Nucleophilic functionalization of thianthrenium salts under basic conditions

In recent years, S-(alkyl)thianthrenium salts have become an important means of functionalizing alcohol compounds. However, additional transition metal catalysts and/or visible light are required. Herein, a direct thioetherification/amination reaction of thianthrenium salts is realized under metal-f...

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Veröffentlicht in:Beilstein journal of organic chemistry 2024-02, Vol.20 (1), p.257-263
Hauptverfasser: Fan, Xinting, Zhang, Duo, Xiu, Xiangchuan, Xu, Bin, Yuan, Yu, Chen, Feng, Gao, Pan
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Sprache:eng
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Zusammenfassung:In recent years, S-(alkyl)thianthrenium salts have become an important means of functionalizing alcohol compounds. However, additional transition metal catalysts and/or visible light are required. Herein, a direct thioetherification/amination reaction of thianthrenium salts is realized under metal-free conditions. This strategy exhibits good functional-group tolerance, operational simplicity, and an extensive range of compatible substrates.
ISSN:1860-5397
1860-5397
DOI:10.3762/bjoc.20.26