Journal of the Chemical Society. Chemical communications p. 236 - 238 (1984)
Update date:2022-08-30
Topics:
Sabbioni, Gabriele
Shea, Marion L.
Jones, J. Bryan
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.
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