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dc.contributor.authorWladislaw, B.-
dc.contributor.authorDiVitta, C.-
dc.contributor.authorMarzorati, L.-
dc.contributor.authorCampos, IPD-
dc.contributor.authorLucchini, V-
dc.date.accessioned2014-05-20T15:21:40Z-
dc.date.accessioned2016-10-25T17:55:11Z-
dc.date.available2014-05-20T15:21:40Z-
dc.date.available2016-10-25T17:55:11Z-
dc.date.issued1997-04-14-
dc.identifierhttp://dx.doi.org/10.1016/S0040-4039(97)00446-2-
dc.identifier.citationTetrahedron Letters. Oxford: Pergamon-Elsevier B.V., v. 38, n. 15, p. 2625-2628, 1997.-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/11449/32789-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/32789-
dc.description.abstract2,3-Bis(methylsulfanyl)norbomenobenzoquinone undergoes reaction with nitrogen, oxygen, sulfur or carbon nucleophiles to give the trisubstituted adducts containing the new substituent at the ring junction. Their configurations are assigned by H-1 NMR spectroscopy and NOE enhancement experiments. (C) 1997 Elsevier B.V. Ltd.en
dc.format.extent2625-2628-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.titleNovel stereoselective addition of some nucleophiles to 2,3-bis(methylsulfanyl) norbornenobenzoquinoneen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUNIV VENICE-
dc.description.affiliationUNIV ESTADUAL PAULISTA,INST CIENCIAS EXATAS & TECNOL,BR-06500970 SANTANA PARNA,SP,BRAZIL-
dc.description.affiliationUNIV VENICE,DIPARTIMENTO SCI AMBIENTALI,I-30123 VENICE,ITALY-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,INST CIENCIAS EXATAS & TECNOL,BR-06500970 SANTANA PARNA,SP,BRAZIL-
dc.identifier.doi10.1016/S0040-4039(97)00446-2-
dc.identifier.wosWOS:A1997WT46400013-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTetrahedron Letters-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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