329897-84-9Relevant academic research and scientific papers
Synthetic studies towards mniopetals (II). A short synthesis of Mniopetal E
Jauch
, p. 87 - 89 (2007/10/03)
A short total synthesis of Mniopetal E in thirteen steps is reported. Key steps are a new and highly diastereoselective lithium phenylselenide induced Baylis-Hillman reaction with Feringa's butenolide, an endo-selective intramolecular Diels-Alder reaction (IMDA) and a new variant of the Parikh-Doering oxidation.
