Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone.

@article{Abe2015StereoselectiveSO,
  title={Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone.},
  author={H. Abe and Yuri Horii and Megumi Hagiwara and Toyoharu Kobayashi and H. Ito},
  journal={Chemical communications},
  year={2015},
  volume={51 28},
  pages={
          6108-10
        }
}
Stereoselective construction of the highly oxygenated decahydrocyclopenta[g]chromene skeleton, which is the tricyclic core of leucosceptrine, which possesses prolylendopeptidase inhibitory activity, and leucosesterterpenone, which exhibits anti-angiogenic activity, from Leucosceptrum canum, was achieved. 
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