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Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols

We report the first Fe(II)‐catalyzed biomimetic aerobic oxidation of alcohols. The principle of this oxidation, which involves several electron‐transfer steps, is reminiscent of biological oxidation in the respiratory chain. The electron transfer from the alcohol to molecular oxygen occurs with the...

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Autores principales: Guðmundsson, Arnar, Schlipköter, Kim Elisabeth, Bäckvall, Jan‐E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154773/
https://www.ncbi.nlm.nih.gov/pubmed/31999013
http://dx.doi.org/10.1002/anie.202000054
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author Guðmundsson, Arnar
Schlipköter, Kim Elisabeth
Bäckvall, Jan‐E.
author_facet Guðmundsson, Arnar
Schlipköter, Kim Elisabeth
Bäckvall, Jan‐E.
author_sort Guðmundsson, Arnar
collection PubMed
description We report the first Fe(II)‐catalyzed biomimetic aerobic oxidation of alcohols. The principle of this oxidation, which involves several electron‐transfer steps, is reminiscent of biological oxidation in the respiratory chain. The electron transfer from the alcohol to molecular oxygen occurs with the aid of three coupled catalytic redox systems, leading to a low‐energy pathway. An iron transfer‐hydrogenation complex was utilized as a substrate‐selective dehydrogenation catalyst, along with an electron‐rich quinone and an oxygen‐activating Co(salen)‐type complex as electron‐transfer mediators. Various primary and secondary alcohols were oxidized in air to the corresponding aldehydes or ketones with this method in good to excellent yields.
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spelling pubmed-71547732020-04-15 Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols Guðmundsson, Arnar Schlipköter, Kim Elisabeth Bäckvall, Jan‐E. Angew Chem Int Ed Engl Communications We report the first Fe(II)‐catalyzed biomimetic aerobic oxidation of alcohols. The principle of this oxidation, which involves several electron‐transfer steps, is reminiscent of biological oxidation in the respiratory chain. The electron transfer from the alcohol to molecular oxygen occurs with the aid of three coupled catalytic redox systems, leading to a low‐energy pathway. An iron transfer‐hydrogenation complex was utilized as a substrate‐selective dehydrogenation catalyst, along with an electron‐rich quinone and an oxygen‐activating Co(salen)‐type complex as electron‐transfer mediators. Various primary and secondary alcohols were oxidized in air to the corresponding aldehydes or ketones with this method in good to excellent yields. John Wiley and Sons Inc. 2020-02-19 2020-03-23 /pmc/articles/PMC7154773/ /pubmed/31999013 http://dx.doi.org/10.1002/anie.202000054 Text en © 2020 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
Guðmundsson, Arnar
Schlipköter, Kim Elisabeth
Bäckvall, Jan‐E.
Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title_full Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title_fullStr Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title_full_unstemmed Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title_short Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols
title_sort iron(ii)‐catalyzed biomimetic aerobic oxidation of alcohols
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154773/
https://www.ncbi.nlm.nih.gov/pubmed/31999013
http://dx.doi.org/10.1002/anie.202000054
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