메뉴 건너뛰기




Volumn 25, Issue 11, 2013, Pages 810-813

Nonaqueous capillary electrophoretic enantioseparation of water insoluble tröger's base derivatives using β-cyclodextrin as chiral selector

Author keywords

cyclodextrin; capillary electrophoresis; enantioseparation; nonaqueous capillary electrophoresis; Tr ger's base

Indexed keywords

ACETIC ACID; BETA CYCLODEXTRIN; CITRATE SODIUM; DRUG ADDITIVE; ELECTROLYTE; FORMAMIDE; HEPTAKIS(2,6 O DIMETHYL) BETA CYCLODEXTRIN; INORGANIC SALT; METHANE; ORGANIC COMPOUND; ORGANIC SOLVENT; POLYMER; SOLVENT; TRIS(HYDROXYMETHYL)AMINOMETHANE ACETATE; TROGER BASE; UNCLASSIFIED DRUG; WATER;

EID: 84886639461     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.22220     Document Type: Article
Times cited : (10)

References (31)
  • 1
    • 65249141725 scopus 로고    scopus 로고
    • Non-aqueous capillary electrophoresis 2005-2008
    • Geiser L, Veuthey JL,. Non-aqueous capillary electrophoresis 2005-2008. Electrophoresis 2009; 30: 36-49.
    • (2009) Electrophoresis , vol.30 , pp. 36-49
    • Geiser, L.1    Veuthey, J.L.2
  • 2
    • 69249215267 scopus 로고    scopus 로고
    • Organic solvents in CE
    • Kenndler E,. Organic solvents in CE. Electrophoresis 2009; 30: S101-S111.
    • (2009) Electrophoresis , vol.30
    • Kenndler, E.1
  • 3
    • 65249094295 scopus 로고    scopus 로고
    • Advances in enantioselective separations using electromigration capillary techniques
    • Preinerstorfer B, Lämmerhofer M, Lindner W,. Advances in enantioselective separations using electromigration capillary techniques. Electrophoresis 2009; 30: 100-132.
    • (2009) Electrophoresis , vol.30 , pp. 100-132
    • Preinerstorfer, B.1    Lämmerhofer, M.2    Lindner, W.3
  • 4
    • 34748924126 scopus 로고    scopus 로고
    • Enantioseparations by using capillary electrophoretic techniques the story of 20 and a few more years
    • Chankvetadze B, Enantioseparations by using capillary electrophoretic techniques The story of 20 and a few more years. J Chromatogr A 2007; 1168: 45-70.
    • (2007) J Chromatogr A , vol.1168 , pp. 45-70
    • Chankvetadze, B.1
  • 6
    • 17644418776 scopus 로고    scopus 로고
    • Chiral separations by capillary electromigration techniques in nonaqueous media I. Enantioselective nonaqueous capillary electrophoresis
    • Lämmerhofer M,. Chiral separations by capillary electromigration techniques in nonaqueous media I. Enantioselective nonaqueous capillary electrophoresis. J Chromatogr A 2005; 1068: 3-30.
    • (2005) J Chromatogr A , vol.1068 , pp. 3-30
    • Lämmerhofer, M.1
  • 7
    • 48949117190 scopus 로고    scopus 로고
    • Cyclodextrins in capillary electrophoresis enantioseparations - Recent developments and applications
    • Scriba GKE,. Cyclodextrins in capillary electrophoresis enantioseparations-Recent developments and applications. J Sep Sci 2008; 31: 1991-2011.
    • (2008) J Sep Sci , vol.31 , pp. 1991-2011
    • Scriba, G.K.E.1
  • 8
    • 69249212318 scopus 로고    scopus 로고
    • Chiral separations by CE employing CDs
    • Fanali S, Chiral separations by CE employing CDs. Electrophoresis 2009; 30: S203-S210.
    • (2009) Electrophoresis , vol.30
    • Fanali, S.1
  • 9
    • 0032806145 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoresis chiral separations with sulfated b-cyclodextrin
    • Wang F, Khaledi MG,. Nonaqueous capillary electrophoresis chiral separations with sulfated b-cyclodextrin. J Chromatogr B 1999; 731: 187-197.
    • (1999) J Chromatogr B , vol.731 , pp. 187-197
    • Wang, F.1    Khaledi, M.G.2
  • 10
    • 0029803925 scopus 로고    scopus 로고
    • Chiral separations by nonaqueous capillary electrophoresis
    • Wang F, Khaledi MG,. Chiral separations by nonaqueous capillary electrophoresis. Anal Chem 1996; 68: 3460-3467.
    • (1996) Anal Chem , vol.68 , pp. 3460-3467
    • Wang, F.1    Khaledi, M.G.2
  • 11
    • 0031832460 scopus 로고    scopus 로고
    • Analyte-additive interactions in nonaqueous capillary electrophoresis: A critical review
    • Bowser MT, Kranack AA, Chen DDY,. Analyte-additive interactions in nonaqueous capillary electrophoresis: a critical review. Trends Anal Chem 1998; 17: 424-434.
    • (1998) Trends Anal Chem , vol.17 , pp. 424-434
    • Bowser, M.T.1    Kranack, A.A.2    Chen, D.D.Y.3
  • 12
    • 0344069454 scopus 로고    scopus 로고
    • Chiral separations in capillary electrophoresis
    • Vespalec R, Boček P,. Chiral separations in capillary electrophoresis. Electrophoresis 1999; 20: 2579-2591.
    • (1999) Electrophoresis , vol.20 , pp. 2579-2591
    • Vespalec, R.1    Boček, P.2
  • 14
    • 1842842535 scopus 로고    scopus 로고
    • Chiral separation of amines with N-benzoxycarbonylglycyl-L-proline as selector in non-aqueous capillary electrophoresis using methanol and 1,2-dichloroethane in the background electrolyte
    • Hedeland Y, Hedeland M, Bondesson U, Pettersson C,. Chiral separation of amines with N-benzoxycarbonylglycyl-L-proline as selector in non-aqueous capillary electrophoresis using methanol and 1,2-dichloroethane in the background electrolyte. J Chromatogr A 2003; 984: 261-271.
    • (2003) J Chromatogr A , vol.984 , pp. 261-271
    • Hedeland, Y.1    Hedeland, M.2    Bondesson, U.3    Pettersson, C.4
  • 15
    • 0029897012 scopus 로고    scopus 로고
    • Chiral separation of dansyl-amino acids in a nonaqueous medium by capillary electrophoresis
    • Valkõ IE, Sirén H, Reikkola M-L,. Chiral separation of dansyl-amino acids in a nonaqueous medium by capillary electrophoresis. J Chromatogr A 1996; 737: 263-272.
    • (1996) J Chromatogr A , vol.737 , pp. 263-272
    • Valkõ, I.E.1    Sirén, H.2    Reikkola, M.-L.3
  • 16
    • 0032860699 scopus 로고    scopus 로고
    • Nonaqueous capillary electrophoretic separation of basic enantiomers using heptakis(2,3-dimethyl-6-sulfato)-ß-cyclodextrin
    • Tacker M, Glukhovskiy P, Cai H, Vigh G,. Nonaqueous capillary electrophoretic separation of basic enantiomers using heptakis(2,3-dimethyl-6- sulfato)-ß-cyclodextrin. Electrophoresis 1999; 20: 2794-2798.
    • (1999) Electrophoresis , vol.20 , pp. 2794-2798
    • Tacker, M.1    Glukhovskiy, P.2    Cai, H.3    Vigh, G.4
  • 17
    • 71949121318 scopus 로고    scopus 로고
    • 6-O-(2-hydroxybutyl)-ß-CD as a chiral selector for nonaqueous capillary electrophoretic separation of chiral drugs
    • Xing W, Wei Y, Yu P, Zhang C, Li J,. 6-O-(2-hydroxybutyl)-ß-CD as a chiral selector for nonaqueous capillary electrophoretic separation of chiral drugs. Front Chem China 2009; 4: 396-401.
    • (2009) Front Chem China , vol.4 , pp. 396-401
