메뉴 건너뛰기




Volumn 10, Issue 5, 1998, Pages 499-504

Enantioselective capillary gas chromatography in the investigation of stereochemical correlations of terpenoids

Author keywords

Cyclodextrin derivatives; Enantioselective capillary gas chromatography; Essential oils; Monoterpenes; Stereochemistry of terpenes

Indexed keywords

ALPHA PHELLANDRENE; CARENE; CYCLODEXTRIN DERIVATIVE; ESSENTIAL OIL; LIMONENE; LINALOOL; PINENE; SABINENE; TERPENE; TERPENE DERIVATIVE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0347596092     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1998)10:5<499::AID-CHIR13>3.0.CO;2-V     Document Type: Article
Times cited : (50)

References (26)
  • 1
    • 0347577170 scopus 로고
    • Separation of enantiomers by gas-liquid chromatography with an optically active stationary phase
    • A.B. Littlewood, ed. London: Institute of Petroleum
    • Gil-Av, E., Feibush, B., Charles-Sigler, R. Separation of enantiomers by gas-liquid chromatography with an optically active stationary phase. In: Gas Chromatography 1966. A.B. Littlewood, ed. London: Institute of Petroleum, 1967:227.
    • (1967) Gas Chromatography 1966 , pp. 227
    • Gil-Av, E.1    Feibush, B.2    Charles-Sigler, R.3
  • 2
    • 0017495101 scopus 로고
    • Rapid gas chromatographic separation of amino acid enantiomers with a novel chiral stationary phase
    • Frank, H., Nicholson, G.J., Bayer, E. Rapid gas chromatographic separation of amino acid enantiomers with a novel chiral stationary phase. J. Chromatogr. Sci. 15:174-176, 1977.
    • (1977) J. Chromatogr. Sci. , vol.15 , pp. 174-176
    • Frank, H.1    Nicholson, G.J.2    Bayer, E.3
  • 4
    • 0012766894 scopus 로고
    • New procedure for gas chromatographic enantiomer separation. Application to chiral amines and hydroxy acids
    • König W.A., Benecke, I., Sievers, S. New procedure for gas chromatographic enantiomer separation. Application to chiral amines and hydroxy acids. J. Chromatogr. 238:427-432, 1982.
    • (1982) J. Chromatogr. , vol.238 , pp. 427-432
    • König, W.A.1    Benecke, I.2    Sievers, S.3
  • 5
    • 24244437218 scopus 로고
    • Phosgene: A versatile reagent for enantiomer separation by capillary gas chromatography
    • König, W.A., Steinbach, E., Ernst, K. Phosgene: A versatile reagent for enantiomer separation by capillary gas chromatography. J. Chromatogr. 301:129-135, 1984.
    • (1984) J. Chromatogr. , vol.301 , pp. 129-135
    • König, W.A.1    Steinbach, E.2    Ernst, K.3
  • 6
    • 2642656977 scopus 로고
    • Separation of chiral ketones by enantioselective gas chromatography
    • König, W.A., Benecke, I., Ernst, K. Separation of chiral ketones by enantioselective gas chromatography. J. Chromatogr. 253:267-270, 1982.
    • (1982) J. Chromatogr. , vol.253 , pp. 267-270
    • König, W.A.1    Benecke, I.2    Ernst, K.3
  • 7
    • 26344448730 scopus 로고    scopus 로고
    • Cyclodextrins as chiral stationary phases with in capillary gas chromatography. Part VII: Cyclodextrins with an inverse substitution pattern; synthesis and enantioselectivity
    • König, W.A., Icheln, D., Runge, T., Pforr, I., Krebs, A. Cyclodextrins as chiral stationary phases with in capillary gas chromatography. Part VII: Cyclodextrins with an inverse substitution pattern; synthesis and enantioselectivity. J. High Res. Chromatogr. 13:702-707.
    • J. High Res. Chromatogr. , vol.13 , pp. 702-707
    • König, W.A.1    Icheln, D.2    Runge, T.3    Pforr, I.4    Krebs, A.5
  • 8
    • 4244194938 scopus 로고
    • Improved gas chromatographic separation of enantiomeric carbohydrate derivatives using a new chiral stationary phase
