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- W1494292007 abstract "A chiral stationary phase (CSP) derived from 3-(4′-glycidyloxyphenyl)-2,3-dihydro-1H-benz[de]isoquinolin-1-one was designed and synthesized according to the reciprocality concept. A coplanar arrangement of possible attractive sites of interaction is due to the rigid conformation of the chiral selector. It was demonstrated that this CSP exhibits a good chiral discrimination ability towards families of racemates such as 3,5-dinitrobenzoyl derivatives of α-amino esters and α-amino-amides. Significant enhancements of selectivity were observed when chloroform was used instead of ethanol as a polar modifier in hexane, emphasizing the major contribution of the nature of the mobile phase to the chiral recognition process." @default.
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- W1494292007 date "1989-01-01" @default.
- W1494292007 modified "2023-09-26" @default.
- W1494292007 title "Design and synthesis of a chiral stationary phase containing a benz[de]isoquinolinone skeleton" @default.
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- W1494292007 doi "https://doi.org/10.1016/s0021-9673(01)89671-0" @default.
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