4.8 Article

TEMPO Oxoammonium Salt-Mediated Dehydrogenative Povarov/Oxidation Tandem Reaction of N-Alkyl Anilines

Journal

ORGANIC LETTERS
Volume 13, Issue 22, Pages 6066-6069

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol202552y

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Funding

  1. Deutsche Forschungsgemeinschaft
  2. Fonds der Chemischen Industrie

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The synthesis of a variety of substituted quinolines from N-alkyl anilines by a one-pot dehydrogenative Povarov/oxidation tandem reaction with mono- and 1,2-disubstituted aryl and alkyl olefins was developed. A simple protocol using cheap and benign iron(111)chloride as the Lewis acid catalyst and a TEMPO oxoammonium salt as a nontoxic, mild, efficient oxidant is reported.

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