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Base-mediated synthesis of aryl enol ethers from α-aryl allylic alcohols and arylsulfonium salts.
Yao, Yu-Fei; Song, Jia-Wei; Zhang, Cheng-Pan.
Affiliation
  • Yao YF; School of Chemistry, Chemical Engineering and Life Science, Hubei Key Laboratory of Nanomedicine for Neurodegenerative Diseases, Wuhan University of Technology, Wuhan 430070, China. cpzhang@whut.edu.cn.
  • Song JW; School of Chemistry, Chemical Engineering and Life Science, Hubei Key Laboratory of Nanomedicine for Neurodegenerative Diseases, Wuhan University of Technology, Wuhan 430070, China. cpzhang@whut.edu.cn.
  • Zhang CP; School of Chemistry, Chemical Engineering and Life Science, Hubei Key Laboratory of Nanomedicine for Neurodegenerative Diseases, Wuhan University of Technology, Wuhan 430070, China. cpzhang@whut.edu.cn.
Org Biomol Chem ; 22(38): 7866-7873, 2024 Oct 02.
Article de En | MEDLINE | ID: mdl-39234762
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.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Biomol Chem / Org. biomol. chem / Organic & biomolecular chemistry Sujet du journal: BIOQUIMICA / QUIMICA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Biomol Chem / Org. biomol. chem / Organic & biomolecular chemistry Sujet du journal: BIOQUIMICA / QUIMICA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni