메뉴 건너뛰기




Volumn 9, Issue 3, 2012, Pages 243-260

Chiral ionic liquids from Carbohydrates: Synthesis and properties

Author keywords

Carbohydrate; Chiral selector; Cyclodextrins; Imidazolium salt; Ionic liquid; Polymers

Indexed keywords

CATALYSTS; CHROMATOGRAPHIC ANALYSIS; CYCLODEXTRINS;

EID: 84867031164     PISSN: 1570193X     EISSN: None     Source Type: Journal    
DOI: 10.2174/1570193X11209030243     Document Type: Article
Times cited : (18)

References (52)
  • 1
    • 12344296667 scopus 로고    scopus 로고
    • Chemical and biochemical transformations in ionic liquids
    • Jain, N.; Kumar, A.; Chauhan, S.; Chauhan, S. M. S. Chemical and biochemical transformations in ionic liquids. Tetrahedron, 2005, 61, 1015-1060.
    • (2005) Tetrahedron , vol.61 , pp. 1015-1060
    • Jain, N.1    Kumar, A.2    Chauhan, S.3    Chauhan, S.M.S.4
  • 2
    • 27944440975 scopus 로고    scopus 로고
    • Ionic liquids in chemical analysis
    • Koel, M. Ionic liquids in chemical analysis. Crit. Rev. Anal. Chem., 2005, 35, 177-192.
    • (2005) Crit. Rev. Anal. Chem , vol.35 , pp. 177-192
    • Koel, M.1
  • 4
    • 28844495851 scopus 로고    scopus 로고
    • Chiral ionic liquids, a renewal for the chemistry of chiral solvents? Design, synthesis and applications for chiral recognition and asymmetric synthesis
    • Baudequin, C.; Bregeon, D.; Levillain, J.; Guillen, F.; Plaquevent, J. C.; Gaumont, A. C. Chiral ionic liquids, a renewal for the chemistry of chiral solvents? Design, synthesis and applications for chiral recognition and asymmetric synthesis. Tetrahedron-Asymmetry, 2005, 16, 3921-3945.
    • (2005) Tetrahedron-Asymmetry , vol.16 , pp. 3921-3945
    • Baudequin, C.1    Bregeon, D.2    Levillain, J.3    Guillen, F.4    Plaquevent, J.C.5    Gaumont, A.C.6
  • 5
    • 42049110530 scopus 로고    scopus 로고
    • Recent advances in the synthesis and application of chiral ionic liquids
    • Winkel, A.; Reddy, P. V. G.; Wilhelm, R. Recent advances in the synthesis and application of chiral ionic liquids. Synthesis-Stuttgart, 2008, 999-1016.
    • (2008) Synthesis-Stuttgart , pp. 999-1016
    • Winkel, A.1    Reddy, P.V.G.2    Wilhelm, R.3
  • 7
    • 70349931637 scopus 로고    scopus 로고
    • From Ionic Liquids to Supramolecular Polymers
    • Craig, S. L. From Ionic Liquids to Supramolecular Polymers. Angew. Chem. Int. Ed., 2009, 48, 2645-2647.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 2645-2647
    • Craig, S.L.1
  • 8
    • 0030963592 scopus 로고    scopus 로고
    • Moisture stable dialkylimidazolium salts as heterogeneous and homogeneous Lewis acids in the Diels-Alder reaction
    • Howarth, J.; Hanlon, K.; Fayne, D.; McCormac, P. Moisture stable dialkylimidazolium salts as heterogeneous and homogeneous Lewis acids in the Diels-Alder reaction. Tetrahedron Lett., 1997, 38, 3097-3100.
    • (1997) Tetrahedron Lett , vol.38 , pp. 3097-3100
    • Howarth, J.1    Hanlon, K.2    Fayne, D.3    McCormac, P.4
  • 9
    • 0033432259 scopus 로고    scopus 로고
    • Diels-Alder reactions in ionic liquids-A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures
    • Earle, M. J.; McCormac, P. B.; Seddon, K. R. Diels-Alder reactions in ionic liquids-A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures. Green Chem., 1999, 1, 23-25.
    • (1999) Green Chem , vol.1 , pp. 23-25
    • Earle, M.J.1    McCormac, P.B.2    Seddon, K.R.3
  • 10
    • 18144373455 scopus 로고    scopus 로고
    • Chiral ionic liquids: Synthesis and applications
    • Ding, J.; Armstrong, D. W. Chiral ionic liquids: Synthesis and applications. Chirality, 2005, 17, 281-292.
    • (2005) Chirality , vol.17 , pp. 281-292
    • Ding, J.1    Armstrong, D.W.2
  • 11
    • 77954761644 scopus 로고    scopus 로고
    • Ionic cyclodextrins in ionic liquid matrices as chiral stationary phases for gas chromatography
    • Huang, K.; Zhang, X.; Armstrong, D. W. Ionic cyclodextrins in ionic liquid matrices as chiral stationary phases for gas chromatography. J Chromatogr A, 2010, 1217, 5261-5273.
    • (2010) J Chromatogr A , vol.1217 , pp. 5261-5273
    • Huang, K.1    Zhang, X.2    Armstrong, D.W.3
  • 12
    • 53749100279 scopus 로고    scopus 로고
    • Applications of chiral ionic liquids
    • Bica, K.; Gaertner, P. Applications of chiral ionic liquids. Eur. J. Org. Chem., 2008, 3235-3250.
    • (2008) Eur. J. Org. Chem , pp. 3235-3250
    • Bica, K.1    Gaertner, P.2
  • 13
    • 37349005208 scopus 로고    scopus 로고
    • Amino acid ionic liquids
    • Ohno, H.; Fukumoto, K. Amino acid ionic liquids. Acc. Chem. Res., 2007, 40, 1122-1129.
    • (2007) Acc. Chem. Res , vol.40 , pp. 1122-1129
    • Ohno, H.1    Fukumoto, K.2
  • 14
    • 61949379658 scopus 로고    scopus 로고
    • Ionic liquids: New targets and media for alpha-amino acid and peptide chemistry
    • Plaquevent, J. C.; Levillain, J.; Guillen, F.; Malhiac, C.; Gaumont, A. C. Ionic liquids: new targets and media for alpha-amino acid and peptide chemistry. Chem. Rev., 2008, 108, 5035-5060.
    • (2008) Chem. Rev , vol.108 , pp. 5035-5060
    • Plaquevent, J.C.1    Levillain, J.2    Guillen, F.3    Malhiac, C.4    Gaumont, A.C.5
  • 15
    • 38549179976 scopus 로고    scopus 로고
    • Synthesis and characterization of novel chiral ionic liquids and investigation of their enantiomeric recognition properties
    • Bwambok, D. K.; Marwani, H. M.; Fernand, V. E.; Fakayode, S. O.; Lowry, M.; Negulescu, I.; Strongin, R. M.; Warner, I. M. Synthesis and characterization of novel chiral ionic liquids and investigation of their enantiomeric recognition properties. Chirality, 2008, 20, 151-158.
    • (2008) Chirality , vol.20 , pp. 151-158
    • Bwambok, D.K.1    Marwani, H.M.2    Fernand, V.E.3    Fakayode, S.O.4    Lowry, M.5    Negulescu, I.6    Strongin, R.M.7    Warner, I.M.8
  • 16
    • 77958503246 scopus 로고    scopus 로고
    • Carbohydrate chemistry and room temperature ionic liquids (RTILs): Recent trends, opportunities, challenges and future perspectives
    • Prasad, V.; Kale, R. R.; Kumar, V.; Tiwari, V. K. Carbohydrate chemistry and room temperature ionic liquids (RTILs): recent trends, opportunities, challenges and future perspectives. Curr. Org. Synthesis, 2010, 7, 506-531.
