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All aboard please! A new reaction of enals and cyclic sulfonylimines, as the nucleophiles(!), is the first highly enantioselective NHC-catalyzed annulation of trisubstituted enals. The catalytically generated α,β-unsaturated acyl azolium undergoes a reaction with the enamine tautomer of the imine via an aza-Claisen rearrangement as the key CC bond-forming step. High yields and enantioselectivities were achieved using β-, α,β-, and β,β′-substituted enals.
Kravina et al. (Tue,) studied this question.
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