52210-15-8Relevant academic research and scientific papers
Enantiocontrolled access to the ionone type bisnorsesquiterpenes. Total syntheses of 3-oxo-α-ionol and related natural products
Kikuchi, Daisuke,Yoshida, Masahiro,Shishido, Kozo
, p. 145 - 147 (2012/01/17)
The enantiocontrolled total syntheses of three ionone type bisnorsesquiterpenes have been accomplished employing a highly diastereoselective intramolecular Heck reaction as the key step.
Megastigmane glycosides from seeds of Trifolium alexandrinum
Mohamed, Khaled M.,Mohamed, Mahmoud H.,Ohtani, Kazuhiro,Kasai, Ryoji,Yamasaki, Kazuo
, p. 859 - 862 (2007/10/03)
Five megastigmane glycosides have been isolated from the seeds of Trifolium alexandrinum L., of which two are known compounds, while three are new compounds showing the presence of apiofuranosyl-(1→2)-glucopyranosyl residue as a sugar moiety. The structures of the isolated compounds were established on the basis of NMR and mass spectral data.
TWO DIASTEREOMERIC 3-OXO-α-IONOL β-D-GLUCOSIDES FROM RASPBERRY FRUIT
Pabst, Anni,Barron, Denis,Semon, Etienne,Schreier, Peter
, p. 1649 - 1652 (2007/10/02)
From a methanolic extract of raspberry fruit two 3'-O-β-D-glucopyranosides of diastereomeric 4-(3'-hydroxy-1'-butenyl)-3,3,5-trimethyl-2-cyclohexen-1-one (3-oxo-α-ionol) were isolated by adsorption chromatography on XAD-2 followed by LC on Sephadex LH-20,
