Answers are grounded in this paper and cite their sources.
Intermolecular reactions of planar chiral 9-membered diallylic amides provide a variety of bicyclic compounds with central chiralities in a stereospecific fashion with high group selectivity. Lewis-acid-promoted intramolecular reactions of the obtained bicyclic compounds provide transannular products in a stereospecific fashion. Furthermore, a direct transannular reaction of diallylic amide involving sequential intermolecular-intramolecular reactions has been developed.
No takes yet. Share an insight, caveat, or question.
Tomooka et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: