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C-H Diselenation and Monoselenation of Electron-Deficient Alkenes via Radical Coupling at Room Temperature.

Yao ChenMengxia LvYuxin ZhangYao WuLinkun YingJielin TangXiangnan GongJianmin ZhouZengqiang Song
Published in: The Journal of organic chemistry (2022)
A new, simple, and metal-free route for the diselenation of maleimides has been first developed employing (bis(trifluoroacetoxy)iodo)benzene (PIFA) at room temperature. The present method is compatible with different functional groups, and various diselenyl maleimides were obtained in moderate to excellent yields. Moreover, this protocol further highlights the unique practical application for the functionalization of biologically relevant molecules and amino acid derivatives. Preliminary mechanism studies suggest that radicals may be involved in this novel transformation. Additionally, this protocol is also applicable for the monoselenation of maleimides by switching the reaction conditions and selenation of other electron-deficient alkenes.
Keyphrases
  • room temperature
  • ionic liquid
  • amino acid
  • randomized controlled trial
  • electron transfer
  • solar cells
  • high intensity
  • wild type
  • electron microscopy