The incorporation of nitrogen in the phenolic ring leads to compounds with very low phenolic O-H bond dissociation enthalpies, and thus high reactivities towards peroxyl radicals, but which are reasonably stable to direct reactions with air. The 3-pyridinols 1 and 2 are extremely effective peroxyl-radical-trapping chain-breaking antioxidants.
6-amino-3-pyridinols: Towards diffusion-controlled chain-breaking antioxidants / Wijtmans M.; Pratt D.A.; Valgimigli L.; DiLabio G.A.; Pedulli G.F.; Porter N.A.. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - STAMPA. - 42:36(2003), pp. 4370-4373. [10.1002/anie.200351881]
6-amino-3-pyridinols: Towards diffusion-controlled chain-breaking antioxidants
Valgimigli L.
;Pedulli G. F.;
2003
Abstract
The incorporation of nitrogen in the phenolic ring leads to compounds with very low phenolic O-H bond dissociation enthalpies, and thus high reactivities towards peroxyl radicals, but which are reasonably stable to direct reactions with air. The 3-pyridinols 1 and 2 are extremely effective peroxyl-radical-trapping chain-breaking antioxidants.File in questo prodotto:
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