Repository logo
 
Publication

Synthesis and antioxidant activity of new methoxylated di(hetero)arylamines derivatives of thieno[3,2-b]pyridines,

dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorCalhelha, Ricardo C.
dc.contributor.authorAbreu, Rui M.V.
dc.contributor.authorFerreira, Isabel C.F.R.
dc.date.accessioned2011-03-22T14:58:54Z
dc.date.available2011-03-22T14:58:54Z
dc.date.issued2008
dc.description.abstractDue to their isosterism with pyrrolopyridines or quinolines, thieno[3,2-b]pyridines have attracted much attention because of their potential biological activity [1]. We have prepared the 6-bromothieno[3,2-b]pyridine 1, following a known method used by us for benzo[b]thiophene compounds [2], as component for palladium-catalyzed Buchwald-Hartwig coupling with methoxylated ani lines. The corresponding di(hetero)arylamines 2a-2d were obtained in good yields and were fully characterized (Scheme 1).por
dc.identifier.citationQueiroz, Maria-João R.P.; Calhelha, Ricardo C.; Abreu, Rui M.V.; Ferreira, Isabel C.F.R. (2008). Synthesis and antioxidant activity of new methoxylated di(hetero)arylamines derivatives of thieno[3,2-b]pyridines. In International Conference in Medicinal Chemistry: Interfacing Chemical Biology, Natural Products and Drug Discovery. Angerspor
dc.identifier.urihttp://hdl.handle.net/10198/3708
dc.language.isoengpor
dc.relationSFRH/BD/27294/2006
dc.relationEVALUATION OF ANTIOXIDANT ACTIVITY OF DI HETEROARYLAMINES AND ANTITUMORAL ACTIVITY OF POLTCYCLIC HETEROAROMATIC COMPOUNDS, INCLUDING MOLECULAR MODELLING STUDIES
dc.titleSynthesis and antioxidant activity of new methoxylated di(hetero)arylamines derivatives of thieno[3,2-b]pyridines,por
dc.typeconference object
dspace.entity.typePublication
oaire.awardTitleEVALUATION OF ANTIOXIDANT ACTIVITY OF DI HETEROARYLAMINES AND ANTITUMORAL ACTIVITY OF POLTCYCLIC HETEROAROMATIC COMPOUNDS, INCLUDING MOLECULAR MODELLING STUDIES
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F27430%2F2006/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCI%2FQUI%2F59407%2F2004/PT
oaire.citation.conferencePlaceAngers, Françapor
oaire.citation.titleInternational Conference in Medicinal Chemistry: Interfacing Chemical Biology, Natural Products and Drug Discoverypor
oaire.fundingStreamPOCI
person.familyNameCalhelha
person.familyNameAbreu
person.familyNameFerreira
person.givenNameRicardo C.
person.givenNameRui M.V.
person.givenNameIsabel C.F.R.
person.identifier144781
person.identifier.ciencia-idF313-E3CE-554E
person.identifier.ciencia-id0F19-0DE2-12A2
person.identifier.ciencia-id9418-CF95-9919
person.identifier.orcid0000-0002-6801-4578
person.identifier.orcid0000-0002-7745-8015
person.identifier.orcid0000-0003-4910-4882
person.identifier.ridJ-2172-2014
person.identifier.ridE-8500-2013
person.identifier.scopus-author-id6507978333
person.identifier.scopus-author-id7003290613
person.identifier.scopus-author-id36868826600
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
relation.isAuthorOfPublication2d5d1a41-7561-4a01-871c-b4c97da35053
relation.isAuthorOfPublicationcadb03a4-5e60-4745-b35f-fc3a97c071bc
relation.isAuthorOfPublicationbd0d1537-2e03-41fb-b27a-140af9c35db8
relation.isAuthorOfPublication.latestForDiscoverybd0d1537-2e03-41fb-b27a-140af9c35db8
relation.isProjectOfPublication0f32cd6d-2cff-4db8-96c9-c646917cd612
relation.isProjectOfPublication524521dd-d586-4707-8194-a22aae8ed9f4
relation.isProjectOfPublication.latestForDiscovery524521dd-d586-4707-8194-a22aae8ed9f4

Files

Original bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
Int_24.pdf
Size:
803.29 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: