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A sterically hindered homoenolate has been generated by the NHC-catalyzed conjugate umpolung of β,β-disubstituted enals and successfully employed in a facile stereoselective annulation with isatins. The strategy provides efficient access to spirocyclic oxindoles bearing two highly congested contiguous quaternary carbon centers. The use of a Brønsted acid cocatalyst was found to be crucial for guaranteeing both excellent reactivity and high stereoselectivity.
Li et al. (Thu,) studied this question.