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A Novel C3/C4-Fused Indole Scaffold through Acid-Catalyzed Cascade Reaction.
Potlitz, Felix; Palm, Gottfried J; Bodtke, Anja; Lammers, Michael; Schade, Dennis; Link, Andreas.
  • Potlitz F; Institute of Pharmacy, University of Greifswald, 17489 Greifswald, Germany.
  • Palm GJ; Institute of Biochemistry, University of Greifswald, 17489 Greifswald, Germany.
  • Bodtke A; Institute of Pharmacy, University of Greifswald, 17489 Greifswald, Germany.
  • Lammers M; Institute of Biochemistry, University of Greifswald, 17489 Greifswald, Germany.
  • Schade D; Institute of Pharmacy, Department of Pharmaceutical and Medicinal Chemistry, Christian-Albrechts-University of Kiel, 24118 Kiel, Germany.
  • Link A; Partner Site Kiel, DZHK, German Center for Cardiovascular Research, 24105 Kiel, Germany.
Molecules ; 29(13)2024 Jun 27.
Article en En | MEDLINE | ID: mdl-38999014
ABSTRACT
3,4-bridged indoles are underrepresented among the vast number of indoles described in the literature. Attempts to access 3,4-macrocyclized indoles led to the unexpected formation of a novel tetracyclic indole through intramolecular acid-catalyzed ring contraction. The herein-established one-step synthetic route provides an excellent medicinal chemistry platform for the construction of screening libraries covering a unique chemical space of indoles.
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