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- W2000639229 abstract "N-Aryl-α-amino esters, 1, may be considered to be acyclic analogues of 2-carboalkoxyindolines, 2. The enantiomers of both types of compounds may be separated chromatographically on chiral stationary phases (CSPs) prepared from N-(3,5-dinitrobenzoyl) derivatives of (S)-leucine and (R)-phenylglycine. The degree of chiral recognition is high. Separation factors greater than 10 have been noted and preparative separations are readily performed. A chiral recognition model is advanced to account for the observed separations and is used to relate elution order to absolute configuration for a series of type 1 and type 2 analytes." @default.
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- W2000639229 title "Chromatographic separation of the enantiomers of 2-carboalkoxyindolines and N-aryl-α-amino esters on chiral stationary phases derived from N-(3,5-dinitrobenzoyl)-α-amino acids" @default.
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- W2000639229 doi "https://doi.org/10.1016/s0021-9673(01)92442-2" @default.
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