Brief introduction of 17557-76-5

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 17557-76-5, Name is 4,4′-Diamino-[1,1′-biphenyl]-2,2′-dicarboxylic acid, formurla is C14H12N2O4. In a document, author is Fukuda, Tsutomu, introducing its new discovery. Product Details of 17557-76-5.

A SYNTHESIS OF LAMELLARINS VIA REGIOSELECTIVE ASSEMBLY OF 1,2,3-DIFFERENTIALLY SUBSTITUTED 5,6-DIHYDROPYRROLO[2,1-a]ISOQUINOLINE CORE

A modular synthesis of the marine natural products lamellarins has been developed. The key reactions utilized are C3-selective Vilsmeier-Haack formylation followed by iterative bromination/cross-coupling of the 5,6-dihydropyrrolo[2,1-a]isoquinoline core. The 1,2-diaryl-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carbaldehyde thus synthesized was readily converted to the lamellarin skeleton by mean of palladium-catalyzed oxidative lactonization.

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Reference:
Isoquinoline – Wikipedia,
,Isoquinoline | C9H7N – PubChem