Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/72925

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dc.contributor.authorRodrigues, Anabelapor
dc.contributor.authorFerreira, Paula M. T.por
dc.contributor.authorMonteiro, Luís S.por
dc.date.accessioned2021-05-27T15:01:32Z-
dc.date.available2021-05-27T15:01:32Z-
dc.date.issued2004-09-13-
dc.identifier.issn0040-4020por
dc.identifier.urihttps://hdl.handle.net/1822/72925-
dc.description.abstractN,N-Bis-(tert-butoxycarbonyl)-2,5-bis-methoxycarbonyl-1,4-dihydropyrazine can be obtained in high yield by treatment of the methyl ester of N-(4-toluenesulfonyl)-N-(tert-butoxycarbonyl)-alpha,beta-didehydroalanine with dimethylaminopyridine and potassium carbonate. This compound was used as substrate in Michael addition reactions with several types of nucleophiles. The electrochemical behaviour of this pyrazine derivative was also studied by cyclic voltammetry and by controlled potential electrolysis.por
dc.description.sponsorshipWe wish to thank the Fundação para a Ciência e a Tecnologia for financial support (project no. POCTI/1999/QUI/32689).por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.relationPOCTI/1999/QUI/32689por
dc.rightsopenAccesspor
dc.subjectDehydroalaninespor
dc.subject1,4-dihydropyrazinepor
dc.subjectPyrazinepor
dc.subjectMichael addditionpor
dc.subjectElectrolysispor
dc.titleSynthesis and reactivity of a 1,4-dihydropyrazine derivativepor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0040402004010464por
oaire.citationStartPage8489por
oaire.citationEndPage8496por
oaire.citationIssue38por
oaire.citationVolume60por
dc.date.updated2021-05-24T15:18:31Z-
dc.identifier.doi10.1016/j.tet.2004.06.127por
dc.subject.wosScience & Technology-
sdum.export.identifier10827-
sdum.journalTetrahedronpor
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