Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/24707

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dc.contributor.authorDuñach, E.-
dc.contributor.authorMedeiros, M. J.-
dc.contributor.authorOlivero, S.-
dc.date.accessioned2013-07-16T13:14:55Z-
dc.date.available2013-07-16T13:14:55Z-
dc.date.issued2013-04-27-
dc.identifier.issn0013-4651por
dc.identifier.urihttps://hdl.handle.net/1822/24707-
dc.description.abstractThe electrochemical intramolecular cyclisation of bromoalkoxylated derivatives 1 was carried out using Ni(II) complexes as the catalysts in ethanol solutions by constant-current electrolysis in one-compartment cell in the absence of sacrificial anodes as an environmentally friendly system. The reduction of the substrates proceeds via one-electron cleavage of the carbon–bromine bond to form radical-type intermediates that undergo cyclisation to afford cyclic ethers in moderate to good yields.por
dc.description.sponsorshipFundação para a Ciência e a Tecnologia (FCT)por
dc.language.isoengpor
dc.publisherThe Electrochemical Societypor
dc.rightsopenAccesspor
dc.subjectCyclizationpor
dc.subjectNickel(II) complexpor
dc.subjectElectroreductionpor
dc.subjectHeterocyclespor
dc.subjectEthanol solventpor
dc.titleElectrochemical catalytic cyclization reactions using environmentally friendly methodologiespor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttp://dx.doi.org/10.1149/2.016307jespor
sdum.publicationstatuspublishedpor
oaire.citationStartPageG3112por
oaire.citationEndPageG3116por
oaire.citationIssue7por
oaire.citationTitleJournal of The Electrochemical Societypor
oaire.citationVolume160por
dc.identifier.doi10.1149/2.016307jespor
dc.subject.wosScience & Technologypor
sdum.journalJournal of The Electrochemical Societypor
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