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Accessing chiral NHC-boranes by abstraction of C6F5 from the B(C6F5)4- weakly coordinating anion
Nicolas Niessen1, Abel Idrice Adjieufack1, Nikolay Tumanov1
1Chemistry Department - Namur Institute of Structured Matter - University of Namur, 61 rue de Bruxelles, 5000 Namur, Belgium. guillaume.berionni@unamur.be.
Abstract:
The prolonged heating of an N-heterocyclic carbene-stabilised borenium cation resulted in the abstraction of a -C6F5 group from its B(C6F5)4- counter-anion. The resulting new chiral NHC-boranes presented an unusual cis/trans isomerism around the newly formed plane. The corresponding borenium cation, due to its Lewis superacidity, is a potentially interesting new chiral organocatalyst.
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