DOI

A method to convert tertiary N -propargylamides into 1,2,4-trisubstituted imidazoles using ammonium chloride and zinc triflate as the catalyst is reported. The method is convenient, practical and employs conventional heating. It is also applicable to N -propargyl lactams and tends to populate the so-called 'lead-like' chemistry space.

Original languageEnglish
Article numberss-2018-z0257-op
Pages (from-to)3048-3058
Number of pages11
JournalSynthesis (Germany)
Volume50
Issue number15
DOIs
StatePublished - 1 Aug 2018

    Scopus subject areas

  • Catalysis
  • Organic Chemistry

    Research areas

  • cyclodehydration, hydroamination, imidazoles, lead-oriented synthesis, Lewis acid catalysis, N -propargylamides, privileged structures

ID: 35632071