Awesome Chemistry Experiments For (S)-N,N-Dimethyl-1-ferrocenylethylamine

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 31886-57-4

Synthetic Route of 31886-57-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.31886-57-4, Name is (S)-N,N-Dimethyl-1-ferrocenylethylamine, molecular formula is C14H19FeN. In a Article£¬once mentioned of 31886-57-4

Substituted ferrrocenecarboxylic acids and esters

The synthesis of Fe(eta-C5H5)(eta-C5H3(CHMeNMe2)(COOH)-1,2), 3a, and its methyl and ethyl esters is described.Esterification of 3a by using RI in DMA affords Fe(eta-C5H5)(eta-C5H3(CHMeOH)(COOR)-1,2), R = Me, Et, with retention of configuration at the chiral center.The variable temperature 1H NMR spectrum of 3a reveals H-bonding between the two functional groups.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 31886-57-4

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