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Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes

Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El(+)/H(–) equivalents in B(C(6)F(5))(3)-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-...

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Detalles Bibliográficos
Autores principales: Keess, Sebastian, Oestreich, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596415/
https://www.ncbi.nlm.nih.gov/pubmed/28936336
http://dx.doi.org/10.1039/c7sc01657c
Descripción
Sumario:Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El(+)/H(–) equivalents in B(C(6)F(5))(3)-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-dash]C/C[triple bond, length as m-dash]C and C[double bond, length as m-dash]O/C[double bond, length as m-dash]N). Surrogates of Si–H/Ge–H, H–H and even C–H bonds have been designed and successfully applied to ionic transfer hydrosilylation/hydrogermylation, hydrogenation and hydro-tert-butylation, respectively. These processes and their basic principles are summarised in this Minireview. The similarities and differences between these transfer reactions as well as the challenges associated with these transformations are discussed.