Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24333
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dc.date.accessioned2022-02-02T08:28:30Z-
dc.date.available2022-02-02T08:28:30Z-
dc.date.issued2005-
dc.identifier.citationCoşkun, N. ve Er, M. (2005). "New alkoxyzinc salts mediated chemoselective transesterification reactions". Turkish Journal of Chemistry, 29(5), 455-461.tr_TR
dc.identifier.issn1300-0527-
dc.identifier.urihttps://journals.tubitak.gov.tr/chem/abstract.htm?id=7857-
dc.identifier.urihttps://journals.tubitak.gov.tr/chem/issues/kim-05-29-5/kim-29-5-1-0505-2.pdf-
dc.identifier.urihttp://hdl.handle.net/11452/24333-
dc.description.abstractA new chemoselective method for the transesterification of alkyl esters in the presence of in situ formed alkoxyzinc salts was developed. Electron-rich esters are less reactive than electron poor ones and this is the basis for the chemoselectivity of the reaction. Suggested mechanisms of the transesterification reactions are discussed.en_US
dc.language.isoenen_US
dc.publisherTÜBİTAKtr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectChemistryen_US
dc.subjectEngineeringen_US
dc.subjectChemoselective transesterificationen_US
dc.subjectZinc bromideen_US
dc.subjectZinc acetateen_US
dc.subjectAlkoxyzinc bromideen_US
dc.subjectAlkoxyzinc acetateen_US
dc.subjectRing-opening reactionsen_US
dc.subjectBeta-ketoestersen_US
dc.subjectEstersen_US
dc.subjectAciden_US
dc.subjectEfficienten_US
dc.subjectCatalysten_US
dc.titleNew alkoxyzinc salts mediated chemoselective transesterification reactionsen_US
dc.typeArticleen_US
dc.identifier.wos000233674200001tr_TR
dc.identifier.scopus2-s2.0-32644474613tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.relation.bap2001-2tr_TR
dc.contributor.orcid0000-0003-3879-0813tr_TR
dc.identifier.startpage455tr_TR
dc.identifier.endpage461tr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalTurkish Journal of Chemistryen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.buuauthorEr, Mustafa-
dc.contributor.researcheridAAK-4577-2020tr_TR
dc.indexed.trdizinTrDizintr_TR
dc.subject.wosChemistry, multidisciplinaryen_US
dc.subject.wosEngineering, chemicalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ2 (Engineering, chemical)en_US
dc.wos.quartileQ3 (Chemistry, multidisciplinary)en_US
dc.contributor.scopusid7004177880tr_TR
dc.contributor.scopusid12244540300tr_TR
dc.subject.scopusNitrones; Cycloaddition Reactions; Hydroxylaminesen_US
Appears in Collections:Scopus
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