Bioorganic and Medicinal Chemistry Letters p. 1267 - 1272 (1999)
Update date:2022-08-10
Topics:
Everett
Naylor
Patel
Stratford
Wardman
2-Nitroimidazoles were synthesised substituted with aspirin or salicylic acid, as leaving groups linked through the (imidazole-5-yl)methyl position. Activation of aqueous solutions by CO2- (a model one-electron reductant) resulted in release of aspirin or salicylate, probably via the 2- hydroxyaminoimidazole. The analogous 2-nitroimidazole with bromide as leaving group eliminated bromide in <1 ms via radical-anion.
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