Issue 24, 1971

Enantiomeric specificity in the cyclohexa-amylose-catalysed hydrolysis of 3-carboxy-2,2,5,5-tetramethylpyrrolidin-1-oxy m-nitrophenyl ester

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.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1621-1622

Enantiomeric specificity in the cyclohexa-amylose-catalysed hydrolysis of 3-carboxy-2,2,5,5-tetramethylpyrrolidin-1-oxy m-nitrophenyl ester

K. Flohr, R. M. Paton and E. T. Kaiser, J. Chem. Soc. D, 1971, 1621 DOI: 10.1039/C29710001621

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