Enantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligands

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dc.contributor.authorColak, Mehmet
dc.contributor.authorDemirel, Nadir
dc.date.accessioned2024-04-24T16:18:27Z
dc.date.available2024-04-24T16:18:27Z
dc.date.issued2008
dc.departmentDicle Üniversitesien_US
dc.description.abstractChiral Schiff-bases 2, 3, 4 and 5 were designed for the enantioselective nitroaldol (Henry) reaction. The highest enantioselectivity was observed for ligand 4 (82% ee) when CH2Cl2 was used as a solvent. (C) 2008 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tetasy.2008.02.005
dc.identifier.endpage639en_US
dc.identifier.issn0957-4166
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-40849094003
dc.identifier.scopusqualityN/A
dc.identifier.startpage635en_US
dc.identifier.urihttps://doi.org/10.1016/j.tetasy.2008.02.005
dc.identifier.urihttps://hdl.handle.net/11468/16101
dc.identifier.volume19en_US
dc.identifier.wosWOS:000254802000018
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.titleEnantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligandsen_US
dc.titleEnantioselective nitroaldol (Henry) reaction catalyzed by chiral Schiff-base ligands
dc.typeArticleen_US

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