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.
2003
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]
Wijtmans M.; Pratt D.A.; Valgimigli L.; DiLabio G.A.; Pedulli G.F.; Porter N.A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/901890
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