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dc.contributor.authorFeberero García, Claudia 
dc.contributor.authorVelasco, Rocío
dc.contributor.authorSanz Díez, Roberto 
dc.date.accessioned2016-11-24T08:10:48Z
dc.date.available2017-11-01T03:45:07Z
dc.date.issued2016-11
dc.identifier.issn1434-193X
dc.identifier.urihttp://hdl.handle.net/10259/4281
dc.description.abstractNew dihalosalicylamides and trihalophenol derivatives have been synthesized from easily available O-(3,n-dihalophenyl) N,N-diethylcarbamates by using a directed ortho-metalation (DoM) strategy. The o-lithiation reactions with sBuLi take place regioselectively at the doubly activated C-2 position, which demonstrates the ability of O-carbamates as directed metalating groups. In addition, highly functionalized arylnitriles were accessed from organolithium intermediates by using a tandem transnitrilation/SNAr reaction sequence.en
dc.description.sponsorshipJunta de Castilla y León (Consejería de Educación) and FEDER (BU237U13 and BU076U16) as well as the Ministerio de Economía y Competitividad (MINECO) and FEDER (CTQ2013-48937-C2-1-P)en
dc.format.mimetypeapplication/pdf
dc.language.isospaes
dc.publisherWiley-VCH Verlagen
dc.relation.ispartofEuropean Journal of Organic Chemistry. 2016, n. 33, p. 5445–5587en
dc.subject.otherChemistry, Organicen
dc.subject.otherQuímica orgánicaes
dc.titleortho-Lithiation Reactions of O-(3,n-Dihalophenyl) N,N-Diethylcarbamates: Synthesis of Dihalosalicylamides and 2,3,n-Trihalophenol Derivativesen
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttp://dx.doi.org/10.1002/ejoc.201600933
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersionen


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