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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/66244
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dc.contributor.authorZim, Danilo-
dc.contributor.authorGruber, Adriane S.-
dc.contributor.authorEbeling, Gunter-
dc.contributor.authorDupont, Jairton-
dc.contributor.authorMonteiro, Adriano L.-
dc.date.accessioned2014-05-27T11:19:57Z-
dc.date.accessioned2016-10-25T18:16:33Z-
dc.date.available2014-05-27T11:19:57Z-
dc.date.available2016-10-25T18:16:33Z-
dc.date.issued2000-09-07-
dc.identifierhttp://dx.doi.org/10.1021/ol0063048-
dc.identifier.citationOrganic Letters, v. 2, n. 18, p. 2881-2884, 2000.-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/11449/66244-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/66244-
dc.description.abstractCyclopalladated compounds derived from the ortho-metalation of benzylic tert-butyl thioethers are excellent catalyst precursors for the Suzuki cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under mild reaction conditions. A broad range of substrates and functional groups are tolerated in this protocol, and highly catalytic activity is attained.en
dc.format.extent2881-2884-
dc.language.isoeng-
dc.sourceScopus-
dc.titleSulfur-containing palladacycles: Efficient phosphine-free catalyst precursors for the Suzuki cross-coupling reaction at room temperatureen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLaboratory of Molecular Catalysis Instituto de Química UFRGS, Av. Bento Gonçalves, 9500 Porto Alegre, RS 91501-970-
dc.description.affiliationCPGQ-UNESP Instituto de Química, Araraquara, SP-
dc.description.affiliationUnespCPGQ-UNESP Instituto de Química, Araraquara, SP-
dc.identifier.doi10.1021/ol0063048-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofOrganic Letters-
dc.identifier.scopus2-s2.0-0001292112-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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