The dioxolenonemethyl moiety of the oral penem prodrug FCE 25199 (1) was found to be a source of photochemical lability in the solid state. Reactions centered on the formation and decomposition of a hydroperoxide (3) have been observed and rationalized. Expedients have been devised to improve the shelf-life of crystalline 1 up to acceptable levels.
Solid state photoreactivity of a dioxolenone methyl ester
ALBINI, ANGELO;FASANI, ELISA;
1995-01-01
Abstract
The dioxolenonemethyl moiety of the oral penem prodrug FCE 25199 (1) was found to be a source of photochemical lability in the solid state. Reactions centered on the formation and decomposition of a hydroperoxide (3) have been observed and rationalized. Expedients have been devised to improve the shelf-life of crystalline 1 up to acceptable levels.File in questo prodotto:
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