    • (2010) Curr. Org. Synthesis , vol.7 , pp. 506-531
    • Prasad, V.1    Kale, R.R.2    Kumar, V.3    Tiwari, V.K.4
  • 17
    • 37049105258 scopus 로고
    • Purines, pyrimidines, and imidazoles.51. New syntheses of some 5-alkyl-aminoimidazoles and 5-dialkyl-aminoimidazoles-3-alkylimidazolium nucleosides and 3-alkylpurines
    • Brown, T.; Kadir, K.; Mackenzie, G.; Shaw, G. Purines, pyrimidines, and imidazoles.51. New syntheses of some 5-alkyl-aminoimidazoles and 5-dialkyl-aminoimidazoles-3-alkylimidazolium nucleosides and 3-alkylpurines. J. Chem. Soc.,Perkin Trans. 1, 1979, 3107-3112.
    • (1979) J. Chem. Soc.,Perkin Trans , vol.1 , pp. 3107-3112
    • Brown, T.1    Kadir, K.2    Mackenzie, G.3    Shaw, G.4
  • 18
    • 57649112536 scopus 로고    scopus 로고
    • Synthesis of chiral carbohydrate ionic liquids
    • Plaza, P. G. J.; Bhongade, B. A.; Singh, G. Synthesis of chiral carbohydrate ionic liquids. Synlett, 2008, 2973-2976.
    • (2008) Synlett , pp. 2973-2976
    • Plaza, P.G.J.1    Bhongade, B.A.2    Singh, G.3
  • 19
    • 19344371650 scopus 로고    scopus 로고
    • The synthesis and applications of asymmetric phase-transfer catalysts derived from isomannide and isosorbide
    • Kumar, S.; Ramachandran, U. The synthesis and applications of asymmetric phase-transfer catalysts derived from isomannide and isosorbide. Tetrahedron, 2005, 61, 4141-4148.
    • (2005) Tetrahedron , vol.61 , pp. 4141-4148
    • Kumar, S.1    Ramachandran, U.2
  • 20
    • 35048815465 scopus 로고    scopus 로고
    • Synthesis and applications of novel bis(ammonium) chiral ionic liquids derived from isomannide
    • Kumar, V.; Olsen, C. E.; Schaffer, S. J. C.; Parmar, V. S.; Malhotra, S. V. Synthesis and applications of novel bis(ammonium) chiral ionic liquids derived from isomannide. Org. Lett., 2007, 9, 3905-3908.
    • (2007) Org. Lett , vol.9 , pp. 3905-3908
    • Kumar, V.1    Olsen, C.E.2    Schaffer, S.J.C.3    Parmar, V.S.4    Malhotra, S.V.5
  • 22
    • 59749098452 scopus 로고    scopus 로고
    • Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels-Alder reaction
    • Van Buu, O. N.; Aupoix, A.; Vo-Thanh, G. Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels-Alder reaction. Tetrahedron, 2009, 65, 2260-2265.
    • (2009) Tetrahedron , vol.65 , pp. 2260-2265
    • van Buu, O.N.1    Aupoix, A.2    Vo-Thanh, G.3
  • 23
    • 70350009893 scopus 로고    scopus 로고
    • Chiral ionic liquids derived from isosorbide: Synthesis, properties and applications in asymmetric synthesis
    • Van Buu, O. N.; Aupoix, A.; Hong, N. D. T.; Vo-Thanh, G. Chiral ionic liquids derived from isosorbide: synthesis, properties and applications in asymmetric synthesis. New J. Chem., 2009, 33, 2060-2072.
    • (2009) New J. Chem , vol.33 , pp. 2060-2072
    • van Buu, O.N.1    Aupoix, A.2    Hong, N.D.T.3    Vo-Thanh, G.4
  • 24
    • 77951585154 scopus 로고    scopus 로고
    • Revisit to imidazolium receptors for the recognition of anions: Highlighted research during 2006-2009
    • Xu, Z.; Kim, S. K.; Yoon, J. Revisit to imidazolium receptors for the recognition of anions: highlighted research during 2006-2009. Chem. Soc. Rev., 2010, 39, 1457-1466.
    • (2010) Chem. Soc. Rev , vol.39 , pp. 1457-1466
    • Xu, Z.1    Kim, S.K.2    Yoon, J.3
  • 25
    • 0035665552 scopus 로고    scopus 로고
    • Sugar-based cationic surfactants: Synthesis and aggregation of methyl 2-acylamido-6-trimethylammonio-2,6-dideoxy-Dglucopyranoside chlorides
    • Bazito, R. C.; El Seoud, O. A. Sugar-based cationic surfactants: Synthesis and aggregation of methyl 2-acylamido-6-trimethylammonio-2,6-dideoxy-Dglucopyranoside chlorides. J. Surfactants Deterg., 2001, 4, 395-400.
    • (2001) J. Surfactants Deterg , vol.4 , pp. 395-400
    • Bazito, R.C.1    El Seoud, O.A.2
  • 26
    • 0035826940 scopus 로고    scopus 로고
    • Sugar-based anionic surfactants: Synthesis and micelle formation of sodium methyl 2-acylamido-2-deoxy-6-O-sulfo-Dglucopyranosides
    • Bazito, R. C.; El Seoud, O. A. Sugar-based anionic surfactants: synthesis and micelle formation of sodium methyl 2-acylamido-2-deoxy-6-O-sulfo-Dglucopyranosides. Carbohydr. Res., 2001, 332, 95-102.
    • (2001) Carbohydr. Res , vol.332 , pp. 95-102
    • Bazito, R.C.1    El Seoud, O.A.2
  • 27
    • 34047111261 scopus 로고    scopus 로고
    • Glucose-derived ionic liquids: Exploring low-cost sources for novel chiral solvents
    • Poletti, L.; Chiappe, C.; Lay, L.; Pieraccini, D.; Polito, L.; Russo, G. Glucose-derived ionic liquids: exploring low-cost sources for novel chiral solvents. Green Chem., 2007, 9, 337-341.
    • (2007) Green Chem , vol.9 , pp. 337-341
    • Poletti, L.1    Chiappe, C.2    Lay, L.3    Pieraccini, D.4    Polito, L.5    Russo, G.6
  • 29
    • 33846248338 scopus 로고    scopus 로고
    • Ionic-liquid-supported synthesis: A novel liquidphase strategy for organic synthesis
    • Miao, W. S.; Chan, T. H. Ionic-liquid-supported synthesis: A novel liquidphase strategy for organic synthesis. Acc. Chem. Res., 2006, 39, 897-908.
    • (2006) Acc. Chem. Res , vol.39 , pp. 897-908
    • Miao, W.S.1    Chan, T.H.2
  • 30
    • 34948888286 scopus 로고    scopus 로고
    • Applications of ionic liquids in carbohydrate chemistry: A window of opportunities
    • El Seoud, O. A.; Koschella, A.; Fidale, L. C.; Dorn, S.; Heinze, T. Applications of ionic liquids in carbohydrate chemistry: A window of opportunities. Biomacromolecules, 2007, 8, 2629-2647.
    • (2007) Biomacromolecules , vol.8 , pp. 2629-2647
    • El Seoud, O.A.1    Koschella, A.2    Fidale, L.C.3    Dorn, S.4    Heinze, T.5
  • 31
    • 77954927291 scopus 로고    scopus 로고
    • A novel liquid-phase strategy for organic synthesis using organic ions as soluble supports
    • Huo, C. D.; Chan, T. H. A novel liquid-phase strategy for organic synthesis using organic ions as soluble supports. Chem. Soc. Rev., 2010, 39, 2977-3006.
    • (2010) Chem. Soc. Rev , vol.39 , pp. 2977-3006
    • Huo, C.D.1    Chan, T.H.2
  • 32
    • 38149031778 scopus 로고    scopus 로고
    • Automated oligosaccharide synthesis
    • Seeberger, P. H. Automated oligosaccharide synthesis. Chem. Soc. Rev., 2008, 37, 19-28.
    • (2008) Chem. Soc. Rev , vol.37 , pp. 19-28
    • Seeberger, P.H.1
  • 33
    • 33749130643 scopus 로고    scopus 로고
    • A novel approach to oligonucleotide synthesis using an imidazolium ion tag as a soluble support
    • Donga, R. A.; Khaliq-Uz-Zaman, S. M.; Chan, T. H.; Damha, M. J. A novel approach to oligonucleotide synthesis using an imidazolium ion tag as a soluble support. J. Org. Chem., 2006, 71, 7907-7910.
