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    Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/4281

    Título
    ortho-Lithiation Reactions of O-(3,n-Dihalophenyl) N,N-Diethylcarbamates: Synthesis of Dihalosalicylamides and 2,3,n-Trihalophenol Derivatives
    Autor
    Feberero García, ClaudiaUBU authority Orcid
    Velasco, Rocío
    Sanz Díez, RobertoUBU authority Orcid
    Publicado en
    European Journal of Organic Chemistry. 2016, n. 33, p. 5445–5587
    Editorial
    Wiley-VCH Verlag
    Fecha de publicación
    2016-11
    ISSN
    1434-193X
    Abstract
    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.
    Materia
    Chemistry, Organic
    Química orgánica
    URI
    http://hdl.handle.net/10259/4281
    Versión del editor
    http://dx.doi.org/10.1002/ejoc.201600933
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    • Artículos SINTORG
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