Visible‐Light‐Induced Mpg‐C<sub>3</sub>N<sub>4</sub> Catalyzed C(sp<sup>2</sup>)−H Thiocyanation of Ketene Dithioacetals

Abstract Using mesoporous graphite carbon nitride (mpg‐C 3 N 4 ) as metal‐free heterogeneous catalyst, the thiocyanation of ketene dithioacetals was achieved under visible light irradiation with oxygen as green oxidant and without any other additives. The present protocol has excellent functional group tolerance and the desired tetrasubstituted alkenyl thiocyanides were obtained in moderate to good yields. Moreover, the recyclable mpg‐C 3 N 4 catalyst could be used at least 6 times without significant loss of activities. A series of mechanistic validation experiments indicated that the reaction involves a radical process.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-12-06
DOI
https://doi.org/10.1002/ejoc.202401180
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.50

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article

Visible‐Light‐Induced Mpg‐C3N4 Catalyzed C(sp2)−H Thiocyanation of Ketene Dithioacetals

Shan Shan Hu, Shifeng Xing, Fumeng Yin, Hongjun Zhu et al.
2 citations
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
0.50
article

Visible‐Light‐Induced Mpg‐C3N4 Catalyzed C(sp2)−H Thiocyanation of Ketene Dithioacetals

Shan Shan Hu, Shifeng Xing, Fumeng Yin, Hongjun Zhu, Shuwei Zhu
article en
2 citations

Abstract

Abstract Using mesoporous graphite carbon nitride (mpg‐C 3 N 4 ) as metal‐free heterogeneous catalyst, the thiocyanation of ketene dithioacetals was achieved under visible light irradiation with oxygen as green oxidant and without any other additives. The present protocol has excellent functional group tolerance and the desired tetrasubstituted alkenyl thiocyanides were obtained in moderate to good yields. Moreover, the recyclable mpg‐C 3 N 4 catalyst could be used at least 6 times without significant loss of activities. A series of mechanistic validation experiments indicated that the reaction involves a radical process.

European Journal of Organic ChemistryVol. 28(4)
Nanjing Tech University (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 37%
Sulfur-Based Synthesis Techniques
0.50
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