Diels-Alder reactions of 6-substituted 1-(p-nitrobenzoyl)-5,6-dihydro-2-pyridinones

dc.creatorDias, LC
dc.creatorFernandes, AMAP
dc.creatorZukerman-Schpector, J
dc.date2002
dc.dateJAN
dc.date2014-11-15T13:57:38Z
dc.date2015-11-26T16:11:28Z
dc.date2014-11-15T13:57:38Z
dc.date2015-11-26T16:11:28Z
dc.date.accessioned2018-03-28T22:59:58Z
dc.date.available2018-03-28T22:59:58Z
dc.identifierSynlett. Georg Thieme Verlag Kg, n. 1, n. 100, n. 104, 2002.
dc.identifier0936-5214
dc.identifierWOS:000173162300022
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/61725
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/61725
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/61725
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1267095
dc.descriptionThe first examples of Diels-Alder cycloaddition reactions of 6-substituted 1-(p-nitrobenzoyl)-5,6-dihydro-2-pyridinones are described. This reaction benefits from the fact that the diene adopts an endo orientation trans to the axial substituent at C-6 due to A(1.3) allylic type strain with the N-PNB protecting group.
dc.descriptiono TEXTO COMPLETO DESTE ARTIGO, ESTARÁ DISPONÍVEL À PARTIR DE AGOSTO DE 2015.
dc.description1
dc.description100
dc.description104
dc.languageen
dc.publisherGeorg Thieme Verlag Kg
dc.publisherStuttgart
dc.publisherAlemanha
dc.relationSynlett
dc.relationSynlett
dc.rightsembargo
dc.sourceWeb of Science
dc.subjectheterocycles
dc.subjectcycloadditions
dc.subjectalpha,beta-unsaturated lactams
dc.subjectA(1,3) allylic strain
dc.subjectcis-hydroisoquinotine
dc.subjectFunctionalized Cis-hydroisoquinolines
dc.subjectManzamine-a
dc.subjectTricyclic Core
dc.subjectDihydropyridinones
dc.titleDiels-Alder reactions of 6-substituted 1-(p-nitrobenzoyl)-5,6-dihydro-2-pyridinones
dc.typeArtículos de revistas


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