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Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex

Novel well-defined NNP and PNP manganese pincer complexes have been synthetized and fully characterized. The catalyst Mn-2 containing an imidazolyaminolphosphino ligand shows high activity and selectivity in the hydrogenation of a wide range of secondary and tertiary amides to the corresponding alco...

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Autores principales: Papa, Veronica, Cabrero-Antonino, Jose R., Alberico, Elisabetta, Spanneberg, Anke, Junge, Kathrin, Junge, Henrik, Beller, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092716/
https://www.ncbi.nlm.nih.gov/pubmed/30155202
http://dx.doi.org/10.1039/c7sc00138j
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author Papa, Veronica
Cabrero-Antonino, Jose R.
Alberico, Elisabetta
Spanneberg, Anke
Junge, Kathrin
Junge, Henrik
Beller, Matthias
author_facet Papa, Veronica
Cabrero-Antonino, Jose R.
Alberico, Elisabetta
Spanneberg, Anke
Junge, Kathrin
Junge, Henrik
Beller, Matthias
author_sort Papa, Veronica
collection PubMed
description Novel well-defined NNP and PNP manganese pincer complexes have been synthetized and fully characterized. The catalyst Mn-2 containing an imidazolyaminolphosphino ligand shows high activity and selectivity in the hydrogenation of a wide range of secondary and tertiary amides to the corresponding alcohols and amines, under relatively mild conditions. For the first time, more challenging substrates like primary aromatic amides including an actual herbicide can also be hydrogenated using this earth-abundant metal-based pincer catalyst.
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spelling pubmed-60927162018-08-28 Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex Papa, Veronica Cabrero-Antonino, Jose R. Alberico, Elisabetta Spanneberg, Anke Junge, Kathrin Junge, Henrik Beller, Matthias Chem Sci Chemistry Novel well-defined NNP and PNP manganese pincer complexes have been synthetized and fully characterized. The catalyst Mn-2 containing an imidazolyaminolphosphino ligand shows high activity and selectivity in the hydrogenation of a wide range of secondary and tertiary amides to the corresponding alcohols and amines, under relatively mild conditions. For the first time, more challenging substrates like primary aromatic amides including an actual herbicide can also be hydrogenated using this earth-abundant metal-based pincer catalyst. Royal Society of Chemistry 2017-05-01 2017-03-08 /pmc/articles/PMC6092716/ /pubmed/30155202 http://dx.doi.org/10.1039/c7sc00138j Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Papa, Veronica
Cabrero-Antonino, Jose R.
Alberico, Elisabetta
Spanneberg, Anke
Junge, Kathrin
Junge, Henrik
Beller, Matthias
Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title_full Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title_fullStr Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title_full_unstemmed Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title_short Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–PNN pincer complex
title_sort efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese–pnn pincer complex
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092716/
https://www.ncbi.nlm.nih.gov/pubmed/30155202
http://dx.doi.org/10.1039/c7sc00138j
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