Sulfenylation of nitroalkanes and hydroxyaryls

dc.creatorBlanco, Guillermo Aldo
dc.creatorBaumgartner, Maria Teresa del V.
dc.date.accessioned2018-10-03T19:15:54Z
dc.date.accessioned2018-11-06T15:42:32Z
dc.date.available2018-10-03T19:15:54Z
dc.date.available2018-11-06T15:42:32Z
dc.date.created2018-10-03T19:15:54Z
dc.date.issued2011-12
dc.identifierBlanco, Guillermo Aldo; Baumgartner, Maria Teresa del V.; Sulfenylation of nitroalkanes and hydroxyaryls; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 52; 52; 12-2011; 7061-7063
dc.identifier0040-4039
dc.identifierhttp://hdl.handle.net/11336/61611
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1900015
dc.description.abstractThe sulfenylation of nitroalkanes and hydroxyaryls in DMSO using aryl disulfides as sulfenylating reagents was studied. The corresponding arylthionitroalkanes and arylthiohydroxyaryls were obtained in moderate to good yields in very mild conditions, thus improving the reported procedures for the synthesis of these compounds. © 2011 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherPergamon-Elsevier Science Ltd
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.tetlet.2011.10.053
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0040403911017825
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectDIMETHYLSULFOXIDE
dc.subjectDISULFIDES
dc.subjectHYDROXYARYLS
dc.subjectNITROALKANES
dc.subjectSULFENYLATION
dc.titleSulfenylation of nitroalkanes and hydroxyaryls
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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