Related Products of 31886-57-4, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.31886-57-4, Name is (S)-N,N-Dimethyl-1-ferrocenylethylamine, molecular formula is C14H19FeN. In a article£¬once mentioned of 31886-57-4
Ferrocene Derivatives, Part 70: Syntheses and Stereochemistry of Chiral 1,1′-Biferrocenyls (Stereochemistry of Metallocenes, Part 55 <1>)
2,2′-Disubstituted 1,1′-biferrocenyls have been prepared by coupling of appropriate ferrocene derivatives.The stereochemistry of the diastereoisomers obtained thereby is discussed on the basis of n.m.r.-spectroscopy and in two cases (2a,b) from X-ray structure analyses.Chiroptical properties of optically active 1,1′-biferrocenyls – obtained from (+)(R)-1-ferrocenyl-N,N-dimethylaminoethane – are reported.Attempts to prepare 2,2′,5,5′-tetrasubstituted biferrocenyls failed.
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