Addition of silylated carbon nucleophiles to iminium and cyclic N-acyliminium ions promoted by InCl3

dc.creatorRussowsky, D
dc.creatorPetersen, RZ
dc.creatorGodoi, MN
dc.creatorPilli, RA
dc.date2000
dc.dateDEC 16
dc.date2014-12-02T16:30:56Z
dc.date2015-11-26T17:41:02Z
dc.date2014-12-02T16:30:56Z
dc.date2015-11-26T17:41:02Z
dc.date.accessioned2018-03-29T00:22:47Z
dc.date.available2018-03-29T00:22:47Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 41, n. 51, n. 9939, n. 9942, 2000.
dc.identifier0040-4039
dc.identifierWOS:000165960100003
dc.identifier10.1016/S0040-4039(00)01828-1
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/76716
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/76716
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/76716
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1286894
dc.descriptionInCl3 was used as Lewis acid in the addition of silyl enolates and allyltrimethylsilane to aromatic aldimines and cyclic N-acyliminium ions derived from 5-acetoxylactams affording beta -aminocarbonyl systems and allyl adducts, respectively, in reasonable to good yields. The diastereofacial selectivity of cyclic N-acyliminium ions was investigated. (C) 2000 Elsevier Science Ltd. All rights reserved.
dc.description41
dc.description51
dc.description9939
dc.description9942
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.subjectMannich-type Reaction
dc.subjectEnol Ethers
dc.subjectComplex
dc.subjectKetones
dc.titleAddition of silylated carbon nucleophiles to iminium and cyclic N-acyliminium ions promoted by InCl3
dc.typeArtículos de revistas


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