1075244-48-2Relevant academic research and scientific papers
Total synthesis of pinnatoxin A
Nakamura, Seiichi,Kikuchi, Fumiaki,Hashimoto, Shunichi
supporting information; experimental part, p. 7091 - 7094 (2009/04/07)
A familiar ring: A ruthenium-catalyzed cycloisomerization of an enyne, synthesized by an exo-selective Diels-Alder reaction with an α-methylene lactone as the dienophile, proved to be highly effective for the construction of the 27-membered carbocycle of pinnatoxin A. The total synthesis was completed upon the formation of the seven-membered cyclicimine by self-catalyzed dehydration. (Chemical Equation Presented).
