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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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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
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author 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
author_facet 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
author_sort Panja, Subir
collection PubMed
description 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.
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spelling pubmed-93837082022-09-08 Non-directed Pd-catalysed electrooxidative olefination of arenes 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 Chem Sci Chemistry 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. The Royal Society of Chemistry 2022-08-05 /pmc/articles/PMC9383708/ /pubmed/36093017 http://dx.doi.org/10.1039/d2sc03288k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
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
Non-directed Pd-catalysed electrooxidative olefination of arenes
title Non-directed Pd-catalysed electrooxidative olefination of arenes
title_full Non-directed Pd-catalysed electrooxidative olefination of arenes
title_fullStr Non-directed Pd-catalysed electrooxidative olefination of arenes
title_full_unstemmed Non-directed Pd-catalysed electrooxidative olefination of arenes
title_short Non-directed Pd-catalysed electrooxidative olefination of arenes
title_sort non-directed pd-catalysed electrooxidative olefination of arenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9383708/
https://www.ncbi.nlm.nih.gov/pubmed/36093017
http://dx.doi.org/10.1039/d2sc03288k
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