dc.creatorSchuchardt, U
dc.creatorMandelli, D
dc.creatorShulpin, GB
dc.date1996
dc.dateSEP 2
dc.date2014-12-16T11:32:22Z
dc.date2015-11-26T17:29:38Z
dc.date2014-12-16T11:32:22Z
dc.date2015-11-26T17:29:38Z
dc.date.accessioned2018-03-29T00:16:36Z
dc.date.available2018-03-29T00:16:36Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 37, n. 36, n. 6487, n. 6490, 1996.
dc.identifier0040-4039
dc.identifierWOS:A1996VE83100018
dc.identifier10.1016/0040-4039(96)01418-9
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/56653
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/56653
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/56653
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1285325
dc.descriptionAlkanes (cyclohexane, cyclooctane, n-heptane) and aromatic compounds (benzene, toluene, and ethylbenzene) are oxidized by anhydrous H2O2 in MeCN in air in the presence of catalytic amounts of MTO. The reaction is accelerated by addition of pyrazine-2-carboxylic acid. Alkanes give alkyl hydroperoxides as main products, as well as alcohols and ketones. Arenes yield predominantly phenols. Copyright (C) 1996 Elsevier Science Ltd
dc.description37
dc.description36
dc.description6487
dc.description6490
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectHydrogen-peroxide
dc.subjectAlkyl Peroxides
dc.subjectAcid Reagent
dc.subjectAlkanes
dc.subjectSystem
dc.subjectCyclohexane
dc.subjectEpoxidation
dc.subjectAlcohols
dc.subjectPhenols
dc.titleMethyltrioxorhenium catalyzed oxidation of saturated and aromatic hydrocarbons by H2O2 in air
dc.typeArtículos de revistas


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