Chiral zwitterionic stationary phases based on Cinchona alkaloids and dipeptides: Application in chiral separation of dipeptides under reversed phase conditions
Author:
Funder
Russian Science Foundation
Canadian Society of Plastic Surgeons
Czech Science Foundation
Publisher
Elsevier BV
Reference30 articles.
1. Сinchona alkaloids for preparing new, easily accessible chiral stationary phases.1. 11-(10,11-dihydro-6′-methoxy-cinchonan-9-ol)-tiopropylsilanized silica;Rosini;Tetrahedron. Lett.,1985
2. A novel application of cinchona alkaloids as chiral auxiliaries: preparation and use of a new family of chiral stationary phases for the chromatographic resolution of racemates;Salvadori;Tetrahedron.,1987
3. Chiral stationary phases based on cinchona alkaloids for the HPLC resolution of racemates;Rosini;Chromatographia,1987
4. Effect of mobile phase composition on the enantioselectivity of chromatographic separation on a quinine-bonded silica stationary phase;Nesterenko;J. Chromatogr. A,1994
5. Quinine and quinidine derivatives as chiral selectors I. Brush type chiral stationary phases for high-performance liquid chromatography based on cinchonan carbamates and their application as chiral anion exchangers;Lämmerhofer;J. Chromatogr. A,1996
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