Abstract
Thiols and thioesters play crucial roles in pharmaceuticals, biology, and material science as essential organosulfur compounds. Leveraging readily available and cost-effective inert alkanes through direct thioetherification holds promise for yielding high-value-added products. Herein, we present a photoinduced strategy for sulfur-containing modification of inert alkanes utilizing decatungstate as hydrogen atom transfer reagent, offering a straightforward and practical approach for synthesizing thioethers and thioesters.
| Original language | English |
|---|---|
| Pages (from-to) | 3420-3424 |
| Number of pages | 5 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 22 |
| Issue number | 17 |
| DOIs | |
| State | Published - 3 Apr 2024 |
| Externally published | Yes |
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Dive into the research topics of 'Photoinduced decatungstate-catalyzed C(sp3)-H thioetherification by sulfinate salts'. Together they form a unique fingerprint.Cite this
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