O-alkylation of pyridine aldo- and ketoximes with dihalohydrins under phase-transfer conditions

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dc.contributor.authorKocak, Abmet
dc.contributor.authorKurbanli, Sultan
dc.contributor.authorMalkondu, Sait
dc.date.accessioned2020-03-26T17:17:46Z
dc.date.available2020-03-26T17:17:46Z
dc.date.issued2007
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractPhase-transfer-catalyzed alkylation of (E)-pyridine aldo- and (E)-ketoximes with dihalohydrins in the benzene (or DMSO)/10% aq. NaOH system in the presence of tetradecylammonium bromide proceeds regiospecifically to afford the corresponding O-halohydrins in good yields. In this study, first O-halohydrin derivatives were converted into glycidyl ether derivatives, and then a new series of amino alcohols were synthesized by the condensation of amines with these glycidyl ethers.en_US
dc.identifier.doi10.1080/00397910701198997en_US
dc.identifier.endpage1165en_US
dc.identifier.issn0039-7911en_US
dc.identifier.issue07.09.2020en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage1155en_US
dc.identifier.urihttps://dx.doi.org/10.1080/00397910701198997
dc.identifier.urihttps://hdl.handle.net/20.500.12395/21498
dc.identifier.volume37en_US
dc.identifier.wosWOS:000247620500013en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.relation.ispartofSYNTHETIC COMMUNICATIONSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectamino alcoholsen_US
dc.subjectcondensationen_US
dc.subjectdihalohydrinsen_US
dc.subjectepoxidesen_US
dc.subjectpyridine aldo- and ketoximesen_US
dc.titleO-alkylation of pyridine aldo- and ketoximes with dihalohydrins under phase-transfer conditionsen_US
dc.typeArticleen_US

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