COMPARISON OF GRAFTING MODES FOR THE PREPARATION OF CHOLIC ACID-BASED STATIONARY PHASES. INFLUENCE ON ENANTIOMER SEPARATIONS IN HIGH PERFORMANCE LIQUID CHROMATOGRAPHY-Reference-Cited by-同舟云学术

COMPARISON OF GRAFTING MODES FOR THE PREPARATION OF CHOLIC ACID-BASED STATIONARY PHASES. INFLUENCE ON ENANTIOMER SEPARATIONS IN HIGH PERFORMANCE LIQUID CHROMATOGRAPHY

Published:2000-08-21 Issue:14 Volume:23 Page:2155-2167
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Vaton-Chanvrier L.¹,Bucaille N.¹,Combret Y.¹,Combret J. -C.¹

Affiliation:

1. a Université de Rouen , Laboratoire d'Hétérochimie Organique, UPRES EA 2659, IRCOF, Mont Saint Aignan Cedex, F-76821, France

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/JLC-100100478

Reference19 articles.

1. Doubly tethered tertiary amide selectors

2. Chiral-bonded silica gel stationary phases obtained from chiral silanes for high-performance liquid chromatography

3. A chiral stationary phase derived from (R,R)-tartramide with broadened scope of application to the liquid chromatographic resolution of enantiomers

4. The influence of end-capping on the enantioselectivity of a chiral phase

5. Investigations of the influence of silanol groups on the separation of enantiomers by liquid and supercritical fluid chromatography

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1. Stereoselective chromatography of cardiovascular drugs: an update;Journal of Biochemical and Biophysical Methods;2002-12

2. Rate of Access to the Binding Sites in Organically Modified Silicates. 1. Amorphous Silica Gels Grafted with Amine or Thiol Groups;Chemistry of Materials;2002-05-10

3. High-performance liquid chromatographic investigation of the enantioselectivity and mechanism of chiral recognition of new cholic acid-based stationary phases;Chromatographia;2001-07

4. Chiral recognition of binaphthyl derivatives: A chiral recognition model on the basis of chromatography, spectroscopy, and molecular mechanistic calculations for the enantioseparation of 1,1?-binaphthyl derivatives on cholic acid-bonded stationary phases;Chirality;2001