217442-59-6

Upstream product

• 115-18-4 2-methyl-3-buten-2-ol 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 24672-82-0 1-[2,4-dihydroxy-3,5-bis-(3-methyl-but-2-enyl)-phenyl]-ethanone 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 217442-57-4 (E)-3-(2,2-dimethyl-2H-chromen-6-yl)-1-[2-hydroxy-3,5-bis(3,3-dimethylallyl)-4-methoxymethyloxyphenyl]-2-propen-1-one 

Relevant academic research and scientific papers

Syntheses of (+/-)-shinflavanone and its structural analogues as potent inhibitors of bone resorption pits formation.

The first total syntheses of (+/-)-shinflavanone and its structural analogues were achieved. (+/-)-Shinflavanone, appears to be a strong inhibitor of bone resorption pits formation by osteoclast-like cell induced by 1alpha, 25-dihydroxy vitamine D3 (IC50 = 0.70 microg/mL).

A short and facile synthetic route to prenylated flavones. Cyclodehydrogenation of prenylated 2'-hydroxychalcones by a hypervalent iodine reagent

The first synthesis of the prenylated flavones kanzonol-D (1), -E (3) and yinyanghuo-C (4) was accomplished by cyclodehydrogenation of the appropriately substituted 2'-hydroxychalcones 16, 14 and 11, respectively, in presence of phenyl-iodine(III) diaceta