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.
![Graphical abstract: Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone](/en/Image/Get?imageInfo.ImageType=GA&imageInfo.ImageIdentifier.ManuscriptID=C5CC00879D&imageInfo.ImageIdentifier.Year=2015)
H. Abe, Y. Horii, M. Hagiwara, T. Kobayashi and H. Ito, Chem. Commun., 2015, 51, 6108 DOI: 10.1039/C5CC00879D
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