A disguised hydride in a butylmagnesium cationElectronic supplementary information (ESI) available: General experimental methods, synthesis and characterisation. CCDC 1837173-1837175. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8cc03127d

The ability of the β-CH functionality in a butylmagnesium cation [Me 6 TREN-Mg- n -Bu] + to quantitatively reduce benzophenone has been demonstrated. The hydridic nature of the β-CH functionality is highlighted by its abstraction using B(C 6 F 5 ) 3 . β-CH abstraction over alkylation in [Me 6 TREN-M...

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Bibliographic Details
Main Authors Banerjee, Sumanta, Ankur, Andrews, Alex, Venugopal, Ajay
Format Journal Article
LanguageEnglish
Published 31.05.2018
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Summary:The ability of the β-CH functionality in a butylmagnesium cation [Me 6 TREN-Mg- n -Bu] + to quantitatively reduce benzophenone has been demonstrated. The hydridic nature of the β-CH functionality is highlighted by its abstraction using B(C 6 F 5 ) 3 . β-CH abstraction over alkylation in [Me 6 TREN-Mg- n -Bu] + is dependent on the nature of the incoming electrophile and the polarity of the solvent. The reactivity of a butylmagnesium cation provides a new perspective on the concept of β-hydride abstraction in s-block chemistry.
Bibliography:For ESI and crystallographic data in CIF or other electronic format see DOI
10.1039/c8cc03127d
Electronic supplementary information (ESI) available: General experimental methods, synthesis and characterisation. CCDC
1837173-1837175
ISSN:1359-7345
1364-548X
DOI:10.1039/c8cc03127d