Login / Signup

Total Synthesis of Bruceolline I.

Dina ScarpiCristina FaggiErnesto G Occhiato
Published in: Journal of natural products (2017)
The first total synthesis of the natural product bruceolline I, isolated in small quantities from the ethanol extract of Brucea mollis stems, was achieved in 29% yield over nine steps and with high enantiomeric purity (>98%). The key step of the process is the tandem gold-catalyzed rearrangement/Nazarov reaction of a propargylic acetate derivative. This synthesis provides a sufficient amount of synthesized bruceolline I for further bioassays.
Keyphrases
  • oxidative stress
  • room temperature
  • capillary electrophoresis
  • anti inflammatory
  • silver nanoparticles
  • water soluble
  • mass spectrometry
  • electron transfer