Synthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation

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dc.contributor.authorSaborit Villarroya, Gisela
dc.contributor.authorCativiela, Carlos
dc.contributor.authorJimenez, Ana I.
dc.contributor.authorBonjoch i Sesé, Josep
dc.contributor.authorBradshaw, Ben
dc.date.accessioned2019-02-13T12:54:14Z
dc.date.available2019-02-13T12:54:14Z
dc.date.issued2018-10-09
dc.date.updated2019-02-13T12:54:14Z
dc.description.abstractA straightforward synthetic entry to functionalized hydrindane compounds based on a rapid assembly of the core nucleus by a Danheiser cycloaddition is reported. Valuable bicyclic building blocks containing the fused five and six-membered carbocyclic ring system can be achieved in only four steps from a simple acyclic β-keto ester. Keywords: alkaloid; Danheiser annulation; decahydroquinoline
dc.format.extent5 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec683225
dc.identifier.issn1860-5397
dc.identifier.pmid30410621
dc.identifier.urihttps://hdl.handle.net/2445/128207
dc.language.isoeng
dc.publisherBeilstein Institute
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3762/bjoc.14.237
dc.relation.ispartofBeilstein Journal of Organic Chemistry, 2018, vol. 14, p. 2597-2601
dc.relation.urihttps://doi.org/10.3762/bjoc.14.237
dc.rightscc-by (c) Saborit Villarroya, Gisela et al., 2018
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject.classificationCiclització (Química)
dc.subject.classificationAlcaloides
dc.subject.classificationSíntesi orgànica
dc.subject.otherRing formation (Chemistry)
dc.subject.otherAlkaloids
dc.subject.otherOrganic synthesis
dc.titleSynthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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