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Ph3P/I2-Mediated Synthesis of N,N',N″-Substituted Guanidines and 2-Iminoimidazolin-4-ones from Aryl Isothiocyanates.

Sirilak WangngaeMookda PattarawarapanWong Phakhodee
Published in: The Journal of organic chemistry (2017)
A convenient one-pot procedure for the synthesis of acyclic and cyclic guanidines mediated by the Ph3P/I2 system is described. Sequential condensation of aryl isothiocyanates with amines followed by dehydrosulfurization and guanylation could lead to both symmetric and unsymmetric N,N',N″-substituted derivatives. Through a tandem guanylation-cyclization, a series of 2-iminoimidazolin-4-ones could also be prepared in good yields from the reaction of aryl isothiocyanates with amino acid methyl esters.
Keyphrases
  • amino acid
  • molecular docking
  • minimally invasive
  • molecular dynamics simulations
  • structure activity relationship
  • electron transfer