Article ID Journal Published Year Pages File Type
7683029 Talanta 2013 10 Pages PDF
Abstract
Oxidation of fluoroquinolones proceeded at piperazine moiety yielding respective hydroxy and oxo analogs, and remaining the quinolone fragment intact. Structures of products formed were assigned on a basis of UPLC/MS/MS fragmentation pathways.
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Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
Preview
Separation and characterization of ciprofloxacin, difloxacin, lomefloxacin, norfloxacin, and ofloxacin oxidation products under potassium permanganate treatment in acidic medium by UPLC-MS/MS
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