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A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: a mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates.

András György NémethGyörgy Miklós KeserűPéter Ábrányi-Balogh
Published in: Beilstein journal of organic chemistry (2019)
A new multicomponent reaction has been developed between isocyanides, sulfur and alcohols or thiols under mild reaction conditions to afford O-thiocarbamates and dithiocarbamates in moderate to good yields. The one-pot reaction cascade involves the formation of an isothiocyanate intermediate, thus a catalyst-free synthesis of isothiocyanates, as valuable building blocks from isocyanides and sulfur is proposed, as well. The synthetic procedure suits the demand of a modern organic chemist, as it tolerates a wide range of functional groups, it is atom economic and easily scalable.
Keyphrases
  • electron transfer
  • room temperature
  • ionic liquid
  • highly efficient
  • reduced graphene oxide
  • molecular dynamics
  • carbon dioxide
  • metal organic framework
  • visible light