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Difluoroisoxazolacetophenone: A Difluoroalkylation Reagent for Organocatalytic Vinylogous Nitroaldol Reactions of 1,2-Diketones.

Yong ZhangJin GeLiang LuoSu-Qiong YanGuo-Wei LaiZu-Qin MeiHai-Qing LuoXiao-Lin Fan
Published in: Organic letters (2020)
Difluoroisoxazolacetophenone (DFIO) is developed as a new difluoroalkylation reagent that can be easily prepared from inexpensive starting materials. In situ remote C-C bond cleavage of DFIO affords γ,γ-difluoroisoxazole nitronate that undergoes base-catalyzed vinylogous nitroaldol additions to isatins, benzothiophene-2,3-dione, unsaturated-α-ketoesters, and cyclic 1,2-diketones. This organocatalytic debenzoate vinylogous nitroaldol reaction provides a new and mild approach for the preparation of various difluoroisoxazole-substituted 3-hydroxy-2-oxindoles.
Keyphrases
  • molecular docking
  • room temperature
  • molecularly imprinted
  • liquid chromatography
  • visible light