메뉴 건너뛰기




Volumn 328, Issue 1-2, 2009, Pages 268-272

Chiral separation of (R,S)-2-phenyl-1-propanol through glutaraldehyde-crosslinked chitosan membranes

Author keywords

(R,S) 2 Phenyl 1 propanol; Chiral separation; Chitosan; Enantioselective membrane; Glutaraldehyde

Indexed keywords

CHEMICAL ANALYSIS; CHIRALITY; CHITIN; CHITOSAN; CROSSLINKING; ENANTIOSELECTIVITY; FOURIER TRANSFORM INFRARED SPECTROSCOPY; PROPANOL; SCANNING ELECTRON MICROSCOPY; STEREOCHEMISTRY;

EID: 67349201474     PISSN: 03767388     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.memsci.2008.12.019     Document Type: Article
Times cited : (49)

References (29)
  • 1
    • 7244236529 scopus 로고    scopus 로고
    • Recent advances in chiral resolution through membrane-based approaches
    • CAM. Afonso, J.G. Crespo, Recent advances in chiral resolution through membrane-based approaches, Angew. Chem. Int. Ed. 43 (2004) 5293-5295.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5293-5295
    • Afonso, C.A.M.1    Crespo, J.G.2
  • 2
    • 0000915204 scopus 로고
    • Useful chiral packing material for high-performance liquid chromatographic resolution. Cellulose triacetate and tribenzoate coated on macroporous silica gel
    • Y. Okamoto, M. Kawashima, K. Hatada, Useful chiral packing material for high-performance liquid chromatographic resolution. Cellulose triacetate and tribenzoate coated on macroporous silica gel, Chem. Lett. (1984) 739-742.
    • (1984) Chem. Lett. , pp. 739-742
    • Okamoto, Y.1    Kawashima, M.2    Hatada, K.3
  • 3
    • 0003012070 scopus 로고
    • Optical resolution of N-benzoyl-cis-2-aminocyclohexanecarboxylic acid by preferential crystallization
    • H. Nohira, K. Watanabe, M. Kurokawa, Optical resolution of N-benzoyl-cis-2-aminocyclohexanecarboxylic acid by preferential crystallization, Chem. Lett. (1976) 299-300.
    • (1976) Chem. Lett. , pp. 299-300
    • Nohira, H.1    Watanabe, K.2    Kurokawa, M.3
  • 4
    • 33746317330 scopus 로고    scopus 로고
    • A practical approach to the resolution of racemic N-benzyl a-amino acids by liquid-liquid extraction with a lipophilic chiral salen-cobalt (III) complex
    • T.B. Reeve, J.P. Cros, C. Gennari, U Piarulli, J.G. de Vries, A practical approach to the resolution of racemic N-benzyl a-amino acids by liquid-liquid extraction with a lipophilic chiral salen-cobalt (III) complex, Angew. Chem. Int. Ed. 45 (2006)2449-2453.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2449-2453
    • Reeve, T.B.1    Cros, J.P.2    Gennari, C.3    Piarulli, U.4    de Vries, J.G.5
  • 5
    • 0242459819 scopus 로고    scopus 로고
    • Separation of drug enantiomer by liquid chromatography and capillary electrophoresis, using immobilized proteins as chiral selectors
    • M.C. Millot, Separation of drug enantiomer by liquid chromatography and capillary electrophoresis, using immobilized proteins as chiral selectors, J. Chromatogr. B 797 (2003) 131-159.
    • (2003) J. Chromatogr. B , vol.797 , pp. 131-159
    • Millot, M.C.1
  • 6
    • 33745685787 scopus 로고    scopus 로고
    • Chiral separation of phenylalanine in ultrafiltration through DNA-immobilized chitosan membranes
    • Y. Matsuoka, N. Kanda, Y.M. Lee, A. Higuchi, Chiral separation of phenylalanine in ultrafiltration through DNA-immobilized chitosan membranes, J. Membr. Sci. 280(2006)116-123.
    • (2006) J. Membr. Sci. , vol.280 , pp. 116-123
    • Matsuoka, Y.1    Kanda, N.2    Lee, Y.M.3    Higuchi, A.4
  • 7
    • 46149127527 scopus 로고    scopus 로고
    • Chiral separation of (R,S)-2-phenyl-1-propanol through cellulose acetate butyrate membranes
    • S.M. Xie, W.F. Wang, P. Ai, L.M. Yuan, Chiral separation of (R,S)-2-phenyl-1-propanol through cellulose acetate butyrate membranes, J. Membr. Sci. 321 (2008)293-298.
    • (2008) J. Membr. Sci. , vol.321 , pp. 293-298
    • Xie, S.M.1    Wang, W.F.2    Ai, P.3    Yuan, L.M.4
  • 8
    • 0037358374 scopus 로고    scopus 로고
    • Optical resolution of a-amino acids through enantioselective polymeric membranes based on polysaccharides
    • J.H. Kim,J.H. Kim,J.Jegal, K.H. Lee, Optical resolution of a-amino acids through enantioselective polymeric membranes based on polysaccharides, J. Membr. Sci. 213 (2003) 273-283.
    • (2003) J. Membr. Sci. , vol.213 , pp. 273-283
    • Kim, J.H.1    Kim, J.H.2    Jegal, J.J.3    Lee, K.H.4
  • 9
    • 0016391473 scopus 로고
    • Enantiomer differentiation in transport through bulk liquid membranes
    • M. Newcomb, R.C. Helgeson, D.J. Cram, Enantiomer differentiation in transport through bulk liquid membranes, J. Am. Chem. Soc. 96(1974) 7367-7369.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 7367-7369
    • Newcomb, M.1    Helgeson, R.C.2    Cram, D.J.3
  • 10
    • 0001399210 scopus 로고
    • Optical resolution through the solid membrane from (+)-poly {1-[dimethyl(10-pinanyl)-silyl]-1-propyne}
    • T. Aoki, K. Shinohara, E. Oikawa, Optical resolution through the solid membrane from (+)-poly {1-[dimethyl(10-pinanyl)-silyl]-1-propyne}, Makromol. Chem. Rapid. Commun. 13 (1992) 565-570.
    • (1992) Makromol. Chem. Rapid. Commun. , vol.13 , pp. 565-570
    • Aoki, T.1    Shinohara, K.2    Oikawa, E.3
  • 11
    • 0041568646 scopus 로고    scopus 로고
    • Chiral separation of phenylalanine by ultrafiltration through immobilized DNA membrane
    • A. Higuchi, Y. Higuchi, K. Furuta, B.O. Yoon, Chiral separation of phenylalanine by ultrafiltration through immobilized DNA membrane, J. Membr. Sci. 221 (2003) 207-218.
    • (2003) J. Membr. Sci. , vol.221 , pp. 207-218
    • Higuchi, A.1    Higuchi, Y.2    Furuta, K.3    Yoon, B.O.4
  • 12
    • 0030826127 scopus 로고    scopus 로고
    • Enantioseparation using apoenzymes immobilized in a porous polymeric membrane
    • B.B. Lakshmi, C.R. Martin, Enantioseparation using apoenzymes immobilized in a porous polymeric membrane, Nature 388 (1997) 758-760.
    • (1997) Nature , vol.388 , pp. 758-760
    • Lakshmi, B.B.1    Martin, C.R.2
  • 13
    • 0036844215 scopus 로고    scopus 로고
    • Staging of affinity ultrafiltration processes for chiral separations
    • J. Romero, A.L. Zydney, Staging of affinity ultrafiltration processes for chiral separations, J. Membr. Sci. 209 (2002) 107-119.
    • (2002) J. Membr. Sci. , vol.209 , pp. 107-119
    • Romero, J.1    Zydney, A.L.2
  • 14
    • 15344340752 scopus 로고    scopus 로고
    • Enantioseparation of D,L-lactic acid by membrane techniques
    • P. Hadika, LP. Szabó, E. Nagy, Zs. Farkas, Enantioseparation of D,L-lactic acid by membrane techniques, J. Membr. Sci. 251 (2005) 223-232.
    • (2005) J. Membr. Sci. , vol.251 , pp. 223-232
    • Hadika, P.1    Szabó, L.P.2    Nagy, E.3    Farkas, Z.4
  • 15
    • 0037376347 scopus 로고    scopus 로고
    • Surface characterization of polysulfone membranes modified by DNA immobilization
