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Nucleophilic functionalization of thianthrenium salts under basic conditions.


ABSTRACT: 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.

SUBMITTER: Fan X 

PROVIDER: S-EPMC10862136 | biostudies-literature | 2024

REPOSITORIES: biostudies-literature

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Nucleophilic functionalization of thianthrenium salts under basic conditions.

Fan Xinting X   Zhang Duo D   Xiu Xiangchuan X   Xu Bin B   Yuan Yu Y   Chen Feng F   Gao Pan P  

Beilstein journal of organic chemistry 20240208


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. ...[more]

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