4.7 Article

The synthesis of diverse benzazepinoindoles via gold-catalyzed post-Ugi alkyne hydroarylation/Michael addition sequence

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 17, Pages 4619-4624

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo00810f

Keywords

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Funding

  1. China Scholarship Council (CSC)
  2. Hercules Foundation [AKUL/09/0035]
  3. Nazarbayev University Faculty-Development Competitive Research Grants Program [11022021FD2903]
  4. FWO [Fund for Scientific Research-Flanders (Belgium)]
  5. Research Council of the KU Leuven
  6. RUDN University Strategic Academic Leadership Program

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A novel gold-catalyzed hydroarylation/Michael addition process has been developed for the efficient construction of benzazepinoindole polycyclic scaffolds from readily accessible multifunctional Ugi adducts. The developed methodology exhibits a broad substrate scope, excellent functional-group tolerance, and high yields of the target benzazepinoindoles.
We have developed a novel gold-catalyzed hydroarylation/Michael addition process, enabling the construction of the benzazepinoindole polycyclic scaffold in a highly efficient manner starting from readily accessible multifunctional Ugi adducts. The developed methodology is characterized by a broad substrate scope, excellent functional-group tolerance and high yields of the target benzazepinoindoles.

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