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Volumn 16, Issue 2, 2011, Pages 1682-1694

Bis-indole derivatives for polysaccharide compositional analysis and chiral resolution of D-, L-monosaccharides by ligand exchange capillary electrophoresis using borate-cyclodextrin as a chiral selector

Author keywords

Cyclodextrin; Enantioseparation; Indole; Ligand exchange capillary electrophoresis (LECE); Monosaccharides

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; 2-HYDROXYPROPYL-BETA-CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; BORIC ACID; INDOLE DERIVATIVE; LIGAND; MONOSACCHARIDE; PLANT EXTRACT; POLYSACCHARIDE;

EID: 79952133888     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16021682     Document Type: Article
Times cited : (17)

References (25)
  • 1
    • 0035937499 scopus 로고    scopus 로고
    • Chemical glycobiology
    • DOI 10.1126/science.1059820
    • Bertozzi, C.R.; Kiessling, L.L. Chemical glycobiology. Science 2001, 291, 2357-2364. (Pubitemid 32231790)
    • (2001) Science , vol.291 , Issue.5512 , pp. 2357-2364
    • Bertozzi, C.R.1    Kiessling, L.L.2
  • 2
    • 77950377779 scopus 로고    scopus 로고
    • Functionalized C-glycoside ketohydrazones: Carbohydrate derivatives that retain the ring integrity of the terminal reducing sugar
    • Price, N.P.J.; Bowman, M.J.; Gall, S.L.; Berhow, M.A.; Kendra, D.F.; Lerouge, P. Functionalized C-glycoside ketohydrazones: Carbohydrate derivatives that retain the ring integrity of the terminal reducing sugar. Anal. Chem. 2010, 82, 2893-2899.
    • (2010) Anal. Chem. , vol.82 , pp. 2893-2899
    • Price, N.P.J.1    Bowman, M.J.2    Gall, S.L.3    Berhow, M.A.4    Kendra, D.F.5    Lerouge, P.6
  • 3
    • 55249085380 scopus 로고    scopus 로고
    • Metal-free one-pot oxidative amidation of aldoses with functionalized amines
    • Colombeau, L.; Traoré, T.; Compain, P.; Martin, O.R. Metal-free one-pot oxidative amidation of aldoses with functionalized amines. J. Org. Chem. 2008, 73, 8647-8650.
    • (2008) J. Org. Chem. , vol.73 , pp. 8647-8650
    • Colombeau, L.1    Traoré, T.2    Compain, P.3    Martin, O.R.4
  • 4
    • 3943087054 scopus 로고
    • Synthesis of some substituted di-indolylmethanes in aqueous medium at room temperature
    • Kamal, A.; Qureshi, A.A. Synthesis of some substituted di-indolylmethanes in aqueous medium at room temperature. Tetrahedron 1963, 19, 513-520.
    • (1963) Tetrahedron , vol.19 , pp. 513-520
    • Kamal, A.1    Qureshi, A.A.2
  • 5
    • 0030600171 scopus 로고    scopus 로고
    • Lewis acid-catalyzed reactions in protic media. Lanthanide-catalyzed reactions of indoles with aldehydes or ketones
    • DOI 10.1016/0040-4039(96)00958-6
    • Chen, D.; Yu, L.; Wang, P.G. Lewis acid-catalyzed reactions in protic media. Lanthanidecatalyzed reactions of indoles with aldehydes or ketones. Tetrahedron Lett. 1996, 37, 4467-4470. (Pubitemid 26257349)
    • (1996) Tetrahedron Letters , vol.37 , Issue.26 , pp. 4467-4470
    • Chen, D.1    Yu, L.2    Wang, P.G.3
  • 6
    • 1042298780 scopus 로고    scopus 로고
    • Facile synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions
    • DOI 10.1016/j.tet.2003.12.060
    • Ji, S.J.; Wang, S.Y.; Zhang, Y.; Loh, T.P. Facil synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions. Tetrahedron 2004, 60, 2051-2055. (Pubitemid 38201586)
    • (2004) Tetrahedron , vol.60 , Issue.9 , pp. 2051-2055
    • Ji, S.-J.1    Wang, S.-Y.2    Zhang, Y.3    Loh, T.-P.4
  • 7
    • 5144231016 scopus 로고    scopus 로고
    • Environmentally friendly C-glycosylation of phloroacetophenone with unprotected d-glucose using scandium(III) trifluoromethanesulfonate in aqueous media: Key compounds for the syntheses of mono- and di-C-glucosylflavonoids
    • DOI 10.1016/j.carres.2004.07.023, PII S0008621504003489
    • Sato, S.; Akiya, T.; Suzuki, T.; Onodera, J. Environmentally friendly C-glycosylation of phloroacetophenone with unprotected D-glucose using scandium (III) trifluoromethanesulfonate in aqueous media: Key compounds for the synthesis of mono- and di-C-glucosylflavonoids. Carbohydr. Res. 2004, 339, 2611-2614. (Pubitemid 39346078)
