Some scientific research about 108-47-4

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.Product Details of 108-47-4, you can also check out more blogs about108-47-4

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 108-47-4. Introducing a new discovery about 108-47-4, Name is 2,4-Dimethylpyridine

Triflic acid-catalyzed C sp3 – H functionalization of 2-methyl azaarenes with a alpha-trifluoromethyl imino ester

A Br¡ãnsted acid promoted Csp3-H functionalization of 2-alkyl azaarenes with alpha-trifluoromethylated imino ester is described. A catalytic amount of triflic acid provided straightforward access to the corresponding trifluoromethylated amino esters via concomitant in situ one step N-alkyl deprotection. On further hydrolysis of ester, synthesis of quinoline derived unnatural trifluoromethylated amino acids has been achieved in a short and efficient manner.

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.Product Details of 108-47-4, you can also check out more blogs about108-47-4

Reference£º
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis¡ªI. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis