Liquid chromatographic resolution of 3-amino-1,4-benzodiazepin-2-one derivatives on various Pirkle-type chiral stationary phases
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.20944/fullpdf
Reference14 articles.
1. Mechanism of action of anxiolytic drugs;Mennini;Prog Drug Res,1987
2. Configurational stability of the chiral centre C(3) in some 1,4-benzodiazepin-2-ones;Sunjic;Tetrahedron Lett,1976
3. Chiral 1,4-benzodiazepin-2-ones: relationship between stereochemistry and pharmacological activity;Salvadori;J Pharm Biomed Anal,1989
4. Application of preparative liquid chromatography to the isolation of enantiomers of a benzodiazepinone derivative;Katti;J Chromatogr,1992
5. Enantiomer resolution of camazepam and its derivatives and enantioselective metabolism of camazepam by human liver microsomes;Lu;J Chromatogr A,1994
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1. Preparation of Two New Diasteromeric Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and (R)- or (S)-1-(1-Naphthyl)ethylamine and Chiral Tethering Group Effect on the Chiral Recognition;Molecules;2016-08-12
2. Separation of benzoxazine enantiomers on β-cyclodextrin bonded chiral stationary phases;Chinese Journal of Chromatography;2013-09-18
3. Liquid chromatographic resolution of 3-amino-1,4-benzodiazepin-2-ones on crown ether-based chiral stationary phases;Chirality;2012-04-16
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