A formal total synthesis of the marine diterpenoid diisocyanoadociane.

@article{Fairweather2006AFT,
  title={A formal total synthesis of the marine diterpenoid diisocyanoadociane.},
  author={K. Fairweather and L. Mander},
  journal={Organic letters},
  year={2006},
  volume={8 15},
  pages={
          3395-8
        }
}
[Structure: see text] A formal total synthesis of diisocyanoadociane, a marine diterpenoid with potent antimalarial properties, has been completed. The synthesis begins with a phenanthrenoid precursor that is transformed into a pyrene-derived intermediate by means of an intramolecular Michael reaction. Nitrogen functionality is introduced via a double Curtius reaction. 
Natural Product Repertoire of the Genus Amphimedon

References

SHOWING 1-10 OF 36 REFERENCES
...
1
2
3
4
...