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A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones

By applying N-doped carbon modified iron-based catalysts, the controlled hydrogenation of N-heteroarenes, especially (iso)quinolones, is achieved. Crucial for activity is the catalyst preparation by pyrolysis of a carbon-impregnated composite, obtained from iron(ii) acetate and N-aryliminopyridines....

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Autores principales: Sahoo, Basudev, Kreyenschulte, Carsten, Agostini, Giovanni, Lund, Henrik, Bachmann, Stephan, Scalone, Michelangelo, Junge, Kathrin, Beller, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238895/
https://www.ncbi.nlm.nih.gov/pubmed/30542564
http://dx.doi.org/10.1039/c8sc02744g
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author Sahoo, Basudev
Kreyenschulte, Carsten
Agostini, Giovanni
Lund, Henrik
Bachmann, Stephan
Scalone, Michelangelo
Junge, Kathrin
Beller, Matthias
author_facet Sahoo, Basudev
Kreyenschulte, Carsten
Agostini, Giovanni
Lund, Henrik
Bachmann, Stephan
Scalone, Michelangelo
Junge, Kathrin
Beller, Matthias
author_sort Sahoo, Basudev
collection PubMed
description By applying N-doped carbon modified iron-based catalysts, the controlled hydrogenation of N-heteroarenes, especially (iso)quinolones, is achieved. Crucial for activity is the catalyst preparation by pyrolysis of a carbon-impregnated composite, obtained from iron(ii) acetate and N-aryliminopyridines. As demonstrated by TEM, XRD, XPS and Raman spectroscopy, the synthesized material is composed of Fe(0), Fe(3)C and FeN(x) in a N-doped carbon matrix. The decent catalytic activity of this robust and easily recyclable Fe-material allowed for the selective hydrogenation of various (iso)quinoline derivatives, even in the presence of reducible functional groups, such as nitriles, halogens, esters and amides. For a proof-of-concept, this nanostructured catalyst was implemented in the multistep synthesis of natural products and pharmaceutical lead compounds as well as modification of photoluminescent materials. As such this methodology constitutes the first heterogeneous iron-catalyzed hydrogenation of substituted (iso)quinolones with synthetic importance.
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spelling pubmed-62388952018-12-12 A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones Sahoo, Basudev Kreyenschulte, Carsten Agostini, Giovanni Lund, Henrik Bachmann, Stephan Scalone, Michelangelo Junge, Kathrin Beller, Matthias Chem Sci Chemistry By applying N-doped carbon modified iron-based catalysts, the controlled hydrogenation of N-heteroarenes, especially (iso)quinolones, is achieved. Crucial for activity is the catalyst preparation by pyrolysis of a carbon-impregnated composite, obtained from iron(ii) acetate and N-aryliminopyridines. As demonstrated by TEM, XRD, XPS and Raman spectroscopy, the synthesized material is composed of Fe(0), Fe(3)C and FeN(x) in a N-doped carbon matrix. The decent catalytic activity of this robust and easily recyclable Fe-material allowed for the selective hydrogenation of various (iso)quinoline derivatives, even in the presence of reducible functional groups, such as nitriles, halogens, esters and amides. For a proof-of-concept, this nanostructured catalyst was implemented in the multistep synthesis of natural products and pharmaceutical lead compounds as well as modification of photoluminescent materials. As such this methodology constitutes the first heterogeneous iron-catalyzed hydrogenation of substituted (iso)quinolones with synthetic importance. Royal Society of Chemistry 2018-09-06 /pmc/articles/PMC6238895/ /pubmed/30542564 http://dx.doi.org/10.1039/c8sc02744g Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Sahoo, Basudev
Kreyenschulte, Carsten
Agostini, Giovanni
Lund, Henrik
Bachmann, Stephan
Scalone, Michelangelo
Junge, Kathrin
Beller, Matthias
A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title_full A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title_fullStr A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title_full_unstemmed A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title_short A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
title_sort robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238895/
https://www.ncbi.nlm.nih.gov/pubmed/30542564
http://dx.doi.org/10.1039/c8sc02744g
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