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Visible-Light-Induced Tandem Radical Addition-Cyclization of Alkenyl Aldehydes Leading to Indanones and Related Compounds.

Danyang LuYimei WanLichun KongGangguo Zhu
Published in: Organic letters (2017)
Herein we describe a novel, visible light-induced tandem radical addition-cyclization of alkenyl aldehydes with α-bromocarbonyl compounds. A set of cyclic ketones, including indanones, cyclopentenones, 3,4-dihydronaphthalen-1(2H)-ones, and chroman-4-ones, are synthesized at room temperature with high efficiency and good functional group compatibility. It represents the first report on the catalytic 1,2-acylalkylation of unactivated alkenes.
Keyphrases
  • room temperature
  • high efficiency
  • visible light
  • ionic liquid
  • high glucose
  • diabetic rats
  • drug induced
  • oxidative stress
  • crystal structure
  • light emitting