Electric Literature of 13104-56-8, 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.13104-56-8, Name is 4′-(4-Methoxyphenyl)-2,2′:6′,2”-terpyridine, molecular formula is C22H17N3O. In a article£¬once mentioned of 13104-56-8
A facile route to sterically hindered and non-hindered 4?-aryl-2, 2?:6?,2?-terpyridines
A facile one-pot synthesis of 4?-aryl-2,2?:6?,2?- terpyridines from aryl aldehydes and 2-acetylpyridine is presented. The synthesis of terpyridines incorporating sterically hindered aryl groups, such as the 9-anthryl group, can also be readily synthesized using this method.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 13104-56-8, and how the biochemistry of the body works.Electric Literature of 13104-56-8
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI