메뉴 건너뛰기




Volumn 12, Issue 2, 2000, Pages 63-70

Preparation and evaluation of chiral stationary phases based on N,N-2,4- (or 4,6)-disubstituted 4,5-(or 2,5)-dichloro-1,3-dicyanobenzene

Author keywords

Brush type CSPs; Chiral recognition; Resolution

Indexed keywords

ANILINE; BENZENE DERIVATIVE; BENZONITRILE; CHLORINE; SILICA GEL;

EID: 0033973276     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(2000)12:2<63::AID-CHIR2>3.0.CO;2-W     Document Type: Article
Times cited : (18)

References (18)
  • 2
    • 0000352907 scopus 로고    scopus 로고
    • Chromatography on chiral stationary phase
    • Allenmark S, Schurig V. Chromatography on chiral stationary phase. J Matern Sci 1997;7:1955-1963.
    • (1997) J Matern Sci , vol.7 , pp. 1955-1963
    • Allenmark, S.1    Schurig, V.2
  • 3
    • 0001090404 scopus 로고    scopus 로고
    • Enantioselective chromatography: An essential and versatile tool for the analytical and preparative separation of enantiomers
    • Francotte ER. Enantioselective chromatography: an essential and versatile tool for the analytical and preparative separation of enantiomers. Chimia 1997;51:717-725.
    • (1997) Chimia , vol.51 , pp. 717-725
    • Francotte, E.R.1
  • 4
    • 0028799796 scopus 로고
    • Preparation and properties of glutathion conjugates of 2,4,5,6-tetrachloro-1,3-dicyanobenzene
    • Hameršak Z, Hollosi M, Kontrec D, Ladešic, Majer Z, Šunjic V. Preparation and properties of glutathion conjugates of 2,4,5,6-tetrachloro-1,3-dicyanobenzene. Tetrahedron 1995;51:2331-2338.
    • (1995) Tetrahedron , vol.51 , pp. 2331-2338
    • Hameršak, Z.1    Hollosi, M.2    Kontrec, D.3    Ladešic4    Majer, Z.5    Šunjic, V.6
  • 5
    • 0033591106 scopus 로고    scopus 로고
    • Chiroptical and conformational properties of (R)-1-phenylethylamine derivatives of persubsituted benzene
    • Kontrec D, Vinkovic V, Lesac A, Šunjic V, Hollosi M. Chiroptical and conformational properties of (R)-1-phenylethylamine derivatives of persubsituted benzene. Tetrahedron Asymm 1999;10:1935-1945.
    • (1999) Tetrahedron Asymm , vol.10 , pp. 1935-1945
    • Kontrec, D.1    Vinkovic, V.2    Lesac, A.3    Šunjic, V.4    Hollosi, M.5
  • 6
    • 0032743610 scopus 로고    scopus 로고
    • Stationary phases based on (R)-1-naphthylelhylamine bound to 2,4,5,6-tetrachloro-1,3-dicyanobenzene
    • in press
    • Kontrec D, Vinkovic V, Šunjic V. Stationary phases based on (R)-1-naphthylelhylamine bound to 2,4,5,6-tetrachloro-1,3-dicyanobenzene. Chirality; in press.
    • Chirality
    • Kontrec, D.1    Vinkovic, V.2    Šunjic, V.3
  • 7
    • 0025801425 scopus 로고
    • Enantiomeric resolution of amino acid derivatives by high-performance liquid chromatography on chiral stationary phases derived from L-proline
    • Daban Haurou C, Declercq G, Ramiandrasoa P, Millet JL. Enantiomeric resolution of amino acid derivatives by high-performance liquid chromatography on chiral stationary phases derived from L-proline. J Chromatogr 1991;547:31-44.
    • (1991) J Chromatogr , vol.547 , pp. 31-44
    • Daban Haurou, C.1    Declercq, G.2    Ramiandrasoa, P.3    Millet, J.L.4
  • 8
    • 0004057301 scopus 로고
    • High-pressure liquid chromatographic resolution of optical isomers
    • Ahuja S, editor. Chiral separation by liquid chromatography
    • Dhanesar SC. High-pressure liquid Chromatographic resolution of optical isomers. In: Ahuja S, editor. Chiral separation by liquid chromatography. ACS Symposium Series 1991;471:183-202.
    • (1991) ACS Symposium Series , vol.471 , pp. 183-202
    • Dhanesar, S.C.1
  • 9
    • 0000858104 scopus 로고
    • Preparation and use of hydantoin-based chiral stationary phases
    • Pirkle WH, Hyun MH. Preparation and use of hydantoin-based chiral stationary phases. J Chromatogr 1985;322:309-320.
