215049-65-3

Upstream product

• 108-24-7 acetic anhydride 
• 1025886-67-2 7-hydroxy-4-methoxy-2-phenyl-benzo[g]quinoline-5,10-dione 
• 115929-62-9 3-bromo-2,5-dimethoxyaniline 
• 244237-08-9 7-bromo-4-methoxy-2-phenylquinoline-5,8-dione 
• 244237-04-5 7-bromo-4,5,8-trimethoxy-2-phenylquinoline 
• 244237-02-3 7-bromo-4-hydroxy-5,8-dimethoxy-2-phenylquinoline 
• 67188-06-1 4-hydroxy-5,8-dimethoxy-2-phenylquinoline 
• 215049-58-4 4-methoxy-2-phenylquinoline-5,8-dione 
• 215049-56-2 4,5,8-trimethoxy-2-phenylquinoline 

Relevant academic research and scientific papers

A chemical evidence of reiochemistry in the Diels-Alder reaction of 4- oxygenated quinolinequinones with 1-methoxy-3-trimethylsilyloxy- 1,3- butadienes

The synthesis of four regioisomeric azaanthraquinones (4a, b and 5a, b) was achieved in a regioselective manner by the Diels-Alder reaction of 4- oxygenated 6-bromo- and 7-bromoquinolinequinones (11 and 15) with 1-methoxy- 3-trimethylsilyloxy-1,3-butadien

A synthesis of 1-azaanthraquinones via Diels-Alder reaction of 4- hydroxy- and 4-methoxy-2-phenylquinolinequinones with 3-trimethylsilyloxy- 1,3-butadienes: Observation of inverse regioselectivity

Diels-Alder reaction of 4-hydroxy-2-phenylquinolinequinone (10a) and 4- methoxy-2-phenylquinolinequinone (10b) with 1-methoxy-3- trimethylsilyloxybutadiene proceeded in a highly regio- and stereoselective manner to give the [4+2] adducts (11) and (14) in