Optical resolution by crystallization from melt using enantiomer derivatives as resolving agents: Nonlinear behavior of resolving agent mixtures

6Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free