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Reductive amination of tertiary anilines and aldehydes



Reductive amination of tertiary anilines and aldehydes



Chemical Communications 49(78): 8866-8868



An unprecedented oxidant-mediated reductive amination of tertiary anilines and aldehydes without external reducing agents was developed via the nucleophilic attack of the oxygen atom of the carbonyl group to in situ generated iminium ions, in which tertiary anilines were used as both nitrogen source and reducing agent for the first time.

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Accession: 055434272

Download citation: RISBibTeXText

PMID: 23963514

DOI: 10.1039/c3cc45084h


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