132018-33-8

Upstream product

• 921942-45-2 2-(4-aminophenyl)-5,7-dimethoxy-4H-chromen-4-one 
• 1609456-12-3 2-acetyl-3,5-dimethoxyphenyl-4-bromobenzoate 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 122-04-3 4-nitro-benzoyl chloride 
• 132018-00-9 methyl 3-<4,6-bis(benzyloxy)-2-hydroxyphenyl>-3-oxopropanoate 
• 132018-30-5 5,7-dihydroxy-2-(4-nitrophenyl)-4-oxo-4H-benzopyran-3-carboxylic acid 
• 18065-05-9 1-[2,4-bis(benzyloxy)-6-hydroxyphenyl]ethanone 
• 110865-14-0 5,7-dihydroxy-2-(4'-nitrophenyl)chromone 
• 132018-14-5 5,7-bis(benzyloxy)-3-(methoxycarbonyl)-2-(4-nitrophenyl)-4H-benzopyran-4-one 

Relevant academic research and scientific papers

Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids

Aminoflavonoids are unique antioxidants comparing to other abundant flavonoids in nature. Their syntheses and biological activities were scarcely reported. An effectively copper-mediated amination of the corresponding bromoflavonoids to synthesize a serie

Synthesis and Protein-Tyrosine Kinase Inhibitory Activities of Flavanoid Analogues

Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with