Issue 20, 1997

Enzymatic cleavage and formation of cyanohydrins: a reaction of biological and synthetic relevance

Abstract

Hydroxynitrile lyases (Hnls) catalyse enantioselectively both the cleavage and formation of cyanohydrins. Besides the well known (R)-selective enzyme from almonds, (S)-Hnls have recently become available in larger quantities by cloning and over-expression. The first three-dimensional structure of a Hnl has been established for the enzyme from Hevea brasiliensis. These results are the basis for a still broader application of Hnls for biocatalytic asymmetric syntheses on a preparative scale.

Article information

Article type
Paper

Chem. Commun., 1997, 1933-1940

Enzymatic cleavage and formation of cyanohydrins: a reaction of biological and synthetic relevance

H. Griengl, A. Hickel, D. V. Johnson, M. Schmidt, C. Kratky and H. Schwab, Chem. Commun., 1997, 1933 DOI: 10.1039/A700907K

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