2,3-di-O-methoxymethyl-6-O-tert-butyldimethylsilyl-beta-cyclodextrin, a useful stationary phase for gas chromatographic separation of enantiomers.

[1]  K. Engel,et al.  2,3-di-O-methoxymethyl-6-O-tert-butyldimethylsilyl-gamma-cyclodextrin: a new class of cyclodextrin derivatives for gas chromatographic separation of enantiomers. , 2005, Journal of chromatography. A.

[2]  V. Schurig,et al.  Extraordinary chiral discrimination in inclusion gas chromatography. thermodynamics of enantioselectivity between a racemic perfluorodiether and a modified gamma-cyclodextrin. , 2003, Journal of chromatography. A.

[3]  S. Brennecke,et al.  METHYL DIHYDROJASMONATE AND ITS STEREOISOMERS: SENSORY PROPERTIES AND ENANTIOSELECTIVE ANALYSIS , 2002 .

[4]  V. Schurig Separation of enantiomers by gas chromatography. , 2001, Journal of chromatography. A.

[5]  A. Mosandl,et al.  Diluted modified cyclodextrins as chiral stationary phases in capillary gas chromatography-octakis(2,3-di-O-propionyl-6-O-tert-butyldimethylsilyl)-?-cyclodextrin , 2000 .

[6]  C. Bicchi,et al.  Cyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields. , 1999, Journal of chromatography. A.

[7]  V. Schurig,et al.  Enantioselective capillary gas chromatography and capillary supercritical fluid chromatography on an immobilized γ-cyclodextrin derivative , 1997 .

[8]  C. Bicchi,et al.  Cyclodextrin derivatives in GC separation of racemic mixtures of volatiles. Part IX. The influence of the different polysiloxanes as diluting phase for 2,3‐di‐O‐acetyl‐6‐O‐t‐butyldimethylsilyl‐β‐cyclodextrin on the separation of some racemates , 1995 .

[9]  P. Sandra,et al.  Retention on mixed cyclodextrin/polysiloxane stationary phases in capillary GC—Evidence for the interaction of cyclodextrin and polysiloxane , 1995 .

[10]  V. Schurig Enantiomer separation by gas chromatography on chiral stationary phases , 1994 .

[11]  A. Mosandl,et al.  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 , 1992 .

[12]  R. Meier,et al.  The separation of enantiomers on modified cyclodextrin columns: Measurements and molecular modeling , 1992 .

[13]  D. Armstrong,et al.  Multiple enantioselective retention mechanisms on derivatized cyclodextrin gas chromatographic chiral stationary phases. , 1992 .

[14]  A. Mosandl,et al.  Influence of derivatization on the chiral selectivity of cyclodextrins: Alkylated/acylated cyclodextrins and γ-/δ-lactones as an example , 1991 .

[15]  H. Nowotny,et al.  Gas Chromatographic Separation of Enantiomers on Cyclodextrin Derivatives , 1990 .

[16]  Péter Fügedi,et al.  Synthesis of heptakis(6-O-tert-butyldimethylsilyl)cyclomaltoheptaose and octakis(6-O-tert-butyldimethylsilyl)cyclomalto-octaose , 1989 .

[17]  W. König,et al.  Cyclodextrins as chiral stationary phases in capillary gas chromatography. Part II: Heptakis(3-O-acetyl-2,6-di-O-pentyl)-ß-cyclodextrin , 1988 .

[18]  K. Grob Making and Manipulating Capillary Columns for Gas Chromatography , 1986 .