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Volumn 15, Issue 5, 2003, Pages 400-408

Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction

Author keywords

Bicyclic selectors; Cycloaddition; Enantioselective liquid chromatography; Hydrosilylation

Indexed keywords

9,10 DIHYDRO 9,10 ETHANOANTHRACENE 11,12 DICARBOXYLIC ACID; 9,10 DIHYDRO 9,10 ETHANOANTHRACENE 11,12 DICARBOXYLIC ACID BISALLYLAMIDE; ANTHRACENE; BENZODIAZEPINE DERIVATIVE; CAMAZEPAM; CHLORMEZANONE; CHLORTALIDONE; CLENBUTEROL; DICARBOXYLIC ACID DERIVATIVE; FUMARIC ACID; IBUPROFEN; KETAZOLAM; KETOPROFEN; LOPIRAZEPAM; LORAZEPAM; OMEPRAZOLE; SILANE DERIVATIVE; SILICON DIOXIDE; TEMAZEPAM; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 0037277068     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10224     Document Type: Article
Times cited : (7)

References (19)
  • 1
    • 0028847071 scopus 로고
    • A new class of network-polymeric chiral stationary phases
    • Allenmark S, Andersson S, Möller P, Sanchez D. A new class of network-polymeric chiral stationary phases. Chirality 1995;7:248-256.
    • (1995) Chirality , vol.7 , pp. 248-256
    • Allenmark, S.1    Andersson, S.2    Möller, P.3    Sanchez, D.4
  • 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
    • 0030602809 scopus 로고    scopus 로고
    • Efficient high-performance liquid chromatographic enantioseparation of five-membered aryl-substituted lactones and cyclic carbamates on a (R,R)-diaminodihydroanthracene-derived chiral stationary phase
    • Maier NM, Uray G. Efficient high-performance liquid chromatographic enantioseparation of five-membered aryl-substituted lactones and cyclic carbamates on a (R,R)-diaminodihydroanthracene-derived chiral stationary phase. J Chromatogr A 1996;740:11-19.
    • (1996) J Chromatogr A , vol.740 , pp. 11-19
    • Maier, N.M.1    Uray, G.2
  • 4
    • 0000916414 scopus 로고
    • Étude des mélanges d'antipodes optiques. Dérivés du dihydro-9,10 éthano-9,10 anthracène
    • Brienne M-J, Jacques J. Étude des mélanges d'antipodes optiques. Dérivés du dihydro-9,10 éthano-9,10 anthracène. Bull Soc Chim Fr 1973;1:190-197.
    • (1973) Bull Soc Chim Fr , vol.1 , pp. 190-197
    • Brienne, M.-J.1    Jacques, J.2
  • 5
    • 0001013175 scopus 로고
    • Asymmetric Diels-Alder reaction. Cooperative blocking effect in organic synthesis
    • Furuta K, Iwanaga K, Yamamoto H. Asymmetric Diels-Alder reaction. Cooperative blocking effect in organic synthesis. Tetrahedron Lett 1986;27:4507-4510.
    • (1986) Tetrahedron Lett , vol.27 , pp. 4507-4510
    • Furuta, K.1    Iwanaga, K.2    Yamamoto, H.3
  • 6
    • 1542544067 scopus 로고
    • The reaction of anthracene with maleic and fumaric acid and their derivatives and with citraconic anhydride and mesaconic acid
    • Bachmann WE, Scott LB. The reaction of anthracene with maleic and fumaric acid and their derivatives and with citraconic anhydride and mesaconic acid. J Am Chem Soc 1948;70:1458-1461.
    • (1948) J Am Chem Soc , vol.70 , pp. 1458-1461
    • Bachmann, W.E.1    Scott, L.B.2
  • 7
    • 1642324310 scopus 로고
    • A modular approach for ligand design for asymmetric allylic alkylation via enantioselective palladium-catalyzed ionizations
    • Trost BM, van Vranken DL, Bingel C. A modular approach for ligand design for asymmetric allylic alkylation via enantioselective palladium-catalyzed ionizations. J Am Chem Soc 1992;114:9327-9343.
    • (1992) J Am Chem Soc , vol.114 , pp. 9327-9343
    • Trost, B.M.1    Van Vranken, D.L.2    Bingel, C.3
  • 8
    • 0027264442 scopus 로고
    • Chiral discrimination by albumin: A mechanistic study of liquid chromatographic optical resolution of nonaromatic carboxylic acids
    • (a) Allenmark S. Chiral discrimination by albumin: a mechanistic study of liquid chromatographic optical resolution of nonaromatic carboxylic acids. Chirality 1993;5:295-299.
    • (1993) Chirality , vol.5 , pp. 295-299
    • Allenmark, S.1
  • 9
    • 0030901324 scopus 로고    scopus 로고
    • Thermodynamic study of an unusual chiral separation. Propranolol enantiomers on an immobilized cellulase
    • (b) Fornstedt T, Sajonz P, Guiochon G. Thermodynamic study of an unusual chiral separation. Propranolol enantiomers on an immobilized cellulase. J Am Chem Soc 1997;119: 1254-1264.
    • (1997) J Am Chem Soc , vol.119 , pp. 1254-1264
    • Fornstedt, T.1    Sajonz, P.2    Guiochon, G.3
  • 10
    • 0032835772 scopus 로고    scopus 로고
    • Discrimination between enantioselective and non-selective binding sites on cellobiohydrolase-based stationary phases by site specific competing ligands
    • (c) Henriksson H, Pettersson G, Johansson G. Discrimination between enantioselective and non-selective binding sites on cellobiohydrolase-based stationary phases by site specific competing ligands. J Chromatogr A 1999;857:107-115.
    • (1999) J Chromatogr A , vol.857 , pp. 107-115
    • Henriksson, H.1    Pettersson, G.2    Johansson, G.3
  • 11
    • 0037844272 scopus 로고    scopus 로고
    • Apparent and true enantioselectivity in enantioseparation
    • (d) Götmar G, Fornstedt T, Guiochon G. Apparent and true enantioselectivity in enantioseparation. Chirality 2000;12:558-564.
    • (2000) Chirality , vol.12 , pp. 558-564
    • Götmar, G.1    Fornstedt, T.2    Guiochon, G.3
  • 12
    • 0025429690 scopus 로고
    • Optically active polyamides consisting of anti head-to-head coumarin dimer and α,ω-alkalenediamine. Odd-even discrimination in chiral recognition ability depending on the methylene number of the diamine component and correlation between the ability and crystallizability
    • (a) Saigo K, Shiwaku T, Hayashi K, Fujioka K, Sukegawa M, Chen Y, Yonezawa N, Hasegawa M. Optically active polyamides consisting of anti head-to-head coumarin dimer and α,ω-alkalenediamine. Odd-even discrimination in chiral recognition ability depending on the methylene number of the diamine component and correlation between the ability and crystallizability. Macromolecules 1990;23:2830-2836.
    • (1990) Macromolecules , vol.23 , pp. 2830-2836
    • Saigo, K.1    Shiwaku, T.2    Hayashi, K.3    Fujioka, K.4    Sukegawa, M.5    Chen, Y.6    Yonezawa, N.7    Hasegawa, M.8
  • 13
    • 0026383673 scopus 로고
    • Chromatographic optical resolution of enantiomers on polyamides containing 1,2-disubstituted cyclohexane moiety as a chiral residue
    • (b) Okamoto Y, Nagamura Y, Fukumoto T, Hatada K. Chromatographic optical resolution of enantiomers on polyamides containing 1,2-disubstituted cyclohexane moiety as a chiral residue. Polym J 1991;23: 1197-1207.
    • (1991) Polym J , vol.23 , pp. 1197-1207
    • Okamoto, Y.1    Nagamura, Y.2    Fukumoto, T.3    Hatada, K.4
  • 14
    • 0001612353 scopus 로고
    • Synthesis of optically active polyamides having axially dissymetric 1,1′-binaphthalene-2,2′-dicarboxylic acid component and their optical resolution ability as chiral adsorbent for HPLC
    • (c) Tamai Y, Matsuzaka Y, Ôi S, Miyano S. Synthesis of optically active polyamides having axially dissymetric 1,1′-binaphthalene-2,2′-dicarboxylic acid component and their optical resolution ability as chiral adsorbent for HPLC. Bull Chem Soc Jpn 1991; 64:2260-2265.
    • (1991) Bull Chem Soc Jpn , vol.64 , pp. 2260-2265
    • Tamai, Y.1    Matsuzaka, Y.2    Ôi, S.3    Miyano, S.4
  • 15
    • 0026726864 scopus 로고
    • HPLC resolution of atropoisomeric compounds on a CSP derived from (1R;2R)-diaminocyclohexane: Thermodynamic data from variable temperature chromatography
    • (d) Galli B, Gasparrini F, Misiti D, Pierini M, Villani C, Bronzetti M. HPLC resolution of atropoisomeric compounds on a CSP derived from (1R;2R)-diaminocyclohexane: Thermodynamic data from variable temperature chromatography. Chirality 1992:4:384-388.
    • (1992) Chirality , vol.4 , pp. 384-388
    • Galli, B.1    Gasparrini, F.2    Misiti, D.3    Pierini, M.4    Villani, C.5    Bronzetti, M.6
  • 16
    • 0033613770 scopus 로고    scopus 로고
    • First example of the solvent effect on absolute conformation of chiral 3,3-disubstituted 1,4-benzodiazepin-2-ones
    • (a) Avdagic A, Lesac A, Sunjic V. First example of the solvent effect on absolute conformation of chiral 3,3-disubstituted 1,4-benzodiazepin-2-ones. Tetrahedron 1999;55:1407-1416.
    • (1999) Tetrahedron , vol.55 , pp. 1407-1416
    • Avdagic, A.1    Lesac, A.2    Sunjic, V.3
  • 17
    • 0032848251 scopus 로고    scopus 로고
    • Ring inversion barrier of diazepam and derivatives: An ab initio study
    • (b) Paizs B, Simonyi M. Ring inversion barrier of diazepam and derivatives: an ab initio study. Chirality 1999;11:651-658.
    • (1999) Chirality , vol.11 , pp. 651-658
    • Paizs, B.1    Simonyi, M.2
  • 18
    • 0021242386 scopus 로고
    • Direct liquid chromatographic separation of benzodiazepinone enantiomers
    • Pirkle WH, Tsipouras A. Direct liquid chromatographic separation of benzodiazepinone enantiomers. J Chromatogr 1984;291:291-298.
    • (1984) J Chromatogr , vol.291 , pp. 291-298
    • Pirkle, W.H.1    Tsipouras, A.2
  • 19
    • 0017041018 scopus 로고
    • A comparison of the determination of partition coefficients of 1,4-benzodiazepines by high-performance liquid chromatography and thin-layer chromatography
    • Hulshoff A, Perrin JH. A comparison of the determination of partition coefficients of 1,4-benzodiazepines by high-performance liquid chromatography and thin-layer chromatography. J Chromatogr 1976;129: 263-276.
    • (1976) J Chromatogr , vol.129 , pp. 263-276
    • Hulshoff, A.1    Perrin, J.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.