    • (2004) Carbohydrate Research , vol.339 , Issue.15 , pp. 2611-2614
    • Sato, S.1    Akiya, T.2    Suzuki, T.3    Onodera, J.-I.4
  • 8
    • 24644492754 scopus 로고    scopus 로고
    • A mild and environmentally friendly scandium(III) trifluoromethanesulfonate-catalyzed synthesis of bis(3′-indolyl)alkanes and bis(3′-indolyl)-1-deoxyalditols
    • DOI 10.1016/j.carres.2005.07.019, PII S0008621505003587
    • Sato, S.; Sato, T. A mild and environmentally friendly scandium (III) trifluoromethanesulfonatecatalyzed synthesis of bis(3'-indolyl)alkanes and bis(3'-indolyl)-1-deoxyalditols. Carbohydr. Res. 2005, 340, 2251-2255. (Pubitemid 41267004)
    • (2005) Carbohydrate Research , vol.340 , Issue.14 , pp. 2251-2255
    • Sato, S.1    Sato, T.2
  • 9
    • 0031588708 scopus 로고    scopus 로고
    • Analysis of monosaccharide composition by capillary electrophoresis
    • DOI 10.1016/S0021-9673(96)00750-9, PII S0021967396007509
    • Guttman, A. Analysis of monosaccharide composition by capillary electrophoresis. J. Chromatogr. A 1997, 763, 271-277. (Pubitemid 27149996)
    • (1997) Journal of Chromatography A , vol.763 , Issue.1-2 , pp. 271-277
    • Guttman, A.1
  • 10
    • 49749141391 scopus 로고    scopus 로고
    • Capillary electrophoresis of complex natural polysaccharides
    • Volpi, N.; Maccari, F.; Linhardt, R.J. Capillary electrophoresis of complex natural polysaccharides. Electrophoresis 2008, 29, 3095-3106.
    • (2008) Electrophoresis , vol.29 , pp. 3095-3106
    • Volpi, N.1    Maccari, F.2    Linhardt, R.J.3
  • 11
    • 77950358068 scopus 로고    scopus 로고
    • 2-Catalyzed oxidative condensation of aldoses with diamines: Synthesis of aldo-naphthimidazoles for carbohydrate analysis
    • 2-catalyzed oxidative condensation of aldoses with diamines: Synthesis of aldo-naphthimidazoles for carbohydrate analysis. Molecules 2010, 15, 1340-1353.
    • (2010) Molecules , vol.15 , pp. 1340-1353
    • Lin, C.1    Hung, W.T.2    Kuo, C.Y.3    Liao, K.S.4    Liu, Y.C.5    Yang, W.B.6
  • 12
    • 45249087710 scopus 로고    scopus 로고
    • Chiral separations
    • DOI 10.1021/ac800662y
    • Ward, T.J.; Baker, B.A. Chiral separations. Anal. Chem. 2008, 80, 4363-4372. (Pubitemid 351842326)
    • (2008) Analytical Chemistry , vol.80 , Issue.12 , pp. 4363-4372
    • Ward, T.J.1    Baker, B.A.2
  • 13
    • 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
  • 14
    • 0036868796 scopus 로고    scopus 로고
    • Derivatization trends in capillary eletrophoresis: An update
    • DOI 10.1002/elps.200290010
    • Underberg, W.J.; Waterval, J.C. Derivatization trends in capillary electrophoresis: An update. Electrophoresis 2002, 23, 3922-3933. (Pubitemid 36041582)
    • (2002) Electrophoresis , vol.23 , Issue.22-23 , pp. 3922-3933
    • Underberg, W.J.M.1    Waterval, J.C.M.2
  • 15
    • 50049127805 scopus 로고    scopus 로고
    • Chiral separation by capillary electromigration techniques
    • Gübitz, G.; Schmid, M.G. Chiral separation by capillary electromigration techniques. J. Chromatogr. A 2008, 1204, 140-156.
    • (2008) J. Chromatogr. A , vol.1204 , pp. 140-156
    • Gübitz, G.1    Schmid, M.G.2
  • 16
    • 0036868789 scopus 로고    scopus 로고
    • Enantiomer migration order in chiral capillary electrophoresis
    • DOI 10.1002/elps.200290016
    • Chankvetadze, B. Enantiomer migration order in chiral capillary electrophoresis. Electrophoresis 2002, 23, 4022-4035. (Pubitemid 36041587)
    • (2002) Electrophoresis , vol.23 , Issue.22-23 , pp. 4022-4035
    • Chankvetadze, B.1
  • 17
    • 0031566984 scopus 로고    scopus 로고
    • Chiral resolution of diols by capillary electrophoresis using borate-cyclodextrin complexation
    • DOI 10.1016/S0021-9673(96)00836-9, PII S0021967396008369
