Abstract
An unexpected time-controlled highly selective C3-or C2-sulfinylation of pyrroles with sulfinamides is reported for the first time. The sulfinylation of indoles with sulfinamides using this protocol is oxidant-free and can be performed under obviously more feasible conditions (1.2 equiv. of indoles, 10 min) in comparison with the precedent procedure (3-20 equiv. of indoles, 16-18 h, ammonium persulfate as oxidant, hv). A variety of functional groups were tolerated, and various C2-thioindoles and C2/3-thiopyrroles were obtained in moderate to excellent yields.
| Original language | English |
|---|---|
| Pages (from-to) | 4789-4800 |
| Number of pages | 12 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 17 |
| Issue number | 19 |
| DOIs | |
| State | Published - 2019 |
| Externally published | Yes |
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