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Palladium-Catalyzed Dearomative syn-1,4-Carboamination.

Mikiko OkumuraAlexander S ShvedDavid Sarlah
Published in: Journal of the American Chemical Society (2017)
A dearomative 1,4-carboamination of arenes has been achieved using arenophile cycloaddition and subsequent palladium-catalyzed substitution with nonstabilized lithium enolates. This protocol delivers products with exclusive syn-1,4-selectivity and can be also conducted in an asymmetric fashion. The method allows rapid dearomative difunctionalization of simple aromatic compounds into functional small molecules amenable to further diversification.
Keyphrases
  • solid state
  • randomized controlled trial
  • amino acid
  • loop mediated isothermal amplification