Abstract
We report studies on the photocatalytic formation of C-S bonds to form benzothiazoles via an intramolecular cyclization and sulfenylated indoles via an intermolecular reaction. Cyclic voltammetry (CV) and density functional theory studies suggest that benzothiazole formation proceeds via a mechanism that involves an electrophilic sulfur radical, while the indole sulfenylation likely proceeds via a nucleophilic sulfur radical adding into a radical cationic indole. These conditions were successfully extended to several thiobenzamides and indole substrates.
| Original language | English |
|---|---|
| Pages (from-to) | 1648-1655 |
| Number of pages | 8 |
| Journal | Synlett |
| Volume | 30 |
| Issue number | 14 |
| DOIs | |
| State | Published - 2019 |
Keywords
- C-H functionalization
- benzothiazole
- indole
- photoredox catalysis
- thiolation
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