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- W4235218744 abstract "A newly developed reversed phase cellulose tris(4-methyl benzoate) known as Chiralcel OJ-R was used to investigate the chiral recognition and enantiomeric separation of eight racemic piperidine-2,6-dione compounds—namely, aminoglutethimide and its major metabolite acetylaminoglutethimide, glutethimide, cyclohexylamino-glutethimide, pyridoglutethimide, thalidomide, phenglutarimide, and 3-phenylacetyl-amino-2,6-piperidinedione (antineoplaston A-10). Chiral separation of these compounds was achieved under varying ratios of the mobile phase, except for phenglutarimide and 3-phenylacetylamino-2,6-piperidinedione, for which separation was unsuccessful. Possible chiral recognition mechanisms are also presented. Chirality 9:10–12, 1997. © 1997 Wiley-Liss, Inc." @default.
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- W4235218744 date "1997-01-01" @default.
- W4235218744 modified "2023-10-14" @default.
- W4235218744 title "Enantiomeric separation of some piperidine‐2,6‐dione drugs using chiralcel OJ‐R column" @default.
- W4235218744 doi "https://doi.org/10.1002/(sici)1520-636x(1997)9:1<10::aid-chir2>3.3.co;2-e" @default.
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