4.8 Article

Palladium-Catalyzed Dearomative syn-1,4-Carboamination

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 49, 页码 17787-17790

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b11663

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资金

  1. University of Illinois
  2. National Science Foundation [CHE-1654110]
  3. NIH/National Institute of General Medical Sciences [R01 GM122891]
  4. Honjo International Scholarship Foundation

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A dearomative 1,4-carboamination of arenes has been achieved using arenophile cycloaddition and subsequent palladium-catalyzed substitution with non stabilized 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.

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