    • (1985) J Chromatogr , vol.322 , pp. 309-320
    • Pirkle, W.H.1    Hyun, M.H.2
  • 10
    • 0013260132 scopus 로고
    • Design, synthesis and evaluation of a brush-type chiral stationary phase with broad generality
    • Welch CJ. Design, synthesis and evaluation of a brush-type chiral stationary phase with broad generality. Chiral 1994;33-37.
    • (1994) Chiral , pp. 33-37
    • Welch, C.J.1
  • 11
    • 0001960612 scopus 로고
    • Commercialy available brush-type chiral selectors for the direct resolution of enantiomers
    • Ahuja S, editor. Chiral separation by liquid chromatography
    • Pirkle WH, Perrin S. Commercialy available brush-type chiral selectors for the direct resolution of enantiomers. In: Ahuja S, editor. Chiral separation by liquid chromatography. ACS Symposium Series 1991; 471:43-68.
    • (1991) ACS Symposium Series , vol.471 , pp. 43-68
    • Pirkle, W.H.1    Perrin, S.2
  • 12
    • 0028928186 scopus 로고
    • Direct enantiomer separations by high-performance liquid chromatography with chiral urea derivatives as stationary phases
    • Ôi N, Kitahara H, Aoki F. Direct enantiomer separations by high-performance liquid chromatography with chiral urea derivatives as stationary phases. J Chromatogr A 1995;694:129-134.
    • (1995) J Chromatogr A , vol.694 , pp. 129-134
    • Ôi, N.1    Kitahara, H.2    Aoki, F.3
  • 13
    • 0024340632 scopus 로고
    • Discussion of a controversial chiral recognition model
    • Pirkle WH, McCune JE. Discussion of a controversial chiral recognition model. J Chromatogr 1989;469:67-75.
    • (1989) J Chromatogr , vol.469 , pp. 67-75
    • Pirkle, W.H.1    McCune, J.E.2
  • 14
    • 0028284222 scopus 로고
    • Use of simultaneous face to face and face to edge π-π interactions to facilitate chiral recognition
    • Pirkle WH, Welch CJ. Use of simultaneous face to face and face to edge π-π interactions to facilitate chiral recognition. Tetrahedron Asymm 1994;5:777-780.
    • (1994) Tetrahedron Asymm , vol.5 , pp. 777-780
    • Pirkle, W.H.1    Welch, C.J.2
  • 15
    • 0030592465 scopus 로고    scopus 로고
    • On the relevance of face-to-edge π-π interactions to chiral recognition
    • Pirkle WH, Liu YL. On the relevance of face-to-edge π-π interactions to chiral recognition. J Chromatogr A 1996;749:19-24.
    • (1996) J Chromatogr A , vol.749 , pp. 19-24
    • Pirkle, W.H.1    Liu, Y.L.2
  • 16
    • 0028277007 scopus 로고
    • Comparison between silicabonded chiral stationary phases from 3,5-disubstituted N-benzoyl-(S)-phenylalanine and (S)-cyclohexylalanine in the resolution of racemic compounds by liquid chromatography
    • Oliveros L, Minguillón C, González T. Comparison between silicabonded chiral stationary phases from 3,5-disubstituted N-benzoyl-(S)-phenylalanine and (S)-cyclohexylalanine in the resolution of racemic compounds by liquid chromatography. J Chromatogr A 1994;672:59-65.
    • (1994) J Chromatogr A , vol.672 , pp. 59-65
    • Oliveros, L.1    Minguillón, C.2    González, T.3
  • 17
    • 0001103847 scopus 로고
    • Preparation and evaluation of a chiral stationary phase bearing both π-acidic and -basic sites
    • Hyun MH, Pirkle WH. Preparation and evaluation of a chiral stationary phase bearing both π-acidic and -basic sites. J Chromatogr 1987;393: 357-365.
    • (1987) J Chromatogr , vol.393 , pp. 357-365
    • Hyun, M.H.1    Pirkle, W.H.2
  • 18
    • 0028220741 scopus 로고
    • Evaluation of chiral stationary phase design in the Pirkle laboratories
    • Welch CJ. Evaluation of chiral stationary phase design in the Pirkle laboratories. J Chromatogr A 1994;666:3-26.
    • (1994) J Chromatogr A , vol.666 , pp. 3-26
    • Welch, C.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.