Liquid Chromatographic Separation of the Enantiomers of Chiral Secondary Alcohols as Their α-Naphthyl Urethane Derivatives
Author:
Publisher
Informa UK Limited
Subject
Molecular Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/01483918808069047
Reference6 articles.
1. Broad spectrum resolution of optical isomers using chiral high-performance liquid chromatographic bonded phases
2. Pasto, D. J. and Johnson, C. R. 1969.Organic Structure Determination, 359Englewood Cliffs: Prentice‐Hall.
3. Design of chiral derivatizing agents for the chromatographic resolution of optical isomers. Asymmetric synthesis of some chiral fluoroalkylated amines
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1. Achiral derivatization as a means of improving the chromatographic resolution of racemic alcohols on benzoylcellulose CSPs;Chirality;1998
2. Diphenylethanediamine derivatives as chiral selectors V1. Efficient normal-phase high-performance liquid chromatographic enantioseparation of underivatized chiral arylalcohols on four differently linked 3,5-dinitrobenzoyldiphenylethanediamine-derived chiral stationary phases;Journal of Chromatography A;1996-05
3. Enantiomeric derivatization for biomedical chromatography;Journal of Chromatography B: Biomedical Sciences and Applications;1994-09
4. Diphenylethanediamine derivatives as chiral selectors;Journal of Chromatography A;1994-04
5. Contribution of preparative chromatographic resolution to the investigation of chiral phenomena;Journal of Chromatography A;1994-04
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