Enantiomeric specificity in the cyclohexa-amylose-catalysed hydrolysis of 3-carboxy-2,2,5,5-tetramethylpyrrolidin-1-oxy m-nitrophenyl ester
- 1 January 1971
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society D: Chemical Communications
- No. 24,p. 1621-1622
- https://doi.org/10.1039/c29710001621
Abstract
The asymmetric catalytic effect in the hydrolysis of racemic 3-carboxy-2,2,5,5-tetramethylpyrrolidin-1-oxy m-nitrophenyl ester by cyclohexa-amylose is the largest found so far in a model-enzyme catalysed hydrolysis of a carboxylic acid ester.Keywords
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