Abstract
Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon-sulfur bonds via a highly efficient decarbonylative process.
Original language | English |
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Pages (from-to) | 3045-3050 |
Number of pages | 6 |
Journal | Synthesis (Germany) |
Volume | 53 |
Issue number | 17 |
DOIs | |
Publication status | Published - Sep 1 2021 |
Keywords
- C-F bond activation
- acyl fluorides
- decarbonylation
- sulfides
- thioetherification
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry