152034-50-9

Upstream product

• 35322-20-4 ethyl 3-(4-methoxybenzoyl)pyruvate 
• 95-55-6 2-amino-phenol 
• 1408243-58-2 3-[3-cyclohexyl-2-cyclohexylimino-6-(4-methoxyphenyl)-4-oxo-3,4-dihydro-2H-1,3-oxazin-5-yl]-2H-1,4-benzoxazin-2-one 
• 152034-31-6 3-(4-Methoxy-benzoyl)-benzo[b]pyrrolo[1,2-d][1,4]oxazine-1,2,4-trione 
• 55558-77-5 4-(4-methoxyphenyl)-2,4-dioxobutanoic acid 

Downstream Products

• 152034-31-6 3-(4-Methoxy-benzoyl)-benzo[b]pyrrolo[1,2-d][1,4]oxazine-1,2,4-trione 

Relevant academic research and scientific papers

Five-membered 2,3-dioxo heterocycles: XCVIII.* [4 + 2]-cycloaddition of alkyl vinyl ethers to 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4- triones. A new synthetic approach to heteroanalogs of 13(14→8)-abeo steroids

3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones reacted with alkyl vinyl ethers according to the [4 + 2]-cycloaddition pattern with formation of substituted (1S*,16R*)- and (1R*,16R*)-16-alkoxy-14- aryl-3,15-dioxa-10-azatetracyclo[8.7.0.01,13.04,9

Five-membered 2,3-dioxo heterocycles: LXXXVIII.* Reaction of 3-aroylpyrrolo[1,2-d][1,4]benzoxazine- 1,2,4(4H)-triones with N,N'-dicyclohexylcarbodiimide under thermolysis conditions

Thermolysis of 3-aroylpyrrolo[1,2-d][1,4]benzoxazine-1,2,4(4H)-triones generates aroyl(2-oxo-1,4- benzoxazin-3-yl)ketenes which react as dienes at the aroylketene fragment in [4 + 2]-cycloaddition at the C=N bond of N,N'-dicyclohexylcarbodiimide with form

Sulfamic acid as an effective catalyst in solvent-free synthesis of β-enaminoketone derivatives and X-ray crystallography of their representatives

Two types of β-enaminoketone derivatives of 3-(2-oxo-2-arylethylidene) -3,4-dihydro-1H-quinoxalin-2-ones and 3-(2-oxo-2-arylethylidene)-3,4-dihydro- benzo[1,4]oxazin-2- ones were effectively and conveniently prepared in good to excellent yields under solv