Issue 11, 1988

Highly enantioselective cleavage of α-amino acid p-nitrophenyl esters by chiral metallomicelles

Abstract

Chiral CuII-chelating micelles of 2-[hexadecyl-N,N-(2-hydroxypropyl)aminomethyl]pyridine are effective and remarkably enantioselective catalysts for the hydrolytic cleavage of p-nitrophenyl esters of α-amino acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 716-718

Highly enantioselective cleavage of α-amino acid p-nitrophenyl esters by chiral metallomicelles

R. Fornasier, P. Scrimin, U. Tonellato and N. Zanta, J. Chem. Soc., Chem. Commun., 1988, 716 DOI: 10.1039/C39880000716

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