The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. HPLC of Formula: C16H16N2O2, 94-93-9, Name is 2,2′-((Ethane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenol, SMILES is OC1=CC=CC=C1C=NCCN=CC2=CC=CC=C2O, in an article , author is Yu, Jie, once mentioned of 94-93-9.
Since L-prolinamide was revealed to have high capacity to catalyze asymmetric aldol reaction, great advances have been made on the design of chiral amino amide catalysts and their applications in asymmetric catalysis. In particular, the enamine-double hydrogen-bonding activation mode has turned out to be a general concept for the proliferation of structurally diverse range of organocatalysts. This review mainly describes asymmetric reactions catalyzed by chiral amino amides containing single hydrogen-bonding donor, double hydrogen-bonding donors and multiple hydrogen-bonding donors, including enantioselective direct aldol reaction, Mannich reaction, Michael addition reaction, cycloaddition reaction, tandem cyclization reaction, Biginelli reaction and others.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 94-93-9, you can contact me at any time and look forward to more communication. HPLC of Formula: C16H16N2O2.
Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare