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Volumn 23, Issue 2, 2011, Pages 113-117

Stereodynamics of tetramezine

Author keywords

chiral drugs; diaziridines; dynamic gas chromatography; interconversion barrier; kinetics; stereogenic nitrogen; unified equation

Indexed keywords

ANTIDEPRESSANT AGENT; TETRAMEZINE; UNCLASSIFIED DRUG;

EID: 78650933919     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20885     Document Type: Article
Times cited : (31)

References (55)
  • 2
    • 26944464251 scopus 로고    scopus 로고
    • Effects of amphazide (a hydrazide of phosphorylated carboxylic acids) and tetramezine (a diaziridine derivative) on central dopaminergic structures
    • Baichurina AZ, Semina II, Garaev RS,. Effects of amphazide (a hydrazide of phosphorylated carboxylic acids) and tetramezine (a diaziridine derivative) on central dopaminergic structures. Bull Exp Biol Med 1996; 121: 584-586.
    • (1996) Bull Exp Biol Med , vol.121 , pp. 584-586
    • Baichurina, A.Z.1    Semina, I.I.2    Garaev, R.S.3
  • 3
    • 0001990714 scopus 로고
    • Synthesis and in vitro activity of some aryl diaziridines as potential monoamine oxidase inhibitors
    • Paget CJ, Davis CS,. Synthesis and in vitro activity of some aryl diaziridines as potential monoamine oxidase inhibitors. J Med Chem 1964; 7: 626-628.
    • (1964) J Med Chem , vol.7 , pp. 626-628
    • Paget, C.J.1    Davis, C.S.2
  • 4
    • 33847780470 scopus 로고    scopus 로고
    • Experimental evaluation of bioavailability of tetramezine from tablets
    • Prokopov AA, Kotlova LI, Berlyand AS,. Experimental evaluation of bioavailability of tetramezine from tablets. Pharm Chem J 2006; 40: 463-464.
    • (2006) Pharm Chem J , vol.40 , pp. 463-464
    • Prokopov, A.A.1    Kotlova, L.I.2    Berlyand, A.S.3
  • 5
    • 28644448952 scopus 로고    scopus 로고
    • Experimental pharmacokinetics of tetramezine in rats
    • Prokopov AA, Kotlova LI, Berlyand AS,. Experimental pharmacokinetics of tetramezine in rats. Pharm Chem J 2005; 39: 345-349.
    • (2005) Pharm Chem J , vol.39 , pp. 345-349
    • Prokopov, A.A.1    Kotlova, L.I.2    Berlyand, A.S.3
  • 7
  • 9
    • 0038518998 scopus 로고    scopus 로고
    • Determination of the enantiomerization barrier of chlorthalidone by dynamic electrokinetic chromatography and computer simulation
    • Schoetz G, Trapp O, Schurig V,. Determination of the enantiomerization barrier of chlorthalidone by dynamic electrokinetic chromatography and computer simulation. J Cap Elec 1999; 6: 169-175.
    • (1999) J Cap Elec , vol.6 , pp. 169-175
    • Schoetz, G.1    Trapp, O.2    Schurig, V.3
  • 10
    • 0034234741 scopus 로고    scopus 로고
    • Dynamic micellar electrokinetic chromatography-determination of the enantiomerization barrier of oxazepam, temazepam and lorazepam
    • Schoetz G, Trapp O, Schurig V,. Dynamic micellar electrokinetic chromatography-determination of the enantiomerization barrier of oxazepam, temazepam and lorazepam. Anal Chem 2000; 72: 2758-2764.
    • (2000) Anal Chem , vol.72 , pp. 2758-2764
    • Schoetz, G.1    Trapp, O.2    Schurig, V.3
  • 11
    • 0033659311 scopus 로고    scopus 로고
    • Determination of the enantiomerization barrier of oxazepam by dynamic micellar electrokinetic chromatography-comparison of experiment and simulation with chromwin 99
    • Schoetz G, Trapp O, Schurig V,. Determination of the enantiomerization barrier of oxazepam by dynamic micellar electrokinetic chromatography-comparison of experiment and simulation with chromwin 99. Enantiomer 2000; 5: 391-396.
