Answers are grounded in this paper and cite their sources.
The macrocyclic molecular catalyst (1) complexes primary ammonium ester salts and displays enhanced rates of intramolecular thiolysis of the bound substrates with structural selectivity for dipeptide esters and high chiral recognition for the (L) antipode of the enantiomeric glycyl–phenyl–alanine esters.
No takes yet. Share an insight, caveat, or question.
Lehn et al. (1978) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: