Newman-Kwart Rearrangement Enabled by Flavin Photoredox Catalysis

High Resolution Image Download MS PowerPoint Slide The Newman-Kwart Rearrangement (NKR) is a valuable transformation for accessing thiophenol derivatives from readily available phenols. Traditional methods for conducting the NKR are often limited by harsh reaction conditions, operational scalability, and reactions run in primarily organic solvents. Herein, we introduce a bioinspired approach to perform the NKR using (–)-riboflavin as a cheap and effective photocatalyst. The reaction has been demonstrated on a broad range of substrates in high yield, with low catalyst loadings, and under blue and green light irradiation. A combination of mechanistic and spectroscopic experiments suggests that the reaction is initiated by a photoinduced single electron transfer event between (–)-riboflavin and the starting O -aryl thiocarbamate. The developed NKR is demonstrated on gram scale and is compatible with biological buffers.

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Publication Details

Journal
ACS Catalysis
Published
2026-06-30
DOI
https://doi.org/10.1021/acscatal.6c02238
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Newman-Kwart Rearrangement Enabled by Flavin Photoredox Catalysis

Courtney D. Glenn, Manik Sharma, Kyle F. Biegasiewicz
ACS Catalysis
Radical Photochemical Reactions
article

Newman-Kwart Rearrangement Enabled by Flavin Photoredox Catalysis

Courtney D. Glenn, Manik Sharma, Kyle F. Biegasiewicz
article en

Abstract

High Resolution Image Download MS PowerPoint Slide The Newman-Kwart Rearrangement (NKR) is a valuable transformation for accessing thiophenol derivatives from readily available phenols. Traditional methods for conducting the NKR are often limited by harsh reaction conditions, operational scalability, and reactions run in primarily organic solvents. Herein, we introduce a bioinspired approach to perform the NKR using (–)-riboflavin as a cheap and effective photocatalyst. The reaction has been demonstrated on a broad range of substrates in high yield, with low catalyst loadings, and under blue and green light irradiation. A combination of mechanistic and spectroscopic experiments suggests that the reaction is initiated by a photoinduced single electron transfer event between (–)-riboflavin and the starting O -aryl thiocarbamate. The developed NKR is demonstrated on gram scale and is compatible with biological buffers.

ACS Catalysis
Emory University (US)
National Science Foundation, Emory University, National Science Foundation Graduate Research Fellowship Program
Openalex Percentile: Top 14%
Radical Photochemical Reactions
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