A Concise Route To The Azaspirodecane Moiety Of Halichlorine And Structurally Related Alkaloids.

dc.creatorde Sousa, Andrea L
dc.creatorPilli, Ronaldo A
dc.date2005-Apr
dc.date2015-11-27T13:02:00Z
dc.date2015-11-27T13:02:00Z
dc.date.accessioned2018-03-29T01:00:39Z
dc.date.available2018-03-29T01:00:39Z
dc.identifierOrganic Letters. v. 7, n. 8, p. 1617-9, 2005-Apr.
dc.identifier1523-7060
dc.identifier10.1021/ol050306g
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/15816766
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/196219
dc.identifier15816766
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1296452
dc.description[reaction: see text] A 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.description1617-9
dc.languageeng
dc.relationOrganic Letters
dc.relationOrg. Lett.
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.subjectAlkaloids
dc.subjectAnimals
dc.subjectMolecular Structure
dc.subjectPorifera
dc.subjectSpiro Compounds
dc.subjectStereoisomerism
dc.titleA Concise Route To The Azaspirodecane Moiety Of Halichlorine And Structurally Related Alkaloids.
dc.typeArtículos de revistas


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