Hot Paper: Chemical synthesis solves structures
25 March 2008
Oxasqualenoids are a family of squalene-derived triterpene polyethers that have been isolated from both marine and terrestrial organisms. It is often difficult to determine their stereostructures, even by modern NMR methods. As a result, synthetic organic chemists have turned to chemical synthesis to determine the stereostructures of these fascinating natural products.
In his Emerging Area, Yoshiki Morimoto at Osaka City University, Japan, reports the total assignments of the previously incomplete stereostructures of three members of the oxasqualenoids, through the first asymmetric total syntheses of the natural products.

Link to journal article
The role of chemical synthesis in structure elucidation of oxasqualenoids
Yoshiki Morimoto, Org. Biomol. Chem., 2008, 6, 1709
DOI: 10.1039/b801126e
Also of interest
Natural products: chemical instruments to apprehend biological symphony
Mathieu Pucheault, Org. Biomol. Chem., 2008, 6, 424
DOI: 10.1039/b713022h
