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Volumn 11, Issue 5-6, 1999, Pages 420-425

Chromatographic resolution of organic acids using the Kromasil-CHI-TBB chiral stationary phase

Author keywords

Chiral chromatography; Hydrogen bonding interaction; Mandelic acid; Optical resolution; Preparative chromatography; Tropic acid

Indexed keywords

3 METHOXYTROPIC ACID; CARBOXYLIC ACID; MANDELIC ACID; UNCLASSIFIED DRUG;

EID: 0033024697     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1999)11:5/6<420::AID-CHIR12>3.0.CO;2-V     Document Type: Conference Paper
Times cited : (10)

References (10)
  • 2
    • 0030576511 scopus 로고    scopus 로고
    • Chromatographic separation of enantiomers on N,N′-diallyl-L-tartardiamide-based network-polymeric chiral stationary phases
    • Andersson S, Allenmark S, Möller P, Persson B, Sanchez D. Chromatographic separation of enantiomers on N,N′-diallyl-L-tartardiamide-based network-polymeric chiral stationary phases. J Chromatogr A 1996;741:23-31.
    • (1996) J Chromatogr A , vol.741 , pp. 23-31
    • Andersson, S.1    Allenmark, S.2    Möller, P.3    Persson, B.4    Sanchez, D.5
  • 3
    • 0000861651 scopus 로고
    • Chiral recognition conducted by tartaric acid derivatives in nonaqueous media
    • Dobashi Y, Dobashi A, Hara S. Chiral recognition conducted by tartaric acid derivatives in nonaqueous media. Tetrahedron Lett 1984;25: 329-332.
    • (1984) Tetrahedron Lett , vol.25 , pp. 329-332
    • Dobashi, Y.1    Dobashi, A.2    Hara, S.3
  • 4
    • 33845379431 scopus 로고
    • Extended scope of chiral recognition applying hydrogen bond associations in nonaqueous media: (R,R)-N,N′-diisopropyltartramide (DIPTA) as a widely applicable resolving agent
    • Dobashi Y, Hara S. Extended scope of chiral recognition applying hydrogen bond associations in nonaqueous media: (R,R)-N,N′-diisopropyltartramide (DIPTA) as a widely applicable resolving agent. J Am Chem Soc 1985;107:3406-3411.
    • (1985) J Am Chem Soc , vol.107 , pp. 3406-3411
    • Dobashi, Y.1    Hara, S.2
  • 5
    • 84963287698 scopus 로고
    • Enantioselectivity of hydrogen-bond association in liquid-solid chromatography
    • Dobashi A, Dobashi Y, Hara S. Enantioselectivity of hydrogen-bond association in liquid-solid chromatography. J Liq Chromatogr 1986;9: 243-267.
    • (1986) J Liq Chromatogr , vol.9 , pp. 243-267
    • Dobashi, A.1    Dobashi, Y.2    Hara, S.3
  • 6
    • 84963165355 scopus 로고
    • Chromatographic resolution of amino acids using tartaric acid mono-N-octylamide as mobile phase additive
    • Lindner WF, Hirschböck I. Chromatographic resolution of amino acids using tartaric acid mono-N-octylamide as mobile phase additive. J Liq Chromatogr 1986;9:551-571.
    • (1986) J Liq Chromatogr , vol.9 , pp. 551-571
    • Lindner, W.F.1    Hirschböck, I.2
  • 7
    • 0025955340 scopus 로고
    • (2R, 3R)-Dicyclohexyl tartrate as chiral mobile phase additive
    • Heldin E, Huyun NH, Pettersson C. (2R, 3R)-Dicyclohexyl tartrate as chiral mobile phase additive. J Chromatogr 1991;585:35-44.
    • (1991) J Chromatogr , vol.585 , pp. 35-44
    • Heldin, E.1    Huyun, N.H.2    Pettersson, C.3
  • 8
    • 0027481051 scopus 로고
    • Enantiomer separation by HPLC on reversed phase silica gel coated with copper(II) complexes of (R,R)-tartaric acid mono-amide derivatives
    • Oi N, Kitahara H, Aoki F. Enantiomer separation by HPLC on reversed phase silica gel coated with copper(II) complexes of (R,R)-tartaric acid mono-amide derivatives. J Liq Chromatogr 1993;16:893-901.
    • (1993) J Liq Chromatogr , vol.16 , pp. 893-901
    • Oi, N.1    Kitahara, H.2    Aoki, F.3
  • 9
    • 0001389993 scopus 로고
    • A chiral stationary phase derived from (R,R)-tartramide with broadened scope of application to the liquid chromatographic resolution of enantiomers
    • Dobashi Y, Hara S. A chiral stationary phase derived from (R,R)-tartramide with broadened scope of application to the liquid chromatographic resolution of enantiomers. J Org Chem 1987;52:2490-2496.
    • (1987) J Org Chem , vol.52 , pp. 2490-2496
    • Dobashi, Y.1    Hara, S.2
  • 10
    • 0028355123 scopus 로고
    • Enantiomer separation by high performance liquid chromatography with (R,R)-tartaric acid mono-amide derivatives as bifunctional chiral selectors
    • Oi N, Kitahara H, Aoki F. Enantiomer separation by high performance liquid chromatography with (R,R)-tartaric acid mono-amide derivatives as bifunctional chiral selectors. J Chromatogr A 1994;666:457-462.
    • (1994) J Chromatogr A , vol.666 , pp. 457-462
    • Oi, N.1    Kitahara, H.2    Aoki, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.