Electric Literature of 20439-47-8, 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.20439-47-8, Name is (1R,2R)-Cyclohexane-1,2-diamine, molecular formula is C6H14N2. In a article，once mentioned of 20439-47-8
The syntheses of chiral anion receptors based on rhenium(I) and ruthenium(II) with amide bipyridine ligands are reported. The rhenium(I) hosts were prepared in moderate to high yields by co-ordinating chiral bipyridine ligands to a Re(CO)3Br centre. The ruthenium(II) receptors were synthesised via the chiral building blocks Lambda- and Delta-[Ru(bpy)2-(py)2]2+ or by chromatographic resolution on a SP Sephadex C-25 cation exchanger. Chiral purity was determined by 1H NMR and circular dichroism spectroscopy and lanthanide shift experiments. 1H NMR titration studies showed that these receptors bind chiral carboxylate anions in DMSO-d6, although significant chiral discrimination was not observed.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 20439-47-8, and how the biochemistry of the body works.Electric Literature of 20439-47-8
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI