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

Chem Asian J. 2022 Apr 14;17(8):e202101394. doi: 10.1002/asia.202101394. Epub 2022 Mar 16.

Abstract

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.

Keywords: Green chemistry; Heterocycle; Organochalcogen; benzo[b]chalcogenophene; photocyclization.

MeSH terms

  • Benzofurans*
  • Catalysis
  • Cyclization
  • Solvents
  • Ultraviolet Rays*

Substances

  • Benzofurans
  • Solvents