    • C.S. Zhao, X.D. Liu, S. Rikimaru, M. Nomizu, N. Nishi, Surface characterization of polysulfone membranes modified by DNA immobilization, J. Membr. Sci. 214 (2003) 179-189.
    • (2003) J. Membr. Sci. , vol.214 , pp. 179-189
    • Zhao, C.S.1    Liu, X.D.2    Rikimaru, S.3    Nomizu, M.4    Nishi, N.5
  • 16
    • 33947301782 scopus 로고    scopus 로고
    • Immobilization of lipase with a special microstructure in composite hydrophilic CA/hydrophobic PTFE membrane for the chiral separation of racemic ibuprofen
    • Y. Wang, Y. Hu, J. Xu, G.S. Luo, Y.Y. Dai, Immobilization of lipase with a special microstructure in composite hydrophilic CA/hydrophobic PTFE membrane for the chiral separation of racemic ibuprofen, J. Membr. Sci. 293 (2007) 133-141.
    • (2007) J. Membr. Sci. , vol.293 , pp. 133-141
    • Wang, Y.1    Hu, Y.2    Xu, J.3    Luo, G.S.4    Dai, Y.Y.5
  • 17
    • 33845309072 scopus 로고    scopus 로고
    • Membrane thickness and preparation temperature as key parameters for controlling the macrovoid structure of chiral activated membranes (CAM)
    • A. Conesa, T. Gumi, C. Palet, Membrane thickness and preparation temperature as key parameters for controlling the macrovoid structure of chiral activated membranes (CAM), J. Membr. Sci. 287 (2007) 29-40.
    • (2007) J. Membr. Sci. , vol.287 , pp. 29-40
    • Conesa, A.1    Gumi, T.2    Palet, C.3
  • 18
    • 38649135406 scopus 로고    scopus 로고
    • Enantioselective permeation of racemic alcohol through polymeric membrane
    • S.Hazarika, Enantioselective permeation of racemic alcohol through polymeric membrane, J. Membr. Sci. 310 (2008) 174-183.
    • (2008) J. Membr. Sci. , vol.310 , pp. 174-183
    • Hazarika, S.H.1
  • 19
    • 16344371109 scopus 로고    scopus 로고
    • Chiral separation of amino acids in ultrafiltration through DNA-immobilized cellulose membranes
    • A. Higuchi, A. Hayashi, N. Kanda, K. Sanui, H. Kitamura, Chiral separation of amino acids in ultrafiltration through DNA-immobilized cellulose membranes, J. Mol. Struct. 739 (2005) 145-152.
    • (2005) J. Mol. Struct. , vol.739 , pp. 145-152
    • Higuchi, A.1    Hayashi, A.2    Kanda, N.3    Sanui, K.4    Kitamura, H.5
  • 20
    • 33745836163 scopus 로고    scopus 로고
    • Preparation and chiral selectivity of BSA-modified ceramic membrane
    • C.L. Su, R.J. Dai, B. Tong, Y.L. Deng, Preparation and chiral selectivity of BSA-modified ceramic membrane, Chin. Chem. Lett. 17 (2006) 649-652.
    • (2006) Chin. Chem. Lett. , vol.17 , pp. 649-652
    • Su, C.L.1    Dai, R.J.2    Tong, B.3    Deng, Y.L.4
  • 21
    • 34547426890 scopus 로고    scopus 로고
    • Crosslinking of chitosan membrane using glutaraldehyde: Effect on ion permeability and water absorption
    • M.M. Beppu, R.S. Vieira, C.G. Aimoli, C.C. Santana, Crosslinking of chitosan membrane using glutaraldehyde: effect on ion permeability and water absorption, J. Membr. Sci. 301 (2007) 126-130.
    • (2007) J. Membr. Sci. , vol.301 , pp. 126-130
    • Beppu, M.M.1    Vieira, R.S.2    Aimoli, C.G.3    Santana, C.C.4
  • 22
    • 33746463466 scopus 로고    scopus 로고
    • Preparation and evaluation of a novel chiral stationary phase based on covalently bonded chitosan for ligand-exchange chromatography
    • Y.Liu, H. Zou,J.Haginaka, Preparation and evaluation of a novel chiral stationary phase based on covalently bonded chitosan for ligand-exchange chromatography, J. Sep. Sci. 29 (2006) 1440-1446.
    • (2006) J. Sep. Sci. , vol.29 , pp. 1440-1446
    • Liu, Y.L.1    Zou, H.2    Haginaka, J.3
  • 23
    • 39749198490 scopus 로고    scopus 로고
    • Enantioseparation using urea- and imide-bearing chitosan phenylcarbamate derivatives as chiral stationary phases for high-performance liquid chromatography
    • C. Yamamoto, M. Fujisawa, M. Kamigaito, Y. Okamoto, Enantioseparation using urea- and imide-bearing chitosan phenylcarbamate derivatives as chiral stationary phases for high-performance liquid chromatography, Chirality 20 (2008) 288-294.
    • (2008) Chirality , vol.20 , pp. 288-294
    • Yamamoto, C.1    Fujisawa, M.2    Kamigaito, M.3    Okamoto, Y.4
  • 24
    • 0032482102 scopus 로고    scopus 로고
    • Polysaccharide derivatives for chromatographic separation of enantiomers
    • Y. Okamoto, E. Yashima, Polysaccharide derivatives for chromatographic separation of enantiomers, Angew. Chem. Int. Ed. 37 (1998) 1021-1043.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1021-1043
    • Okamoto, Y.1    Yashima, E.2
  • 25
    • 0032625962 scopus 로고    scopus 로고
    • Crosslinking of chitosan fibers with dialdehydes: Proposal of a new reaction mechanism
    • Z.J. Knaull, S.M. Hudson, A.M.K. Creber, Crosslinking of chitosan fibers with dialdehydes: proposal of a new reaction mechanism, J. Polym. Sci. B: Polym. 37 (1999) 1079-1094.
    • (1999) J. Polym. Sci. B: Polym. , vol.37 , pp. 1079-1094
    • Knaull, Z.J.1    Hudson, S.M.2    Creber, A.M.K.3
  • 26
    • 0344131947 scopus 로고    scopus 로고
    • Some studies of crosslinking-glutaraldehyde interactionin ahomogeneous system
    • O.A.C. Monteiro Jr., C. Airoldi, Some studies of crosslinking-glutaraldehyde interactionin ahomogeneous system, Int. J. Biol. Macromol.26(1999) 119-128.
    • (1999) Int. J. Biol. Macromol. , vol.26 , pp. 119-128
    • Monteiro Jr., O.A.C.1    Airoldi, C.2
  • 27
    • 33646096979 scopus 로고    scopus 로고
    • Interaction of natural and crosslinked chitosan membranes with Hg (II) ions
    • R.S. Vieira, M.M. Beppu, Interaction of natural and crosslinked chitosan membranes with Hg (II) ions, Colloids Surf. A 279 (2006) 196-207.
    • (2006) Colloids Surf. A , vol.279 , pp. 196-207
    • Vieira, R.S.1    Beppu, M.M.2
  • 28
    • 34548008162 scopus 로고    scopus 로고
    • Development of novel blocked diisocyanate crosslinked chitosan membranes for pervaporation separation of water-isopropanol mixtures
    • S.K. Choudhari,A.A.Kittur, M.Y.Kariduraganavar, Development of novel blocked diisocyanate crosslinked chitosan membranes for pervaporation separation of water-isopropanol mixtures, J. Membr. Sci. 302 (2007) 197-206.
    • (2007) J. Membr. Sci. , vol.302 , pp. 197-206
    • Choudhari, S.K.1    Kittur, A.A.2    Kariduraganavar, M.Y.3
  • 29
    • 34548012401 scopus 로고    scopus 로고
    • Anovel methodtoprepare high chitosan contentblend hollow fiber membranes using a non-acidic dope solvent for highly enhanced adsorptive performance
    • W.Han, C.X. Liu,R.B. Bai,Anovel methodtoprepare high chitosan contentblend hollow fiber membranes using a non-acidic dope solvent for highly enhanced adsorptive performance, J. Membr. Sci. 302 (2007) 150-159.
    • (2007) J. Membr. Sci. , vol.302 , pp. 150-159
    • Han, W.H.1    Liu, C.X.2    Bai, R.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.