Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/10646

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Campo DCValorIdioma
dc.contributor.authorSalaheldin, Abdellatif M.-
dc.contributor.authorCampos, Ana M. F. Oliveira-
dc.contributor.authorParpot, Pier-
dc.contributor.authorRodrigues, Lígia M.-
dc.contributor.authorOliveira, M. Manuel-
dc.contributor.authorPeixoto, Francisco-
dc.date.accessioned2010-06-07T13:33:37Z-
dc.date.available2010-06-07T13:33:37Z-
dc.date.issued2010-02-
dc.identifier.citation“Helvetica Chimica Acta”. ISSN 0018-019X. 93:2 (Febr. 2010) 242-248.por
dc.identifier.issn0018-019Xpor
dc.identifier.urihttps://hdl.handle.net/1822/10646-
dc.description.abstractAn easy preparation of 4-aminopyrrole-3-carbonitrile derivatives, and their transformation into new substituted pyrrolo[3,2-b]pyridines is described, in one step, via Friedländer reaction under microwave irradiation and classical heating methods. The use of microwave irradiation led to high conversion and shorter times.por
dc.description.sponsorshipFundação para a Ciência e a Tecnologia (FCT) - NMR Network, REEQ/ 630/QUI/2005, SFRH/BPD/31490/2006por
dc.description.sponsorshipFundo Europeu de Desenvolvimento Regional (FEDER)por
dc.language.isoengpor
dc.publisherVerlag Helvetica Chimica Actapor
dc.rightsopenAccesspor
dc.subjectTacrinepor
dc.subjectFriedländer reactionpor
dc.subjectAlzheimer diseasepor
dc.subjectAcetylcholinesterasepor
dc.subjectThorpe-Ziegler cyclizationpor
dc.subjectMicrowave irradiationpor
dc.titleSynthesis of new tacrine analogues from 4-amino-1H-pyrrole-3-carbonitrilepor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage242por
oaire.citationEndPage248por
oaire.citationIssue2por
oaire.citationVolume93por
dc.identifier.eissn1522-2675-
dc.identifier.doi10.1002/hlca.200900190por
dc.subject.wosScience & Technologypor
sdum.journalHelvetica Chimica Actapor
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