Abstract
Inversion of configuration at the tetrahedral carbon centres of dipolar spiro-σ-complexes formed by coupling 2-(N-benzylamino)tropone, 2-(N-benzylamino)thiotropone or N,N’-dibenzyl-2-aminotroponimine with electrophilic aromatic and heterocyclic compounds has been found to occur intramolecularly with energy barriers accessible to measurement by means of dynamic 1H NMR spectral techniques.
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