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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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