Total synthesis of cis-solamin

Org Lett. 2002 Apr 4;4(7):1083-5. doi: 10.1021/ol0102803.

Abstract

[structure: see text] A convergent total synthesis of cis-solamin and its diastereomer was accomplished using VO(acac)2-catalyzed diastereoselective epoxidation followed by cyclization of bis-homoallylic alcohol as the key step. By comparison of the optical rotation of two possible diastereomers, it is suggested that the absolute configuration of natural cis-solamin is 1a.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Annonaceae / chemistry*
  • Benzethonium / chemical synthesis*
  • Cyclization
  • Epoxy Compounds / chemical synthesis
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Optical Rotation
  • Stereoisomerism

Substances

  • Epoxy Compounds
  • Indicators and Reagents
  • Benzethonium