Under the action of an excess of trifluoromethanesulfonic acid, 1-aryl-5-phenylpent-4-en-2-yn-1-ones cyclize intramolecularly to 6-aryl-2-phenyl-2,3-dihydropyran-4-ones. The reaction proceeds at room temperature for 1 h with 50-60% yields.

Original languageEnglish
Pages (from-to)953-956
Number of pages4
JournalChemistry of Heterocyclic Compounds
Volume56
Issue number7
DOIs
StatePublished - 1 Jul 2020

    Research areas

  • carbocations, conjugated enynones, cyclization, dihydropyranones, trifluoromethanesulfonic acid, CONJUGATED ENYNONES

    Scopus subject areas

  • Organic Chemistry

ID: 69889836