The first examples of the enantioselective Heck-Matsuda reaction: arylation of unactivated cyclic olefins using chiral bisoxazolines

dc.creatorCorreia, CRD
dc.creatorOliveira, CC
dc.creatorSalles, AG
dc.creatorSantos, EAF
dc.date2012
dc.date46539
dc.date2014-07-30T19:41:15Z
dc.date2015-11-26T16:55:34Z
dc.date2014-07-30T19:41:15Z
dc.date2015-11-26T16:55:34Z
dc.date.accessioned2018-03-28T23:43:00Z
dc.date.available2018-03-28T23:43:00Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 53, n. 26, n. 3325, n. 3328, 2012.
dc.identifier0040-4039
dc.identifierWOS:000304851500031
dc.identifier10.1016/j.tetlet.2012.04.079
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/73651
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/73651
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1277160
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionSuccessful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96% isolated yields and in enantiomeric excesses of 54% up to 84%. (C) 2012 Elsevier Ltd. All rights reserved.
dc.description53
dc.description26
dc.description3325
dc.description3328
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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.subjectEnantioselective Heck-Matsuda
dc.subjectBisoxazolines
dc.subjectArenediazonium salts
dc.subjectCatalytic Asymmetric-synthesis
dc.subjectBis(oxazoline) Copper(ii) Complexes
dc.subjectDiazonium Salts
dc.subjectDecalin Derivatives
dc.subjectPalladium
dc.subjectMichael
dc.subjectAnalogs
dc.subjectLigand
dc.subjectEster
dc.subjectIons
dc.titleThe first examples of the enantioselective Heck-Matsuda reaction: arylation of unactivated cyclic olefins using chiral bisoxazolines
dc.typeArtículos de revistas


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