Login / Signup

UVA Light-promoted Catalyst-free Cyclization of Vinyl Selenides: Green and Efficient Synthesis of C3-Unsubstituted 2-Selanyl Benzochalcogenophenes.

Gelson PerinThiago J PeglowFilipe PenteadoPatrick C NobreKrigor B SilvaGuilherme StachThiago BarcellosEder J LenardãoJuliano A Roehrs
Published in: Chemistry, an Asian journal (2022)
A metal- and catalyst-free photo-promoted cyclization of properly substituted vinyl selenides was developed using UVA irradiation. A total of eighteen new C3-unsubstituted 2-selanyl benzochalcogenophenes (benzofurans, benzothiophenes and benzoselenophenes) were prepared in 30-86% yield after irradiation with UVA at room temperature. The usefulness of the title compounds was demonstrated in the easy functionalization of the remaining free C-H bond of the benzochalcogenophenes to form new C-Se and C-Br bonds by simple procedures. Furthermore, the reaction can be performed under natural sunlight irradiation and the solvent is easily reused further in several subsequent runs.
Keyphrases
  • room temperature
  • ionic liquid
  • radiation induced
  • highly efficient
  • reduced graphene oxide
  • molecular docking
  • radiation therapy
  • electron transfer
  • metal organic framework