Login / Signup

Rhodium-Catalyzed Annulation of α-Imino Carbenes with α,β-Unsaturated Ketones: Construction of Multisubstituted 2,3-Dihydropyrrole/pyrrole Rings.

Xueji MaLi LiuJiaying WangXianglin XiXuemei XieHangxiang Wang
Published in: The Journal of organic chemistry (2018)
An efficient annulation of α-imino rhodium carbenes with α,β-unsaturated ketones has been developed to generate multisubstituted 2,3-dihydropyrrole derivatives. Using the optimized catalyst, this approach is compatible with both cyclic and normal linear α,β-unsaturated ketones. Further detosylation in the presence of base could produce multisubstituted pyrroles. The new method has the potential to enable the rapid construction of bioactive molecules containing pyrrole rings.
Keyphrases
  • room temperature
  • ionic liquid
  • highly efficient
  • reduced graphene oxide
  • human health
  • loop mediated isothermal amplification