Login / Signup

Catalyst/Metal/Solvent-Free Markovnikov Hydrothiolation of Unactivated Alkenes with Dithiocarbamic Acids.

Azim Ziyaei HalimehjaniZiya DağalanZahra MarjaniFigen GündüzArif DastanBilal Nişancı
Published in: The Journal of organic chemistry (2024)
Catalyst-free Markovnikov-selective hydrothiolation of unactivated alkenes still remains a great challenge. Herein, we develop a catalyst/metal/solvent-free methodology for the Markovnikov hydrothiolation of unactivated alkenes with in situ prepared dithiocarbamic acids, providing a wide array of alkyl dithiocarbamates. A variety of terminal, internal, cyclic, and acyclic unactivated alkenes were applied successfully in this protocol. This three-component thiol-ene reaction can be considered as a new family of click reactions.
Keyphrases
  • ionic liquid
  • room temperature
  • reduced graphene oxide
  • highly efficient
  • visible light
  • metal organic framework
  • randomized controlled trial
  • carbon dioxide
  • high resolution
  • gold nanoparticles
  • high density