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Iodine promoted cyclization of <i>N</i>,<i>N</i>'-diphenylthiocarbamides with enaminones: a protocol for the synthesis of poly-substituted 2-iminothiazolines.

Xiao-Hu XuZhi-Bing Dong
Published in: Organic & biomolecular chemistry (2022)
An iodine promoted cyclization reaction between <i>N</i>,<i>N</i>'-diphenylthiocarbamides and enaminones was achieved, providing a series of poly-substituted 2-iminothiazolines. This protocol is transition metal free and simple to perform, with a broad functional group tolerance and good to excellent yields under mild reaction conditions, showing potential synthetic value for the preparation of a diversity of biologically and pharmaceutically active compounds.
Keyphrases
  • molecular docking
  • randomized controlled trial
  • dual energy
  • molecularly imprinted
  • electron transfer
  • risk assessment
  • mass spectrometry
  • molecular dynamics simulations
  • high resolution