Highly efficient enantioselective hydrolysis of short chain N-acetyl amino acid p-nitrophenyl esters catalysed by esterase models
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 3,p. 666-667
- https://doi.org/10.1039/p19890000666
Abstract
An enantioselectivity (L/D) of 167 ± 21 (pH 7.68; ionic strength = 0.01; 298 K) has been achieved for the hydrolysis of the short chain substrate, N-acetylphenylalanine p-nitrophenyl ester in the catalytic vesicular system of Nα-(N-benzyloxycarbonyl-L-Ieucyl)-L-histidine (Z-L-Leu-L-His) and N,N-ditetradecyl-N,N-dimethylammonium bromide.Keywords
This publication has 1 reference indexed in Scilit:
- Origins of micellar diastereoselectivityJournal of the American Chemical Society, 1984