𝔖 Bobbio Scriptorium
✦   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

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

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