Unsymmetrical 1,1-diborated multisubstituted sp(3)-carbons formed via a metal-free concerted-asynchronous mechanism

Ana B. Cuenca, Jessica Cid, Diego García-López, Jorge J. Carbó, Elena Fernández

Producción científica: Artículo en revista indizadaArtículorevisión exhaustiva

63 Citas (Scopus)

Resumen

We have experimentally proved the unsymmetrical 1,1-diboration of diazo compounds, formed in situ from aldehydes and cyclic and non-cyclic ketones, in the absence of any transition metal complex. The heterolytic cleavage of the mixed diboron reagent, Bpin-Bdan, and the formation of two geminal C-Bpin and C-Bdan bonds has been rationalised based on DFT calculations to occur via a concerted-asynchronous mechanism. Diastereoselection is attained on substituted cyclohexanones and DFT studies provide understanding on the origin of the selectivity. The alkoxide-assisted selective deborylation of Bpin from multisubstituted sp3-carbon and generation of a Bdan stabilized carbanion, easily conducts a selective protodeboronation sequence.

Idioma originalInglés
Páginas (desde-hasta)9659-9664
Número de páginas6
PublicaciónOrganic and Biomolecular Chemistry
Volumen13
N.º37
DOI
EstadoPublicada - 29 jul 2015
Publicado de forma externa

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