4.8 Article

Copper-catalyzed coupling of arylboronic acids and amines

Journal

ORGANIC LETTERS
Volume 3, Issue 13, Pages 2077-2079

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol0160396

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Funding

  1. NCI NIH HHS [T32CA09112] Funding Source: Medline
  2. NIGMS NIH HHS [GM46059] Funding Source: Medline

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[GRAPHICS] A general catalytic coupling of arylboronic acids and amines is reported. This room-temperature coupling was realized through the use of catalytic copper(II) acetate, 2,6-lutidine as base, and myristic acid as an additive. Functionalized aniline substrates provided the diarylamine coupling products in good yield (58-91%), A variety of alkylamines were also successfully coupled to give N-alkyl anilines in moderate yield (50-64%).

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