    • König, WA, Mischnick-Lübbecke, P., Brassat, B., Lutz, S. Improved gas chromatographic separation of enantiomeric carbohydrate derivatives using a new chiral stationary phase. Carbohydr. Res. 183:11-17, 1988.
    • (1988) Carbohydr. Res. , vol.183 , pp. 11-17
    • König, W.A.1    Mischnick-Lübbecke, P.2    Brassat, B.3    Lutz, S.4
  • 9
    • 84986500332 scopus 로고
    • Cyclodextrins as chiral stationary phases in capillary gas chromatography, Part V: Octakis(3-O-butyryl-2,6-di-O-pentyl)-γ-cyclodextrin
    • König, W.A., Krebber, R., Mischnick, P. Cyclodextrins as chiral stationary phases in capillary gas chromatography, Part V: Octakis(3-O-butyryl-2,6-di-O-pentyl)-γ-cyclodextrin. J. High Res. Chromatogr. 12: 732-738, 1989.
    • (1989) J. High Res. Chromatogr. , vol.12 , pp. 732-738
    • König, W.A.1    Krebber, R.2    Mischnick, P.3
  • 11
    • 0345847991 scopus 로고    scopus 로고
    • Enantiomeric composition of the chiral constituents of essential oils. Part 3: Diterpene hydrocarbons
    • Pietsch, M., König, W.A. Enantiomeric composition of the chiral constituents of essential oils. Part 3: Diterpene hydrocarbons. J. High Res. Chromatogr. 20:257-260, 1997.
    • (1997) J. High Res. Chromatogr. , vol.20 , pp. 257-260
    • Pietsch, M.1    König, W.A.2
  • 12
    • 84985258733 scopus 로고
    • Enantiomeric composition of the chiral constituents in essential oils. Part 1: Monoterpene hydrocarbons
    • König, WA., Krüger, A., Icheln, D., Runge, T. Enantiomeric composition of the chiral constituents in essential oils. Part 1: Monoterpene hydrocarbons. J. High Res. Chromatogr. 15:184-189, 1992.
    • (1992) J. High Res. Chromatogr. , vol.15 , pp. 184-189
    • König, W.A.1    Krüger, A.2    Icheln, D.3    Runge, T.4
  • 13
    • 84985258160 scopus 로고
    • New, selectively substituted cyclodextrins as stationary phases for the analysis of chiral constituents of essential oils
    • König, W.A., Gehrcke, B., Icheln, D., Evers, P., Dönnecke, J., Wang, W. New, selectively substituted cyclodextrins as stationary phases for the analysis of chiral constituents of essential oils. J. High Res. Chromatogr. 17:367-372, 1992.
    • (1992) J. High Res. Chromatogr. , vol.17 , pp. 367-372
    • König, W.A.1    Gehrcke, B.2    Icheln, D.3    Evers, P.4    Dönnecke, J.5    Wang, W.6
  • 14
    • 84985233025 scopus 로고
    • Stereoisomeric flavor compounds. Part LVIII: The use of heptakis(2,3-di-O-methyl-6-O-tert.butyldimethylsilyl)-β-cyclodextrin as a chiral stationary phase in flavor analysis
    • Dietrich, A., Maas, B., Messer, W., Bruche, G., Karl, V., Kaunzinger, A., Mosandl, A. Stereoisomeric flavor compounds. Part LVIII: The use of heptakis(2,3-di-O-methyl-6-O-tert.butyldimethylsilyl)-β-cyclodextrin as a chiral stationary phase in flavor analysis. J. High Res. Chromatogr. 15:590-593, 1992.
    • (1992) J. High Res. Chromatogr. , vol.15 , pp. 590-593
    • Dietrich, A.1    Maas, B.2    Messer, W.3    Bruche, G.4    Karl, V.5    Kaunzinger, A.6    Mosandl, A.7
  • 16
    • 0021463335 scopus 로고
    • Multidimensional capillary gas chromatography: Enantiomeric separations of selected cuts using a chiral second column
    • Schomburg, G., Husmann, H., Hübinger, E., König, W.A. Multidimensional capillary gas chromatography: Enantiomeric separations of selected cuts using a chiral second column. J. High Res. Chromatogr. Chromatogr. Commun. 7:404-410, 1984.
    • (1984) J. High Res. Chromatogr. Chromatogr. Commun. , vol.7 , pp. 404-410
    • Schomburg, G.1    Husmann, H.2    Hübinger, E.3    König, W.A.4
  • 17
    • 0028813228 scopus 로고
