Abstract:
:The resolution of four racemic 3-hydroxy-1,4-benzodiazepin-2-ones, widely used in therapeutics, by means of a chiral stationary phase is described. The chiral selector used is (S)-N-(3,5-dinitrobenzoyl)phenylalanine. This chiral stationary phase showed both good enantioselectivity and efficiency for the compounds. Elution times were in all cases shorter than those previously reported for such compounds on different stationary phases. Racemic oxazepam was used to evaluate the loading capacity of the chiral stationary phase.
journal_name
J Pharm Biomed Analjournal_title
Journal of pharmaceutical and biomedical analysisauthors
Oliveros L,Minguillon C,Billaud Cdoi
10.1016/0731-7085(91)80100-nsubject
Has Abstractpub_date
1992-10-01 00:00:00pages
925-30issue
10-12eissn
0731-7085issn
1873-264Xpii
0731-7085(91)80100-Njournal_volume
10pub_type
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