Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/1971

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dc.contributor.authorRodrigues, Lígia M.-
dc.contributor.authorCampos, Ana M. F. Oliveira-
dc.contributor.authorKaja, Martin-
dc.contributor.authorHrdina, Radim-
dc.date.accessioned2005-06-06T12:32:56Z-
dc.date.available2005-06-06T12:32:56Z-
dc.date.issued2004-05-
dc.identifier.citationINTERNATIONAL CONFERENCE ON DYES PIGMENTS AND FUNCTIONAL DYES, 10, Pardubice, República Checa, 2004. [S.l. : s.n.], [2004?].eng
dc.identifier.urihttps://hdl.handle.net/1822/1971-
dc.description.abstractDiazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with two carbon sources and base gave the corresponding new 4-amino-3-cyanopyrazoles, in moderate yields. In one case the corresponding oxo-pyrazolopyrimidine was prepared.eng
dc.description.sponsorshipFundação para a Ciência e Tecnologia - Programa Sócrates.eng
dc.language.isoengeng
dc.publisherResearch Institute of Organic Synthesiseng
dc.rightsopenAccesseng
dc.subjectCyanopyrazoleeng
dc.subjectOxo-pyrazolopyrimidineeng
dc.subjectPyrazoleeng
dc.titleSynthesis of novel derivatives of a versatile synthon : 4-amino-3-cyanopyrazoleeng
dc.typeconferencePapereng
dc.peerreviewedyeseng
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