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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/128156
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dc.contributor.authorGómez Palomino, Alejandro-
dc.contributor.authorRomea, Pedro-
dc.contributor.authorUrpí Tubella, Fèlix-
dc.date.accessioned2019-02-12T10:48:08Z-
dc.date.available2019-07-01T05:10:16Z-
dc.date.issued2018-07-01-
dc.identifier.issn0039-7881-
dc.identifier.urihttp://hdl.handle.net/2445/128156-
dc.description.abstractA novel approach to synthesize enantiomerically pure α-hydroxy carboxylic derivatives is reported. A highly stereoselective oxidation of titanium(IV) enolates from chiral N-acyloxazolidinones is performed with oxygen under simple experimental conditions that do not require any reducing steps. The success of this approach depends on the biradical character of titanium(IV) enolates.-
dc.format.extent6 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherGeorg Thieme Verlag-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1055/s-0037-1609966-
dc.relation.ispartofSynthesis. Journal of Synthetic Organic Chemistry, 2018, vol. 50, num. 14, p. 2721-2726-
dc.relation.urihttps://doi.org/10.1055/s-0037-1609966-
dc.rights(c) Georg Thieme Verlag, 2018-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationTitani-
dc.subject.classificationEstereoquímica-
dc.subject.classificationQuiralitat-
dc.subject.otherTitanium-
dc.subject.otherStereochemistry-
dc.subject.otherChirality-
dc.titleStereoselective oxidation of titanium(IV) enolates with oxygen-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec681108-
dc.date.updated2019-02-12T10:48:08Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
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