Improved and General Manganese‐Catalyzed N‐Methylation of Aromatic Amines Using Methanol

A novel lutidine‐based manganese PNP‐pincer complex has been synthesized for the selective N‐methylation of aromatic amines with methanol. Using borrowing hydrogen methodology, a selection of differently functionalized aniline derivatives is selectively methylated in good yields. Mn lends a hydrogen...

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Veröffentlicht in:Chemistry : a European journal 2017-04, Vol.23 (23), p.5410-5413
Hauptverfasser: Neumann, Jacob, Elangovan, Saravanakumar, Spannenberg, Anke, Junge, Kathrin, Beller, Matthias
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container_end_page 5413
container_issue 23
container_start_page 5410
container_title Chemistry : a European journal
container_volume 23
creator Neumann, Jacob
Elangovan, Saravanakumar
Spannenberg, Anke
Junge, Kathrin
Beller, Matthias
description A novel lutidine‐based manganese PNP‐pincer complex has been synthesized for the selective N‐methylation of aromatic amines with methanol. Using borrowing hydrogen methodology, a selection of differently functionalized aniline derivatives is selectively methylated in good yields. Mn lends a hydrogen: A manganese pincer complex has been employed for the selective N‐methylation of aromatic amines using methanol and borrowing hydrogen methodology. A selection of differently functionalized aniline derivatives is selectively mono‐methylated in good yields.
doi_str_mv 10.1002/chem.201605218
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source Wiley Journals
subjects Amines
Aniline
borrowing hydrogen
Chemical Sciences
Chemistry
Derivatives
Hydrogen
Manganese
Methodology
Methyl alcohol
methylation
pincer complex
Synthesis
title Improved and General Manganese‐Catalyzed N‐Methylation of Aromatic Amines Using Methanol
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