Substituted racemic 1-phenylethylamine derivatives were reacted in molten phase with chiral N-substituted 1-phenylethylamine dicarboxylic acid derivatives (4-9), and their mixtures (e.g., 4+6, 7+8, etc.) in different ratios, and the crystalline quasi-racemic diastereomers so formed were separated. Nonlinear behavior of the mixtures of resolving agents having related structure and considerable positive and negative chiral-chiral interactions were observed. © 2005 Wiley-Liss, Inc.
CITATION STYLE
Schindler, J., Egressy, M., Bálint, J., Hell, Z., & Fogassy, E. (2005). Optical resolution by crystallization from melt using enantiomer derivatives as resolving agents: Nonlinear behavior of resolving agent mixtures. Chirality, 17(9), 565–569. https://doi.org/10.1002/chir.20207
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