The important role of 144222-34-4

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 144222-34-4, you can also check out more blogs about144222-34-4

Synthetic Route of 144222-34-4, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 144222-34-4, Name is N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzenesulfonamide, molecular formula is C21H22N2O2S. In a Article，once mentioned of 144222-34-4

A series of mono- and dialkylated derivatives of C2-symmetric N-tosyl-1,2-diphenylethylene diamines have been prepared and used as ligands for the enantiomeric control of the addition of diethylzinc to aldehydes. Addition products of up to 79% ee were formed.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 144222-34-4, you can also check out more blogs about144222-34-4

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