4.8 Article

N-Arylation of Tertiary Amines under Mild Conditions

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ORGANIC LETTERS
卷 18, 期 5, 页码 980-983

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00078

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  1. Technion Start-up Grant
  2. Schulich Foundation

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A transition-metal-free procedure for the N-arylation of tertiary amines to spa quaternary ammonium salts is described. The presented conditions allow for the isolation of trialkylaryl, dialkyldiaryl, and novel triarylalkyl ammonium salts, including N-chiral quaternary ammonium salts. The reaction works at room temperature, open to air with electron rich or -poor benzyne precursors and different tertiary amines, allowing the synthesis of a broad range of N-aryl ammonium salts that have applications in a variety of fields.

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