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2-Arylpropionic acids stationary phase

Alcaro, S. et al., Enantioselective semi-preparative HPLC of two 2-arylpropionic acids on glycopeptides containing chiral stationary phases, Tetrahedron Asymmetry, 13, 69, 2002. [Pg.164]

Okamoto, Y., Aburatani, R., Kaida, Y., Hatada, K., Inotsume, N., and Nakano, M. (1989) Direct chromatographic separation of 2-arylpropionic acid enantiomers using tris(3,5-dimethylphenylcarbamate)s of cellulose and amylose as chiral stationary phases, Chirality 1, 239-242. [Pg.321]

The enantiomeric purity of 2-arylpropionic acids used as pharmaceuticals was determined after derivatizing to the corresponding amides with various PAA and HAA. End analysis was by HPLC-UVD, with simultaneous measurement at 230 and 254 nm, using a cellulose-based stationary phase. The best derivative for routine determinations was chosen in each case after establishing the chromatographic parameters of the enantiomeric pair of derivatives197. [Pg.674]

Calleri, E., Massolini, G., Loiodice, F., Fracchiolla, G.,Temporini, C., Felix, G., Tortorella, P., Caccialanza, G. Evaluation of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxyalkanoic acids, isosteric analogs and 2-arylpropionic acids,/. Chromatogr. A, 2002,958, 131-140. [Pg.254]

Van Overbeke, A. Baeyens, W. Van den Bossche, W. Dewaele, C. Separation of 2-arylpropionic acids on a cellulose based chiral stationary phase by RP-HPLC. J.Pharm.BiomedAnal., 1994, 12, 901-909... [Pg.762]

Figure 7 Chiral HPLC separation of 2-arylpropionic acid derivatives on nonimprinted (a) and (5)-naproxen-imprinted stationary phase (b). (1) Racemic ketoprofen, (2) racemic ibu-profen, (3) (R)-naproxen, (4) (5)-naproxen. Mobile phase, 20 mM phosphate buffer pH 3.2 -acetonitrile 1 + lv/v. Columns 100 x 4.6 mm. Flow rate, ImL/min. Detection, UV 254 nm. Reproduced from Ref. 45, with permission. Figure 7 Chiral HPLC separation of 2-arylpropionic acid derivatives on nonimprinted (a) and (5)-naproxen-imprinted stationary phase (b). (1) Racemic ketoprofen, (2) racemic ibu-profen, (3) (R)-naproxen, (4) (5)-naproxen. Mobile phase, 20 mM phosphate buffer pH 3.2 -acetonitrile 1 + lv/v. Columns 100 x 4.6 mm. Flow rate, ImL/min. Detection, UV 254 nm. Reproduced from Ref. 45, with permission.
Aboul-Enein, H.Y. El-Awady, M.I. Heard, C.H. Enantiomeric resolution of some 2-arylpropionic acids using L-(-)serine impregnated silica as stationary phase by thin layer chromatography. J. Pharm. Biomed. Anal. 2003, 32,1055-1059. [Pg.754]

Aboul-Enien, H.Y., El-Awady, M.I., and Heard, C.M., Thin layer chromatographic resolution of some 2-arylpropionic acid enantiomers using L-(—)-serine, L-(—)-threonine and a mixture of L-(—)-serine, L-(-)-threonine-impregnated sihca gel as stationary phases, Biomed. Chromatogr., 17, 325, 2003. [Pg.354]


See other pages where 2-Arylpropionic acids stationary phase is mentioned: [Pg.201]    [Pg.676]    [Pg.676]    [Pg.288]   
See also in sourсe #XX -- [ Pg.239 , Pg.240 , Pg.241 , Pg.242 , Pg.243 ]




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Arylpropionic acids

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