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Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles

Herein, an iron(II)‐catalyzed biomimetic oxidation of N‐heterocycles under aerobic conditions is described. The dehydrogenation process, involving several electron‐transfer steps, is inspired by oxidations occurring in the respiratory chain. An environmentally friendly and inexpensive iron catalyst...

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Detalles Bibliográficos
Autores principales: Manna, Srimanta, Kong, Wei‐Jun, Bäckvall, Jan‐E.
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/PMC8518507/
https://www.ncbi.nlm.nih.gov/pubmed/34324754
http://dx.doi.org/10.1002/chem.202102483
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author Manna, Srimanta
Kong, Wei‐Jun
Bäckvall, Jan‐E.
author_facet Manna, Srimanta
Kong, Wei‐Jun
Bäckvall, Jan‐E.
author_sort Manna, Srimanta
collection PubMed
description Herein, an iron(II)‐catalyzed biomimetic oxidation of N‐heterocycles under aerobic conditions is described. The dehydrogenation process, involving several electron‐transfer steps, is inspired by oxidations occurring in the respiratory chain. An environmentally friendly and inexpensive iron catalyst together with a hydroquinone/cobalt Schiff base hybrid catalyst as electron‐transfer mediator were used for the substrate‐selective dehydrogenation reaction of various N‐heterocycles. The method shows a broad substrate scope and delivers important heterocycles in good‐to‐excellent yields.
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spelling pubmed-85185072021-10-21 Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles Manna, Srimanta Kong, Wei‐Jun Bäckvall, Jan‐E. Chemistry Communications Herein, an iron(II)‐catalyzed biomimetic oxidation of N‐heterocycles under aerobic conditions is described. The dehydrogenation process, involving several electron‐transfer steps, is inspired by oxidations occurring in the respiratory chain. An environmentally friendly and inexpensive iron catalyst together with a hydroquinone/cobalt Schiff base hybrid catalyst as electron‐transfer mediator were used for the substrate‐selective dehydrogenation reaction of various N‐heterocycles. The method shows a broad substrate scope and delivers important heterocycles in good‐to‐excellent yields. John Wiley and Sons Inc. 2021-09-06 2021-10-01 /pmc/articles/PMC8518507/ /pubmed/34324754 http://dx.doi.org/10.1002/chem.202102483 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Manna, Srimanta
Kong, Wei‐Jun
Bäckvall, Jan‐E.
Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title_full Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title_fullStr Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title_full_unstemmed Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title_short Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
title_sort iron(ii)‐catalyzed aerobic biomimetic oxidation of n‐heterocycles
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518507/
https://www.ncbi.nlm.nih.gov/pubmed/34324754
http://dx.doi.org/10.1002/chem.202102483
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