Resolution and determination of enantiomeric purity of new chiral derivatives of xanthones using polysaccharide-based stationary phases

被引:26
|
作者
Fernandes, Carla [1 ,2 ]
Brandao, Pedro [1 ,2 ]
Santos, Alexandre [1 ,2 ]
Tiritan, Maria Elizabeth [1 ,3 ]
Afonso, Carlos [1 ,2 ]
Cass, Quezia B. [4 ]
Pinto, Madalena M. [1 ,2 ]
机构
[1] Univ Porto CEQUIMED UP, Ctr Quim Med, P-4050313 Oporto, Portugal
[2] Univ Porto, Fac Farm, Dept Ciencias Quim, Lab Quim Organ & Farmaceut, P-4050313 Oporto, Portugal
[3] Inst Super Ciencias Saude N CICS ISCS N, Ctr Invest Ciencias Saude, P-4585116 Gandra Prd, Portugal
[4] Univ Fed Sao Carlos, SP, Dept Quim, Sao Carlos, SP, Brazil
关键词
Chiral derivatives of xanthones; Polysaccharide-based stationary phases; Multimodal elution; Enantioselectivity; Enantiomeric purity; PERFORMANCE LIQUID-CHROMATOGRAPHY; MULTIMODAL ELUTION; MULTIMILLIGRAM ENANTIORESOLUTION; MICROPOROUS SILICA; IN-VITRO; HPLC; ENANTIOSEPARATION; ANTICONVULSANT; RECOGNITION; INHIBITORS;
D O I
10.1016/j.chroma.2012.07.058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The enantioresolution and determination of the enantiomeric purity of 24 new chiral derivatives of xanthones (CDXs) were investigated on polysaccharide-based chiral stationary phases (CSPs). The tris-3.5-dimethylphenylcarbamates of cellulose and amylose and tris-3,5-dimethoxyphenylcarbamate of amylose were selected as CSPs for this work. The separation of enantiomeric mixtures of CDXs was explored under multimodal elution conditions. All the enantiomeric mixtures of CDXs were enantioseparated with very high enantioselectivity and resolution with a and R-S ranging from 1.43 to 12.41 and from 1.48 to 10.29, respectively. The best performances were achieved on amylose tris-3,5-dimethylphenylcarbamate stationary phase under polar organic elution conditions. Furthermore the enantiomeric purity for all the CDXs was measured, achieving values higher than 99%. Based on the obtained results, the influence of the mobile phases and structural features of the CSPs and CDXs on chiral discrimination are also discussed. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 153
页数:11
相关论文
共 50 条
  • [1] Enantiomeric resolution, thermodynamic parameters, and modeling of clausenamidone and neoclausenamidone on polysaccharide-based chiral stationary phases
    Luo, Xuna
    Fang, Chengqiao
    Mi, Junru
    Xu, Jingzi
    Lin, Hansen
    [J]. CHIRALITY, 2019, 31 (06) : 423 - 433
  • [2] Enantiomeric separation of cyclopropane derivatives on a polysaccharide-based chiral stationary phase
    Ghanem, A
    Hoenen, H
    Müller, P
    Aboul-Enein, HY
    [J]. ANALYTICA CHIMICA ACTA, 2005, 538 (1-2) : 15 - 24
  • [3] Separation of piracetam derivatives on polysaccharide-based chiral stationary phases
    Kazoka, H.
    Koliskina, O.
    Veinberg, G.
    Vorona, M.
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2013, 1281 : 160 - 165
  • [4] Chromatographic enantioseparation of chiral sulfinamide derivatives on polysaccharide-based chiral stationary phases
    Zeng, Qingle
    Wen, Quan
    Xiang, Yao
    Zhang, Lei
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2018, 1571 : 240 - 244
  • [5] Enantiomeric separation of several oxirane derivatives by high performance liquid chromatography on polysaccharide-based chiral stationary phases
    Zhou, Wei
    Liu, Bing
    Yang, Guo-Sheng
    Koppenhoefer, Bernhard
    Aboul-Enein, Hassan Y.
    [J]. JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2008, 31 (18) : 2879 - 2891
  • [6] HPLC separation of enantiomeric pyrrolidine alcohols and their precursors on polysaccharide-based chiral stationary phases
    Zhou, Ailing
    Lindsay, Harriet A.
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248
  • [7] Preparative enantiomeric separation of new aromatase inhibitors by HPLC on polysaccharide-based chiral stationary phases: Determination of enantiomeric purity and assignment of absolute stereochemistry by X-ray structure analysis
    Danel, C
    Foulon, C
    Guelzim, A
    Park, CH
    Bonte, JP
    Vaccher, C
    [J]. CHIRALITY, 2005, 17 (09) : 600 - 607
  • [8] Development and validation of a chiral LC-MS method for the enantiomeric resolution of (+) and (-)-medetomidine in equine plasma by using polysaccharide-based chiral stationary phases
    Kal, Abdul Khader Karakka
    Nalakath, Jahfar
    Karatt, Tajudheen Kunhamu
    Perwad, Zubair
    Mathew, Binoy
    Subhahar, Michael
    [J]. CHIRALITY, 2020, 32 (03) : 314 - 323
  • [9] Enantiomer resolution screening strategy using multiple immobilised polysaccharide-based chiral stationary phases
    Zhang, Tong
    Nguyen, Dung
    Franco, Pilar
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2008, 1191 (1-2) : 214 - 222
  • [10] Immobilized Polysaccharide-Based Chiral Stationary Phases for HPLC
    Tomoyuki Ikai
    Chiyo Yamamoto
    Masami Kamigaito
    Yoshio Okamoto
    [J]. Polymer Journal, 2006, 38 : 91 - 108