Use of quantitative structure-enantioselective retention relationship for the liquid chromatography chiral separation prediction of the series of pyrrolidin-2-one compounds-Reference-Cited by-同舟云学术

Use of quantitative structure-enantioselective retention relationship for the liquid chromatography chiral separation prediction of the series of pyrrolidin-2-one compounds

Published:2011-11-26 Issue:1 Volume:24 Page:72-77
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Rasulev Bakhtiyor,Turabekova Malakhat,Gorska Magdalena,Kulig Katarzyna,Bielejewska Anna,Lipkowski Janusz,Leszczynski Jerzy

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference39 articles.

1. Search for new antiarrhythmic and hypotensive compounds. Synthesis, antiarrhythmic, antihypertensive, and α-adrenoceptor blocking activity of novel 1-[(2-hydroxy-3-amino)]-propylpyrrolidin-2-one derivatives;Filipek;Arch Pharm Pharm Med Chem,1997

2. Synthesis, antiarrhythmic, and antihypertensive effects of novel 1-substituted pyrrolidin-2-one and pyrrolidine derivatives with adrenolytic activity;Malawska;Eur J Med Chem,2002

3. Synthesis and development of new 2-substituted 1-[3-(4-arylpiperazin-1-yl)propyl]-pyrrolidin-2-one derivatives with antiarrhythmic, hypotensive, and α-adrenolytic activity;Malawska;Farmaco,2005

4. Stereocontrolled synthesis of the enantiomers of 1-[2-hydroxy-3-(4-phenyl-1-piperazinyl)-propyl]-pyrrolidin-2-one;Kulig;Tetrahedron Asymmetry,2001

5. Polysaccharide derivatives for chromatographic separation of enantiomers;Okamoto;Angew Chem Int Ed Engl,1998

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