dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorWladislaw, B.
dc.creatorDiVitta, C.
dc.creatorMarzorati, L.
dc.creatorCampos, IPD
dc.creatorLucchini, V
dc.date2014-05-20T15:21:40Z
dc.date2016-10-25T17:55:11Z
dc.date2014-05-20T15:21:40Z
dc.date2016-10-25T17:55:11Z
dc.date1997-04-14
dc.date.accessioned2017-04-05T23:32:45Z
dc.date.available2017-04-05T23:32:45Z
dc.identifierTetrahedron Letters. Oxford: Pergamon-Elsevier B.V., v. 38, n. 15, p. 2625-2628, 1997.
dc.identifier0040-4039
dc.identifierhttp://hdl.handle.net/11449/32789
dc.identifierhttp://acervodigital.unesp.br/handle/11449/32789
dc.identifier10.1016/S0040-4039(97)00446-2
dc.identifierWOS:A1997WT46400013
dc.identifierhttp://dx.doi.org/10.1016/S0040-4039(97)00446-2
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/877056
dc.description2,3-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.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationTetrahedron Letters
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleNovel stereoselective addition of some nucleophiles to 2,3-bis(methylsulfanyl) norbornenobenzoquinone
dc.typeOtro


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