62885-78-3Relevant academic research and scientific papers
FeCl3-Catalyzed Intramolecular Michael Reaction of Styrenes for the Synthesis of Highly Substituted Indenes
Dethe, Dattatraya H.,Murhade, Ganesh M.,Ghosh, Sourav
, p. 8367 - 8376 (2015/09/01)
An intramolecular FeCl3-catalyzed Michael addition reaction of styrene, a poor nucleophile, onto α,β-unsaturated ketones was developed for the synthesis of highly substituted indene derivatives. The method was further applied to the total synthesis of the sesquiterpene natural products (±)-jungianol and 1-epi-jungianol.
