Asymmetric reduction of acetophenone using lithium aluminium hydride modified with some novel amino alcohol Schiff bases

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dc.contributor.authorTümerdem, R
dc.contributor.authorTopal, G
dc.contributor.authorTurgut, Y
dc.date.accessioned2024-04-24T16:18:26Z
dc.date.available2024-04-24T16:18:26Z
dc.date.issued2005
dc.departmentDicle Üniversitesien_US
dc.description.abstractSome new chiral Schiff bases have been prepared in good yields from various carbonyl groups and two 2-amino alcohols. LiAlH4 was treated with different equivalents of the Schiff bases. Enantioselective reduction of acetophenone is achieved in high chemical yield (up to 93%) with moderate enantiomeric excess (up to 22%) by use of the new reducing agents. (C) 2005 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tetasy.2004.12.020
dc.identifier.endpage868en_US
dc.identifier.issn0957-4166
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-13844275046
dc.identifier.scopusqualityN/A
dc.identifier.startpage865en_US
dc.identifier.urihttps://doi.org/10.1016/j.tetasy.2004.12.020
dc.identifier.urihttps://hdl.handle.net/11468/16095
dc.identifier.volume16en_US
dc.identifier.wosWOS:000227266700016
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedron-Asymmetry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleAsymmetric reduction of acetophenone using lithium aluminium hydride modified with some novel amino alcohol Schiff basesen_US
dc.titleAsymmetric reduction of acetophenone using lithium aluminium hydride modified with some novel amino alcohol Schiff bases
dc.typeArticleen_US

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