143264-39-5Relevant academic research and scientific papers
Catalytic asymmetric total synthesis of (S)-(-)-zearalenone, a novel lipoxygenase inhibitor
Baggelaar, Marc P.,Huang, Yange,Feringa, Ben L.,Dekker, Frank J.,Minnaard, Adriaan J.
, p. 5271 - 5274 (2013/09/02)
A catalytic asymmetric synthesis of (S)-(-)-zearalenone is reported using asymmetric allylic alkylation for the introduction of the stereocenter. (S)-(-)-Zearalenone turned out to be a novel lipoxygenase inhibitor.
First stereoselective total synthesis of isoaspinonene through a Baylis-Hillman/olefin cross-metathesis protocol
Radha Krishna, Palakodety,Alivelu, Munagala,Prabhakar Rao, Tadikamalla
, p. 616 - 622 (2012/03/10)
The first stereoselective and efficient total synthesis of isoaspinonene by using Baylis-Hillman reaction, chelation-controlled vinyl Grignard reaction, Wittig olefination, and olefin cross-metathesis reaction of a hitherto unreported substrate as the key
