Issue 22, 1985

Preparation of chiral hydroxyester synthons vis stereoselective porcine pancreatic lipase-catalysed hydrolyses of meso-diesters

Abstract

Stereoselective porcine pancreatic lipase-catalysed hydrolyses of monocyclic meso-1,2-diesters provides a flexible and convenient preparative route to chiral hydroxyesters and lactones of asymmetric synthetic value.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1563-1564

Preparation of chiral hydroxyester synthons vis stereoselective porcine pancreatic lipase-catalysed hydrolyses of meso-diesters

W. Kasel, P. G. Hultin and J. B. Jones, J. Chem. Soc., Chem. Commun., 1985, 1563 DOI: 10.1039/C39850001563

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