Synthesis of unexpected six-membered imides by free-radical carbocyclisation on carbohydrate templates

dc.creatorde Oliveira, RB
dc.creatorde Souza, JD
dc.creatorPrado, MAF
dc.creatorEberlin, MN
dc.creatorMeurer, EC
dc.creatorSantos, LS
dc.creatorAlves, RJ
dc.date2004
dc.dateOCT 25
dc.date2014-11-15T15:56:24Z
dc.date2015-11-26T17:20:41Z
dc.date2014-11-15T15:56:24Z
dc.date2015-11-26T17:20:41Z
dc.date.accessioned2018-03-29T00:08:16Z
dc.date.available2018-03-29T00:08:16Z
dc.identifierTetrahedron. Pergamon-elsevier Science Ltd, v. 60, n. 44, n. 9901, n. 9908, 2004.
dc.identifier0040-4020
dc.identifierWOS:000224333000011
dc.identifier10.1016/j.tet.2004.08.039
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/79271
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/79271
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/79271
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1283196
dc.descriptionFree-radical reactions of amido-esters anchored to a carbohydrate derived from methyl alpha-D-glucopyranoside afforded unexpected six-membered cyclic imides. Their structures were elucidated by ESI-MS/MS and NMR spectral analyses, and a mechanism for the formation of these imides is proposed. (C) 2004 Elsevier Ltd. All rights reserved.
dc.description60
dc.description44
dc.description9901
dc.description9908
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron
dc.relationTetrahedron
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectradical cyclisation
dc.subjectcarbohydrate
dc.subjectimides
dc.subjectCyclization
dc.subjectBenzomacrolactam
dc.subjectMacrocyclization
dc.subjectSugars
dc.titleSynthesis of unexpected six-membered imides by free-radical carbocyclisation on carbohydrate templates
dc.typeArtículos de revistas


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