13222-07-6

Upstream product

• 132246-43-6 8-(3,3-dimethylallyl)-5,7,3',4'-tetrakis(methoxymethoxy)flavanone 
• 6515-06-6 3,4-bis-methoxymethoxy-benzaldehyde 
• 132246-42-5 5'-(3,3-dimethylallyl)-6'-hydroxy-3,4,2',4'-tetrakis(methoxymethoxy)chalcone 
• 84092-45-5 2',4'-bis(methoxymethoxy)-5'-(3,3-dimethylallyl)-6'-hydroxyacetophenone 

Downstream Products

• 132339-94-7 6,6-dimethyl-4,5-dihydropyrano(2,3:7,8)-5,3',4'-trihydroxyflavanone 
• 132339-92-5 6,6-dimethyl-4,5-dihydropyrano(2,3:7,6)-5,3',4'-trihydroxyflavanone 

Relevant academic research and scientific papers

8-Prenylflavanones through Microwave Promoted Tandem Claisen Rearrangement/6-endo-trig Cyclization and Cross Metathesis

Prenylated flavanones were obtained from ortho-allyloxy chalcones through a one-pot sequence of Claisen rearrangement and 6-endo-trig cyclization, followed by olefin cross metathesis of the intermediate allyl flavanones with 2-methyl-2-butene. The synthet

STRUCTURE OF 6- OR 8-ISOPRENOID SUBTITUTED FLAVANONE: CHEMICAL SHIFT OF THE HYDROGEN-BONDED HYDROXYL GROUP

The proton signal of the hydrogen-bonded hydroxyl group of the 6-isoprenoid substituted flavanone was shifted more downfield than that of 6-nonsubstituted flavanone.By comparison of the chemical shifts of the hydrogen-bonded hydroxyl groups of 8-(3",3"-di