Fast resolutions of racemic compounds (sulfoxides, amino alcohols, and α-methylarylacetic acids derivatives) were achieved on a chiral microbore column using carbon dioxide and a polar methanol/dioxane modifier. The stationary phase used in this study contains the 3,5-dinitrobenzoyl derivative of R,R(−)-1,2-diaminocyclohexane (DACH-DNB) as the chiral moiety, anchored to a silica gel surface by covalent bonds. Both thermodynamic and kinetic separation performances were improved by using a super- or subcritical carbon dioxide mobile phase (SFC, SubFC).
Direct resolution of racemic compounds on chiral microbore columns by Sub- and Supercritical Fluid Chromatography / Gasparrini, Francesco; Misiti, Domenico; Villani, Claudio. - In: HRC- JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY. - ISSN 0935-6304. - STAMPA. - 13:3(1990), pp. 182-184. [10.1002/jhrc.1240130309]
Direct resolution of racemic compounds on chiral microbore columns by Sub- and Supercritical Fluid Chromatography
GASPARRINI, Francesco;MISITI, Domenico;VILLANI, Claudio
1990
Abstract
Fast resolutions of racemic compounds (sulfoxides, amino alcohols, and α-methylarylacetic acids derivatives) were achieved on a chiral microbore column using carbon dioxide and a polar methanol/dioxane modifier. The stationary phase used in this study contains the 3,5-dinitrobenzoyl derivative of R,R(−)-1,2-diaminocyclohexane (DACH-DNB) as the chiral moiety, anchored to a silica gel surface by covalent bonds. Both thermodynamic and kinetic separation performances were improved by using a super- or subcritical carbon dioxide mobile phase (SFC, SubFC).I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.