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DOI: 10.1055/a-2416-2206
The Synthesis of Unsymmetrical Arylated Tetrathiafulvalenes Extended with an Anthraquinoid Spacer via Pd-Catalyzed C–H Arylation
This work was supported by the Japan Society for the Promotion of Science (JSPS KAKENHI, Grant Number JP21K14696) and by Grant-in-Aid for Research Promotion to The Research Unit for Development of Organic Superconductors.

Abstract
We synthesized diarylated 10-(1,3-dithiol-2-ylidene)anthracene-9-(10H)-one derivatives, which serve as important precursors of unsymmetrical arylated TTFAQs, via the palladium-catalyzed direct C–H arylation. Unsymmetrical diarylated TTFAQs were synthesized by the Horner–Wadsworth–Emmons reaction using diarylated 10-(1,3-dithiol-2-ylidene)anthracene-9-(10H)-one as the starting materials. Additionally, we have successfully synthesized unsymmetrical tetraarylated TTFAQs by a second palladium-catalyzed C–H arylation of diarylated TTFAQs.
Key words
tetrathiafulvalene - extended TTF - anthraquinoid spacer - unsymmetrical arylated compounds - palladium-catalyzed direct C–H arylation - X-ray structure analysis - redox behaviorSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2416-2206.
- Supporting Information
Publikationsverlauf
Eingereicht: 06. Juli 2024
Angenommen nach Revision: 16. September 2024
Accepted Manuscript online:
16. September 2024
Artikel online veröffentlicht:
10. Oktober 2024
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