    • Jira, T.; Bunke, A.; Schmid, M.G.; Gubitz, G. Chiral resolution of diols by capillary electrophoresis using borate-cyclodextrin complexation. J. Chromatogr. A 1997, 761, 269-275. (Pubitemid 27113424)
    • (1997) Journal of Chromatography A , vol.761 , Issue.1-2 , pp. 269-275
    • Jira, T.1    Bunke, A.2    Schmid, M.G.3    Gubitz, G.4
  • 18
    • 0000471859 scopus 로고
    • Electrophoretic resolution of monosaccharide enantiomers in borateoligosaccharide complexation media
    • Stefansson, M.; Novotny, M. Electrophoretic resolution of monosaccharide enantiomers in borateoligosaccharide complexation media. J. Am. Chem. Soc. 1993, 115, 11573-11580.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 11573-11580
    • Stefansson, M.1    Novotny, M.2
  • 19
    • 33845571580 scopus 로고    scopus 로고
    • Chiral resolution of monosaccharides as 1-phenyl-3-methyl-5-pyrazolone derivatives by ligand-exchange CE using borate anion as a central ion of the chiral selector
    • DOI 10.1002/elps.200600140
    • Kodama, S.; Aizawa, S.; Taga, A.; Yamashita, T.; Yamamoto, A. Chiral resolution of monosaccharides as 1-phenyl-3-methyl-5-pyrazolone derivatives by ligand-exchange CE using borate anion as a central ion of the chiral selector. Electrophoresis 2006, 27, 4730-4734. (Pubitemid 44932696)
    • (2006) Electrophoresis , vol.27 , Issue.23 , pp. 4730-4734
    • Kodama, S.1    Aizawa, S.-I.2    Taga, A.3    Yamashita, T.4    Yamamoto, A.5
  • 20
    • 79251478776 scopus 로고    scopus 로고
    • Monosaccharide-NAIM derivatives for D-,Lconfigurational analysis
    • Lin, C.; Kuo, C.Y.; Liao, K.S.; Yang, W.B. Monosaccharide-NAIM derivatives for D-, Lconfigurational analysis. Molecules 2011, 16, 652-664.
    • (2011) Molecules , vol.16 , pp. 652-664
    • Lin, C.1    Kuo, C.Y.2    Liao, K.S.3    Yang, W.B.4
  • 22
    • 4444246162 scopus 로고    scopus 로고
    • Structural characterization of a 2-O-acetylglucomannan from Dendrobium officinale stem
    • DOI 10.1016/j.carres.2004.05.034, PII S000862150400271X
    • Hua, Y.; Zhang, M.; Fu, C.; Chen, Z.; Chan, G.Y.S. Structural characterization of a 2-Oacetylglucomannan from Dendrobium officinale stem. Carbohydr. Res. 2004, 339, 2219-2224. (Pubitemid 39165111)
    • (2004) Carbohydrate Research , vol.339 , Issue.13 , pp. 2219-2224
    • Hua, Y.-F.1    Zhang, M.2    Fu, C.-X.3    Chen, Z.-H.4    Chan, G.Y.S.5
  • 23
    • 9744248320 scopus 로고    scopus 로고
    • The traditional Chinese medicine Cordyceps sinensis and its effects on apoptotic homeostasis
    • DOI 10.1016/j.jep.2004.09.029, PII S0378874104004696
    • Buenz, E.J.; Bauer, B.A.; Osmundson, T.W.; Motley, T.J. The traditional Chinese medicine Cordyceps sinensis and its effects on apoptotic homeostasis. J. Ethnopharmacol. 2005, 96, 19-29. (Pubitemid 39585156)
    • (2005) Journal of Ethnopharmacology , vol.96 , Issue.1-2 , pp. 19-29
    • Buenz, E.J.1    Bauer, B.A.2    Osmundson, T.W.3    Motley, T.J.4
  • 24
    • 85047686650 scopus 로고    scopus 로고
    • Cordyceps fungi: Natural products, pharmacological functions and developmental products
    • Zhou, X.; Gong, Z.; Su, Y.; Lin, J.; Tang, K. Cordyceps fungi: Natural products, pharmacological functions and developmental products. J. Pharm. Pharmacol. 2009, 61, 279-291.
    • (2009) J. Pharm. Pharmacol. , vol.61 , pp. 279-291
    • Zhou, X.1    Gong, Z.2    Su, Y.3    Lin, J.4    Tang, K.5
  • 25
    • 79952151783 scopus 로고    scopus 로고
    • A potent sphingomyelinase inhibitor from Cordyceps mycelia contributes to its cytoprotective effect against oxidative stress in macrophages
    • Wang, S.H.; Yang, W.B.; Liu, Y.C.; Chiu, Y.H.; Chen, C.T.; Kao, P.F.; lin, C.M. A potent sphingomyelinase inhibitor from Cordyceps mycelia contributes to its cytoprotective effect against oxidative stress in macrophages. J. Lipid Res. 2011, 52, 471-479.
    • (2011) J. Lipid Res. , vol.52 , pp. 471-479
    • Wang, S.H.1    Yang, W.B.2    Liu, Y.C.3    Chiu, Y.H.4    Chen, C.T.5    Kao, P.F.6    Lin, C.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.