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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