Cu-mediated selective O-arylation on C-6 substituted pyridin-2-ones

  • Taijie Chen
  • , Qingqing Huang
  • , Yu Luo*
  • , Youhong Hu
  • , Wei Lu
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

A practical and mild strategy has been developed for the selective O-arylation on C-6 substituted pyridin- 2-ones with a series of arylboronic acids, using Cu(OTf)2 as the catalyst, DABCO as the ligand, Et3N as the base, and K2HPO4 as the additive. This method affords O-arylated pyridin-2-ones with good selectivity and yields.

Original languageEnglish
Pages (from-to)1401-1404
Number of pages4
JournalTetrahedron Letters
Volume54
Issue number11
DOIs
StatePublished - 13 Mar 2013

Keywords

  • Arylboronic acids
  • Chan-Evans-Lam cross-coupling
  • O-arylation
  • Pyridin-2-ones
  • Selectivity

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