38736-62-8

Upstream product

• 36340-49-5 5,6-epoxy-trans-β-ionone 
• 79-77-6 (E)-β-ionone 
• 127-41-3 alpha-ionone 

Downstream Products

• 38736-64-0 ethyl (2E,4E)-1'-hydroxy-α-ionylideneacetate 
• 219972-48-2 (2E,4E)-ethyl 2-fluoro-5-(1'-hydroxy-2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-3-methyl-2,4-pentadienoate 
• 28714-00-3 (2E,4E)-5-(1-Hydroxy-2,6,6-trimethyl-cyclohex-2-enyl)-3-methyl-penta-2,4-dienoic acid 
• 28713-99-7 (+/-)-4-deoxoabscisic acid 
• 23043-31-4 methyl-2-cis-1'-hydroxy-α-ionylidene acetate 
• 30167-18-1 methyl-2-trans-1'-hydroxy-α-ionylidene acetate 

Relevant academic research and scientific papers

2-Fluoroabscisic acid analogues: Their synthesis and biological activities

Fluorine was introduced into the 2-position of the side chain of abscisic acid (ABA) analogues by Wittig reaction of α-ionone derivatives with ethyl triethylphosphono-2-fluoroacetate. The effects of the fluorinated analogues were evaluated on inhibition o

BIOSYTESIS OF ABSCISIC ACID FROM &α-IONYLIDENEETHANOL IN CERCOSPORA PINI-DENSIFLORAE

2H-labelled α-ionylideneethanol was efficiently incorporated into the 1',4'-trans-diol of ABA via (1'R)-4'S-hydroxy-α-ionylideneacetic acid by Cercospora pini-densiflorae, and 2H-labelled α-ionylideneacetic acid was incorporated into 1'-deoxyABA via (1'R)

THE METABOLISM OF α-IONYLIDENE COMPOUNDS BY CERCOSPORA ROSICOLA

α-Ionylidene ethanol was converted to 4'hydroxy-α-ionylidene acetic acid, 1'-deoxy-ABA and ABA by Cerospora rosicola.Both the 4'-(R)- and 4'-(S)-epimers of 4'-hydroxy-α-ionylidene acetic acid were detected but the configuration of the 1'-position was not