Addition of carbon nucleophiles to substituted N-acyliminium ions. A stereoselective route to trans-fused decahydroquinoline systems

dc.creatorMaldaner, AO
dc.creatorPilli, RA
dc.date2000
dc.dateOCT 7
dc.date2014-12-02T16:30:28Z
dc.date2015-11-26T16:44:24Z
dc.date2014-12-02T16:30:28Z
dc.date2015-11-26T16:44:24Z
dc.date.accessioned2018-03-28T23:29:45Z
dc.date.available2018-03-28T23:29:45Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 41, n. 41, n. 7843, n. 7846, 2000.
dc.identifier0040-4039
dc.identifierWOS:000089809800012
dc.identifier10.1016/S0040-4039(00)01362-9
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/76709
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/76709
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/76709
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1273914
dc.descriptionA stereoselective route to trans-fused 2-substituted decahydroquinoline hydrochloride 11 featuring the addition of allyl tri-n-butyltin to a disubstituted N-acyliminium ion derived from glutarimide, followed by ring-closing metathesis is described (seven steps, 13% overall yield from lactam 4). (C) 2000 Elsevier Science Ltd. All rights reserved.
dc.description41
dc.description41
dc.description7843
dc.description7846
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectN-acyliminium ions
dc.subjectmetathesis
dc.subjectpiperidinones
dc.subjectdecahydroquinolines
dc.subjectDendrobatid Poison Frogs
dc.subjectAlkaloids
dc.subjectLactams
dc.subjectCis
dc.titleAddition of carbon nucleophiles to substituted N-acyliminium ions. A stereoselective route to trans-fused decahydroquinoline systems
dc.typeArtículos de revistas


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