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EDA Complex-Enabled Annulation to Access CF2-Containing Tetralones and Quinazolinones Using Persulfates as Electron Donors.
Zhang, Shu-Peng; Guo, Da-Wei; Yang, Mei-Ling; Xia, Yun-Tao; Yang, Wen-Chao.
Afiliación
  • Zhang SP; Guangling College and School of Plant Protection, Yangzhou University, Yangzhou 225009, P. R. China.
  • Guo DW; Guangling College and School of Plant Protection, Yangzhou University, Yangzhou 225009, P. R. China.
  • Yang ML; Guangling College and School of Plant Protection, Yangzhou University, Yangzhou 225009, P. R. China.
  • Xia YT; College of Chemistry & Chemical Engineering, Henan University of Technology, Academician Workstation for Natural Medicinal Chemistry of Henan Province, Zhengzhou 450001, China.
  • Yang WC; Guangling College and School of Plant Protection, Yangzhou University, Yangzhou 225009, P. R. China.
J Org Chem ; 89(15): 10614-10623, 2024 Aug 02.
Article en En | MEDLINE | ID: mdl-39051432
ABSTRACT
A photocatalyst-free and EDA complex-enabled radical cascade cyclization reaction of inactive alkenes with bromodifluoroacetamides was reported for the divergent synthesis of fluorine-containing tetralones and quinazolinones. In this transformation, persulfates as electron donors and difluoro bromamide as electron acceptors generate the EDA complex. This is a promising photochemical method with advantages such as mild reaction conditions, simple operation, being metal-free, and excellent functional group tolerance.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article