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Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones
A catalytic system based on complexes comprising abundant and cheap manganese together with readily available aminotriazole ligands is reported. The new Mn(I) complexes are catalytically competent in transfer hydrogenation of ketones with 2‐propanol as hydrogen source. The reaction proceeds under mi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220868/ https://www.ncbi.nlm.nih.gov/pubmed/30443274 http://dx.doi.org/10.1002/cctc.201800953 |
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author | Martínez‐Ferraté, Oriol Werlé, Christophe Franciò, Giancarlo Leitner, Walter |
author_facet | Martínez‐Ferraté, Oriol Werlé, Christophe Franciò, Giancarlo Leitner, Walter |
author_sort | Martínez‐Ferraté, Oriol |
collection | PubMed |
description | A catalytic system based on complexes comprising abundant and cheap manganese together with readily available aminotriazole ligands is reported. The new Mn(I) complexes are catalytically competent in transfer hydrogenation of ketones with 2‐propanol as hydrogen source. The reaction proceeds under mild conditions at 80 °C for 20 h with 3 % of catalyst loading using either KO(t)Bu or NaOH as base. Good to excellent yields were obtained for a wide substrate scope with broad functional group tolerance. The obtained results by varying the substitution pattern of the ligand are consistent with an out‐sphere mechanism for the H‐transfer. |
format | Online Article Text |
id | pubmed-6220868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62208682018-11-13 Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones Martínez‐Ferraté, Oriol Werlé, Christophe Franciò, Giancarlo Leitner, Walter ChemCatChem Communications A catalytic system based on complexes comprising abundant and cheap manganese together with readily available aminotriazole ligands is reported. The new Mn(I) complexes are catalytically competent in transfer hydrogenation of ketones with 2‐propanol as hydrogen source. The reaction proceeds under mild conditions at 80 °C for 20 h with 3 % of catalyst loading using either KO(t)Bu or NaOH as base. Good to excellent yields were obtained for a wide substrate scope with broad functional group tolerance. The obtained results by varying the substitution pattern of the ligand are consistent with an out‐sphere mechanism for the H‐transfer. John Wiley and Sons Inc. 2018-10-11 2018-10-23 /pmc/articles/PMC6220868/ /pubmed/30443274 http://dx.doi.org/10.1002/cctc.201800953 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Martínez‐Ferraté, Oriol Werlé, Christophe Franciò, Giancarlo Leitner, Walter Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title | Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title_full | Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title_fullStr | Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title_full_unstemmed | Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title_short | Aminotriazole Mn(I) Complexes as Effective Catalysts for Transfer Hydrogenation of Ketones |
title_sort | aminotriazole mn(i) complexes as effective catalysts for transfer hydrogenation of ketones |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220868/ https://www.ncbi.nlm.nih.gov/pubmed/30443274 http://dx.doi.org/10.1002/cctc.201800953 |
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