925231-82-9Relevant academic research and scientific papers
Total synthesis of (-)-amphidinolide E
Kim, Chan Hyuk,An, Hyo Jung,Shin, Won Kyo,Yu, Wei,Woo, Sang Kook,Jung, Soon Kyu,Lee, Eun
, p. 8019 - 8021 (2007/10/03)
The unique structural features of the cytotoxic marine macrolide (-)-amphidinolide E make it an intriguing synthetic target. Its total synthesis has now been completed by employing a radical cyclization of a β-alkoxy acrylate to form the oxolane ring, a Kocienski-Julia olefination to create the E C=C bond, and a lactonization reaction to close the macrocyclic ring. (Chemical Equation Presented).
