More research is needed about 102490-05-1

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.Application of 102490-05-1, you can also check out more blogs about102490-05-1

Application of 102490-05-1, 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. 102490-05-1, Name is (S)-3,3′-Diphenyl-[1,1′-binaphthalene]-2,2′-diol, molecular formula is C32H22O2. In a Article，once mentioned of 102490-05-1

A series of monophosphite ligands derived from D-fructose and D-glucose have been synthesized and employed in Rh-catalyzed asymmetric hydrogenation of alpha- and beta-dehydroamino acid esters. A variety of chiral alpha- and beta-amino acid esters have been obtained in excellent enantiomeric excess (up to 98.4% ee).

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.Application of 102490-05-1, you can also check out more blogs about102490-05-1

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