A practical synthesis of chiral 3-aryloxy-1,2-propanediols

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dc.contributor.authorKarakaplan, M
dc.contributor.authorTurgut, Y
dc.contributor.authorHosgören, H
dc.date.accessioned2024-04-24T17:33:11Z
dc.date.available2024-04-24T17:33:11Z
dc.date.issued2005
dc.departmentDicle Üniversitesien_US
dc.description.abstractChiral 3-aryloxy-1,2-propanediols (1-5) of > 96% ee were obtained in high yield by the nucleophilic addition of substituted phenols to chiral glycidol in the presence of piperidine hydrochloride as catalyst.en_US
dc.identifier.endpage42en_US
dc.identifier.issn1747-5198
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-17144407934
dc.identifier.scopusqualityQ3
dc.identifier.startpage41en_US
dc.identifier.urihttps://hdl.handle.net/11468/20512
dc.identifier.wosWOS:000228312800011
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherScience Reviews 2000 Ltden_US
dc.relation.ispartofJournal of Chemical Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChiral 3-Aryloxy-1,2-Propanediolsen_US
dc.subjectRing Opening Of Glycidolen_US
dc.titleA practical synthesis of chiral 3-aryloxy-1,2-propanediolsen_US
dc.titleA practical synthesis of chiral 3-aryloxy-1,2-propanediols
dc.typeArticleen_US

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