Photoredox Autocatalysis: Towards a Library of Generally Applicable Sulfonamide Reductive Photocatalysts
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.
Authors
- Mark John P. Mandigma (ORCID: https://orcid.org/0000-0003-0272-0768)
- Joshua P. Barham (ORCID: https://orcid.org/0000-0003-1675-9399)
- Nakul Abhay Bapat (ORCID: https://orcid.org/0009-0001-3815-3729)
- Jaspreet Kaur (ORCID: https://orcid.org/0000-0003-1606-3017)
Institutions
- University of Strathclyde (GB)
- University of Bristol (GB)
- University of Regensburg (DE)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2025-02-18
- DOI
- https://doi.org/10.1002/anie.202423190
- Citations
- 4
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 3.74