The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4488-22-6, Name is [1,1′-Binaphthalene]-2,2′-diamine, molecular formula is C20H16N2. In a Article£¬once mentioned of 4488-22-6, Quality Control of: [1,1′-Binaphthalene]-2,2′-diamine
The synthesis of homochiral hybrid diamines derived from 1,1?-binaphthyl-2,2?-diamine and alpha-amino acids
A convenient procedure for the preparation of homochiral diamines is presented. Coupling of racemic 1, 1?-binaphthyl-2,2?-diamine with natural N-protected amino acids afforded the corresponding diastereomeric precursors which, following chromatographic separation and deprotection, gave the desired products in good yields. These compounds, called herein hybrid compounds, possess two different stereogenic elements, i.e., the centre containing the L-amino acid residues and the C2 axis, resulting from the 1,1?-binaphthyl moiety. Georg Thieme Verlag Stuttgart.
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.Quality Control of: [1,1′-Binaphthalene]-2,2′-diamine, you can also check out more blogs about4488-22-6
Reference£º
Chiral Catalysts,
Chiral catalysts – SlideShare