4.8 Article

Transition-Metal-Free Electrophilic Amination between Aryl Grignard Reagents and N-Chloroamines

Journal

ORGANIC LETTERS
Volume 12, Issue 7, Pages 1516-1519

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol100235b

Keywords

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Funding

  1. Synergistic Effects for Creation of Functional Molecules [18064006]
  2. Chemistry of Concerto Catalysis [20037033]
  3. JSPS
  4. MEXT
  5. Uehara Memorial Foundation
  6. Tosoh Organic Chemical and Finechem Corps
  7. [2075003]
  8. [2175098]

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In the presence of N,N,N,N-tetramethylethylenediamine (TMEDA) as an additive, easily prepared and handled N-chloroamines react with aryl Grignard reagents to give a variety of arylamines in good to excellent yields. Functional groups such as ester and nitrile are compatible under the reaction conditions.

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