Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/26848
DC FieldValueLanguage
dc.contributor.authorPereira, Nelson A. M.-
dc.contributor.authorLemos, Américo-
dc.contributor.authorSerra, Arménio C.-
dc.contributor.authorMelo, Teresa M. V. D. Pinho e-
dc.date.accessioned2014-09-23T10:32:29Z-
dc.date.available2014-09-23T10:32:29Z-
dc.date.issued2013-03-20-
dc.identifier.citationPEREIRA, Nelson A. M. [et al.] - Functionalization of dipyrromethanes via hetero-Diels–Alder reaction with azo- and nitrosoalkenes. "Tetrahedron Letters". ISSN 0040-4039. Vol. 54 Nº 12 (2013) p. 1553-1557por
dc.identifier.issn0040-4039-
dc.identifier.urihttps://hdl.handle.net/10316/26848-
dc.description.abstract5,5′-Diethyl- and 5-phenyldipyrromethanes participate in cycloadditions with azo- and nitrosoalkenes giving dipyrromethanes with side chains containing open chain oximes and hydrazones. By controlling reaction stoichiometry it is possible to get mono or 1,9-disubstituted derivatives. The reported methodology gave access to a range of dipyrromethanes with good structural features for various applications. It was demonstrated that reduction of dipyrromethanes containing α-oximino ester groups opens the way to new α-amino esters.por
dc.language.isoengpor
dc.publisherElsevierpor
dc.rightsopenAccesspor
dc.subjectDipyrromethanespor
dc.subjectAzoalkenespor
dc.subjectNitrosoalkenespor
dc.subjectHetero-Diels–Alder reactionpor
dc.titleFunctionalization of dipyrromethanes via hetero-Diels–Alder reaction with azo- and nitrosoalkenespor
dc.typearticlepor
degois.publication.firstPage1553por
degois.publication.lastPage1557por
degois.publication.issue12por
degois.publication.titleTetrahedron Letterspor
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0040403913000683por
dc.peerreviewedYespor
dc.identifier.doi10.1016/j.tetlet.2013.01.032-
degois.publication.volume54por
uc.controloAutoridadeSim-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCEMMPRE - Centre for Mechanical Engineering, Materials and Processes-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-1891-9010-
crisitem.author.orcid0000-0001-9588-4555-
crisitem.author.orcid0000-0001-8664-2757-
crisitem.author.orcid0000-0003-3256-4954-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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