Login / Signup

Hypervalent Iodine(III)-Promoted Radical Oxidative C-H Annulation of Arylamines with α-Keto Acids.

Lipeng LongJieyan WangLiuqing GuShiguang YangLiang QiaoGuotian LuoZhengwang Chen
Published in: The Journal of organic chemistry (2021)
A novel catalyst-free radical oxidative C-H annulation reaction of arylamines with α-keto acids toward benzoxazin-2-ones synthesis under mild conditions was developed. This hypervalent iodine(III)-promoted process eliminated the use of a metal catalyst or additive with high levels of functional group tolerance. Hypervalent iodine(III) was both an oxidant and a radical initiator for this reaction. The synthetic utility of this method was confirmed by the synthesis of the natural product cephalandole A.
Keyphrases
  • dual energy
  • ionic liquid
  • room temperature
  • highly efficient
  • reduced graphene oxide
  • carbon dioxide
  • computed tomography
  • visible light
  • magnetic resonance imaging
  • magnetic resonance
  • anti inflammatory