✦ LIBER ✦

Enantioseparation on 3,5-dichloro- and 3,5-dimethylphenylcarbamates of polysaccharides as chiral stationary phases for high-performance liquid chromatography

✍ Scribed by Yoshio Okamoto; Junko Noguchi; Eiji Yashima

Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 538 KB
Volume: 37
Category: Article
ISSN: 1381-5148
DOI: 10.1016/s1381-5148(97)00135-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enantioseparations in nonaqueous capilla

Enantioseparations in nonaqueous capillary liquid chromatography and capillary electrochromatography using cellulose tris(3,5-dimethylphenylcarbamate) as chiral stationary phase

✍ Lali Chankvetadze; Irma Kartozia; Chiyo Yamamoto; Bezhan Chankvetadze; Gottfried 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 801 KB

3,5-Dimethylphenylcarbamates of cellulos

3,5-Dimethylphenylcarbamates of cellulose and amylose regioselectively bonded to silica gel as chiral stationary phases for high-performance liquid chr

✍ Eiji Yashima; Hiroyasu Fukaya; Yoshio Okamoto 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 753 KB

Dimethyl-, dichloro- and chloromethylphe

Dimethyl-, dichloro- and chloromethylphenylcarbamates of amylose as chiral stationary phases for high-performance liquid chromatography

✍ Bezhan Chankvetadze; Eiji Yashima; Yoshio Okamoto 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 556 KB

Enantioseparation on 4-halogen-substitut

Enantioseparation on 4-halogen-substituted phenylcarbamates of amylose as chiral stationary phases for high-performance liquid chromatography

✍ Eiji Yashima; Eiji Kasashima; Yoshio Okamoto 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 263 KB 👁 2 views

Enantioseparation of 2-aryl-1,3-dicarbon

Enantioseparation of 2-aryl-1,3-dicarbonyl analogues by high performance liquid chromatography using polysaccharide type chiral stationary phase

✍ Zhe Xu; Zuoding Ding; Xu Xu; Xiaoan Xie 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 96 KB

Dichloro-, dimethyl-, and chloromethylph

Dichloro-, dimethyl-, and chloromethylphenylcarbamate derivatives of cyclodextrins as chiral stationary phases for high-performance liquid chromatography

✍ Bezhan Chankvetadze; Eiji Yashima; Yoshio Okamoto 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 521 KB

New dichloro-, dimethyl-, and chloromethylphenylcarbamate derivatives of cyclodextrins (CDs) were prepared and their enantiomeric recognition abilities were evaluated as chiral stationary phases (CSPs) in normal phase high-performance liquid chromatography (HPLC). The effects of the type of cyclodex