Highly enantioselective cleavage of α-amino acid p-nitrophenyl esters by chiral metallomicelles
- 1 January 1988
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 11,p. 716-718
- https://doi.org/10.1039/c39880000716
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.Keywords
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