Some scientific research about 17057-04-4

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 17057-04-4, and how the biochemistry of the body works.Electric Literature of 17057-04-4

Electric Literature of 17057-04-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.17057-04-4, Name is 4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-benzoicacid, molecular formula is C11H7NO4. In a Article£¬once mentioned of 17057-04-4

Synthesis and antibacterial activity of new 2,5-diaryl-3-styryl-4H,2,3,3a, 5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-diones

The synthesis of some biologically interesting pyrrolo-isoxazolidine derivatives has been accomplished by the 1,3-dipolar cycloaddition reaction of substituted open chain conjugated azomethine N-oxides 1 with substituted N-aryl maleimides 2 leading to the formation of new stereoisomeric 2,5-diaryl-3-styryl- 4H,2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-dione derivatives 3 in excellent yields. These stereoisomers have been characterized as cis-3A and trans-3B on the basis of their 1H-NMR spectral measurements. The synthesized compounds have been screened for their antibacterial activities and have been found to be active against the bacteria Escherichia coli and Pseudomonas aeruginosa up to a significant extent.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 17057-04-4, and how the biochemistry of the body works.Electric Literature of 17057-04-4

Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem