Issue 4, 1984

Preparations of bicyclic chiral lactone synthons via stereospecific pig liver esterase-catalysed hyderolyses of meso-diesters. Ring-size induced reversal of stereospecificity

Abstract

Stereospecific pig liver esterase-catalysed hydrolysis of monocyclic meso-1,2-diesters provides a convenient preparative route to both enantiomers of useful chiral lactones and demonstrates a sharply defined and unprecedented ring-size-mediated reversal of stereospecificity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 236-238

Preparations of bicyclic chiral lactone synthons via stereospecific pig liver esterase-catalysed hyderolyses of meso-diesters. Ring-size induced reversal of stereospecificity

G. Sabbioni, M. L. Shea and J. B. Jones, J. Chem. Soc., Chem. Commun., 1984, 236 DOI: 10.1039/C39840000236

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