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Oxidative decarbonylative coupling of aliphatic aldehydes with methacryloyl benzamides to generate isoquinoline-1,3(2H,4H)-diones.

Changduo PanChaoyue ChenJin-Tao Yu
Published in: Organic & biomolecular chemistry (2018)
Alkyl-substituted isoquinoline-1,3(2H,4H)-diones were prepared by decarbonylative coupling of N-alkyl-N-methacryloylbenzamides and aliphatic aldehydes under metal-free conditions. The reaction undergoes subsequent decarbonylation, radical addition and cyclization processes with aliphatic aldehydes as the cheap and abundant alkyl radical source. This procedure offers a complementary approach to the convenient generation of alkyl-substituted isoquinoline-1,3(2H,4H)-diones.
Keyphrases
  • ionic liquid
  • room temperature
  • molecular docking
  • visible light
  • minimally invasive
  • electron transfer
  • molecular dynamics simulations
  • transition metal