35491-99-7

Upstream product

• 60237-54-9 1-(2,4-dimethoxy-6-(methoxymethoxy)phenyl)ethan-1-one 
• 123-11-5 4-methoxy-benzaldehyde 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 

Downstream Products

• 130322-28-0 (-)-(αR,βS)-4,4',6'-trimethoxy-2'-O-methoxymethylchalcone epoxide 

Relevant academic research and scientific papers

ENANTIOSELECTIVE SYNTHESIS OF FLAVONOIDS. PART 1. POLY-OXYGENATED CHALCONE EPOXIDES

Epoxidation of a series of poly-oxygenated chalcones with H2O2 in the presence of poly-α-aminoacid catalysts afforded chiral aromatic oxygenated epoxides in moderate to high optical yields; their absolute configurations were determined by CD spectroscopy.These chalcone epoxides could, in principle, be used as chirons for enantiomerically enriched dihydroflavonols.