869586-20-9Relevant academic research and scientific papers
Stereocontrolled total synthesis of (-)-eudistomin C
Yamashita, Tohru,Kawai, Nobutaka,Tokuyama, Hidetoshi,Fukuyama, Tohru
, p. 15038 - 15039 (2005)
A stereocontrolled total synthesis of (-)-eudistomin C was accomplished in 18-step sequence with an overall yield of 7.7%. The synthesis features the diastereoselective Pictet-Spengler reaction of a tryptamine derivative and the Garner aldehyde catalyzed
