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Tandem palladium-catalyzed borylation and suzuki coupling (BSC) to thienocarbazole precursors

dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorKirsch, Gilbert
dc.date.accessioned2008-09-12T13:08:20Z
dc.date.available2008-09-12T13:08:20Z
dc.date.issued2003
dc.description.abstractSubstituted 2-methyl-2'-nitro diaryl compounds in the benzo[b]thiophene series were prepared by palladium-catalyzed, two-step, one-pot borylation/Suzuki coupling (BSC) reaction in good to high yields. The borylation reaction was performed on methylated 6-bromobenzo[b]thiophenes using pinacolborane and was followed by in situ Suzuki coupling with substituted (CF3, OMe) 2-bromonitrobenzenes. The compounds obtained were cyclized to the corresponding ring A substituted thienocarbazoles which can have biological activity or/and be used as biomarkers due to their fluorescence properties and possible DNA intercalation.en
dc.identifier.citationFerreira, Isabel C.F.R.; Queiroz, Maria João R.P.; Kirsch, Gilbert (2003). Tandem palladium-catalyzed borylation and suzuki coupling (BSC) to thienocarbazole precursors. Tetrahedron Letters. ISSN 0040-4039. 44:23 (2003) p. 4327-4329en
dc.identifier.doi10.1016/S0040-4039(03)00952-3
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10198/819
dc.language.isoengen
dc.publisherElsevieren
dc.subjectPalladiumen
dc.subjectBorylationen
dc.subjectSuzuki couplingen
dc.subject2-methyl-2'-nitro biarylsen
dc.subjectBenzo[b]thiophenesen
dc.titleTandem palladium-catalyzed borylation and suzuki coupling (BSC) to thienocarbazole precursorsen
dc.typejournal article
dspace.entity.typePublication
person.familyNameFerreira
person.givenNameIsabel C.F.R.
person.identifier144781
person.identifier.ciencia-id9418-CF95-9919
person.identifier.orcid0000-0003-4910-4882
person.identifier.ridE-8500-2013
person.identifier.scopus-author-id36868826600
rcaap.rightsopenAccess
rcaap.typearticleen
relation.isAuthorOfPublicationbd0d1537-2e03-41fb-b27a-140af9c35db8
relation.isAuthorOfPublication.latestForDiscoverybd0d1537-2e03-41fb-b27a-140af9c35db8

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