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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....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-6238895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
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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
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title_short | A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones
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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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