| Literature DB >> 28608589 |
Carla Fernandes1,2, Maria Elizabeth Tiritan1,2,3, Sara Cravo1,2, Ye' Zaw Phyo4, Anake Kijjoa2,4, Artur M S Silva5, Quezia B Cass6, Madalena M M Pinto1,2.
Abstract
Six chiral derivatives of xanthones (CDXs) were covalently bonded to silica, yielding the corresponding xanthonic chiral stationary phases (XCSPs). The new XCSPs were packed into stainless-steel columns with 150 x 4.6 mm i.d. Moreover, the greening of the chromatographic analysis by reducing the internal diameter (150 x 2.1 mm i.d.) of the liquid chromatography (LC) columns was also investigated. The enantioselective capability of these phases was evaluated by LC using different chemical classes of chiral compounds, including several types of drugs. A library of CDXs was evaluated in order to explore the principle of reciprocity as well as the chiral self-recognition phenomenon. The separation of enantiomeric mixtures of CDXs was investigated under multimodal elution conditions. The XCSPs provided high specificity for the enantiomeric mixtures of CDXs evaluated mainly under normal-phase elution conditions. Furthermore, two XCSPs were prepared with both enantiomers of the same xanthonic selector in order to confirm the inversion order elution.Entities:
Keywords: chiral derivatives of xanthones; chiral stationary phase; enantioselectivity; liquid chromatography
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Year: 2017 PMID: 28608589 DOI: 10.1002/chir.22706
Source DB: PubMed Journal: Chirality ISSN: 0899-0042 Impact factor: 2.437