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dc.creatorSouza, Marcus .V. N. de-
dc.creatorAlmeida, Mauro Vieira de-
dc.date.accessioned2019-02-22T13:14:04Z-
dc.date.available2019-02-20-
dc.date.available2019-02-22T13:14:04Z-
dc.date.issued2002-02-
dc.citation.volume25pt_BR
dc.citation.issue1pt_BR
dc.citation.spage89pt_BR
dc.citation.epage98pt_BR
dc.identifier.doihttp://dx.doi.org/10.1590/S0100-40422002000100016pt_BR
dc.identifier.urihttps://repositorio.ufjf.br/jspui/handle/ufjf/9155-
dc.description.abstractIn this paper we describe a powerful methodology for the regiospecific construction of polysubstituted aromatic and heteroaromatic compounds. The DoM reaction (direct ortho-metalation) comprises the deprotonation in position ortho of a aromatic or heteroaromatic containing DMG (directed metalation group) by strong bases, normally an alkyllithium reagent, leading to an ortho-lithiated species. These species, upon treatment with electrophilic reagents, gives 1,2 disubstituted products.pt_BR
dc.description.resumo-pt_BR
dc.languageporpt_BR
dc.publisher-pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.initials-pt_BR
dc.relation.ispartofQuímica Novapt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectOrtho-metalationpt_BR
dc.subjectDirected metallation grouppt_BR
dc.subjectHeteroaromatic compoundspt_BR
dc.subject.cnpq-pt_BR
dc.titleReações de Ortometalacão em Piridinaspt_BR
dc.typeArtigo de Periódicopt_BR
Appears in Collections:Artigos de Periódicos



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