9/23/21 News Top Picks: new discover of (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine

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 In Synthesis of (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine, you can also check out more blogs about894493-95-9

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.894493-95-9, Name is (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine, molecular formula is C8H18N2. In a Article,once mentioned of 894493-95-9, Application In Synthesis of (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine

Asymmetric direct vinylogous aldol reactions of furan-2(5H)-one with aldehydes in the presence of a catalytic amount of novel squaramide-sulfonamide organocatalyst resulted in the corresponding addition products with high to excellent enantioselectivities. This is the first successful report illustrating an example of highly stereoselective reactions using a squaramide-sulfonamide organocatalyst.

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 In Synthesis of (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine, you can also check out more blogs about894493-95-9

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare