Journal of the American Chemical Society, Vol.130, No.24, 7566-7566, 2008
Total synthesis of (-)-corilagin
The synthesis of corilagin was achieved by the integration of the development of the oxidative coupling of the symmetrically protected gallates and the temporarily ring-opened synthetic route for the 3.6-hexahydroxydiphenoyl (HHDP) bridge. This is the first total synthesis of the C-1(4)/B-ellagitannins, which contain ring-flipped glucose.