Synthetic Route 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
Novel optically active salen ligands and their cobalt(II) complexes were synthesized on the basis of 1,3-dioxolane. Spectral parameters of the complexes and their catalytic activity in enantioselective reduction of carbonyl and unsaturated compounds with sodium tetrahydridoborate were studied. The catalytic reduction of acetophenone is characterized by quantitative yield, the optical yields ranging from 0 to 42%. Benzil and ethyl benzoylformate undergo noncatalytic reduction. The catalytic activity and enantioselectivity in the reduction prochiral C=C bond strongly depend on the solvent and change from low to moderate values in the reduction of methyl 2-acetylamino-3-phenylprop-2- enoate. Dimethyl 2-methylidenebutane-1,4-dioate is reduced in DMF and its mixtures with ethanol and toluene in quantitative yield; in chloroform, the optical yield reaches 89%, but the chemical yield sharply decreases.
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.Synthetic Route of 29841-69-8
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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI