Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/5861
DC FieldValueLanguage
dc.contributor.authorSilvestre, Samuel M.-
dc.contributor.authorSalvador, Jorge A. R.-
dc.date.accessioned2008-09-26T17:43:04Z-
dc.date.available2008-09-26T17:43:04Z-
dc.date.issued2007en_US
dc.identifier.citationTetrahedron. 63:11 (2007) 2439-2445en_US
dc.identifier.urihttp://hdl.handle.net/10316/5861-
dc.description.abstractVarious allylic and benzylic substrates were selectively oxidized to the corresponding enones in good yields using sodium chlorite, either in combination with tert-butyl hydroperoxide in stoichiometric conditions, or associated with N-hydroxyphthalimide as catalyst. These oxidation reactions were effectively and economically performed under mild, transition-metal free conditions and therefore the dual challenge of cost effectiveness and benign nature of the processes was met with.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6THR-4MT5JX3-5/1/64e51e9b1aae448b3f47f8c2efad85afen_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectSodium chloriteen_US
dc.subjectAllylic oxidationen_US
dc.subjectBenzylic oxidationen_US
dc.subjectTransition-metal freeen_US
dc.titleAllylic and benzylic oxidation reactions with sodium chloriteen_US
dc.typearticleen_US
dc.identifier.doi10.1016/j.tet.2007.01.012-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptFaculty of Pharmacy-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-4297-5108-
crisitem.author.orcid0000-0003-0779-6083-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
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