Studies toward the total synthesis of fusidilactone C

ORGN 422

Sunil K. Ghosh, sghosh2@wisc.edu, Yonggang Wei, ywei2@wisc.edu, Jiashi Wang, and Richard P. Hsung. School of Pharmacy, UW Madison, 777 Highland Ave., Madison, WI 53705
The progress of the total synthesis of Fusidilactone C is described here. A rare ketal-tethered intramolecular Diels-Alder cycloaddition is involved for the synthesis of the 2-oxadecalin spiroketal core of Fusidilactone C.

 

New Reactions and Methodology, Total Synthesis, Materials, Devices and Switches, Lipids, Nucleotides and Mimetics
8:00 PM-10:00 PM, Tuesday, March 27, 2007 Hyatt Regency Chicago -- Riverside Center, Poster

Division of Organic Chemistry

The 233rd ACS National Meeting, Chicago, IL, March 25-29, 2007