803-15-6

Upstream product

• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 1122-91-4 4-bromo-benzaldehyde 
• 18600-53-8 2-(4-bromophenyl)-4H-benzo[d][1,3]oxazine-4-one 
• 611-73-4 Benzoylformic acid 

Relevant academic research and scientific papers

Radical-Induced, Palladium-Catalyzed C–H Activation: An Approach to Functionalize 4H-Benzo[d][1,3]oxazin-4-one Derivatives by Using Toluenes, Aldehydes, and Benzyl Alcohols

Toluenes, aldehydes, and benzyl alcohols have been utilized in the radical-induced direct functionalization of 4H-benzo[d][1,3]oxazin-4-one derivatives by using a palladium-catalyzed C–H activation strategy. The stability, low toxicity, and ease of access

Palladium-Catalyzed Decarboxylative Synthesis of 5H-Benzo[4,5][1,3]oxazino[2,3-a]isoindole-5,11(6aH)-Diones using 2-Phenyl-4H-Benzo[d][1,3]oxazin-4-Ones and α-Oxo Carboxylic Acids

A Pd-catalyzed novel and efficient protocol has been developed for the direct functionalization of 2-phenyl-4H-benzo[d][1,3]oxazin-4-ones with α-oxo carboxylic acids resulting in 5H-benzo[4,5][1,3]oxazino[2,3-a]isoindole-5,11(6aH)-diones using (NH4/