Abstract
A copper(II) triflate catalyzed transfer hydromethylthiolation of alkenes has been developed using commercially available and easy-to-handle β-methylthioketone as the methanethiol donor under air. This method exclusively provides Markovnikov products. The reaction demonstrates a broad substrate scope and excellent functional group tolerance, including compatibility with natural product derivatives. Furthermore, methylthioethers synthesized by this protocol were successfully applied to the preparation of diverse sulfur-containing compounds as well as bioactive molecules.
| Original language | English |
|---|---|
| Pages (from-to) | 9637-9642 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 27 |
| Issue number | 35 |
| DOIs | |
| Publication status | Published - 5 Sept 2025 |
| Externally published | Yes |