    • (2000) Enantiomer , vol.5 , pp. 391-396
    • Schoetz, G.1    Trapp, O.2    Schurig, V.3
  • 12
    • 0024312032 scopus 로고
    • The FDA perspective on the development of stereoisomers
    • de Camp WH,. The FDA perspective on the development of stereoisomers. Chirality 1989; 1: 2-6.
    • (1989) Chirality , vol.1 , pp. 2-6
    • De Camp, W.H.1
  • 13
    • 0018620980 scopus 로고
    • Chromatographische Racemattrennungen von Thalidomid und teratogene Wirkung der Enantiomere
    • Blaschke G, Kraft HP, Fickentscher K, Köhler F,. Chromatographische Racemattrennungen von Thalidomid und teratogene Wirkung der Enantiomere. Arzneim-Forsch [Drug Res] 1979; 29: 1640-1642.
    • (1979) Arzneim-Forsch [Drug Res] , vol.29 , pp. 1640-1642
    • Blaschke, G.1    Kraft, H.P.2    Fickentscher, K.3    Köhler, F.4
  • 14
    • 0028220747 scopus 로고
    • Investigations on the in vitro racemization of thalidomide by high-performance liquid chromatography
    • Knoche B, Blaschke G,. Investigations on the in vitro racemization of thalidomide by high-performance liquid chromatography. J Chromatogr A 1994; 666: 235-240.
    • (1994) J Chromatogr A , vol.666 , pp. 235-240
    • Knoche, B.1    Blaschke, G.2
  • 15
    • 0345191687 scopus 로고    scopus 로고
    • Enantiomers of thalidomide: Blood distribution and the influence of serum albumin on chiral inversion and hydrolysis
    • Eriksson T, Björkman S, Roth B, Fyge A, Höglund P,. Enantiomers of thalidomide: blood distribution and the influence of serum albumin on chiral inversion and hydrolysis. Chirality 1998; 10: 223-228.
    • (1998) Chirality , vol.10 , pp. 223-228
    • Eriksson, T.1    Björkman, S.2    Roth, B.3    Fyge, A.4    Höglund, P.5
  • 16
    • 0029990823 scopus 로고    scopus 로고
    • Enantioselective inhibition of TNF-α release by thalidomide and thalidomide-analogues
    • Wnendt S, Finkam M, Winter W, Ossig J, Raabe G, Zwingenberger K,. Enantioselective inhibition of TNF-α release by thalidomide and thalidomide-analogues. Chirality 1996; 8: 390-396.
    • (1996) Chirality , vol.8 , pp. 390-396
    • Wnendt, S.1    Finkam, M.2    Winter, W.3    Ossig, J.4    Raabe, G.5    Zwingenberger, K.6
  • 17
    • 0034784563 scopus 로고    scopus 로고
    • Determination of the enantiomerization barrier of thalidomide by dynamic capillary electrokinetic chromatography
    • DOI 10.1002/1522-2683(200109)22:15<3185::AID-ELPS3185>3.0.CO;2-V
    • Schoetz G, Trapp O, Schurig V,. Determination of the enantiomerization barrier of thalidomide by dynamic electrokinetic chromatography. Electrophoresis 2001; 22: 3185-3190. (Pubitemid 32936705)
    • (2001) Electrophoresis , vol.22 , Issue.15 , pp. 3185-3190
    • Schoetz, G.1    Trapp, O.2    Schurig, V.3
  • 18
    • 0037080475 scopus 로고    scopus 로고
    • Stereointegrity of thalidomide: Gas-chromatographic determination of the enantiomerization barrier
    • Trapp O, Schoetz G, Schurig V,. Stereointegrity of thalidomide: gas-chromatographic determination of the enantiomerization barrier. J Pharm Biomed Anal 2002; 27: 497-505.
    • (2002) J Pharm Biomed Anal , vol.27 , pp. 497-505
    • Trapp, O.1    Schoetz, G.2    Schurig, V.3
  • 19
    • 33747713254 scopus 로고    scopus 로고
    • The unified equation for the evaluation of degenerated first-order reactions in dynamic electrophoresis
    • DOI 10.1002/elps.200500907
    • Trapp O,. The unified equation for the evaluation of degenerated first order reactions in dynamic electrophoresis. Electrophoresis 2006; 27: 2999-3006. (Pubitemid 44269516)
    • (2006) Electrophoresis , vol.27 , Issue.15 , pp. 2999-3006
    • Trapp, O.1
  • 20
    • 84981751097 scopus 로고
    • Diaziridine aus Aminalen des Formaldehyds
    • Ohme R, Schmitz E, Dolge P,. Diaziridine aus Aminalen des Formaldehyds. Chem Ber 1966; 99: 2104-2109.
    • (1966) Chem Ber , vol.99 , pp. 2104-2109
    • Ohme, R.1    Schmitz, E.2    Dolge, P.3
  • 21
    • 0000844121 scopus 로고
    • Determination of enantiomerization barriers by computer simulation of interconversion profiles: Enantiomerization of diaziridines during chiral inclusion gas chromatography
    • Jung M, Schurig V,. Determination of enantiomerization barriers by computer simulation of interconversion profiles: enantiomerization of diaziridines during chiral inclusion gas chromatography. J Am Chem Soc 1992; 114: 529-534.
    • (1992) J Am Chem Soc , vol.114 , pp. 529-534
    • Jung, M.1    Schurig, V.2
  • 22
    • 25044479784 scopus 로고
    • Präparative Trennung enantiomerer Diaziridine durch Säulenchromatographie an Triacetylcellulose
    • Häkli H, Mannschreck A,. Präparative Trennung enantiomerer Diaziridine durch Säulenchromatographie an Triacetylcellulose. Angew Chem 1977; 89: 419.
    • (1977) Angew Chem , vol.89 , pp. 419
    • Häkli, H.1    Mannschreck, A.2
  • 23
    • 0001537154 scopus 로고
    • Nitrogen inversion-experiment and theory
    • Lehn JM,. Nitrogen inversion-experiment and theory. Top Curr Chem 1970; 15: 311-377.
    • (1970) Top Curr Chem , vol.15 , pp. 311-377
    • Lehn, J.M.1
  • 25
    • 1542378820 scopus 로고    scopus 로고
    • The control of the nitrogen inversion in alkylsubstituted diaziridines
    • Trapp O, Schurig V, Kostyanovsky RG,. The control of the nitrogen inversion in alkylsubstituted diaziridines. Chem-Eur J 2004; 10: 951-957.
    • (2004) Chem-Eur J , vol.10 , pp. 951-957
    • Trapp, O.1    Schurig, V.2    Kostyanovsky, R.G.3
  • 26
    • 0006473992 scopus 로고
    • Nuclear magnetic resonance studies of rate processes and conformations. V. Synchronous inversion at two nitrogens
    • Anderson JE, Lehn JM,. Nuclear magnetic resonance studies of rate processes and conformations. V. Synchronous inversion at two nitrogens. J Am Chem Soc 1967; 89: 81-87.
    • (1967) J Am Chem Soc , vol.89 , pp. 81-87
    • Anderson, J.E.1    Lehn, J.M.2
  • 27
    • 74749102946 scopus 로고    scopus 로고
    • The stereodynamics of 1,2-dipropyldiaziridines
    • Trapp O, Sahraoui L, Hofstadt W, Könen W,. The stereodynamics of 1,2-dipropyldiaziridines. Chirality 2010; 22: 284-291.
    • (2010) Chirality , vol.22 , pp. 284-291
    • Trapp, O.1    Sahraoui, L.2    Hofstadt, W.3    Könen, W.4
  • 28
    • 74049094391 scopus 로고    scopus 로고
    • Chromatographic peak deconvolution of constitutional isomers by multiple reaction monitoring mass spectrometry
    • Trapp O,. Chromatographic peak deconvolution of constitutional isomers by multiple reaction monitoring mass spectrometry. J Chromatogr A 2010; 1217: 1010-1016.
    • (2010) J Chromatogr A , vol.1217 , pp. 1010-1016
    • Trapp, O.1
  • 29
    • 0034899754 scopus 로고    scopus 로고
    • Determination of enantiomerization barriers by dynamic and stopped-flow chromatographic methods
    • DOI 10.1002/chir.1052
    • Trapp O, Schoetz G, Schurig V,. Determination of enantiomerization barriers by dynamic and stopped flow chromatographic methods. Chirality 2001; 13: 403-414. (Pubitemid 32729794)
    • (2001) Chirality , vol.13 , Issue.8 , pp. 403-414
    • Trapp, O.1    Schoetz, G.2    Schurig, V.3
  • 30
    • 0000651610 scopus 로고
    • Quantitative resolution of pyramidal nitrogen invertomers by complexation chromatography
    • Schurig V, Bürkle W, Zlatkis A, Poole CF,. Quantitative resolution of pyramidal nitrogen invertomers by complexation chromatography. Naturwissenschaften 1979; 66: 423-424.
    • (1979) Naturwissenschaften , vol.66 , pp. 423-424
    • Schurig, V.1    Bürkle, W.2    Zlatkis, A.3    Poole, C.F.4
  • 31
    • 0003037941 scopus 로고
    • Dynamic phenomena during enantiomer resolution by complexation gas chromatography
    • Bürkle W, Karfunkel H, Schurig V,. Dynamic phenomena during enantiomer resolution by complexation gas chromatography. J Chromatogr 1984; 288: 1-14.
    • (1984) J Chromatogr , vol.288 , pp. 1-14
    • Bürkle, W.1    Karfunkel, H.2    Schurig, V.3
  • 32
    • 0034000649 scopus 로고    scopus 로고
    • Stereointegrity of tröger's base: Gas-chromatographic determination of the enantiomerization barrier
    • Trapp O, Schurig V,. Stereointegrity of tröger's base: gas-chromatographic determination of the enantiomerization barrier. J Am Chem Soc 2000; 122: 1424-1430.
    • (2000) J Am Chem Soc , vol.122 , pp. 1424-1430
    • Trapp, O.1    Schurig, V.2
  • 33
    • 0034746004 scopus 로고    scopus 로고
    • Chromwin-a computer program for the determination of enantiomerization barriers in dynamic chromatography
    • Trapp O, Schurig V,. Chromwin-a computer program for the determination of enantiomerization barriers in dynamic chromatography. Comput Chem 2001; 25: 187-195.
    • (2001) Comput Chem , vol.25 , pp. 187-195
    • Trapp, O.1    Schurig, V.2
  • 34
    • 0035896457 scopus 로고    scopus 로고
    • Approximation function for the direct calculation of rate constants and Gibbs activation energies of enantiomerization of racemic mixtures from chromatographic parameters in dynamic chromatography
    • Trapp O, Schurig V,. Approximation function for the direct calculation of rate constants and Gibbs activation energies of enantiomerization of racemic mixtures from chromatographic parameters in dynamic chromatography. J Chromatogr A 2001; 911: 167-175.
    • (2001) J Chromatogr A , vol.911 , pp. 167-175
    • Trapp, O.1    Schurig, V.2
  • 35
    • 0036313224 scopus 로고    scopus 로고
    • Novel direct access to enantiomerization barriers from peak profiles in enantioselective dynamic chromatography: Enantiomerization of dialkyl-1,3-allenedicarboxylates
    • Trapp O, Schurig V,. Novel direct access to enantiomerization barriers from peak profiles in enantioselective dynamic chromatography: enantiomerization of dialkyl-1,3-allenedicarboxylates. Chirality 2002; 14: 465-470.
    • (2002) Chirality , vol.14 , pp. 465-470
    • Trapp, O.1    Schurig, V.2
  • 36
    • 22244434936 scopus 로고    scopus 로고
    • Stereolabile chiral compounds: Analysis by dynamic chromatography and stopped-flow methods
    • Wolf C,. Stereolabile chiral compounds: analysis by dynamic chromatography and stopped-flow methods. Chem Soc Rev 2005; 34: 595-608.
    • (2005) Chem Soc Rev , vol.34 , pp. 595-608
    • Wolf, C.1
  • 37
    • 33746408979 scopus 로고    scopus 로고
    • Dynamic HPLC on chiral stationary phases: A powerful tool for the investigation of stereomutation processes
    • D'Acquarica I, Gasparrini F, Pierini M, Villani C, Zappia G,. Dynamic HPLC on chiral stationary phases: a powerful tool for the investigation of stereomutation processes. J Sep Sci 2006; 29: 1508-1516.
    • (2006) J Sep Sci , vol.29 , pp. 1508-1516
    • D'Acquarica, I.1    Gasparrini, F.2    Pierini, M.3    Villani, C.4    Zappia, G.5
  • 39
    • 40649128956 scopus 로고    scopus 로고
    • Methods for studying reaction kinetics in gas chromatography, exemplified by using the 1-chloro-2,2-dimethylaziridine interconversion reaction
    • Krupcik J, Mydlova J, Majek P, Simon P, Armstrong DW,. Methods for studying reaction kinetics in gas chromatography, exemplified by using the 1-chloro-2,2-dimethylaziridine interconversion reaction. J Chromatogr A 2008; 1186: 144-160.
    • (2008) J Chromatogr A , vol.1186 , pp. 144-160
    • Krupcik, J.1    Mydlova, J.2    Majek, P.3    Simon, P.4    Armstrong, D.W.5
  • 40
    • 77649099532 scopus 로고    scopus 로고
    • Investigation of the stereodynamics of molecules and catalyzed reactions by CE
    • Trapp O,. Investigation of the stereodynamics of molecules and catalyzed reactions by CE. Electrophoresis 2010; 31: 786-813.
    • (2010) Electrophoresis , vol.31 , pp. 786-813
    • Trapp, O.1
  • 41
    • 54049129637 scopus 로고    scopus 로고
    • Enantiomerization of chiral 2,3,3a,4-tetrahydro-1h-pyrrolo[2,1-c][1,2,4] benzothiadiazine 5,5-dioxide by stopped-flow multidimensional HPLC
    • Cannazza G, Carrozzo MM, Braghiroli D, Parenti C,. Enantiomerization of chiral 2,3,3a,4-tetrahydro-1h-pyrrolo[2,1-c][1,2,4] benzothiadiazine 5,5-dioxide by stopped-flow multidimensional HPLC. J Chromatogr B 2008; 875: 192-199.
    • (2008) J Chromatogr B , vol.875 , pp. 192-199
    • Cannazza, G.1    Carrozzo, M.M.2    Braghiroli, D.3    Parenti, C.4
  • 42
    • 39749203611 scopus 로고    scopus 로고
    • Gas chromatographic high-throughput screening techniques in catalysis
    • Trapp O,. Gas chromatographic high-throughput screening techniques in catalysis. J Chromatogr A 2008; 1184: 160-190.
    • (2008) J Chromatogr A , vol.1184 , pp. 160-190
    • Trapp, O.1
  • 43
    • 30044437787 scopus 로고    scopus 로고
    • Unified equation for access to rate constants of first-order reactions in dynamic and on-column reaction chromatography
    • Trapp O,. Unified equation for access to rate constants of first-order reactions in dynamic and on-column reaction chromatography. Anal Chem 2006; 78: 189-198.
    • (2006) Anal Chem , vol.78 , pp. 189-198
    • Trapp, O.1
  • 44
    • 32844457214 scopus 로고    scopus 로고
    • The unified equation for the evaluation of first order reactions in dynamic electrophoresis
    • DOI 10.1002/elps.200500708
    • Trapp O,. The unified equation for the evaluation of first order reactions in dynamic electrophoresis. Electrophoresis 2006; 27: 534-541. (Pubitemid 43250766)
    • (2006) Electrophoresis , vol.27 , Issue.3 , pp. 534-541
    • Trapp, O.1
  • 45
    • 33745426581 scopus 로고    scopus 로고
    • Fast and precise access to enantiomerization rate constants in dynamic chromatography
    • Trapp O,. Fast and precise access to enantiomerization rate constants in dynamic chromatography. Chirality 2006; 18: 489-497.
    • (2006) Chirality , vol.18 , pp. 489-497
    • Trapp, O.1
  • 46
    • 70449587517 scopus 로고    scopus 로고
    • Accessing reaction rate constants in on-column reaction chromatography: An extended unified equation for reaction educts and products with different response factors
    • Trapp O, Bremer S, Weber SK,. Accessing reaction rate constants in on-column reaction chromatography: an extended unified equation for reaction educts and products with different response factors. Anal Bioanal Chem 2009; 395: 1673-1679.
    • (2009) Anal Bioanal Chem , vol.395 , pp. 1673-1679
    • Trapp, O.1    Bremer, S.2    Weber, S.K.3
  • 47
    • 34948854924 scopus 로고    scopus 로고
    • High-throughput screening of catalysts by combining reaction and analysis
    • Trapp O, Weber SK, Bauch S, Hofstadt W,. High-throughput screening of catalysts by combining reaction and analysis. Angew Chem Int Ed Engl 2007; 46: 7307-7310.
