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.

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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
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article

Photoredox Autocatalysis: Towards a Library of Generally Applicable Sulfonamide Reductive Photocatalysts

Mark John P. Mandigma, Joshua P. Barham, Nakul Abhay Bapat, Jaspreet Kaur
4 citations
Angewandte Chemie International Edition
Radical Photochemical Reactions
3.74
article

Photoredox Autocatalysis: Towards a Library of Generally Applicable Sulfonamide Reductive Photocatalysts

Mark John P. Mandigma, Joshua P. Barham, Nakul Abhay Bapat, Jaspreet Kaur
article en
4 citations

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.

Angewandte Chemie International EditionVol. 64(22)
University of Strathclyde (GB), University of Bristol (GB), University of Regensburg (DE)
Openalex Percentile: Top 8%
Radical Photochemical Reactions
3.74
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