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<dc:title>ortho-Lithiation Reactions of O-(3,n-Dihalophenyl) N,N-Diethylcarbamates: Synthesis of Dihalosalicylamides and 2,3,n-Trihalophenol Derivatives</dc:title>
<dc:creator>Feberero, Claudia</dc:creator>
<dc:creator>Velasco, Rocío</dc:creator>
<dc:creator>Sanz Díez, Roberto</dc:creator>
<dc:description>New 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.</dc:description>
<dc:date>2016-11-24T08:10:48Z</dc:date>
<dc:date>2017-11-01T03:45:07Z</dc:date>
<dc:date>2016-11</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>1434-193X</dc:identifier>
<dc:identifier>http://hdl.handle.net/10259/4281</dc:identifier>
<dc:language>spa</dc:language>
<dc:relation>European Journal of Organic Chemistry. 2016, n. 33, p. 5445–5587</dc:relation>
<dc:relation>http://dx.doi.org/10.1002/ejoc.201600933</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Wiley-VCH Verlag</dc:publisher>
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