123973-57-9Relevant 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 (1992)
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
