Diastereoisomeric enrichment through fractional crystallisation of C-nitrobenzoate derivatives of alpha-ionol, and enantioselective enzyme-mediated reactions of alpha-ionol and alpha-ionol acetate, were usefully combined to optimise two different procedures to enantiopure (S)- and (R)-ionone.

Enzyme-mediated synthesis of (R)- and (S)-alpha-ionone.

SERRA STEFANO
1998

Abstract

Diastereoisomeric enrichment through fractional crystallisation of C-nitrobenzoate derivatives of alpha-ionol, and enantioselective enzyme-mediated reactions of alpha-ionol and alpha-ionol acetate, were usefully combined to optimise two different procedures to enantiopure (S)- and (R)-ionone.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/202408
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