Photocatalytic Synthesis of Thioesters from Thianthrenium Salts with Sodium Hydrosulfide

Abstract Sodium hydrosulfide (NaSH), as an inexpensive, weakly toxic, odorless, and atom-economical inorganic sulfur source, shows great potential for application in the synthesis of sulfur-containing compounds. Herein, we report a practical method for the preparation of sulfur ester compounds, using sodium hydrosulfide as the sulfur source and visible-light-induced catalysis of thianthrenium salts. The reaction proceeds through visible-light-driven EDA (electron donor–acceptor) complexation, with sodium hydrosulfide serving as the sulfur source and no transition metals involved. This method is characterized by mild reaction conditions, excellent functional group compatibility, and simple operation, thus providing a novel approach for the green and efficient synthesis of sulfur ester compounds.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-09-18
DOI
https://doi.org/10.1021/acs.joc.6c01784
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Photocatalytic Synthesis of Thioesters from Thianthrenium Salts with Sodium Hydrosulfide

Bin Zhao, Dan He, Xinyu Liu, Guo-Qin Hu et al.
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Photocatalytic Synthesis of Thioesters from Thianthrenium Salts with Sodium Hydrosulfide

Bin Zhao, Dan He, Xinyu Liu, Guo-Qin Hu, Jia-Yi Shang, Jing-Hui Liu, Yan Li
article en

Abstract

Abstract Sodium hydrosulfide (NaSH), as an inexpensive, weakly toxic, odorless, and atom-economical inorganic sulfur source, shows great potential for application in the synthesis of sulfur-containing compounds. Herein, we report a practical method for the preparation of sulfur ester compounds, using sodium hydrosulfide as the sulfur source and visible-light-induced catalysis of thianthrenium salts. The reaction proceeds through visible-light-driven EDA (electron donor–acceptor) complexation, with sodium hydrosulfide serving as the sulfur source and no transition metals involved. This method is characterized by mild reaction conditions, excellent functional group compatibility, and simple operation, thus providing a novel approach for the green and efficient synthesis of sulfur ester compounds.

The Journal of Organic Chemistry
Zhengzhou University (CN)
National Natural Science Foundation of China, Zhengzhou University, Science and Technology Department of Henan Province
Openalex Percentile: Top 21%
Sulfur-Based Synthesis Techniques
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