Synthesis
DOI: 10.1055/a-2787-1393
Paper

Synthetic Access to Indolo[2,3-d]tropone-Derived Tolanes and Synthesis of Indolo[2,3-d]tropolones

Authors

  • Lars Benedix

    1   Fakultät für Chemie und Chemische Biologie, Technische Universitat Dortmund, Dortmund, Germany (Ringgold ID: RIN14311)
  • David Mross

    1   Fakultät für Chemie und Chemische Biologie, Technische Universitat Dortmund, Dortmund, Germany (Ringgold ID: RIN14311)
  • Martin Hiersemann

    1   Fakultät für Chemie und Chemische Biologie, Technische Universitat Dortmund, Dortmund, Germany (Ringgold ID: RIN14311)

Supported by: Deutsche Forschungsgemeinschaft 426847721, 452669591, 452669688

Indolo[2,3-d]tropones or indolo[2,3-d]tropolones are formally assembled by an annulative merger of tropone or α-tropolone and indole. Although indolo[2,3-d]tropone or indolo[2,3-d]tropolone are derivatives of the popular cyclohepta[b]indole, their chemical, biological and physical properties have not yet been evaluated. We reveal a modular, robust and scalable synthetic access to indolo[2,3-d]tropone-derived tolanoids by adapting established chemistry, namely the alkyne-de Mayo reaction and the Sonogashira coupling. Furthermore, a method for the single-step oxidation of 6,7-dihydroindolo[2,3-d]tropones to indolo[2,3-d]tropolones is introduced.



Publication History

Received: 05 December 2025

Accepted after revision: 12 January 2026

Accepted Manuscript online:
13 January 2026

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