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Rh(III)-Catalyzed [5 + 1] Annulation of Indole-enaminones with Diazo Compounds To Form Highly Functionalized Carbazoles.

Zhidong JiangJianhui ZhouHaoran ZhuHong LiuYu Zhou
Published in: Organic letters (2021)
A novel Rh(III)-catalyzed C-H activation/annulation cascade of indole-enaminones with diazo compounds was reported to construct diversely functionalized carbazole frameworks. The most notable characteristic is that this transformation could smoothly furnish a novel [5 + 1] cyclization product with good to excellent yields (up to 95%), accompanied by the thorough removal of acetyl and N,N-dimethyl groups of two substrates from the target products, rather than the normally expected [4 + 2] cyclization products.
Keyphrases
  • room temperature
  • quantum dots
  • molecularly imprinted
  • high resolution
  • liquid chromatography