Login / Signup

Regioselective synthesis of N-containing polycyclic compounds via radical annulation cyclization of 1,7-dienes with aldehydes.

Jia-Li SuiLong-Jin ZhongBi-Quan XiongKe-Wen TangYu Liu
Published in: Chemical communications (Cambridge, England) (2024)
A convenient method for oxidant-promoted radical cascade acylation or decarbonylative alkylation of 1,7-dienes with aldehydes has been established. This method allows for the rapid construction of N-containing polycyclic skeletons in a highly regio- and stereoselective manner. This transformation provides a simple and efficient method for the preparation of a range of tetrahydro-6 H -indeno[2,1- c ]quinolinone derivatives by sequential formation of three new carbon-carbon bonds. Additionally, this radical cascade cyclization can selectively convert aldehydes into aroyl/primary aliphatic acyl radicals and secondary or tertiary alkyl radicals.
Keyphrases
  • ionic liquid
  • fatty acid
  • structure activity relationship