Abstract
A catalyst- and photo-free strategy for the divergent synthesis of thioethers and thioimidate esters from thiophenols/thiols and aryldiazonium salts has been developed. The reaction pathway is precisely controlled by temperature and bases. The electron donor-acceptor (EDA) complex-initiated cross-coupling of aryl and thiyl radicals was achieved at 0 °C in the presence of a base. The EDA complex initiated cascade aryl radical addition to acetonitrile, followed by coupling with thiyl radical, was realized at 70 °C in the absence of base. Both transformations feature broad substrate scope, good functional group tolerance, large-scale synthesis, along with metal- and photo-free conditions. Detailed mechanistic studies indicated that the corresponding radicals can be generated precisely and react in situ to avoid self-coupling under catalyst- and photo-free conditions.
| Original language | English |
|---|---|
| Journal | Green Synthesis and Catalysis |
| DOIs | |
| State | Accepted/In press - 2026 |
Keywords
- Aryldiazonium salts
- Divergent synthesis
- EDA complexes
- Thioethers
- Thioimidate esters
- Thiols/thiophenols
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