Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/51975

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dc.contributor.authorMarinho, Elina Margarida Ribeiropor
dc.contributor.authorProença, M. Fernanda R. P.por
dc.date.accessioned2018-03-09T15:49:16Z-
dc.date.available2018-03-09T15:49:16Z-
dc.date.issued2015-
dc.identifier.issn0039-7881por
dc.identifier.urihttps://hdl.handle.net/1822/51975-
dc.description.abstract2-Substituted 4-(arylamino) quinazolines were prepared from 2-(acylamino) benzonitriles and primary arylamines by refluxing in either ethanol using trifluoroacetic acid as a catalyst or acetic acid. The 2-aminobenzonitrile was acylated by reaction with anhydrides, isocyanates, or ethyl chloroformate at room temperature.por
dc.description.sponsorshipWe gratefully acknowledge the financial support by the University of Minho and FCT through the Portuguese NMR network (RNRMN), the Project F-COMP-01-00124-FEDER-022716 (ref. FCT PEst-C/QUI/UI0686/2011) FEDER-COMPETE, and a PhD grant awarded to Elina Marinho (SFRH/BD/73659/2010).por
dc.language.isoengpor
dc.publisherGeorg Thieme Verlagpor
dc.relationPEst-C/QUI/UI0686/2011por
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F73659%2F2010/PTpor
dc.rightsrestrictedAccesspor
dc.subjectacylationpor
dc.subjectcyclizationpor
dc.subjectheterocyclespor
dc.subject4-aminoquinazolinespor
dc.subject2-aminobenzonitrilepor
dc.titleThe reaction of 2-(Acylamino) benzonitriles with primary aromatic amines: A convenient synthesis of 2-substituted 4-(Arylamino) quinazolinespor
dc.typearticle-
dc.peerreviewedyespor
oaire.citationStartPage1623por
oaire.citationEndPage1632por
oaire.citationIssue11por
oaire.citationVolume47por
dc.date.updated2018-03-09T15:37:32Z-
dc.identifier.doi10.1055/s-0034-1380322por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technology-
sdum.export.identifier4343-
sdum.journalSynthesispor
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