1373498-17-9Relevant academic research and scientific papers
Total synthesis of (±)-3-hydroxy-β-ionone through a ring-closing enyne metathesis
Kikuchi, Daisuke,Yoshida, Masahiro,Shishido, Kozo
, p. 577 - 580 (2012/04/11)
The total synthesis of (±)-3-hydroxy - ionone, a bisnor-sesquiterpene having allelopathic activity, has been accomplished employing an enyne metathesis for the construction of the C1-C8 segment and two-carbon elongation via a nitrile oxide-alkene [3+2] cycloaddition as the key steps. Georg Thieme Verlag Stuttgart · New York.
