Selenium-promoted oxidations enable a broad range of valuable oxidative functional group interconversions. Anilines are oxidised with hydrogen peroxide in water in the presence of selenium catalysts. The selenium catalyst determines the nature of the oxidation product; whereas nitroarenes are obtained employing diphenyl diselenide or benzeneseleninic acid, azoxyarenes are formed using selenium dioxide or sodium seleninate. The reaction mechanism relies on the reactivity of Se(IV) active oxidants, while Se(VI) species have been demonstrated not to be involved in.
Synthesis of nitroarenes and azoxyarenes through the selenium-mediated on water oxidation of aryl amines / Capperucci, Antonella; Dalia, Camilla; Cenni, Alessio; Tanini, Damiano. - In: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS. - ISSN 1042-6507. - ELETTRONICO. - 198:(2023), pp. 526-531. [10.1080/10426507.2023.2166044]
Synthesis of nitroarenes and azoxyarenes through the selenium-mediated on water oxidation of aryl amines
Capperucci, Antonella;Tanini, Damiano
2023
Abstract
Selenium-promoted oxidations enable a broad range of valuable oxidative functional group interconversions. Anilines are oxidised with hydrogen peroxide in water in the presence of selenium catalysts. The selenium catalyst determines the nature of the oxidation product; whereas nitroarenes are obtained employing diphenyl diselenide or benzeneseleninic acid, azoxyarenes are formed using selenium dioxide or sodium seleninate. The reaction mechanism relies on the reactivity of Se(IV) active oxidants, while Se(VI) species have been demonstrated not to be involved in.File | Dimensione | Formato | |
---|---|---|---|
Tanini - PSSi.pdf
accesso aperto
Tipologia:
Preprint (Submitted version)
Licenza:
Tutti i diritti riservati
Dimensione
244.71 kB
Formato
Adobe PDF
|
244.71 kB | Adobe PDF |
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.