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Novel stereoselective addition of some nucleophiles to 2,3-bis(methylsulfanyl) norbornenobenzoquinone

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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.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUNIV VENICE
dc.date.accessioned2014-05-20T15:21:40Z
dc.date.available2014-05-20T15:21:40Z
dc.date.issued1997-04-14
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.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.format.extent2625-2628
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.doi10.1016/S0040-4039(97)00446-2
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/11449/32789
dc.identifier.wosWOS:A1997WT46400013
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofTetrahedron Letters
dc.relation.ispartofjcr2.125
dc.relation.ispartofsjr0,683
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleNovel stereoselective addition of some nucleophiles to 2,3-bis(methylsulfanyl) norbornenobenzoquinoneen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication

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