Related Products of 14871-92-2, 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.14871-92-2, Name is (2,2¡ä-Bipyridine)dichloropalladium(II), molecular formula is C10H8Cl2N2Pd. In a article£¬once mentioned of 14871-92-2
In situ generated cationic Pd(II)/bipyridine-catalyzed addition of arylboronic acids to N-sulfonyl-arylaldimines
An in situ generated cationic Pd(II)/bipyridine-catalyzed nucleophilic addition of arylboronic acids to N-sulfonyl arylaldimines was developed and optimized, and the reaction was proceeded highly efficiently and conveniently in CH3NO2. A series of arylboronic acids and N-sulfonyl arylaldimines were surveyed, and 12 of 13 examples gave 90?96% yields.
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 14871-92-2
Reference£º
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method