272773-95-2

Upstream product

• 272773-90-7 N-(5,7-dimethoxy-4-oxo-2-phenyl-4H-chromen-8-yl)-N-isopropyl-2,4-dinitro-benzenesulfonamide 
• 105173-18-0 5,7-dihydroxy-8-nitro-2-phenyl-4H-chromen-4-one 
• 88503-22-4 5,7-dimethoxy-8-nitroflavone 
• 272773-89-4 N-(5,7-dimethoxy-4-oxo-2-phenyl-4H-chromen-8-yl)-2,4-dinitro-benzenesulfonamide 
• 272773-88-3 8-amino-5,7-dimethoxyflavone 
• 480-40-0 5,7-dihydroxy-2-phenyl-chromen-4-one 

Downstream Products

• 272774-05-7 5-hydroxy-6-isopropylamino-7-methoxy-2-phenyl-chromen-4-one 

Relevant academic research and scientific papers

A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro

A series of 8-alkylamino-5,7-dihydroxyflavones was prepared from chrysine via a seven step sequence. The synthesis of their 6-alkylamino isomers could be subsequently accomplished through a convenient extension of the Wessely-Moser rearrangement. These compounds were found to be efficient neuroprotective agents in vitro. (C) 2000 Elsevier Science Ltd. All rights reserved.