New Advances in Chemical Research, April 2021. Related Products of 98796-51-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 98796-51-1, Name is 5′-O-[Bis(4-Methoxyphenyl)phenylmethyl]-thymidine 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], SMILES is O=C(NC(C(C)=C1)=O)N1[C@H](O2)C[C@H](OP(N(C(C)C)C(C)C)OCCC#N)[C@H]2COC(C3=CC=C(OC)C=C3)(C4=CC=C(OC)C=C4)C5=CC=CC=C5, belongs to naphthyridine compound. In a article, author is Ma, Yong-Gang, introduce new discover of the category.
Consecutive Knoevenagel condensation, Michael addition, cyclization, and Ullmann Csp(2)-N coupling reactions took place in the Domino reaction of o-halogenated benzaldehydes, tert-butyl 2,4-dioxopiperidine-1-carboxylate, and 1H-indazol-6-amine or 3H-benzo[d]imidazol-5-amine catalyzed by CuI. It gave series of fused hexacyclic heterocycles containing naphthyridine, acridine, and pyrazole (imidazole) moieties in one-pot under ligand-free conditions. [GRAPHICS]
Related Products of 98796-51-1, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 98796-51-1 is helpful to your research.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem