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Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol

We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, a...

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Detalles Bibliográficos
Autores principales: Schlagbauer, Martin, Kallmeier, Fabian, Irrgang, Torsten, Kempe, Rhett
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003965/
https://www.ncbi.nlm.nih.gov/pubmed/31743576
http://dx.doi.org/10.1002/anie.201912055
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author Schlagbauer, Martin
Kallmeier, Fabian
Irrgang, Torsten
Kempe, Rhett
author_facet Schlagbauer, Martin
Kallmeier, Fabian
Irrgang, Torsten
Kempe, Rhett
author_sort Schlagbauer, Martin
collection PubMed
description We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer.
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spelling pubmed-70039652020-02-11 Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol Schlagbauer, Martin Kallmeier, Fabian Irrgang, Torsten Kempe, Rhett Angew Chem Int Ed Engl Communications We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer. John Wiley and Sons Inc. 2019-12-12 2020-01-20 /pmc/articles/PMC7003965/ /pubmed/31743576 http://dx.doi.org/10.1002/anie.201912055 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Schlagbauer, Martin
Kallmeier, Fabian
Irrgang, Torsten
Kempe, Rhett
Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title_full Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title_fullStr Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title_full_unstemmed Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title_short Manganese‐Catalyzed β‐Methylation of Alcohols by Methanol
title_sort manganese‐catalyzed β‐methylation of alcohols by methanol
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003965/
https://www.ncbi.nlm.nih.gov/pubmed/31743576
http://dx.doi.org/10.1002/anie.201912055
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AT kemperhett manganesecatalyzedbmethylationofalcoholsbymethanol