Issue 21, 1978

Molecular catalysis: enhanced rates of thiolysis with high structural and chiral recognition in complexes of a reactive macrocyclic receptor molecule

Abstract

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 949-951

Molecular catalysis: enhanced rates of thiolysis with high structural and chiral recognition in complexes of a reactive macrocyclic receptor molecule

J. Lehn and C. Sirlin, J. Chem. Soc., Chem. Commun., 1978, 949 DOI: 10.1039/C39780000949

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