Application of an unusual ninhydrin-based reaction for the indirect chiral resolution of d,l-penicillamine

Volume: 85, Issue: 4, Pages: 1783 - 1785
Published: Sep 1, 2011
Abstract
An unusual reaction involving ninhydrin and aminothiols was exploited to set an indirect method for the chiral recognition of stereoisomers of penicillamine. Separation of diastereoisomers was achieved on a C18 column in isocratic mode by using a mixture of propionic acid (pH 3.0)/acetonitrile/water (10:10:80, v/v/v) as a mobile phase. Diastereoisomers were detected by a fluorescence detector in fairly short times (about 7 min) and with a good...
Paper Details
Title
Application of an unusual ninhydrin-based reaction for the indirect chiral resolution of d,l-penicillamine
Published Date
Sep 1, 2011
Journal
Volume
85
Issue
4
Pages
1783 - 1785
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