A concise route to the azaspirodecane moiety of halichlorine and structurally related alkaloids

dc.creatorde Sousa, AL
dc.creatorPilli, RA
dc.date2005
dc.dateAPR 14
dc.date2014-11-19T05:08:51Z
dc.date2015-11-26T17:57:40Z
dc.date2014-11-19T05:08:51Z
dc.date2015-11-26T17:57:40Z
dc.date.accessioned2018-03-29T00:41:13Z
dc.date.available2018-03-29T00:41:13Z
dc.identifierOrganic Letters. Amer Chemical Soc, v. 7, n. 8, n. 1617, n. 1619, 2005.
dc.identifier1523-7060
dc.identifierWOS:000228344200046
dc.identifier10.1021/ol050306g
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/53011
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/53011
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/53011
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1291543
dc.descriptionA tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrangement provided the corresponding [5.4.0] azaspirobicyclodecane, a key intermediate in our synthetic route to the marine alkaloid halichlorine (1).
dc.description7
dc.description8
dc.description1617
dc.description1619
dc.languageen
dc.publisherAmer Chemical Soc
dc.publisherWashington
dc.publisherEUA
dc.relationOrganic Letters
dc.relationOrg. Lett.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectPinnaic Acid
dc.subjectSpirocyclic Core
dc.subject(+/-)-pinnaic Acid
dc.subjectTricyclic Core
dc.subjectDaphniphyllum Alkaloids
dc.subject(+/-)-halichlorine
dc.subjectConstruction
dc.subjectEntry
dc.subject(&/-)-perhydrohistrionicotoxin
dc.subjectCyclopentanones
dc.titleA concise route to the azaspirodecane moiety of halichlorine and structurally related alkaloids
dc.typeArtículos de revistas


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