Improvement of chiral stationary phases based on cinchona alkaloids bonded to crown ethers by chiral modification-Reference-Cited by-同舟云学术

Improvement of chiral stationary phases based on cinchona alkaloids bonded to crown ethers by chiral modification

Published:2015-10-15 Issue:22 Volume:38 Page:3884-3890
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Science

Author:

Zhao Jianchao¹,Wu Haixia¹,Wang Dongqiang¹,Wu Haibo¹,Cheng Lingping¹,Jin Yu¹,Ke Yanxiong¹,Liang Xinmiao¹²

Affiliation:

1. Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy; East China University of Science and Technology; Shanghai China

2. Dalian Institute of Chemical Physics; Chinese Academy of Sciences; Dalian China

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jssc.201500834/fullpdf

Reference40 articles.

1. Chiral HPLC for efficient resolution of enantiomers

2. Chiral Separations

3. Direct High-Performance Liquid Chromatographic Separation of Peptide Enantiomers: Study on Chiral Recognition by Systematic Evaluation of the Influence of Structural Features of the Chiral Selectors on Enantioselectivity

4. Elucidation of the Chiral Recognition Mechanism of Cinchona Alkaloid Carbamate-type Receptors for 3,5-Dinitrobenzoyl Amino Acids

5. Unexpected enantioseparation of mandelic acids and their derivatives on 1,2,3-triazolo-linked quinine tert-butyl carbamate anion exchange-type chiral stationary phase

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