526217-82-3Relevant academic research and scientific papers
Total synthesis of elisabethin A: Intramolecular Diels-Alder reaction under biomimetic conditions
Heckrodt, Thilo J.,Mulzer, Johann
, p. 4680 - 4681 (2007/10/03)
We describe the first total synthesis of the marine diterpenoid elisabethin A. The synthesis uses (S)-hydroxy-2-methyl-propionate as the chiral starting material, which is elaborated into a dienyl-iodide and added to an aryl acetic acid ester via enolate
