Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/34586
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorPérez Bosch, Maria-
dc.contributor.authorMinaglia, Annamaria Tania-
dc.contributor.authorCasamitjana i Badia, Núria-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2013-04-15T16:48:33Z-
dc.date.available2013-04-15T16:48:33Z-
dc.date.issued2005-07-25-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://hdl.handle.net/2445/34586-
dc.description.abstractAn enantioselective route to cis-perhydroisoquinolines, involving a cyclocondensation reaction of (R)-phenylglycinol with a racemic oxoester, a stereoselective conjugate addition to an unsaturated bicyclic lactam, and the closure of the carbocyclic ring by a ring-closing metathesis as the key steps is reported. This route allows the preparation of 3-cyano derivatives as well as cis-octahydroisoquinolines bearing a quaternary center at the C4-position.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1021/ol051242c-
dc.relation.ispartofOrganic Letters, 2005, vol. 7, num. 17, p. 3653-3656-
dc.relation.urihttp://dx.doi.org/10.1021/ol051242c-
dc.rights(c) American Chemical Society , 2005-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationIsoquinolina-
dc.subject.otherIsoquinoline-
dc.titleAn enantioselective entry to cis-perhydroisoquinolines-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec568510-
dc.date.updated2013-04-15T16:48:33Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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