A series of functionalized 4,5-bis(arylethynyl)triazoles were prepared by a copper-catalyzed cycloaddition of 1-iodobuta-1,3-diynes and azides and subsequent Sonogashira reaction of iodoethynyltriazoles with substituted arylacetylenes. The iodine-promoted cyclization of 4,5-bis(arylethynyl)triazoles involved only one triple bond and led to the formation of 2-triazolyl-3-iodoheteroindenes or 5-(4-iodoisochromeno)triazoles. © 2025 Elsevier B.V., All rights reserved.
Original languageEnglish
Pages (from-to)3318-3323
Number of pages6
JournalRussian Chemical Bulletin
Volume73
Issue number11
DOIs
StatePublished - 2024

    Research areas

  • 1,3-dipolar cycloaddition, 1-iodobuta-1,3-diynes, azides, enediynes, iodine-promoted cyclization, iodoheterocyclic compounds, Sonogashira reaction, triazoles

ID: 143413128