Anodic coupling reactions: probing the stereochemistry of tetrahydrofuran formation. A short, convenient synthesis of linalool oxide

Org Lett. 2001 Aug 23;3(17):2685-8. doi: 10.1021/ol0162670.

Abstract

[reaction: see text]. Intramolecular coupling reactions between enol ether radical cations and oxygen nucleophiles are primarily governed by stereoelectronics. By taking advantage of this observation, a tetrahydrofuran building block for use in constructing (+)-linalool oxide and rotundisine has been synthesized in four steps from a commercially available starting material. The synthesis of (+)-linalool oxide has been completed.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acyclic Monoterpenes
  • Furans / chemical synthesis*
  • Furans / chemistry
  • Magnetic Resonance Spectroscopy
  • Monoterpenes*
  • Stereoisomerism
  • Terpenes / chemical synthesis*
  • Terpenes / chemistry

Substances

  • Acyclic Monoterpenes
  • Furans
  • Monoterpenes
  • Terpenes
  • tetrahydrofuran
  • linalool