Chirality in diarylether heptanoids: synthesis of myricatomentogenin, jugcathanin, and congeners.

@article{Salih2012ChiralityID,
  title={Chirality in diarylether heptanoids: synthesis of myricatomentogenin, jugcathanin, and congeners.},
  author={M. Q. Salih and C. Beaudry},
  journal={Organic letters},
  year={2012},
  volume={14 15},
  pages={
          4026-9
        }
}
  • M. Q. Salih, C. Beaudry
  • Published 2012
  • Chemistry, Medicine
  • Organic letters
  • The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported. Synthetic material was used to measure their optical activities and free energy of activation for racemization. The natural enantiomers of myricatomentogenin, jugcathanin, galeon, and pterocarine were determined to have the same pR absolute stereochemistry. Acerogenins L and C are achiral compounds. 
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