Login / Signup

α-Acyloxylation of Ketones/Cyclic Ethers Mediated by Hypervalent Iodine(III) Reagents as Oxidants and Nucleophilic Sources.

Hao JiaNan LiChunmei TangWenjing NiXinru ZhaoJing SunFufang WuXiaobao ShenHongbin Zhai
Published in: The Journal of organic chemistry (2024)
This study describes a catalyst-free α-acyloxylation of ketones and a KBr-mediated α-acyloxylation of cyclic ethers. These conversions are effectively mediated by hypervalent iodine(III) reagents serving dual roles as the oxidant and nucleophilic source. Consequently, esters are produced directly in moderate to excellent yields. The proposed method features good functional group compatibility, a broad substrate scope, and high synthetic efficiency and is remarkably environmentally friendly.
Keyphrases
  • magnetic resonance imaging
  • ionic liquid
  • computed tomography
  • room temperature
  • gold nanoparticles
  • highly efficient
  • carbon dioxide