_TR
dc.typeArticletr_TR
dc.identifier.wosA1997WG44300001tr_TR
dc.identifier.scopus2-s2.0-1842291552tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage1tr_TR
dc.identifier.endpage9tr_TR
dc.identifier.volume27tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalSynthetic Communicationstr_TR
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.buuauthorTirli, Fatma-
dc.subject.wosChemistry, organictr_TR
dc.indexed.wosSCIEtr_TR
dc.indexed.scopusScopustr_TR
dc.wos.quartileQ3tr_TR
dc.contributor.scopusid7004177880tr_TR
dc.contributor.scopusid6505555336tr_TR
dc.subject.scopusTetrahydroisoquinoline Derivative; Synthetic Chemistry Techniques; Isolationtr_TR
dc.subject.emtreeAcetamide derivativetr_TR
dc.subject.emtreeAmidetr_TR
dc.subject.emtreeDrug synthesistr_TR
dc.subject.emtreeIn vitro studytr_TR
dc.subject.emtreeInfrared spectrophotometrytr_TR
dc.subject.emtreeMethodologytr_TR
dc.subject.emtreeNuclear magnetic resonancetr_TR
dc.subject.emtreeReaction analysistr_TR
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