Hg(OTf)2-catalyzed arylene cyclization

Org Lett. 2008 May 1;10(9):1767-70. doi: 10.1021/ol800450x. Epub 2008 Apr 9.

Abstract

Novel Hg(OTf) 2-catalyzed arylene cyclization was achieved with highly efficient catalytic turnover (up to 200 times). The reaction takes place via protonation of allylic hydroxyl group by in situ formed TfOH of an organomercuric intermediate to generate a cationic species. Subsequent smooth demercuration regenerates the catalyst.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cyclization
  • Mercury Compounds / chemistry*
  • Molecular Structure
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / chemistry

Substances

  • Mercury Compounds
  • Naphthalenes