dc.creatorLarghi, Enrique Leandro
dc.creatorKaufman, Teodoro Saul
dc.date.accessioned2021-07-21T12:12:53Z
dc.date.accessioned2022-10-15T10:25:44Z
dc.date.available2021-07-21T12:12:53Z
dc.date.available2022-10-15T10:25:44Z
dc.date.created2021-07-21T12:12:53Z
dc.date.issued2008-10
dc.identifierLarghi, Enrique Leandro; Kaufman, Teodoro Saul; A combined RCM-Bischler-Napieralski strategy towards the synthesis of the carbon skeleton of excentricine and related stephaoxocanes; Pergamon-Elsevier Science Ltd; Tetrahedron; 64; 42; 10-2008; 9921-9927
dc.identifier0040-4020
dc.identifierhttp://hdl.handle.net/11336/136553
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4375422
dc.description.abstractA convenient synthetic approach to a cyclodeca[ij]isoquinoline derivative, which embodies the carbon skeleton of excentricine and related stephaoxocanes, is described. The synthesis involves the combined use of ring closing metathesis and Bischler-Napieralski cyclizations for the construction of the homocyclic and nitrogen-bearing rings, respectively.
dc.languageeng
dc.publisherPergamon-Elsevier Science Ltd
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0040402008014531
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.tet.2008.08.005
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectBISCHLER-NAPIERALSKI
dc.subjectEXCENTRICINE ANALOGUE
dc.subjectMACROLACTAM CYCLIZATION
dc.subjectRCM
dc.subjectSTEPHAOXOCANES
dc.titleA combined RCM-Bischler-Napieralski strategy towards the synthesis of the carbon skeleton of excentricine and related stephaoxocanes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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