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Development of HPLC Chiral Stationary Phases Based on (+)‐(18‐Crown‐6)‐2,3,11,12‐tetracarboxylic Acid and Their Applications
Authors:Myung Ho Hyun
Institution:Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan, Republic of Korea
Abstract:Crown ether‐based chiral stationary phases (CSPs) have been known to be useful for the resolution of racemic primary amino compounds. In particular, CSPs based on (+)‐(18‐crown‐6)‐2,3,11,12‐tetracarboxylic acid have been reported to be useful for the resolution of secondary amino compounds as well as primary amino compounds. In this article, the process of developing various CSPs based on (+)‐(18‐crown‐6)‐2,3,11,12‐tetracarboxylic acid to improve the chiral recognition efficiency and/or the stability of the CSPs and their applications to the resolution of various primary and nonprimary amino compounds are reviewed. Chirality 27:576588, 2015. © 2015 Wiley Periodicals, Inc.
Keywords:chiral stationary phase  enantiomer separation  liquid chromatography  (18‐crown‐6)‐2  3  11  12‐tetracarboxylic acid
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