DOI

[3+2]-Cycloaddition of arenediazonium salts with diazo compounds (earlier exemplified only for trimethylsilyldiazomethane and 2,2,2-trifluorodiazoethane) has been developed to include a wide range of readily available α-diazocarbonyl compounds. The resulting 2-aryl-5-acyl-2 H -tetrazoles are of high value in medicinal chemistry.

Original languageEnglish
Pages (from-to)3998-4005
JournalSynthesis (Germany)
Volume51
Issue number21
Early online date12 Aug 2019
DOIs
StatePublished - 2019

    Scopus subject areas

  • Catalysis
  • Organic Chemistry

    Research areas

  • arenediazonium tosylates, silver nitrate, tetrazoles, [3+2]-cycloaddition, α-diazocarbonyl compounds, 5-SUBSTITUTED 1H-TETRAZOLES, ACID, ISOCYANIDES, DIAZO-COMPOUNDS, REGIOSELECTIVE 3+2 CYCLOADDITION, MEDICINAL CHEMISTRY, NITRILES, alpha-diazocarbonyl compounds, DIAZOKETONES, INHIBITORS, ACCESS

ID: 49033698