| Autor: |
Cizmáriková R; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University, Bratislava, Slovak Republic. cizmarikova@fpharm.uniba.sk, Bruchatá K, Pastírová Z, Lehotay J, Hrobonová K |
| Jazyk: |
angličtina |
| Zdroj: |
Die Pharmazie [Pharmazie] 2010 May; Vol. 65 (5), pp. 387-8. |
| Abstrakt: |
An enantioseparation study of nitro-substituted aryloxyaminopropanols was performed using HPLC on a teicoplanin chiral stationary phase and TLC impregnated with L-aspartic and L-tartaric acid as chiral selectors. The type of substituent on the nitrogen in the hydrophilic part of molecule is essential for excellent separation by HPLC. L-aspartic acid seems to be a suitable chiral selector for enantioseparation by TLC. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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