Reference of 29841-69-8, 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.29841-69-8, Name is (1S,2S)-(-)-1,2-Diphenylethylenediamine, molecular formula is C14H16N2. In a article£¬once mentioned of 29841-69-8
Ir(III) complexes of diamine ligands for asymmetric ketone hydrogenation
The use of a combination of IrCl3 with a series of ligands derived from the C2-symmetric diamine diphenylethanediamine (DPEN) forms a catalyst capable of the asymmetric hydrogenation of ketones in up to 85% ee.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 29841-69-8, and how the biochemistry of the body works.Reference of 29841-69-8
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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI