Answers are grounded in this paper and cite their sources.
Benzotetramisole (1) promotes the reaction of ammonium enolates derived from arylacetic acids with N-tosyl-α,β-unsaturated ketimines, thus giving dihydropyridones with high diastereo- and enantiocontrol (see scheme). These products readily undergo N- to C-sulfonyl photoisomerization and are derivatized to afford stereodefined piperidines and tetrahydropyrans.
No takes yet. Share an insight, caveat, or question.
Simal et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: