A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a C-13 NMR chemical shift/structure correlation.
- supramolecular host systems
- 2-directional chain synthesis
- natural product syntheses
- fused polycyclic ethers
Sheldrake, H. M., Jamieson, C., Pascu, S. I., & Burton, J. W. (2009). Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula. Organic and Biomolecular Chemistry, 7(2), 238-252. https://doi.org/10.1039/b814953d