    • Xing, W.1    Wei, Y.2    Yu, P.3    Zhang, C.4    Li, J.5
  • 18
    • 0035942142 scopus 로고    scopus 로고
    • Chiral separations of 1,3,4-thia- and 1,3,4-selenadiazine derivatives by use of non-aqueous capillary electrophoresis
    • Karbaum A, Jira T,. Chiral separations of 1,3,4-thia- and 1,3,4-selenadiazine derivatives by use of non-aqueous capillary electrophoresis. J Biochem Biophys Methods 2001; 48: 155-162.
    • (2001) J Biochem Biophys Methods , vol.48 , pp. 155-162
    • Karbaum, A.1    Jira, T.2
  • 19
    • 34547872371 scopus 로고    scopus 로고
    • Nonaqueous and aqueous-organic media for the enantiomeric separations of neutral organophosphorus pesticides by CE
    • Huang L, Lin J, Xu L, Chen G,. Nonaqueous and aqueous-organic media for the enantiomeric separations of neutral organophosphorus pesticides by CE. Electrophoresis 2007; 28: 2758-2764.
    • (2007) Electrophoresis , vol.28 , pp. 2758-2764
    • Huang, L.1    Lin, J.2    Xu, L.3    Chen, G.4
  • 20
    • 84860454327 scopus 로고    scopus 로고
    • Oligo Tröger's bases - New molecular scaffolds
    • Dolenský B, Havlík M, Král V,. Oligo Tröger's bases-new molecular scaffolds. Chem Soc Rev 2012; 41: 3839-3858.
    • (2012) Chem Soc Rev , vol.41 , pp. 3839-3858
    • Dolenský, B.1    Havlík, M.2    Král, V.3
  • 21
    • 0034615951 scopus 로고    scopus 로고
    • Troger's base molecular scaffolds in dicarboxylic acid recognition
    • Goswami S, Ghosh K, Dasgupta S,. Troger's base molecular scaffolds in dicarboxylic acid recognition. J Org Chem 2000; 65: 1907-1914.
    • (2000) J Org Chem , vol.65 , pp. 1907-1914
    • Goswami, S.1    Ghosh, K.2    Dasgupta, S.3
  • 22
    • 33846865575 scopus 로고    scopus 로고
    • Enantioseparation of tetrahydropalmatine and Troger's base by molecularly imprinted monolith in capillary electrochromatography
    • Ou J, Dong J, Tian T, Hu J, Ye M, Zou H,. Enantioseparation of tetrahydropalmatine and Troger's base by molecularly imprinted monolith in capillary electrochromatography. J Biochem Biophys Methods 2007; 70: 71-76.
    • (2007) J Biochem Biophys Methods , vol.70 , pp. 71-76
    • Ou, J.1    Dong, J.2    Tian, T.3    Hu, J.4    Ye, M.5    Zou, H.6
  • 23
    • 0343885449 scopus 로고
    • Approaches to quantitative supramolecular chemistry. Hydrogen-bond-based molecular recognition phenomena and sigmoidal behavior in multicomponent mixtures
    • Wilcox CS, Adrian JC, Webb TH, Zawacki FJ,. Approaches to quantitative supramolecular chemistry. Hydrogen-bond-based molecular recognition phenomena and sigmoidal behavior in multicomponent mixtures. J Am Chem Soc 1992; 114: 10189-10197.
    • (1992) J Am Chem Soc , vol.114 , pp. 10189-10197
    • Wilcox, C.S.1    Adrian, J.C.2    Webb, T.H.3    Zawacki, F.J.4
  • 24
    • 0037119309 scopus 로고    scopus 로고
    • Probing the stereointegrity of Troger's base - A dynamic electrokinetic chromatographic study
    • Trapp O, Trapp G, Kong J, Hahn U, Vogtle F, Schurig V,. Probing the stereointegrity of Troger's base-A dynamic electrokinetic chromatographic study. Chem Eur J 2002; 8: 3629-3634.
    • (2002) Chem Eur J , vol.8 , pp. 3629-3634
    • Trapp, O.1    Trapp, G.2    Kong, J.3    Hahn, U.4    Vogtle, F.5    Schurig, V.6
  • 25
    • 0001081015 scopus 로고
