Comparative Studies on Enantiomer Resolution of α-Amino Acids and Their Esters Using (18-Crown-6)-tetracarboxylic acid as a Chiral Crown Ether Selector by NMR Spectroscopy and High-Performance Liquid Chromatography
Author:
Publisher
Korean Chemical Society
Subject
General Chemistry
Link
http://ocean.kisti.re.kr/downfile/crosscheck/chemical/JAKO201231434109111.pdf
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Effective enantiomeric identification of aromatic amines by tyrosine-modified pillar[5]arenes as chiral NMR solvating agents;Organic Chemistry Frontiers;2021
2. Michael addition reactions of chiral glycine Schiff base Ni (II)‐complex with 1‐(1‐phenylsulfonyl)benzene;Chirality;2020-02-24
3. Enantiodiscrimination Using a Chiral Crown Ether as a Chiral Solvating Agent Using NMR Spectroscopy;Natural Product Communications;2019-05-01
4. REFERENCES;Differentiation of Chiral Compounds Using NMR Spectroscopy;2018-06-15
5. Chiral separation using chiral crown ethers as chiral selectors in chirotechnology;Journal of Pharmaceutical Investigation;2017-07-13
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