    • (2006) J. Org. Chem , vol.71 , pp. 7907-7910
    • Donga, R.A.1    Khaliq-Uz-Zaman, S.M.2    Chan, T.H.3    Damha, M.J.4
  • 34
    • 33645874206 scopus 로고    scopus 로고
    • A novel and efficient ionic liquid supported synthesis of oligosaccharides
    • Huang, J. Y.; Lei, M.; Wang, Y. G. A novel and efficient ionic liquid supported synthesis of oligosaccharides. Tetrahedron Lett., 2006, 47, 3047-3050.
    • (2006) Tetrahedron Lett , vol.47 , pp. 3047-3050
    • Huang, J.Y.1    Lei, M.2    Wang, Y.G.3
  • 35
    • 33744488831 scopus 로고    scopus 로고
    • Ionic-tag-assisted oligosaccharide synthesis
    • He, X.; Chan, T. H. Ionic-tag-assisted oligosaccharide synthesis. Synthesis-Stuttgart, 2006, 1645-1651.
    • (2006) Synthesis-Stuttgart , pp. 1645-1651
    • He, X.1    Chan, T.H.2
  • 36
    • 38349176562 scopus 로고    scopus 로고
    • Oligomannan synthesis using ionic liquid supported glycosylation
    • Pathak, A. K.; Yerneni, C. K.; Young, Z.; Pathak, V. Oligomannan synthesis using ionic liquid supported glycosylation. Org. Lett., 2008, 10, 145-148.
    • (2008) Org. Lett , vol.10 , pp. 145-148
    • Pathak, A.K.1    Yerneni, C.K.2    Young, Z.3    Pathak, V.4
  • 37
    • 70349113505 scopus 로고    scopus 로고
    • Imidazolium cation supported solution-phase assembly of homolinear alpha(1-6)-linked octamannoside: An efficient alternate approach for oligosaccharide synthesis
    • Yerneni, C. K.; Pathak, V.; Pathak, A. K. Imidazolium cation supported solution-phase assembly of homolinear alpha(1-6)-linked octamannoside: an efficient alternate approach for oligosaccharide synthesis. J. Org. Chem., 2009, 74, 6307-6310.
    • (2009) J. Org. Chem , vol.74 , pp. 6307-6310
    • Yerneni, C.K.1    Pathak, V.2    Pathak, A.K.3
  • 38
    • 77951788498 scopus 로고    scopus 로고
    • Preparation of composite materials composed of icarrageenan and polymeric ionic liquids
    • Prasad, K.; Kadokawa, J. Preparation of composite materials composed of icarrageenan and polymeric ionic liquids. Polymer Composites, 2010, 31, 799-806.
    • (2010) Polymer Composites , vol.31 , pp. 799-806
    • Prasad, K.1    Kadokawa, J.2
  • 39
    • 0024647404 scopus 로고
    • Electrokinetic chromatography-An interface between electrophoresis and chromatography
    • Terabe, S. Electrokinetic chromatography-An interface between electrophoresis and chromatography. TrAc. Trends Anal. Chem., 1989, 8, 129-134.
    • (1989) TrAc. Trends Anal. Chem , vol.8 , pp. 129-134
    • Terabe, S.1
  • 40
    • 27344447904 scopus 로고    scopus 로고
    • Synthesis and application of mono-6-ammonium-6-deoxy-beta-cyclodextrin chloride as chiral selector for capillary electrophoresis
    • Tang, W.; Muderawan, I. W.; Ng, S. C.; Chan, H. S. O. Synthesis and application of mono-6-ammonium-6-deoxy-beta-cyclodextrin chloride as chiral selector for capillary electrophoresis. J. Chromatogr. A, 2005, 1094, 187-191.
    • (2005) J. Chromatogr. A , vol.1094 , pp. 187-191
    • Tang, W.1    Muderawan, I.W.2    Ng, S.C.3    Chan, H.S.O.4
  • 41
    • 13744261937 scopus 로고    scopus 로고
    • Synthesis of ammonium substituted beta-cyclodextrins for enantioseparation of anionic analytes
    • Muderawan, I. W.; Ong, T. T.; Tang, W.; Young, D. J.; Ching, C. B.; Ng, S. C. Synthesis of ammonium substituted beta-cyclodextrins for enantioseparation of anionic analytes. Tetrahedron Lett., 2005, 46, 1747-1749.