    • Enantiomeric composition of sesquiterpene hydrocarbons of the essential oil of Cedrela odorata L.
    • Hardt, I.H., Rieck, A., Fricke, C., König, W.A. Enantiomeric composition of sesquiterpene hydrocarbons of the essential oil of Cedrela odorata L. Flavour Fragr. J. 10:165-171, 1995.
    • (1995) Flavour Fragr. J. , vol.10 , pp. 165-171
    • Hardt, I.H.1    Rieck, A.2    Fricke, C.3    König, W.A.4
  • 18
    • 0028294669 scopus 로고
    • Preparative enantiomer separation with modified cyclodextrins as chiral stationary phases
    • Hardt, I., König, W.A. Preparative enantiomer separation with modified cyclodextrins as chiral stationary phases. J. Chromatogr. A, 666: 611-615, 1994.
    • (1994) J. Chromatogr. A , vol.666 , pp. 611-615
    • Hardt, I.1    König, W.A.2
  • 19
    • 0000132982 scopus 로고
    • Separation of α- And β-pinene into enantiomers in gas-liquid chromatography systems via α-cyclodextrin inclusion complexes
    • Koscielski, T., Sybilska, D., Jurczak, J. Separation of α-and β-pinene into enantiomers in gas-liquid chromatography systems via α-cyclodextrin inclusion complexes. J. Chromatogr. 280:131-134, 1983.
    • (1983) J. Chromatogr. , vol.280 , pp. 131-134
    • Koscielski, T.1    Sybilska, D.2    Jurczak, J.3
  • 20
    • 0003671612 scopus 로고
    • Ätherische Öle-Gepanschte Seelen
    • Becker, S., Ätherische Öle-Gepanschte Seelen. Öko-Test, 10:41-49, 1995.
    • (1995) Öko-Test , vol.10 , pp. 41-49
    • Becker, S.1
  • 21
    • 0000084686 scopus 로고
    • Melissenöle, Untersuchungen zur Echtheit mittels enantioselektiver Gaschromatographie und Isotopenverhältnis-Massenspektrometrie
    • Schultze, W., König, W.A., Hilker, A., Richter, R., Melissenöle, Untersuchungen zur Echtheit mittels enantioselektiver Gaschromatographie und Isotopenverhältnis-Massenspektrometrie. Dtsch. Apoth. Ztg. 135:567-575, 1995.
    • (1995) Dtsch. Apoth. Ztg. , vol.135 , pp. 567-575
    • Schultze, W.1    König, W.A.2    Hilker, A.3    Richter, R.4
  • 22
    • 84988115601 scopus 로고
    • Enantiomeric composition of the chiral constituents of essential oils, Part 2: Sesquiterpene hydrocarbons
    • König, W.A., Rieck, A., Hardt, I., Gehrcke, B., Kubeczka, K.-H. Muhle, H. Enantiomeric composition of the chiral constituents of essential oils, Part 2: Sesquiterpene hydrocarbons. J. High Res. Chromatogr. 17:315-320, 1994.
    • (1994) J. High Res. Chromatogr. , vol.17 , pp. 315-320
    • König, W.A.1    Rieck, A.2    Hardt, I.3    Gehrcke, B.4    Kubeczka, K.-H.5    Muhle, H.6
  • 24
    • 0001048824 scopus 로고
    • Inhaltsstoffe der Moose, III. Über die vergleichende gas- Und dünnschicht-chromatographisch Untersuchung der ätherischen Öle einiger Lebermoose und die Isolierung von (-)-Longifolen und (-)-Longiborneol aus Scapania undulata (L.) Dum
    • Huneck, S., Klein, E. Inhaltsstoffe der Moose, III. Über die vergleichende gas-und dünnschicht-chromatographisch Untersuchung der ätherischen Öle einiger Lebermoose und die Isolierung von (-)-Longifolen und (-)-Longiborneol aus Scapania undulata (L.) Dum. Phytochem. 6:383-390, 1967.
    • (1967) Phytochem. , vol.6 , pp. 383-390
    • Huneck, S.1    Klein, E.2
  • 25
    • 0000115051 scopus 로고
    • Germacrene D, a key intermediate of cadinene group compounds and bourbonenes
    • Yoshihara, K., Ohta, Y., Sakai, T., Hirose, Y. Germacrene D, a key intermediate of cadinene group compounds and bourbonenes. Tetrahedron Lett. 27:2263-2264, 1969.
    • (1969) Tetrahedron Lett. , vol.27 , pp. 2263-2264
    • Yoshihara, K.1    Ohta, Y.2    Sakai, T.3    Hirose, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.