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Stable and Storable N(CF(3))(2) Transfer Reagents
Fluorinated groups are essential for drug design, agrochemicals, and materials science. The bis(trifluoromethyl)amino group is an example of a stable group that has a high potential. While the number of molecules containing perfluoroalkyl, perfluoroalkoxy, and other fluorinated groups is steadily in...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361714/ https://www.ncbi.nlm.nih.gov/pubmed/33978273 http://dx.doi.org/10.1002/chem.202101436 |
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author | Schneider, Leon N. Tanzer Krauel, Eva‐Maria Deutsch, Carl Urbahns, Klaus Bischof, Tobias Maibom, Kristina A. M. Landmann, Johannes Keppner, Fabian Kerpen, Christoph Hailmann, Michael Zapf, Ludwig Knuplez, Tanja Bertermann, Rüdiger Ignat'ev, Nikolai V. Finze, Maik |
author_facet | Schneider, Leon N. Tanzer Krauel, Eva‐Maria Deutsch, Carl Urbahns, Klaus Bischof, Tobias Maibom, Kristina A. M. Landmann, Johannes Keppner, Fabian Kerpen, Christoph Hailmann, Michael Zapf, Ludwig Knuplez, Tanja Bertermann, Rüdiger Ignat'ev, Nikolai V. Finze, Maik |
author_sort | Schneider, Leon N. |
collection | PubMed |
description | Fluorinated groups are essential for drug design, agrochemicals, and materials science. The bis(trifluoromethyl)amino group is an example of a stable group that has a high potential. While the number of molecules containing perfluoroalkyl, perfluoroalkoxy, and other fluorinated groups is steadily increasing, examples with the N(CF(3))(2) group are rare. One reason is that transfer reagents are scarce and metal‐based storable reagents are unknown. Herein, a set of Cu(I) and Ag(I) bis(trifluoromethyl)amido complexes stabilized by N‐ and P‐donor ligands with unprecedented stability are presented. The complexes are stable solids that can even be manipulated in air for a short time. They are bis(trifluoromethyl)amination reagents as shown by nucleophilic substitution and Sandmeyer reactions. In addition to a series of benzylbis(trifluoromethyl)amines, 2‐bis(trifluoromethyl)amino acetate was obtained, which, upon hydrolysis, gives the fluorinated amino acid N,N‐bis(trifluoromethyl)glycine. |
format | Online Article Text |
id | pubmed-8361714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83617142021-08-17 Stable and Storable N(CF(3))(2) Transfer Reagents Schneider, Leon N. Tanzer Krauel, Eva‐Maria Deutsch, Carl Urbahns, Klaus Bischof, Tobias Maibom, Kristina A. M. Landmann, Johannes Keppner, Fabian Kerpen, Christoph Hailmann, Michael Zapf, Ludwig Knuplez, Tanja Bertermann, Rüdiger Ignat'ev, Nikolai V. Finze, Maik Chemistry Full Papers Fluorinated groups are essential for drug design, agrochemicals, and materials science. The bis(trifluoromethyl)amino group is an example of a stable group that has a high potential. While the number of molecules containing perfluoroalkyl, perfluoroalkoxy, and other fluorinated groups is steadily increasing, examples with the N(CF(3))(2) group are rare. One reason is that transfer reagents are scarce and metal‐based storable reagents are unknown. Herein, a set of Cu(I) and Ag(I) bis(trifluoromethyl)amido complexes stabilized by N‐ and P‐donor ligands with unprecedented stability are presented. The complexes are stable solids that can even be manipulated in air for a short time. They are bis(trifluoromethyl)amination reagents as shown by nucleophilic substitution and Sandmeyer reactions. In addition to a series of benzylbis(trifluoromethyl)amines, 2‐bis(trifluoromethyl)amino acetate was obtained, which, upon hydrolysis, gives the fluorinated amino acid N,N‐bis(trifluoromethyl)glycine. John Wiley and Sons Inc. 2021-06-09 2021-07-26 /pmc/articles/PMC8361714/ /pubmed/33978273 http://dx.doi.org/10.1002/chem.202101436 Text en © 2021 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 | Full Papers Schneider, Leon N. Tanzer Krauel, Eva‐Maria Deutsch, Carl Urbahns, Klaus Bischof, Tobias Maibom, Kristina A. M. Landmann, Johannes Keppner, Fabian Kerpen, Christoph Hailmann, Michael Zapf, Ludwig Knuplez, Tanja Bertermann, Rüdiger Ignat'ev, Nikolai V. Finze, Maik Stable and Storable N(CF(3))(2) Transfer Reagents |
title | Stable and Storable N(CF(3))(2) Transfer Reagents |
title_full | Stable and Storable N(CF(3))(2) Transfer Reagents |
title_fullStr | Stable and Storable N(CF(3))(2) Transfer Reagents |
title_full_unstemmed | Stable and Storable N(CF(3))(2) Transfer Reagents |
title_short | Stable and Storable N(CF(3))(2) Transfer Reagents |
title_sort | stable and storable n(cf(3))(2) transfer reagents |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361714/ https://www.ncbi.nlm.nih.gov/pubmed/33978273 http://dx.doi.org/10.1002/chem.202101436 |
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