1,3,3-Trimethyl-3,4-dihydroisoquinolines and their crown-containing derivatives react with 6-nitro-2-polyfluoroalkylchromones in THF at room temperature with the formation of zwitterionic axially chiral 6H,7H-pyrido[2,1-a]isoquinolinium derivatives, which were converted to 2,6-diaryl-4-polyfluoroalkylpyridines, including those with the benzocrown-ether fragment. © 2014 Springer Science+Business Media New York.
Original languageEnglish
Pages (from-to)1337-1343
Number of pages7
JournalRussian Chemical Bulletin
Volume63
Issue number6
DOIs
Publication statusPublished - 1 Jan 2014

    Research areas

  • 1 3 3-trimethyl-3 4-dihydroisoquinolines, 2 6-diaryl-4-poly-fluoroalkylpyridines, 2-polyfluoroalkylchromones, atropisomerism, benzocrown ethers, pyrido[2 1-a]isoquinolinium zwitterions

    ASJC Scopus subject areas

  • Chemistry(all)

    WoS ResearchAreas Categories

  • Chemistry, Multidisciplinary

ID: 315195