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Volumn 6 B, Issue 1, 2005, Pages 74-78

Separation and identification of cis and trans isomers of 2-butene-1,4-diol and lafutidine by HPLC and LC-MS

Author keywords

(S, S) Whelk O 1; 2 butene 1,4 diol; ChiraSpher; Isomers separation; Lafutidine; LC MS

Indexed keywords

BUTENES; ETHANOL; ISOMERS; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY;

EID: 12444337533     PISSN: 10093095     EISSN: None     Source Type: Journal    
DOI: 10.1631/jzus.2005.B0074     Document Type: Article
Times cited : (16)

References (8)
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    • Boonen, G., Beck, M., Haberlein, H., 1997. Contribution to the quantitative and enantioselective determination of kavapyrones by high-performance liquid chromatography on ChiraSpher NT material. Journal of Chromatography B, 702: 240.
    • (1997) Journal of Chromatography B , vol.702 , pp. 240
    • Boonen, G.1    Beck, M.2    Haberlein, H.3
  • 2
    • 12444316685 scopus 로고    scopus 로고
    • Lafutidine, a novel antiulcer drug
    • Chinese source
    • Chen, W.Q., Xu, D.Y., 2003. Lafutidine, a novel antiulcer drug. Chinese J. New Drugs Clin. Rem., 4: 247-250 (in Chinese).
    • (2003) Chinese J. New Drugs Clin. Rem. , vol.4 , pp. 247-250
    • Chen, W.Q.1    Xu, D.Y.2
  • 3
    • 0032940574 scopus 로고    scopus 로고
    • Enantioseparations in normal- and reversed-phase nano-high-performance liquid chromatography and capillary electrochromatography using polyacrylamide and polysaccharide derivatives as chiral stationary phases
    • Krause, K., Girod, M., Chankvetadze, B., Blaschke, G., 1999. Enantioseparations in normal- and reversed-phase nano-high-performance liquid chromatography and capillary electrochromatography using polyacrylamide and polysaccharide derivatives as chiral stationary phases. J. Chromatogr. A, 837: 51-63.
    • (1999) J. Chromatogr. A , vol.837 , pp. 51-63
    • Krause, K.1    Girod, M.2    Chankvetadze, B.3    Blaschke, G.4
  • 5
    • 0026651356 scopus 로고
    • An improved chiral stationary phase for the chromatographic-separation of underivatized naproxen enantiomers
    • Pirkle, W.H., Welch, C.J., 1992, An improved chiral stationary phase for the chromatographic-separation of underivatized naproxen enantiomers. J. Liq. Chromatogr., 15: 1947-1955.
    • (1992) J. Liq. Chromatogr. , vol.15 , pp. 1947-1955
    • Pirkle, W.H.1    Welch, C.J.2
  • 6
    • 0037080856 scopus 로고    scopus 로고
    • Enantioseparation of Gantofiban precursors on chiral stationary phases of the poly-(N-acryloyl amino acid derivative)-type
    • Schulte, M., Devent, R., Grosser, R., 2002. Enantioseparation of Gantofiban precursors on chiral stationary phases of the poly-(N-acryloyl amino acid derivative)-type. Journal of Pharmaceutical and Biomedical Analysis, 27: 627-637.
    • (2002) Journal of Pharmaceutical and Biomedical Analysis , vol.27 , pp. 627-637
    • Schulte, M.1    Devent, R.2    Grosser, R.3
  • 7
    • 11244276129 scopus 로고    scopus 로고
    • Comparison of enantioseparation and chiral recognition mechanism of racemic naproxen esters on (S, S)-whelk-O 1 and CDMPC chiral columns
    • Shao, B.H., Xu, X.Z., Lu, J.D., Cai, X.J., Zou, L., Fu, X.Y., 2003. Comparison of enantioseparation and chiral recognition mechanism of racemic naproxen esters on (S, S)-whelk-O 1 and CDMPC chiral columns. Acta Chim. Sinica, 61: 1635-1640.
    • (2003) Acta Chim. Sinica , vol.61 , pp. 1635-1640
    • Shao, B.H.1    Xu, X.Z.2    Lu, J.D.3    Cai, X.J.4    Zou, L.5    Fu, X.Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.