Self-assembly of an organocatalyst for the enantioselective synthesis of Michael adducts and ?-aminoxy alcohols in a nonpolar medium

dc.authorid0000-0002-6311-1918
dc.contributor.authorBasçeken, Sinan
dc.date.accessioned2019-05-13T08:58:23Z
dc.date.available2019-05-13T08:58:23Z
dc.date.issued2013
dc.departmentHitit Üniversitesi, Fen Edebiyat Fakültesi, Kimya Bölümü
dc.description.abstractA proline-thiourea host-guest complex is described as a self-assembled organocatalyst for the enantioselective Michael addition of aldehydes to nitroolefins and for the asymmetric ?-aminoxylation of both aldehydes and ketones. The Michael adducts were obtained in good yields of up to 80%, high diastereoselectivities of up to 5:95, and high enantiomeric excesses of up to 98%. The optically active aminoxy alcohols were synthesized in 60-85% yields with 94-99% enantiomeric excesses after reduction of the ?-oxidation products using NaBH4. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citationDemir, A. S., Basçeken, S. (2013). Self-assembly of an organocatalyst for the enantioselective synthesis of Michael adducts and ?-aminoxy alcohols in a nonpolar medium. Tetrahedron: Asymmetry, 24(19), 1218-1224.
dc.identifier.doi10.1016/j.tetasy.2013.08.008
dc.identifier.endpage1224en_US
dc.identifier.issn0957-4166
dc.identifier.issue19en_US
dc.identifier.scopusqualityN/A
dc.identifier.startpage1218en_US
dc.identifier.urihttps://doi.org/10.1016/j.tetasy.2013.08.008
dc.identifier.urihttps://hdl.handle.net/11491/1127
dc.identifier.volume24en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.relation.ispartofTetrahedron Asymmetry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject[Belirlenecek]en_US
dc.titleSelf-assembly of an organocatalyst for the enantioselective synthesis of Michael adducts and ?-aminoxy alcohols in a nonpolar medium
dc.typeArticle

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