Application of 3340-78-1, 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.3340-78-1, Name is 2-Phenyl-1,2,3,4-tetrahydroisoquinoline, molecular formula is C15H15N. In a article£¬once mentioned of 3340-78-1
CeO2-Catalyzed C-H Functionalization of N-Aryltetrahydroisoquinolines: An Aerobic Cross-Dehydrogenative Coupling Reaction between Two sp3 C-H Bonds
CeO2 has been used as heterogeneous catalyst for carbon-carbon bond formation via cross-dehydrogenative coupling (CDC). It works efficiently for oxidative C?C bond formation between N-aryltetrahydroisoquinoline derivatives and a carbon nucleophile nitroalkane and acetone under aerobic conditions. This is the first report of CeO2 as a low temperature catalyst for the carbon-carbon bond formation reaction between two sp3 C?H bonds.
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 3340-78-1
Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem