Four chiral stationary phases (CSPs) derived from N-(3,5-dinitrobenzoyl)tyrosine have been synthesized. They differ by the substituent nature (methyl, ethyl, isopropyl, tert-butyl) of the aliphatic amide function. The enantiorecognition ability of these CSPs was evaluated with 10 racemates. For the
✦ LIBER ✦
Improvement of the enantiorecognition ability of tyrosine-derived chiral stationary phases: Direct resolution of 1,2-amino-alcohols (β-blockers)
✍ Scribed by A. Tambute; L. Siret; A. Begos; M. Caude
- Book ID
- 102797962
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 594 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Steric hindrance influence on the enanti
✍
L. Siret; A. Tambuté; A. Bégos; J. Rouden; M. Caude
📂
Article
📅
1991
🏛
John Wiley and Sons
🌐
English
⚖ 735 KB
Evaluation of π-acid chiral stationary p
✍
M. Liene; P. Macaudìre; M. Caude; R. Rosset; A. Tambut´
📂
Article
📅
1989
🏛
John Wiley and Sons
🌐
English
⚖ 977 KB
Chromatographic applications of three novel chiral stationary phases (CSPs) deriving from (S)-(N)-(3,5-dinitrobenzoyl)tyrosine are reported, under liquid chromatographic (LC) and subcritical fluid chromatographic (SubFC) conditions. Two grafting modes of the chiral moiety have been experimented star
Direct high-performance liquid chromatog
✍
F. Gasparrini; D. Misiti; C. Villani; M. Pierini; F. La Torre
📂
Article
📅
1993
🏛
Elsevier Science
🌐
English
⚖ 448 KB