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Transition Metal-Free Synthesis of Carbo- and Heterocycles via Reaction of Alkynes with Organylchalcogenides.

Gilson Rogério ZeniBenhur GodoiCarla K JurinicAndrei L BelladonaRicardo F Schumacher
Published in: Chemical record (New York, N.Y.) (2021)
This manuscript intends to overview the most recent advances in the synthesis of carbo- and heterocycles through reactions of alkynes with organyl chalcogenides (S, Se, Te) under metal-free conditions. Firstly, the use of electrophilic chalcogenyl halides as a selective reagent for alkyne carbon-carbon triple bond activation will be presented. After that, radical cyclization protocols employing electrochemical oxidative conditions, light-induced photoredox catalysis, or mild oxidants with direct chalcogenyl group installation will be discussed accompanied by the proposed mechanisms.
Keyphrases
  • transition metal
  • gold nanoparticles
  • visible light
  • electron transfer
  • ionic liquid
  • label free
  • mass spectrometry