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About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions
Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052091/ https://www.ncbi.nlm.nih.gov/pubmed/35498499 http://dx.doi.org/10.1039/d0ra02673e |
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author | Beil, Sebastian B. Breiner, Manuel Schulz, Lara Schüll, Aaron Müller, Timo Schollmeyer, Dieter Bomm, Alexander Holtkamp, Michael Karst, Uwe Schade, Wolfgang Waldvogel, Siegfried R. |
author_facet | Beil, Sebastian B. Breiner, Manuel Schulz, Lara Schüll, Aaron Müller, Timo Schollmeyer, Dieter Bomm, Alexander Holtkamp, Michael Karst, Uwe Schade, Wolfgang Waldvogel, Siegfried R. |
author_sort | Beil, Sebastian B. |
collection | PubMed |
description | Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl–aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks. |
format | Online Article Text |
id | pubmed-9052091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90520912022-04-29 About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions Beil, Sebastian B. Breiner, Manuel Schulz, Lara Schüll, Aaron Müller, Timo Schollmeyer, Dieter Bomm, Alexander Holtkamp, Michael Karst, Uwe Schade, Wolfgang Waldvogel, Siegfried R. RSC Adv Chemistry Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl–aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks. The Royal Society of Chemistry 2020-04-08 /pmc/articles/PMC9052091/ /pubmed/35498499 http://dx.doi.org/10.1039/d0ra02673e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Beil, Sebastian B. Breiner, Manuel Schulz, Lara Schüll, Aaron Müller, Timo Schollmeyer, Dieter Bomm, Alexander Holtkamp, Michael Karst, Uwe Schade, Wolfgang Waldvogel, Siegfried R. About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title | About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title_full | About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title_fullStr | About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title_full_unstemmed | About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title_short | About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions |
title_sort | about the selectivity and reactivity of active nickel electrodes in c–c coupling reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052091/ https://www.ncbi.nlm.nih.gov/pubmed/35498499 http://dx.doi.org/10.1039/d0ra02673e |
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