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Carbene-Catalyzed Atroposelective Construction of Chiral Diaryl Ethers.
Liu, Yuheng; Yuan, Lutong; Dai, Linlong; Zhu, Qiaohong; Zhong, Guofu; Zeng, Xiaofei.
Afiliación
  • Liu Y; College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, Zhejiang, China.
  • Yuan L; Kharkiv Institute at Hangzhou Normal University, Hangzhou Normal University, Hangzhou 311121, Zhejiang, China.
  • Dai L; College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, Zhejiang, China.
  • Zhu Q; Department of Chemistry, Eastern Institute for Advanced Study, Ningbo 315200, Zhejiang, China.
  • Zhong G; College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, Zhejiang, China.
  • Zeng X; Department of Chemistry, Eastern Institute for Advanced Study, Ningbo 315200, Zhejiang, China.
J Org Chem ; 89(11): 7630-7643, 2024 Jun 07.
Article en En | MEDLINE | ID: mdl-38738853
ABSTRACT
Atropoisomeric chemotypes of diaryl ethers-related scaffolds are prevalent in naturally active compounds. Nevertheless, there remains considerable research to be carried out on the catalytic asymmetric synthesis of these axially chiral molecules. In this instance, we disclose an N-heterocyclic carbene (NHC)-catalyzed synthesis of axially chiral diaryl ethers via atroposelective esterification of dialdehyde-containing diaryl ethers. NHC desymmetrization produces axially chiral diaryl ether atropisomers with high yields and enantioselectivities in moderate circumstances. Chiral diaryl ether compounds may be precursors for highly functionalized diaryl ethers with bioactivity and chiral ligands for asymmetric catalysis.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China