Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols

Research output: Contribution to journalArticlepeer-review

Abstract

O-Tetrafluoropyridin-4-yl-protected naphthols undergo regioselective reduction with cyclohexane in the presence of aluminium chloride to afford the corresponding 5,6,7,8-tetrahydronaphthyl ethers.

Original languageEnglish
Pages (from-to)190-191
Number of pages2
JournalMendeleev Communications
Volume30
Issue number2
DOIs
Publication statusPublished - 1 Mar 2020

Keywords

  • 5,6,7,8-tetrahydronaphthols
  • cyclohexane
  • ionic hydrogenation
  • naphthyl ethers
  • organofluorine compounds
  • polyfluoropyridines

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