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hal.structure.identifierSynthèse et réactivité des substances naturelles [SRSN]
dc.contributor.authorDELATOUCHE, Régis
hal.structure.identifierSynthèse et réactivité des substances naturelles [SRSN]
dc.contributor.authorLESAGE, Aurélien
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorCOLLETTE, Floraine
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorHÉROGUEZ, Valérie
hal.structure.identifierSynthèse et réactivité des substances naturelles [SRSN]
dc.contributor.authorBERTRAND, Philippe
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2011
dc.identifier.issn0004-9425
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20364
dc.description.abstractEnThe copper-catalyzed reaction of 1,1-dimethyl-O-propargyl aniline carbamates was studied and revealed the unexpected formation of oxazolidin-2-ones and alkylamines. An in-depth study of the reaction conditions showed that the formation of these products was highly dependent on the solvent, copper catalyst and aniline substituents. The reaction can be oriented towards oxazolidinones in pyridine and alkylamines in ethanol, whereas cycloaddition can be achieved in dry tetrahydrofuran.
dc.language.isoen
dc.publisherCSIRO Publishing
dc.subject.enISOCYANATES
dc.subject.en4-METHYLENE-2-OXAZOLIDINONES
dc.subject.enALCOHOLS
dc.subject.enCLICK CHEMISTRY
dc.subject.enCATALYZED CYCLIZATION
dc.subject.enPROPARGYL CARBONATES
dc.subject.enCONVENIENT SYNTHESIS
dc.subject.enMILD CONDITIONS
dc.subject.enAMINES
dc.subject.enBOND
dc.title.enInvestigations into Competitive Cycloaddition/Cyclization or Elimination from 1,1-Dimethyl-propargylcarbamates of Anilines
dc.typeArticle de revue
dc.identifier.doi10.1071/CH10344
dc.subject.halChimie/Polymères
bordeaux.journalAustralian Journal of Chemistry
bordeaux.page166-173
bordeaux.volume64
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue2
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00947153
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00947153v1
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