109681-06-3Relevant academic research and scientific papers
Second approach to the construction of a pentacyclic ring system for neosurugatoxin
Okada,Mizuno,Tanino,Kakoi,Inoue
, p. 1110 - 1115 (2007/10/02)
The Diels-Alder adduct obtained from (E)-6-bromo-3-ethoxycarbonylmethylene-2-oxoindoline and trans-1,3-pentadiene was successfully transformed into the diacetate of the aglycone of neosurugatoxin, which is the key intermediate in our first total synthesis
TOTAL SYNTHESIS OF NEOSURUGATOXIN
Inoue, Shoji,Okada, Kunisuke,Tanino, Hideo,Kakoi, Hisae
, p. 5225 - 5228 (2007/10/02)
Total synthesis of neosurugatoxin, having a strong affinity for nicotinic receptors, is described.
