308087-55-0

Upstream product

• 92549-46-7 1-(2,4-dihydroxy-phenyl)-2-(2-methoxy-phenyl)-ethanone 
• 75-36-5 acetyl chloride 
• 610758-61-7 3-(2-methoxyphenyl)-2-methyl-4-oxo-4H-chromen-7-yl acetate 

Downstream Products

• 1379467-42-1 2-methyl-3-(2-methoxyphenyl)-9-[(1S,9aR)-octahydro-2H-quinolizin-1-ylmethyl]-9,10-dihydro-4H,8H-chromeno[8,7-e][1,3]oxazin-4-one 
• 855627-28-0 7-acetoxy-3-(2-acetoxy-phenyl)-2-methyl-chromen-4-one 
• 112553-72-7 8-allyl-7-hydroxy-3-(2-methoxy-phenyl)-2-methyl-chromen-4-one 
• 97575-50-3 7-hydroxy-2-hydroxymethyl-3-(2-hydroxy-phenyl)-chromen-4-one 
• 855627-29-1 7-hydroxy-3-(2-hydroxy-phenyl)-2-methyl-chromen-4-one 
• 70387-00-7 7-methoxy-3-(2-methoxy-phenyl)-2-methyl-chromen-4-one 
• 112553-73-8 7-allyloxy-3-(2-methoxy-phenyl)-2-methyl-chromen-4-one 
• 610758-61-7 3-(2-methoxyphenyl)-2-methyl-4-oxo-4H-chromen-7-yl acetate 
• 610758-44-6 3-(2-methoxyphenyl)-2-methyl-4-oxo-4H-chromen-7-yl 5-ethoxy-2-phenyl-1-benzofuran-3-carboxylate 

Relevant academic research and scientific papers

Synthesis of 2-alkylisoflavones under phase-transfer catalysis conditions

2-alkyl isoflavones were synthesised with the aliphatic acid chloride and 2-hydroxydeoxybenzoins under phase-transfer catalysis in acetone-K 2CO3 medium involves the modified Baker-VenKataraman transformation.

COMPOUNDS FOR IMMUNOPOTENTIATION

Methods of stimulating an immune response and treating patients responsive thereto with 3,4-di(1H-indol-3-yl)-1H-pyrrole-2,5-diones, staurosporine analogs, derivatized pyridazines, chromen-4-ones, indolinones, quinazolines, nucleoside analogs, and other small molecules are disclosed.