Chiral separation of three agrochemical toxins enantiomers by high-performance liquid chromatography on a vancomycin crystalline degradation products-chiral stationary phase
โ Scribed by Mohammad Majid Mojtahedi; Sohila Chalavi; Alireza Ghassempour; Kourosh Tabar-Heydar; Seyed Javad Ghotb Sharif; Maryam Malekzadeh; Hassan Y. Aboul-Enein
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 214 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0269-3879
- DOI
- 10.1002/bmc.732
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
A sensitive enantioselective high-performance chromatographic (HPLC) method was developed and validated to determine low levels of (-)-R and (+)-S-albuterol in plasma. Baseline resolution was achieved by using a teicoplanin-based chiral stationary phase with a polar organic mobile phase consisting o
Enantiomeric separation of d-/l-norepinephrine (NE) and d-/l-epinephrine (E) was investigated with various mobile phases by high-performance liquid chromatography using a โค-cyclodextrin type chiral stationary phase as a chiral column. The mobile phase of 2.5 M phosphate buffer (pH 3.0) gave separati
Penicillamine enantiomers derivatized with N-[4-(6-dimethylamino-2-benzofuranyl)phenyl]maleimide (DBPM) were separated and determined by high-performance liquid chromatography. A fluorogenic reagent, DBPM easily reacted with 1)-or L-penicillamine to give each two kinds of strong fluorescent derivati