27181-65-3

Upstream product

• 500-99-2 3,5-dimethoxyphenol 
• 54107-66-3 5,7-dimethoxy-4-chromanone 
• 123-11-5 4-methoxy-benzaldehyde 
• 854678-45-8 β-(3,5-dimethoxyphenoxy)propionic acid 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 59887-91-1 5,7-dimethoxy-4H-chromen-4-one 
• 115240-92-1 methyl 2-[hydroxy(4-methoxyphenyl)methyl]prop-2-enoate 
• 1013631-83-8 C₁₂H₁₃BrO₃ 

Downstream Products

• 3791-75-1 2'-hydroxy-4,4',6'-trimethoxydihydrochalcone 
• 22395-14-8 3-methyl-5,7,4′-trimethoxyflavone 
• 34811-77-3 3-(4-methyloxybenzyl)-5,7-dimethoxychromen-4-one 
• 132435-34-8 (R)-5,7-dimethoxy-3-(4-methoxybenzyl)chroman-4-one 
• 17934-14-4 (S)-5,7-dimethoxy-3-(4-methoxybenzyl)chroman-4-one 
• 246244-10-0 rac-5,7-dimethoxy-3-(4-methoxybenzyl)-chroman-4-one 

Relevant academic research and scientific papers

Novel homoisoflavanone derivatives, preparation method thereof, and pharmaceutical composition for use in preventing or treating ischemic brain damage and multiple sclerosis containing the same as an active ingredient

The present invention relates to: a homoisoflavanone compound; a manufacturing method thereof; and a pharmaceutical composition for preventing or treating ischemic brain damage and multiple sclerosis containing the homoisoflavanone compound as an active i

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.

Synthesis and NMR elucidation of homoisoflavanone analogues

A series of five homoisoflavanone analogues have been synthesized from the corresponding 3,5-methoxy phenols via chroman-4-one in three steps. The complete NMR elucidation of these homoisoflavanone analogues is reported. The use of 2D NMR techniques (COSY, NOESY, HSQC and HMBC) proved to be very useful tools in the elucidation of homoisoflavanone analogues. The homoisoflavanone analogues exhibit an AA0BB0 spin pattern in the ring B of the homoisoflavanone. These homoisoflavanone analogues are potential antifungal and anti-inflammatory agents. Springer Science+Business Media, LLC 2010.