Abstract
An efficient photoinduced phenolate organocatalytic methodology for the synthesis of isoindoloindolones was developed, demonstrating a broad substrate scope with high yields and excellent functional group tolerance. Mechanistic studies confirmed a direct single-electron transfer pathway facilitated by an excited phenolate catalyst to N-iodobenzoyl indoles, validated through UV–vis spectroscopy, fluorescence quenching, and cyclic voltammetry. This approach enables the synthesis of biologically significant derivatives including melatonin MT3and 5-HT6receptor ligands.
| Original language | English |
|---|---|
| Pages (from-to) | 12507-12513 |
| Number of pages | 7 |
| Journal | Journal of Organic Chemistry |
| Volume | 90 |
| Issue number | 36 |
| DOIs | |
| Publication status | Published - 12 Sept 2025 |
Bibliographical note
Publisher Copyright:© 2025 American Chemical Society
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