    • (2007) Angew Chem Int Ed Engl , vol.46 , pp. 7307-7310
    • Trapp, O.1    Weber, S.K.2    Bauch, S.3    Hofstadt, W.4
  • 48
    • 53849126519 scopus 로고    scopus 로고
    • High throughput kinetic study of hydrogenations over palladium nanoparticles-combination of reaction and analysis
    • Trapp O, Weber SK, Bauch S, Bäcker T, Hofstadt W, Spliethoff B,. High throughput kinetic study of hydrogenations over palladium nanoparticles-combination of reaction and analysis. Chem-Eur J 2008; 14: 4657-4666.
    • (2008) Chem-Eur J , vol.14 , pp. 4657-4666
    • Trapp, O.1    Weber, S.K.2    Bauch, S.3    Bäcker, T.4    Hofstadt, W.5    Spliethoff, B.6
  • 49
    • 77649188800 scopus 로고    scopus 로고
    • Integration of reaction and separation in a micro capillary column reactor-palladium nanoparticle catalyzed c-c bond forming reactions
    • Weber SK, Bremer S, Trapp O,. Integration of reaction and separation in a micro capillary column reactor-palladium nanoparticle catalyzed c-c bond forming reactions. J Chem Eng Sci 2010; 65: 2410-2416.
    • (2010) J Chem Eng Sci , vol.65 , pp. 2410-2416
    • Weber, S.K.1    Bremer, S.2    Trapp, O.3
  • 50
    • 37749025270 scopus 로고    scopus 로고
    • Synthesis and structure of 1-[ω-(3,3-dialkyldiaziridin-1-yl)alkyl]- 3,3-dialkyldiaziridines
    • Petukhova VY, Strelenko YA, Lyssenko KA, Makhova NN,. Synthesis and structure of 1-[ω-(3,3-dialkyldiaziridin-1-yl)alkyl]-3,3- dialkyldiaziridines. Russ Chem Bull Int Ed 2007; 56: 1550-1554.
    • (2007) Russ Chem Bull Int Ed , vol.56 , pp. 1550-1554
    • Petukhova, V.Y.1    Strelenko, Y.A.2    Lyssenko, K.A.3    Makhova, N.N.4
  • 51
    • 37049169670 scopus 로고
    • Amidines. Part IX. Preparation of substituted amidines from ketoxime sulphonates and ammonia or amines
    • Oxley F, Short WF,. Amidines. Part IX. Preparation of substituted amidines from ketoxime sulphonates and ammonia or amines. J Chem Soc 1948: 1514-1527.
    • (1948) J Chem Soc , pp. 1514-1527
    • Oxley, F.1    Short, W.F.2
  • 52
    • 84986769133 scopus 로고
    • Tert-butyldimethylsilyl-substituted cyclodextrin derivatives as versatile chiral stationary phases in capillary GC
    • Maas B, Dietrich A, Karl V, Kaunzinger A, Lehmann D, Köpke T, Mosandl A,. tert-butyldimethylsilyl-substituted cyclodextrin derivatives as versatile chiral stationary phases in capillary GC. J Microcol Sep 1993; 5: 421-427.
    • (1993) J Microcol Sep , vol.5 , pp. 421-427
    • Maas, B.1    Dietrich, A.2    Karl, V.3    Kaunzinger, A.4    Lehmann, D.5    Köpke, T.6    Mosandl, A.7
  • 53
    • 54049092753 scopus 로고    scopus 로고
    • A Novel Software Tool for high throughput measurements of interconversion barriers: DCXplorer
    • Trapp O,. A Novel Software Tool for high throughput measurements of interconversion barriers: DCXplorer. J Chromatogr B 2008; 875: 42-47.
    • (2008) J Chromatogr B , vol.875 , pp. 42-47
    • Trapp, O.1
  • 54
    • 1342296307 scopus 로고
    • The activated complex and the absolute rate of chemical reactions
    • Eyring H,. The activated complex and the absolute rate of chemical reactions. Chem Rev 1935; 1: 65-77.
    • (1935) Chem Rev , vol.1 , pp. 65-77
    • Eyring, H.1
  • 55
    • 0031950709 scopus 로고    scopus 로고
    • Peak coalescence phenomena in enantioselective chromatography
    • Schurig V,. Peak coalescence phenomena in enantioselective chromatography. Chirality 1998; 10: 140-146.
    • (1998) Chirality , vol.10 , pp. 140-146
    • Schurig, V.1


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