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Volumn 1363, Issue , 2014, Pages 101-108

Direct enantioseparation of underivatized aliphatic 3-hydroxyalkanoic acids with a quinine-based zwitterionic chiral stationary phase

Author keywords

3 Hydroxyalkanoic acids, liquid chromatography; Cinchona based zwitterionic chiral stationary phase; Enantiomer separation; Natural compounds, polar organic mode; Underivatized 3 hydroxycarboxylic acids

Indexed keywords

DRUG PRODUCTS; ENANTIOMERS; ION EXCHANGE RESINS; IONS; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY;

EID: 84908092154     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2014.03.060     Document Type: Article
Times cited : (52)

References (49)
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    • Elsevier Science, Amsterdam, E.M. Carreira, H. Yamamoto (Eds.)
    • Natalini B., Sardella R. Comprehensive Chirality 2012, 115. Elsevier Science, Amsterdam. E.M. Carreira, H. Yamamoto (Eds.).
    • (2012) Comprehensive Chirality , pp. 115
    • Natalini, B.1    Sardella, R.2
  • 42
    • 85018195944 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim, E. Francotte, W. Lindner (Eds.)
    • Maier N.M., Lindner W. Chirality in Drug Research 2006, p189. Wiley-VCH, Weinheim. E. Francotte, W. Lindner (Eds.).
    • (2006) Chirality in Drug Research , pp. p189
    • Maier, N.M.1    Lindner, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.