In a biomimetic transformation, the selective oxidation of catechol (2) to Z,Z-muconic acid (3) has been achieved under extremely mild conditions using methyl(trifluoromethyl)dioxirane (1b). Both dioxirane 1b and dimethyldioxirane (1a) have been applied to the oxidation of 2,6-di-tert-butylphenol (4); the product natures suggest the incursion of radical pathways.

Oxidation of catechol and of 2,6-di-tert-butylphenol by dioxiranes

Fusco C;
1991

Abstract

In a biomimetic transformation, the selective oxidation of catechol (2) to Z,Z-muconic acid (3) has been achieved under extremely mild conditions using methyl(trifluoromethyl)dioxirane (1b). Both dioxirane 1b and dimethyldioxirane (1a) have been applied to the oxidation of 2,6-di-tert-butylphenol (4); the product natures suggest the incursion of radical pathways.
1991
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Methyl(trifluoromethyl)dioxirane
Epoxidation
Dimethyldioxirane
Oxyfunctionalization
Phenols
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/118456
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