DOI

Copper-catalyzed azide–alkyne cycloaddition is a useful tool for the synthesis of both 1,2,3-triazoles and 5-iodo-1H-1,2,3-triazoles starting from either terminal alkynes or iodoalkynes. 5-Iodotriazoles have been recognized as very useful building blocks for the synthesis of diverse 1,4,5-trisubstituted 1,2,3-triazoles. Synthetic application of 5-iodo-1,2,3-triazoles through the creation of a new C–C, C–heteroatom, or C–D(T) bond along with the application areas of both iodotriazoles and products of their modification including radiolabeled compounds are discussed.
Original languageEnglish
Pages (from-to)1874–1896
Number of pages23
JournalSynthesis
Volume52
Issue number13
DOIs
StatePublished - 1 Jul 2020

    Research areas

  • CuAAC, 5-iodo-1,2,3-triazoles, iodoacetylenes, cross-coupling, hetero-coupling, halogen exchange, radiolabeling, ONE-POT REACTION, ORGANIC AZIDES, SUBSTITUTED 1,2,3-TRIAZOLES, ALKYNE, CROSS-COUPLING REACTIONS, IN-VITRO, 1,3-DIPOLAR CYCLOADDITION, REGIOSELECTIVE SYNTHESIS, CLICK-CHEMISTRY, METAL-FREE

    Scopus subject areas

  • Catalysis
  • Organic Chemistry

ID: 54236200