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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9383708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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