    • (2005) Tetrahedron Lett , vol.46 , pp. 1747-1749
    • Muderawan, I.W.1    Ong, T.T.2    Tang, W.3    Young, D.J.4    Ching, C.B.5    Ng, S.C.6
  • 42
    • 33846563587 scopus 로고    scopus 로고
    • Effect of alkylimidazolium substituents on enantioseparation ability of single-isomer alkylimidazolium-beta-cyclodextrin derivatives in capillary electrophoresis
    • Tang, W. H.; Ong, T. T.; Muderawan, I. W.; Ng, S. C. Effect of alkylimidazolium substituents on enantioseparation ability of single-isomer alkylimidazolium-beta-cyclodextrin derivatives in capillary electrophoresis. Anal. Chim. Acta, 2007, 585, 227-233.
    • (2007) Anal. Chim. Acta , vol.585 , pp. 227-233
    • Tang, W.H.1    Ong, T.T.2    Muderawan, I.W.3    Ng, S.C.4
  • 43
    • 77953556389 scopus 로고    scopus 로고
    • Chiral capillary electrophoresis with cationic pyrrolidiniumbeta-cyclodextrin derivatives as chiral selectors
    • Xiao, Y.; Wang, Y.; Ong, T. T.; Ge, L. Y.; Tan, S. N.; Young, D. J.; Tan, T. T. Y.; Ng, S. C. Chiral capillary electrophoresis with cationic pyrrolidiniumbeta-cyclodextrin derivatives as chiral selectors. J. Sep. Sci., 2010, 33, 1797-1805.
    • (2010) J. Sep. Sci , vol.33 , pp. 1797-1805
    • Xiao, Y.1    Wang, Y.2    Ong, T.T.3    Ge, L.Y.4    Tan, S.N.5    Young, D.J.6    Tan, T.T.Y.7    Ng, S.C.8
  • 44
    • 38549105605 scopus 로고    scopus 로고
    • Synthesis and application of mono-6-(3-methylimidazolium)-6-deoxyperphenylcarbamoyl-betacyclodextrin chloride as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography
    • Ong, T. T.; Wang, R. Q.; Muderawan, I. W.; Ng, S. C. Synthesis and application of mono-6-(3-methylimidazolium)-6-deoxyperphenylcarbamoyl-betacyclodextrin chloride as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography. J. Chromatogr. A, 2008, 1182, 136-140.
    • (2008) J. Chromatogr. A , vol.1182 , pp. 136-140
    • Ong, T.T.1    Wang, R.Q.2    Muderawan, I.W.3    Ng, S.C.4
  • 45
    • 58149156498 scopus 로고    scopus 로고
    • Monosubstituted positively charged cyclodextrins: Synthesis and applications in chiral separation
    • Tang, W. H.; Ng, S. C. Monosubstituted positively charged cyclodextrins: Synthesis and applications in chiral separation. J. Sep. Sci., 2008, 31, 3246-3256.
    • (2008) J. Sep. Sci , vol.31 , pp. 3246-3256
    • Tang, W.H.1    Ng, S.C.2
  • 46
    • 74049119746 scopus 로고    scopus 로고
    • Application of charged single isomer derivatives of cyclodextrins in capillary electrophoresis for chiral analysis
    • Cucinotta, V.; Contino, A.; Giuffrida, A.; Maccarrone, G.; Messina, M. Application of charged single isomer derivatives of cyclodextrins in capillary electrophoresis for chiral analysis. J. Chromatogr. A, 1217, 953-967.
    • J. Chromatogr. A , vol.1217 , pp. 953-967
    • Cucinotta, V.1    Contino, A.2    Giuffrida, A.3    Maccarrone, G.4    Messina, M.5
  • 47
    • 77954226662 scopus 로고    scopus 로고
    • Cyclodextrin-ionic liquid polyurethanes for application in drinking water treatment
    • Malefetse, T. J.; Mamba, B. B.; Krause, R. W.; Mahlambi, M. M. Cyclodextrin-ionic liquid polyurethanes for application in drinking water treatment. Water Sa, 2009, 35, 729-734.
