Electric Literature of 107484-69-5, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.107484-69-5, Name is 5-Chloro-8-iodo-1,6-naphthyridine, molecular formula is C8H4ClIN2. In a article£¬once mentioned of 107484-69-5
The iodonation and subsequent dehydroxychlorination of 1,6-naphthyridin-5(6H)-one gave 5-chloro-8-iodo-1,6-naphthyridine, wich was converted to the 5-methoxy derivative.Starting from this compound, didehydromatrine was synthesized by using palladium-catalyzed cross-coupling reactions with ethyl acrylate and 3-butyn-1-ol, as key reactions.Similarly, nordehydro-alpha-matrinidine was synthesized through four steps from 8-bromo-1,6-naphthyridine, obtained by the bromination of unsubstituted 1,6-naphthyridine.Keywords – synthesis; matrine; didehydromatrine; nordehydro-alpha-matrinidine; palladium-catalyzed reaction; 1,6-naphthyridine; ethyl acrylate; 3-butyn-1-ol
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 107484-69-5
Reference£º
1,744-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N738 – PubChem