The primary drawback to
natural-product derived chemotherapeutics is the typical, miniscule
natural abundance. Thus, new synthetic meathods are required to
investigate their viability as drug candidates.
Though a synthesis may be achieved, the length and complexity
of it may be industrially prohibitive from an economic stand-point.
As many natural products are synthesized by a similar
biosynthetic pathway in nature, it would be beneficial to create
syntheses that exploit these common features to create different
chemical architectures in a highly rapid fashion, thereby increasing
industrial feasibility.
Therefore, the goals of this project are to:
- Develop a general method for the synthesis of furan-bridged, ten-membered rings
- Develop a general method for the synthesis of fused heterocycles
- Complete the total syntheses of furan-bridged, ten-membered ring natural products