Chiral stationary phases, 9-anthryl

Asnin, L., Goetmar, G., Guiochon, G. Chromatographic behavior of the enantiomers of 2,2,2-trifluoro-l-(9-anthryl) ethanol on a quinidine-carbamate chiral stationary phase, J. Chromatogr. A, 2005, 1091, 183-186. 

Anthryl trlfluoromethyl carblnol, chiral stationary phase uses, 103 Antibody production, te(dinlque in two-dimensional gel electrophoresis, 254 Aromatic compounds... 

By incorporating into the stationary phase a chiral charge transfer reagent also capable of hydrogen bonding, such as 2,2,2-trifluoro-l-[(10-methyl)-9-anthryl] ethanol, Pirkle and coworkers [18] have resolved substances which either contain a CT complexing moiety in their molecule, e.g. aromatic sulphoxides and lactones, or possess a function through which such a moiety can be introduced, e.g. alcohols, mercaptans, amines, amino alcohols, amino acids, hydroxy acids and esters. 

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