Abstract
Dichotomous thinking dominates the field of synthetic photochemistry—either a reaction needs a photocatalyst or not. Herein, we report the identification of a photoredox autocatalytic pathway - an alternative to the existing mechanistic paradigms - to access cyclic biaryl sulfonamides (BASNs). This reaction does not require exogenous catalyst as the visible light absorbing deprotonated product - with potent excited state reductive power - acts as the photocatalyst for its own synthesis. This finding implicated BASN as a novel organophotocatalyst architecture and allowed a rapid, modular, and low-cost combinatorial synthesis of a BASN library that expedited optimal photocatalyst screening. Furthermore, BASN was revealed as a widely applicable organophotocatalyst for diverse transition metal-free transformations such as: intramolecular (spiro)-cyclizations, defunctionalizations, and C−C / C-heteroatom couplings.
| Original language | English |
|---|---|
| Article number | e202423190 |
| Number of pages | 12 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 64 |
| Issue number | 22 |
| Early online date | 29 Mar 2025 |
| DOIs | |
| Publication status | Published - 26 May 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Keywords
- Combinatorial Library
- Flow Chemistry
- Sulfonamides
- Photocatalysis
- Autocatalysis
Fingerprint
Dive into the research topics of 'Photoredox Autocatalysis: Towards a Library of Generally Applicable Sulfonamide Reductive Photocatalysts'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver