Login / Signup

[3 + 2] Cycloaddition Reaction of Vinylsulfonium Salts with Hydrazonoyl Halides: Synthesis of Pyrazoles.

Wen-Jing LuoXiuwen LiangMaizhuo ChenKe-Hu WangDanfeng HuangJunjiao WangDong-Ping ChenYulai Hu
Published in: The Journal of organic chemistry (2024)
An efficient [3 + 2] cycloaddition reaction between in situ generated nitrile imines from hydrazonoyl halides and vinylsulfonium salts is developed. The nitrile imines are demonstrated to be a new class of reaction partner for vinylsulfonium salts to conduct the [3 + 2] cycloaddition reaction. The process provides a concise and efficient method for the construction of pyrazole derivatives under mild reaction conditions with broad substrate scope, good product yields, and high regioselectivity.
Keyphrases
  • ionic liquid
  • molecular docking
  • hiv infected
  • amino acid
  • hiv testing