Issue 16, 1993

Studies on the stereospecificity of the clavaminic acid synthase catalysed hydroxylation reaction

Abstract

Incubation of (2S,3S)-5-guanidino[2,3-2H2]-2-(2′-oxoazetidin-1′-yl)pentanoic acid and (2S,3R)-5-guanidino-[3-2H1]-2-(2′-oxoazetidin-1′-yl)pentanoic acid with clavaminic acid synthase resulted in highly stereospecific hydroxylation at C-3, with removal of the pro-R hydrogen or deuterium, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1301-1302

Studies on the stereospecificity of the clavaminic acid synthase catalysed hydroxylation reaction

J. E. Baldwin, K. D. Merritt, C. J. Schofield, S. W. Elson and K. H. Baggaley, J. Chem. Soc., Chem. Commun., 1993, 1301 DOI: 10.1039/C39930001301

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