The scale-up of the HPLC separation of the enantiomers of the flavour norterpenoid ketones alpha-ionone and alpha-damascone from analytical to preparative scale was achieved using the chromatographic simulated moving bed (SMB) technique. Commercial HPLC columns. with heptakis-(2,3,6-per-O-methyl)-beta-cyclodextrin bound to silica gel as chiral stationary phase, were employed for the separation. High-purity enantiomers of both chiral compounds have been obtained with a rather satisfactory productivity. Copyright (C) 2002 John Wiley Sons, Ltd.

Scale-up of analytical chromatography to the simulated moving bed separation of the enantiomers of the flavour norterpenoids alpha-ionone and alpha-damascone

MORBIDELLI, MASSIMO
2002-01-01

Abstract

The scale-up of the HPLC separation of the enantiomers of the flavour norterpenoid ketones alpha-ionone and alpha-damascone from analytical to preparative scale was achieved using the chromatographic simulated moving bed (SMB) technique. Commercial HPLC columns. with heptakis-(2,3,6-per-O-methyl)-beta-cyclodextrin bound to silica gel as chiral stationary phase, were employed for the separation. High-purity enantiomers of both chiral compounds have been obtained with a rather satisfactory productivity. Copyright (C) 2002 John Wiley Sons, Ltd.
2002
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/659683
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