Related Products of 767-69-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 767-69-1, Name is 6-Bromo-7H-purine, SMILES is BrC1=NC=NC2=C1NC=N2, belongs to piperidines compound. In a article, author is Zhao, Qun, introduce new discover of the category.
One-Pot Four-Component Synthesis of 5,10-Diarylpyrido[4,3-b][1,6] Naphthyridine Derivatives in Ionic Liquids Catalyzed by TsOH
A one-pot four-component reaction of aldehyde, aromatic amine, and two equivalents of piperidine-2,4-dione was treated in ionic liquids of [BMIm]Br catalyzed by TsOH (p-toluenesulfonic acid), and gave a series of 5,10-diarylpyrido[4,3-b][1,6]naphthyridine derivatives in good yields. This procedure has the advantages of mild reaction conditions, good yields, one-pot, and environmentally benign.
Related Products of 767-69-1, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 767-69-1.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem