Synthetic Route of 96568-07-9, 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.96568-07-9, Name is Ethyl 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate, molecular formula is C14H12ClFN2O3. In a article£¬once mentioned of 96568-07-9
Cyclic beta-tributylstannyl-alpha,beta-unsaturated ketones, alcohols, and amines have been prepared by a highly efficient process. These reagents undergo palladium-catalyzed, intermolecular vinylic cross-coupling with 7-quinolyltriflates and 7-chloro-1,8-naphthyridines under very mild conditions. Cyclic beta-tributylstannyl-alpha,beta-unsaturated ketones, alcohols, and amines undergo palladium-catalyzed, vinylic cross-coupling with 7-quinolytriflates and 7-chloro-1,8-naphthyridines in very good yields. (Chemical Equation Presented).
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 96568-07-9
Reference£º
1,764-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N758 – PubChem