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Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes
The para‐selective fluorination reaction of anilides using electrochemically generated hypervalent ArIF(2) is reported, with Et(3)N ⋅ 5HF serving as fluoride source and as supporting electrolyte. This electrochemical reaction is characterized by a simple set‐up, easy scalability and affords a broad...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401020/ https://www.ncbi.nlm.nih.gov/pubmed/35510825 http://dx.doi.org/10.1002/chem.202201029 |
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author | Berger, Michael Lenhard, Marola S. Waldvogel, Siegfried R. |
author_facet | Berger, Michael Lenhard, Marola S. Waldvogel, Siegfried R. |
author_sort | Berger, Michael |
collection | PubMed |
description | The para‐selective fluorination reaction of anilides using electrochemically generated hypervalent ArIF(2) is reported, with Et(3)N ⋅ 5HF serving as fluoride source and as supporting electrolyte. This electrochemical reaction is characterized by a simple set‐up, easy scalability and affords a broad variety of fluorinated anilides from easily accessible anilides in good yields up to 86 %. |
format | Online Article Text |
id | pubmed-9401020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94010202022-08-26 Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes Berger, Michael Lenhard, Marola S. Waldvogel, Siegfried R. Chemistry Research Articles The para‐selective fluorination reaction of anilides using electrochemically generated hypervalent ArIF(2) is reported, with Et(3)N ⋅ 5HF serving as fluoride source and as supporting electrolyte. This electrochemical reaction is characterized by a simple set‐up, easy scalability and affords a broad variety of fluorinated anilides from easily accessible anilides in good yields up to 86 %. John Wiley and Sons Inc. 2022-06-07 2022-07-20 /pmc/articles/PMC9401020/ /pubmed/35510825 http://dx.doi.org/10.1002/chem.202201029 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Berger, Michael Lenhard, Marola S. Waldvogel, Siegfried R. Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title |
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title_full |
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title_fullStr |
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title_full_unstemmed |
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title_short |
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes |
title_sort | para‐fluorination of anilides using electrochemically generated hypervalent iodoarenes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401020/ https://www.ncbi.nlm.nih.gov/pubmed/35510825 http://dx.doi.org/10.1002/chem.202201029 |
work_keys_str_mv | AT bergermichael parafluorinationofanilidesusingelectrochemicallygeneratedhypervalentiodoarenes AT lenhardmarolas parafluorinationofanilidesusingelectrochemicallygeneratedhypervalentiodoarenes AT waldvogelsiegfriedr parafluorinationofanilidesusingelectrochemicallygeneratedhypervalentiodoarenes |