Cu2O-catalyzed tandem ring-opening/coupling cyclization process for the synthesis of 2,3-dihydro-1,4-benzodioxins

Org Lett. 2008 Sep 4;10(17):3899-902. doi: 10.1021/ol801444p. Epub 2008 Jul 30.

Abstract

2,3-Dihydro-1,4-benzodioxins can be prepared in a tandem one-pot procedure by reaction of o-iodophenols with epoxides catalyzed by Cu2O/1,10-phenanthroline/Cs2CO3 system. The reaction is suggested to occur via a novel ring-opening/coupling mechanism, giving moderate to good yields. Moreover, both aryl and aliphatic epoxides are tolerated under these conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Copper / chemistry
  • Cyclization
  • Dioxins / chemical synthesis*
  • Epoxy Compounds / chemistry
  • Oxides / chemistry
  • Phenanthrolines / chemistry

Substances

  • Dioxins
  • Epoxy Compounds
  • Oxides
  • Phenanthrolines
  • Copper