    • (2009) Water Sa , vol.35 , pp. 729-734
    • Malefetse, T.J.1    Mamba, B.B.2    Krause, R.W.3    Mahlambi, M.M.4
  • 48
    • 28844445262 scopus 로고    scopus 로고
    • Enantioselective separation in capillary electrophoresis using a novel mono-6(A)-propylammonium-beta-cyclodextrin as chiral selector
    • Tang, W. H.; Muderawan, I. W.; Ng, S. C.; Chan, H. S. O. Enantioselective separation in capillary electrophoresis using a novel mono-6(A)-propylammonium-beta-cyclodextrin as chiral selector. Anal. Chim. Acta, 2006, 555, 63-67.
    • (2006) Anal. Chim. Acta , vol.555 , pp. 63-67
    • Tang, W.H.1    Muderawan, I.W.2    Ng, S.C.3    Chan, H.S.O.4
  • 49
    • 34547228730 scopus 로고    scopus 로고
    • Facile synthesis of positively charged monosubstituted alpha-and gamma-cyclodextrins for chiral resolution of anionic racemates
    • Tang, W. H.; Muderawan, I. W.; Ong, T. T.; Ng, S. C. Facile synthesis of positively charged monosubstituted alpha-and gamma-cyclodextrins for chiral resolution of anionic racemates. Tetrahedron-Asymmetry, 2007, 18, 1548-1553.
    • (2007) Tetrahedron-Asymmetry , vol.18 , pp. 1548-1553
    • Tang, W.H.1    Muderawan, I.W.2    Ong, T.T.3    Ng, S.C.4
  • 50
    • 48949101239 scopus 로고    scopus 로고
    • Synthesis of cationic beta-cyclodextrin derivatives and their applications as chiral stationary phases for highperformance liquid chromatography and supercritical fluid chromatography
    • Wang, R. Q.; Ong, T. T.; Ng, S. C. Synthesis of cationic beta-cyclodextrin derivatives and their applications as chiral stationary phases for highperformance liquid chromatography and supercritical fluid chromatography. J. Chromatogr. A, 2008, 1203, 185-192.
    • (2008) J. Chromatogr. A , vol.1203 , pp. 185-192
    • Wang, R.Q.1    Ong, T.T.2    Ng, S.C.3
  • 51
    • 85086606248 scopus 로고    scopus 로고
    • Asymmetric reduction of acetophenones with NaBH4 in the presence of mono-6-(1-methyl-3-imidazolium)-6-deoxy-beta-cyclodextrin tosylate
    • Tang, W. H.; Tang, J.; Ng, S. C.; Chan, H. S. O. Asymmetric reduction of acetophenones with NaBH4 in the presence of mono-6-(1-methyl-3-imidazolium)-6-deoxy-beta-cyclodextrin tosylate. J. Inclusion Phenom. Macrocyclic Chem., 2006, 56, 287-290.
    • (2006) J. Inclusion Phenom. Macrocyclic Chem , vol.56 , pp. 287-290
    • Tang, W.H.1    Tang, J.2    Ng, S.C.3    Chan, H.S.O.4
  • 52
    • 38849155827 scopus 로고    scopus 로고
    • Synthesis and stability of fluorescent gold nanoparticles by sodium borohydride in the presence of mono-6-deoxy-6-pyridinium-beta-cyclodextrin chloride
    • Male, K. B.; Li, J. J.; Bun, C. C.; Ng, S. C.; Luong, J. H. T. Synthesis and stability of fluorescent gold nanoparticles by sodium borohydride in the presence of mono-6-deoxy-6-pyridinium-beta-cyclodextrin chloride. J. Phys. Chem. C, 2008, 112, 443-451.
    • (2008) J. Phys. Chem. C , vol.112 , pp. 443-451
    • Male, K.B.1    Li, J.J.2    Bun, C.C.3    Ng, S.C.4    Luong, J.H.T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.