Application of cyanuric chloride-based six new chiral derivatizing reagents having amino acids and amino acid amides as chiral auxiliaries for enantioresolution of proteinogenic amino acids by reversed-phase high-performance liquid chromatography
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s00726-011-0832-3.pdf
Reference30 articles.
1. Bhushan R, Agarwal C (2010) Reversed-phase liquid chromatographic resolution of diastereomers of protein and non-protein amino acids prepared with newly synthesized chiral derivatizing reagents based on cyanuric chloride. Amino Acids. doi: 10.1007/s00726-010-5050650-z
2. Bhushan R, Dixit S (2010a) Microwave-assisted synthesis and reversed-phase high-performance liquid chromatographic separation of diastereomers of (R,S)-baclofen using ten chiral derivatizing reagents designed from trichloro-s-triazine. J Chromatogr A 1217:6382–6387
3. Bhushan R, Dixit S (2010b) Reversed-phase high-performance liquid chromatographic separation of diastereomers of (R,S)-mexiletine prepared by microwave irradiation with four new chiral derivatizing reagents based on trichloro-s-triazine having amino acids as chiral auxiliaries and ten others having amino acid amides. J Chromatogr A 1217:7669–7676
4. Bhushan R, Kumar V (2008) Indirect enantioseparation of α-amino acids by reversed-phase liquid chromatography using new chiral derivatizing reagents synthesized from s-triazine chloride. J Chromatogr A 1201:35–42
5. Bhushan R, Martens J (2010) Amino acids: chromatographic separation and enantioresolution. HNB Publishing, New York
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