201049-16-3

Upstream product

• 124555-63-1 4-methoxy-2-methoxymethoxy benzaldehyde 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 121133-27-5 1-(3,4-dimethoxyphenyl)-3-(4-methoxy-2-methoxymethoxyphenyl)-2-propen-1-one 

Downstream Products

• 201049-39-0 (2S)-3t-Acetoxy-2r-(3,4-dimethoxy-phenyl)-7-methoxy-chroman 
• 69127-06-6 (2R)-3t-Acetoxy-2r-(3,4-dimethoxy-phenyl)-7-methoxy-chroman 
• 201049-35-6 (1R,2R)-1-(3,4-Dimethoxy-phenyl)-3-(4-methoxy-2-methoxymethoxy-phenyl)-propane-1,2-diol 
• 201049-24-3 (1S,2S)-1-(3,4-Dimethoxy-phenyl)-3-(4-methoxy-2-methoxymethoxy-phenyl)-propane-1,2-diol 
• 888712-57-0 (S)-2-(3,4-Dimethoxy-phenyl)-7-methoxy-chroman-3-ol 
• 201049-20-9 (E)-1-(3',4'-Dimethoxyphenyl)-3-(2''-methoxymethyl-4''-methoxyphenyl)propene 
• 201049-31-2 3-Acetoxy-3',4',7-trimethoxy-2,3-cis-flavan 

Relevant academic research and scientific papers

Enantioselective synthesis of flavonoids. Part 3. trans- and cis-flavan-3-ol methyl ether acetates

Asymmetric dihydroxylation of a series of polyoxygenated 1,3-diarylpropenes with AD-mix-α or AD-mix-β in the presence of methanesulfonamide and subsequent acid-catalysed cyclization, affords for the first time synthetic access to trans- and cis-flavan-3-ol derivatives, essentially enantiopure and in good yield.