86788-64-9

Upstream product

• 100-39-0 benzyl bromide 
• 4047-24-9 1-[2-(benzyloxy)-6-hydroxyphenyl]ethanone 
• 699-83-2 2,6-dihydroxylacetophenone 
• 110168-74-6 6'-benzyloxy-4,2'-bis(methoxymethoxy)chalcone 
• 110168-72-4 6'-benzyloxy-2'-methoxymethoxyacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 110168-79-1 1-6''-benzyloxy-2''-methoxymethoxyphenyl-2,3-epoxy-3-4'-methoxymethoxyphenylpropanone 
• 86788-63-8 (E)-1-(2-(benzyloxy)-6-hydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 

Downstream Products

• 86788-68-3 (+/-)-fistacacidin tetraacetate 
• 86788-67-2 Acetic acid (2S,3S,4S)-3-acetoxy-5-methoxy-2-(4-methoxy-phenyl)-chroman-4-yl ester 
• 86788-69-4 [(2S,3S,4S)-3-Hydroxy-5-methoxy-2-(4-methoxy-phenyl)-chroman-4-ylsulfanyl]-acetic acid methyl ester 
• 86788-66-1 (2S,3R,4S)-5-Methoxy-2-(4-methoxy-phenyl)-chroman-3,4-diol 
• 21187-77-9 (+/-)-2,3-trans-3,4-trans-3,4,5,4'-tetrahydroxyflavan 
• 86788-70-7 (+/-)-2,3-trans-5',4-dimethoxyflavan-3-ol 
• 86788-65-0 (2R^*,3R^*)-5,4'-dihydroxyflavanonol 

Relevant academic research and scientific papers

Heterocycles. XX. Reactions of 2''-Methoxymethoxychalcone Epoxides under Acidic Conditions

The effect of substituents on the formation of products in the reactions of 2''-methoxymethoxychalcone epoxides under acidic conditions has been examined.Regardless of the 6''-substituent, the presence of a 4'-hydroxyl group results in the exlusive format

HETEROCYCLES. XIX. REACTION OF 2'-HYDROXYCHALCONES WITH ALKALINE HYDROGEN PEROXIDE

Reaction of 2'-hydroxychalcones, which contain the hydroxyl and/or the methoxyl group at the 4- and 6'-positions, with alkaline hydrogen peroxide has been examined.It is observed that these substituents intricately influence the formation of the products.

Synthesis of (+/-)-Fistacacidin

Synthesis of fistacacidin and (+/-)-2,3-trans-5,4'-dimethoxyflavan-3-ol (XVII) are reported.Synthesis of XII, starting from monobenzyl ether of 2,6-dihydroxyacetophenone (I) involves the reacti