Photoinduced Pyridine N-Oxide Catalysis for C–H Alkylation of Azauracils and Quinoxalinones with Alkyl Boronic Acids

Abstract A photoinduced pyridine N-oxide-catalyzed C–H alkylation of azauracils and quinoxalinones with alkyl boronic acids has been developed. The transformation proceeds under transition-metal-free aerobic conditions without requiring a separate photoredox catalyst or photosensitizer and exhibits broad substrate scope, including late-stage functionalization of biorelevant molecules and gram-scale synthesis. Mechanistic studies support alkyl radical generation from alkyl boronic acids by photoexcited pyridine N-oxide. This study highlights the potential of pyridine N-oxide organophotocatalysis for radical-mediated synthetic transformations.

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Publication Details

Journal
Organic Letters
Published
2026-08-20
DOI
https://doi.org/10.1021/acs.orglett.6c02705
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoinduced Pyridine N-Oxide Catalysis for C–H Alkylation of Azauracils and Quinoxalinones with Alkyl Boronic Acids

Parthasarathy Gandeepan, Lusina Mantry, S. Sudharsan, Malati Das
Organic Letters
Radical Photochemical Reactions
article

Photoinduced Pyridine N-Oxide Catalysis for C–H Alkylation of Azauracils and Quinoxalinones with Alkyl Boronic Acids

Parthasarathy Gandeepan, Lusina Mantry, S. Sudharsan, Malati Das
article en

Abstract

Abstract A photoinduced pyridine N-oxide-catalyzed C–H alkylation of azauracils and quinoxalinones with alkyl boronic acids has been developed. The transformation proceeds under transition-metal-free aerobic conditions without requiring a separate photoredox catalyst or photosensitizer and exhibits broad substrate scope, including late-stage functionalization of biorelevant molecules and gram-scale synthesis. Mechanistic studies support alkyl radical generation from alkyl boronic acids by photoexcited pyridine N-oxide. This study highlights the potential of pyridine N-oxide organophotocatalysis for radical-mediated synthetic transformations.

Organic Letters
Indian Institute of Technology Tirupati (IN)
Ministry of Education, India, Science and Engineering Research Board
Openalex Percentile: Top 18%
Radical Photochemical Reactions
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