    • Molecular recognition in aqueous media. Conformationally restricted water-soluble cyclophanes derived from 6H, 12H-5,11-methanodibenzo[b,f][1,5] diazocine.
    • Cowart MD, Sucholeiki I, Bukownik RR, Wilcox CS,. Molecular recognition in aqueous media. Conformationally restricted water-soluble cyclophanes derived from 6H, 12H-5,11-methanodibenzo[b,f][1,5]diazocine. J Am Chem Soc 1988; 110: 6204-6210.
    • (1988) J Am Chem Soc , vol.110 , pp. 6204-6210
    • Cowart, M.D.1    Sucholeiki, I.2    Bukownik, R.R.3    Wilcox, C.S.4
  • 26
    • 0000838835 scopus 로고
    • General effects of binding site water exclusion on hydrogen bond based molecular recognition systems: A "closed" binding site is less affected by environmental changes than an "open" site
    • Adrian JC, Wilcox CS,. General effects of binding site water exclusion on hydrogen bond based molecular recognition systems: a "closed" binding site is less affected by environmental changes than an "open" site. J Am Chem Soc 1992; 114: 1398-1403.
    • (1992) J Am Chem Soc , vol.114 , pp. 1398-1403
    • Adrian, J.C.1    Wilcox, C.S.2
  • 27
    • 33846020000 scopus 로고    scopus 로고
    • Cavity effect amplification in the recognition of dicarboxylic acids by initial ditopic H-bond formation followed by kinetic trapping
    • Brotherhood PR, Wu RAS, Turner P, Crossley MJ,. Cavity effect amplification in the recognition of dicarboxylic acids by initial ditopic H-bond formation followed by kinetic trapping. Chem Commun 2007: 225-227.
    • (2007) Chem Commun , pp. 225-227
    • Brotherhood, P.R.1    Wu, R.A.S.2    Turner, P.3    Crossley, M.J.4
  • 28
    • 84879415359 scopus 로고    scopus 로고
    • Enantioseparation of Tröger's base derivatives by capillary electrophoresis using cyclodextrins as chiral selectors
    • Řezanka P, Ryšavá H, Havlík M, Jakubek M, Sýkora D, Král V,. Enantioseparation of Tröger's base derivatives by capillary electrophoresis using cyclodextrins as chiral selectors. Chirality 2013; 25: 379-383.
    • (2013) Chirality , vol.25 , pp. 379-383
    • Řezanka, P.1    Ryšavá, H.2    Havlík, M.3    Jakubek, M.4    Sýkora, D.5    Král, V.6
  • 29
    • 84876101868 scopus 로고    scopus 로고
    • The study of enantioselectivity of all regioisomers of mono-carboxymethyl-ß-cyclodextrins used as additives in capillary electrophoresis
    • Navrátilová K, Řezanka P, Řezanka M, Sýkora D, Jindřich J, Král V,. The study of enantioselectivity of all regioisomers of mono-carboxymethyl-ß- cyclodextrins used as additives in capillary electrophoresis. J Sep Sci 2013; 36: 1270-1274.
    • (2013) J Sep Sci , vol.36 , pp. 1270-1274
    • Navrátilová, K.1    Řezanka, P.2    Řezanka, M.3    Sýkora, D.4    Jindřich, J.5    Král, V.6
  • 30
    • 84860338749 scopus 로고    scopus 로고
    • Impact of substituent position in monosubstituted a-cyclodextrins on enantioselectivity in capillary electrophoresis
    • Řezanka M, Řezanka P, Sýkora D, Jindřich J, Král V,. Impact of substituent position in monosubstituted a-cyclodextrins on enantioselectivity in capillary electrophoresis. J Sep Sci 2012; 35: 811-815.
    • (2012) J Sep Sci , vol.35 , pp. 811-815
    • Řezanka, M.1    Řezanka, P.2    Sýkora, D.3    Jindřich, J.4    Král, V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.