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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164139
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorNavío, Laura-
dc.contributor.authorLlor Brunés, Núria-
dc.contributor.authorMolins, Elies-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2020-06-03T09:40:22Z-
dc.date.available2020-06-03T09:40:22Z-
dc.date.issued2012-01-06-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/2445/164139-
dc.description.abstractStarting from 4-substituted cyclohexanones, a practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines has been developed, the key steps being a stereoselective cyclocondensation of an unsaturated δ-keto ester derivative with (R)-phenylglycinol and the stereoselective hydrogenation of the resulting tricyclic oxazoloquinolone lactams.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/ol2030058-
dc.relation.ispartofOrganic Letters, 2012, vol. 14, num. 1, p. 210-213-
dc.relation.urihttps://doi.org/10.1021/ol2030058-
dc.rights(c) American Chemical Society , 2012-
dc.subject.classificationSíntesi orgànica-
dc.subject.classificationLactames-
dc.subject.classificationEnantiòmers-
dc.subject.classificationCompostos heterocíclics-
dc.subject.otherOrganic synthesis-
dc.subject.otherLactams-
dc.subject.otherEnantiomers-
dc.subject.otherHeterocyclic compounds-
dc.titleA practical synthetic route to enantiopure 6-substituted cis-decahydroquinolines-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec603300-
dc.date.updated2020-06-03T09:40:22Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid22133083-
Appears in Collections:Articles publicats en revistes (Institut de Biomedicina (IBUB))
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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