17934-14-4

Upstream product

• 3791-75-1 2'-hydroxy-4,4',6'-trimethoxydihydrochalcone 
• 123-11-5 4-methoxy-benzaldehyde 
• 27181-65-3 5,7-dimethoxy-3-(4'-methoxybenzylidene)chroman-4-one 
• 1013631-83-8 C₁₂H₁₃BrO₃ 
• 115240-92-1 methyl 2-[hydroxy(4-methoxyphenyl)methyl]prop-2-enoate 
• 3420-72-2 flavokawain A 
• 34811-77-3 3-(4-methyloxybenzyl)-5,7-dimethoxychromen-4-one 

Relevant academic research and scientific papers

A highly enantioselective synthesis of (R)- and (S)-5,7-odimethyleucomol

Both (R)- and (S)-5,7-O-dimethyleucomol 1b (R = Me) were synthesized in 57% overall yield in>96% enantiomeric excess. The key step involves the enantioselective α hydroxylation of the lithium enolate of 8 by readily available (+)- and (-)-[(8,8-dimethoxyc

Asymmetric Synthesis of Eucomol via Enantioselective Oxidation of Enol Phosphate

Stereoselective synthesis of a few derivatives of the homoisoflavanone class of natural products is described.