Structure re-assignment of a metabolite of ampicillin and amoxycillin and epimerization of their penicilloic acids
作者： A. E. BIRD , E. A. CUTMORE , K. R. JENNINGS , A. C. MARSHALL
DOI: 10.1111/J.2042-7158.1983.TB04292.X
关键词:
摘要: Products formed in-vitro from ampicillin and amoxycillin penicilloates have been examined by high-performance liquid chromatography, ultraviolet nuclear magnetic resonance spectroscopy thiol group determination were found to be the 5S epimers of penicilloic acids. This is in contrast a published claim that corresponding penamaldic acids treatment used.
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