Issue 38, 2024

Base-mediated synthesis of aryl enol ethers from α-aryl allylic alcohols and arylsulfonium salts

Abstract

A concise synthesis of aryl enol ethers from allylic alcohols and arylsulfonium salts by simply using an inorganic base as a mediator is described. The reaction enabled the facile conversion of various α-aryl allylic alcohols into the corresponding aryl enol ethers in good yields with excellent selectivity. The results demonstrated that both symmetric triarylsulfonium triflate and 10-methyl-5-aryl-5,10-dihydrophenothiazin-5-ium salts were effective arylation reagents for the base-initiated selective O-arylation and isomerization of α-aryl allylic alcohols. This reaction represents the first use of arylsulfonium salts as arylation reagents to access aryl enol ethers directly from allylic alcohols.

Graphical abstract: Base-mediated synthesis of aryl enol ethers from α-aryl allylic alcohols and arylsulfonium salts

Supplementary files

Article information

Article type
Paper
Submitted
24 Jul 2024
Accepted
29 Aug 2024
First published
30 Aug 2024

Org. Biomol. Chem., 2024,22, 7866-7873

Base-mediated synthesis of aryl enol ethers from α-aryl allylic alcohols and arylsulfonium salts

Y. Yao, J. Song and C. Zhang, Org. Biomol. Chem., 2024, 22, 7866 DOI: 10.1039/D4OB01220H

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