Enantioselective Syntehsis of Alkaloids from Phenylglycinol-derived lactams

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dc.contributor.authorAmat Tusón, Mercedes
dc.contributor.authorLlor Brunés, Núria
dc.contributor.authorGriera Farres, Rosa
dc.contributor.authorPérez Bosch, Maria
dc.contributor.authorBosch Cartes, Joan
dc.date.accessioned2020-12-16T10:16:35Z
dc.date.available2020-12-16T10:16:35Z
dc.date.issued2011-04
dc.date.updated2020-12-16T10:16:35Z
dc.description.abstractThis review is focused on recent synthetic achievements and ongoing work in our laboratory using phenylglycinol-derived oxazolopiperidone lactams as starting materials for the enantioselective synthesis of piperidine-containing alkaloids: madangamines, 2,5-disubstituted decahydroquinoline and 1-substituted tetrahydroisoquinoline alkaloids, the indole alkaloids 20S- and 20R-dihydrocleavamine and quebrachamine, and indole alkaloids of the uleine and silicine groups. Keywords: alkaloids, piperidine, indole, lactams, total synthesis, phenylglycinol.
dc.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec597770
dc.identifier.issn1934-578X
dc.identifier.urihttps://hdl.handle.net/2445/172794
dc.language.isoeng
dc.publisherNatural Product
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1039/b400987h
dc.relation.ispartofNatural Product Communications, 2011, vol. 6, num. 4, p. 515-526
dc.relation.urihttps://doi.org/10.1039/b400987h
dc.rights(c) Natural Product, 2011
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject.classificationAlcaloides
dc.subject.classificationLactames
dc.subject.classificationSíntesi orgànica
dc.subject.otherAlkaloids
dc.subject.otherLactams
dc.subject.otherOrganic synthesis
dc.titleEnantioselective Syntehsis of Alkaloids from Phenylglycinol-derived lactams
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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