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Non-directed Pd-catalysed electrooxidative olefination of arenes

The Fujiwara–Moritani reaction is a powerful tool for the olefination of arenes by Pd-catalysed C–H activation. However, the need for superstoichiometric amounts of toxic chemical oxidants makes the reaction unattractive from an environmental and atom-economical view. Herein, we report the first non...

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Detalles Bibliográficos
Autores principales: Panja, Subir, Ahsan, Salman, Pal, Tanay, Kolb, Simon, Ali, Wajid, Sharma, Sulekha, Das, Chandan, Grover, Jagrit, Dutta, Arnab, Werz, Daniel B., Paul, Amit, Maiti, Debabrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9383708/
https://www.ncbi.nlm.nih.gov/pubmed/36093017
http://dx.doi.org/10.1039/d2sc03288k
Descripción
Sumario:The Fujiwara–Moritani reaction is a powerful tool for the olefination of arenes by Pd-catalysed C–H activation. However, the need for superstoichiometric amounts of toxic chemical oxidants makes the reaction unattractive from an environmental and atom-economical view. Herein, we report the first non-directed and regioselective olefination of simple arenes via an electrooxidative Fujiwara–Moritani reaction. The versatility of this operator-friendly approach was demonstrated by a broad substrate scope which includes arenes, heteroarenes and a variety of olefins. Electroanalytical studies suggest the involvement of a Pd(ii)/Pd(iv) catalytic cycle via a Pd(iii) intermediate.