Brasilane-type sesquiterpenoids from Laurencia obtusa

Org Lett. 2002 Sep 19;4(19):3263-6. doi: 10.1021/ol026506z.

Abstract

[structure: see text] Three novel halogenated rearranged sesquiterpenes (1-3) have been isolated along with brasilenol (4) and epibrasilenol (5) from the organic extract of the red alga Laurencia obtusa, collected at Symi island in the Aegean Sea, Greece. The new metabolites possess the unusual skeleton of brasilane and contain the unprecedented 1,6-epoxy moiety. The structures of the new natural products, as well as their relative stereochemistry, were established by means of spectral data analyses, including two-dimensional NMR experiments along with molecular calculations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Molecular Conformation
  • Molecular Structure
  • Rhodophyta / chemistry*
  • Sesquiterpenes / chemistry*
  • Sesquiterpenes / isolation & purification*

Substances

  • Sesquiterpenes
  • brasilane