✦ LIBER ✦

Chromatographic resolution of the chiral isomers of several β-blockers over cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase

✍ Scribed by C.B. Ching; B.G. Lim; E.J.D. Lee; S.C. Ng

Publisher: John Wiley and Sons
Year: 1992
Tongue: English
Weight: 339 KB
Volume: 4
Category: Article
ISSN: 0899-0042
DOI: 10.1002/chir.530040308

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Optical resolution of glycerin sulfides

Optical resolution of glycerin sulfides and glycerin selenides on the chiral stationary phase of cellulose-tris(3,5-dimethylphenylcarbamate)

✍ Yu Zhaowen; Jiang Shengxiang; Liu Xia; Chen Liren 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB

Cellulose-tris(3,5-dimethylphenylcarbamate) was prepared after a reported method and was coated onto an aminopropylated mesopore spherical silica gel. The final product was used as a chiral stationary phase of high performance liquid chromatography for the enantioseparation of a series of glycerin s

Preparation and Evaluation of a Novel Ce

Preparation and Evaluation of a Novel Cellulose Tris(N-3,5-dimethylphenylcarbamate) Chiral Stationary Phase

✍ Jin GE; Liang ZHAO; Yan-Ping SHI 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 125 KB

## Abstract A novel cellulose tris(__N__‐3,5‐dimethylphenylcarbamate) (CDMPC) chiral stationary phase (CSP) was prepared by coating CDMPC on TiO~2~/SiO~2~, which was prepared by coating titania nanoparticles on silica through a self‐assemble technique. At first, 2‐hydroxyl‐phenyl acetonitrile and _

Direct chromatographic separation of 2-a

Direct chromatographic separation of 2-arylpropionic acid enantiomers using tris(3,5-dimethylphenylcarbamate)s of cellulose and amylose as chiral stationary phases

✍ Yoshio Okamoto; Ryo Aburatani; Yuriko Kaida; Koichi Hatada; Nobuo Inotsume; Masa 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB 👁 2 views

Direct resolution of novel tetrahedral m

Direct resolution of novel tetrahedral metal clusters on a cellulose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase by high-performance liquid chromatography

✍ Xinyi Zhu; Yingchun Cai; Weiqiang Zhang; Liren Chen; Yongmin Li 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 417 KB

## Abstract Direct optical resolution of five novel tetrahedral heterometal cluster enantiomers has been achieved for the first time on a cellulose tris‐(3,5‐dimethylphenylcarbamate) chiral stationary phase, using hexane as the mobile phase with various alcohols as modifiers. UV detection was carri

Chiral recognition ability and solvent v

Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: Enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

✍ Ashraf Ghanem; Ebtessam Al-Humaidi 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 192 KB

Cellulose tris(3,5-dimethylphenylcarbama

Cellulose tris(3,5-dimethylphenylcarbamate)-based chiral stationary phases as effective tools for enantioselective HPLC separation of structurally different disubstituted binaphthyls

✍ Lucie Loukotková; Milena Rambousková; Zuzana Bosáková; Eva Tesařová 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 122 KB