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Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Chemically Bonded to Silica Gel*

Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and... Abstract Cellulose was bonded chemically to 3-aminopropyl silica gel with diisocyanates and then allowed to react with a large excess of 3,5-dimethylphenyl- or 3,5-dichlorophenylisocyanate. Optical resolving power of these chiral stationary phases was compared with that of the cellulose triphenylcarbamate derivatives coated on silica gel. *Chromatographic Resolution XV, for part XIV, see Y. Okamoto, R. Aburatani, and K. Hatada, J. Chromatogr., in press. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Liquid Chromatography Taylor & Francis

Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Chemically Bonded to Silica Gel*

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Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Chemically Bonded to Silica Gel*

Okamoto, Yoshio; Aburatani, Ryo; Miura, Shin-Ichi; Hatada, Koichi
Journal of Liquid Chromatography , Volume 10 (8-9): 16 – Jun 1, 1987

Abstract

Abstract Cellulose was bonded chemically to 3-aminopropyl silica gel with diisocyanates and then allowed to react with a large excess of 3,5-dimethylphenyl- or 3,5-dichlorophenylisocyanate. Optical resolving power of these chiral stationary phases was compared with that of the cellulose triphenylcarbamate derivatives coated on silica gel. *Chromatographic Resolution XV, for part XIV, see Y. Okamoto, R. Aburatani, and K. Hatada, J. Chromatogr., in press.

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References (3)

Publisher
Taylor & Francis
Copyright
Copyright Taylor & Francis Group, LLC
ISSN
0148-3919
DOI
10.1080/01483918708066791
Publisher site
See Article on Publisher Site

Abstract

Abstract Cellulose was bonded chemically to 3-aminopropyl silica gel with diisocyanates and then allowed to react with a large excess of 3,5-dimethylphenyl- or 3,5-dichlorophenylisocyanate. Optical resolving power of these chiral stationary phases was compared with that of the cellulose triphenylcarbamate derivatives coated on silica gel. *Chromatographic Resolution XV, for part XIV, see Y. Okamoto, R. Aburatani, and K. Hatada, J. Chromatogr., in press.

Journal

Journal of Liquid Chromatography – Taylor & Francis

Published: Jun 1, 1987

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