1. Universidade do Minho
  2. Escola de Ciências | School of Sciences
  3. Centro\Departamento de Química
  4. CDQuim - Artigos (Papers)
Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/10658

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Campo DCValorIdioma
dc.contributor.authorRaposo, M. Manuela M.-
dc.contributor.authorSampaio, Ana M. B. A.-
dc.contributor.authorKirsch, G.-
dc.date.accessioned2010-06-11T11:22:54Z-
dc.date.available2010-06-11T11:22:54Z-
dc.date.issued2005-
dc.identifier.citation"Synthesis : Journal of Synthetic Organic Chemistry". ISSN 0039-7881. 2 (Febr. 2005) 199-210.por
dc.identifier.issn0039-7881por
dc.identifier.urihttps://hdl.handle.net/1822/10658-
dc.description.abstract1-Aryl-2-thienyl-substituted pyrroles and/or 5-arylamino-2,2´-bithiophenes were synthesized by treatment of arylaminothieno-oxobutanamides with Lawesson’s reagent. These in turn were prepared by direct amidation of 4-oxo-(2-thienyl)butanoic acid through DCC–BtOH mediated reactions.por
dc.description.sponsorshipFundação para a Ciência e Tecnologia (FCT)por
dc.language.isoengpor
dc.publisherGeorg Thieme Verlagpor
dc.rightsopenAccesspor
dc.subjectSynthesispor
dc.subjectAmidespor
dc.subjectPyrrolespor
dc.subjectBithiophenespor
dc.subjectFriedel-Crafts reactionpor
dc.subjectLawesson´s reagentpor
dc.subjectAylamino-thieno-oxobutanamidespor
dc.subjectPi-conjugated systemspor
dc.subjectPrecursors of nonlinear optical (NLO) materialspor
dc.subjectPrecursors of organic conductive polymerspor
dc.subjectheterocyclespor
dc.subjectsubstituent effectspor
dc.subjectbicyclic compoundspor
dc.titleArylamino-thieno-oxobutanamides under Lawesson’s conditions : competition between thienylpyrrole and bithiophene formationpor
dc.typearticlepor
dc.peerreviewedyespor
sdum.pagination199-210por
sdum.publicationstatuspublishedpor
sdum.volume2por
oaire.citationStartPage199por
oaire.citationEndPage210por
oaire.citationIssue2por
dc.identifier.doi10.1055/s-2004-834952por
dc.subject.wosScience & Technologypor
sdum.journalSynthesispor
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