Comparative HPLC enantioseparation of new chiral hydantoin derivatives on three different polysaccharide type chiral stationary phases

被引:31
作者
Kartozia, I
Kanyonyo, M
Happaerts, T
Lambert, DM
Scriba, GKE
Chankvetadze, B
机构
[1] Univ Munster, Inst Pharmaceut Chem, D-48149 Munster, Germany
[2] Catholic Univ Louvain, Unit Pharmaceut Chem & Radiopharm, CMFA 73 40, B-1200 Brussels, Belgium
[3] Univ Jena, Dept Pharmaceut Chem, D-07743 Jena, Germany
[4] Tbilisi State Univ, Sch Chem, Mol Recognit & Separat Sci Lab, GE-380028 Tbilisi, Georgia
关键词
chiral hydantoins; enantioseparations; HPLC; polysaccharide-type chiral; stationary phases; Chiralcel OD; Chiralpak AD; Chiralcel OJ;
D O I
10.1016/S0731-7085(01)00649-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The enantioseparation of eighteen new chiral hydantoin derivatives was studied on three different polysaccharide type chiral stationary phases (CSP) Chiralpak AD, Chiralcel OD and Chiralcel OJ in the normal-phase HPLC mode. Chiralpak AD material exhibited the most universal chiral resolving ability and allowed the enantioseparation of 17 out of 18 compounds followed by Chiralcel OD (10 enantioseparations of 12 tested compounds) and Chiralcel OJ (eight enantioseparation from 13 tested analytes). Some complementary separations were observed and all of 18 compounds could be resolved at least with one of the three chiral CSP under the conditions of this study. With regard to the structure of the analytes, bulky electron rich substituents at C5 of the hydantoin nucleus appear to favor stereoselective interactions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:457 / 465
页数:9
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