Synergistic Tetrabutylammonium Decatungstate/Persulfate Photocatalysis in Pure Water: A Platform for Diversifying Unactivated Alkenes Into N‐Heterocycles

A photocatalytic strategy for the synthesis of N‐heterocycles under mild conditions using water as the reaction medium is described. Leveraging a synergistic tetrabutylammonium decatungstate (TBADT)/Na 2 S 2 O 8 catalytic system in the presence of PEG‐600 under near‐UV irradiation, this method enables the decarboxylative cyclization of oxalamic acids with unactivated alkenes, providing efficient access to 3‐substituted indolines, tetrahydroquinolines, and dihydroquinolinones. Mechanistic studies indicate that TBADT effectively drives the decarboxylation of oxalamic acids under light to generate the key carbamoyl radical. This protocol features mild conditions, operational simplicity, and broad substrate scope, and its utility is demonstrated through the late‐stage diversification of theophylline and a gram‐scale preparation.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-04-30
DOI
https://doi.org/10.1002/adsc.70476
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Synergistic Tetrabutylammonium Decatungstate/Persulfate Photocatalysis in Pure Water: A Platform for Diversifying Unactivated Alkenes Into N‐Heterocycles

Guohua Zheng, Ming Yuan, Zhenpeng Qiu, Baohui Zhang et al.
Advanced Synthesis & Catalysis
Radical Photochemical Reactions
article

Synergistic Tetrabutylammonium Decatungstate/Persulfate Photocatalysis in Pure Water: A Platform for Diversifying Unactivated Alkenes Into N‐Heterocycles

Guohua Zheng, Ming Yuan, Zhenpeng Qiu, Baohui Zhang, Junjie Hu, Zhongmei Bai, Shuangying Yin, Ming Yao, Haidong Cao, Yanbin Lu
article en

Abstract

A photocatalytic strategy for the synthesis of N‐heterocycles under mild conditions using water as the reaction medium is described. Leveraging a synergistic tetrabutylammonium decatungstate (TBADT)/Na 2 S 2 O 8 catalytic system in the presence of PEG‐600 under near‐UV irradiation, this method enables the decarboxylative cyclization of oxalamic acids with unactivated alkenes, providing efficient access to 3‐substituted indolines, tetrahydroquinolines, and dihydroquinolinones. Mechanistic studies indicate that TBADT effectively drives the decarboxylation of oxalamic acids under light to generate the key carbamoyl radical. This protocol features mild conditions, operational simplicity, and broad substrate scope, and its utility is demonstrated through the late‐stage diversification of theophylline and a gram‐scale preparation.

Advanced Synthesis & CatalysisVol. 368(9)
Hubei University of Chinese Medicine (CN), Huanggang Central Hospital (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 10%
Radical Photochemical Reactions
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