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DOI: 10.1055/a-2787-1393
Synthetic Access to Indolo[2,3-d]tropone-Derived Tolanes and Synthesis of Indolo[2,3-d]tropolones
Authors
Partially funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – Projektnummern 426847721, 452669591, 452669688.

Abstract
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.
Keywords
Tropone - Cyclohepta[b]indole - de Mayo reaction - Sonogashira coupling - Tropolone - Tolane - Indolo[2,3-d]tropone - Indolo[2,3-d]tropolonePublication History
Received: 05 December 2025
Accepted after revision: 12 January 2026
Accepted Manuscript online:
13 January 2026
Article published online:
02 February 2026
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For the synthesis of indolo[3,2-d]tropolone, see:
For indole-derived tolanoids, see:
For indole-derived tolanoids, see:
For indole-derived tolanoids, see:
For indole-derived tolanoids, see:
For an early report on ortho-bis(tolanes), see:
The oxoammonium salt 15 was synthesized according to
4-Iodo-N-phenylphthalimide was synthesized according to
4-Iodothiazole was synthesized according to
Our 1H and 13C NMR data for tert-butyl 3-iodo-9H-carbazole-9-carboxylate matched those reported in the Supporting Information of
Our 1H and 13C NMR data for tert-butyl 3,6-diiodo-9H-carbazole-9-carboxylate matched those reported in the Supporting Information of