Application of cinchona-sulfonate-based chiral zwitterionic ion exchangers for the separation of proline-containing dipeptide rotamers and determination of on-column isomerization parameters from dynamic elution profiles
Author:
Publisher
Elsevier BV
Subject
Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry
Reference57 articles.
1. Synergistic Effects on Enantioselectivity of Zwitterionic Chiral Stationary Phases for Separations of Chiral Acids, Bases, and Amino Acids by HPLC
2. Increments to chiral recognition facilitating enantiomer separations of chiral acids, bases, and ampholytes using Cinchona -based zwitterion exchanger chiral stationary phases
3. Mechanistic investigations of cinchona alkaloid-based zwitterionic chiral stationary phases
4. Versatility of cinchona-based zwitterionic chiral stationary phases: Enantiomer and diastereomer separations of non-protected oligopeptides utilizing a multi-modal chiral recognition mechanism
5. The hunchback and its neighbours: proline as an environmental modulator
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