Properties and Exciting Facts About 6-Methyl-2,2′-bipyridine

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 56100-22-2

Reference of 56100-22-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.56100-22-2, Name is 6-Methyl-2,2′-bipyridine, molecular formula is C11H10N2. In a Article£¬once mentioned of 56100-22-2

Functionalized 2,2?-bipyridines and 2,2?:6?,2?-terpyridines via stille-type cross-coupling procedures

Stille-type cross-coupling procedures are utilized in order to prepare a variety of functionalized 2,2?-bipyridines and 2,2?:6?,2?-terpyridines. Such N-heterocyclic compounds are of great interest as chelating ligands for transitionmetal ions in the field of supramolecular chemistry. Various mono- and disubstitued 2,2?-bipyridines were synthesized in high yields and multigram scales using a modular design principle. The terpyridines may be functionalized in one step with different substituents at the outer pyridine rings and at the 4?-position of the centered ring, leading to multifunctionalized compounds. The initially obtained methyl ester and ethyl ester groups can be simply converted into bromomethyl and hydroxymethyl groups which allow further functionalization reactions.

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 56100-22-2

Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI