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pubmed-article:9589553pubmed:abstractTextSeveral derivatives of lotoprednol etabonate (1), a soft corticosteroid antiinflammatory drug, are formed during the synthesis and sterilization process. Some of these contaminants of 1 result from side reactions taking place on the steroid ring C including oxidation, dehydration, chlorination and chlorohydroxylation. The products have been identified, synthesized, and fully characterized by 1H and 13C NMR spectroscopy.lld:pubmed
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pubmed-article:9589553pubmed:volume63lld:pubmed
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pubmed-article:9589553pubmed:pagination193-201lld:pubmed
pubmed-article:9589553pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9589553pubmed:year1998lld:pubmed
pubmed-article:9589553pubmed:articleTitleChemistry of loteprednol etabonate and related steroids. II. Reactions at ring C and NMR structural studies of the resulting compounds.lld:pubmed
pubmed-article:9589553pubmed:affiliationPharmos Corporation, Alachua, Florida 32615, USA.lld:pubmed
pubmed-article:9589553pubmed:publicationTypeJournal Articlelld:pubmed