Tandem RCM-isomerization-cyclopropanation reactions

Org Lett. 2008 Feb 21;10(4):597-600. doi: 10.1021/ol702766h. Epub 2008 Jan 24.

Abstract

A new triple tandem process has been discovered in which simple acyclic substrates can be transformed into bicyclic compounds via RCM-double bond isomerization-cyclopropanation. This process is catalyzed by second generation Grubb's catalyst without the requirement of other reactives or additives. In addition, a one-pot RCM-isomerization reaction followed by cyclopropanation with CHCl3/NaOH allows the synthesis of products related to iNOS (nitric oxide synthase) inhibitors, which are currently under clinical evaluation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bridged Bicyclo Compounds, Heterocyclic / chemical synthesis*
  • Catalysis
  • Cyclization
  • Cyclopropanes / chemistry*
  • Molecular Structure
  • Nitric Oxide Synthase / antagonists & inhibitors*
  • Stereoisomerism

Substances

  • Bridged Bicyclo Compounds, Heterocyclic
  • Cyclopropanes
  • Nitric Oxide Synthase