Synthetic Route of 23364-44-5, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 23364-44-5, Name is (1S,2R)-2-Amino-1,2-diphenylethanol, molecular formula is C14H15NO. In a Article£¬once mentioned of 23364-44-5
A stereodivergent synthesis of chiral 4,5-disubstituted bis(oxazolines)
Bis(oxazolines), disubstituted in the 4 and 5 positions, are synthesized from dimethylmalonyl bis-diamides of the suitable 1,2-disubstituted chiral aminoethanol. Starting from the same diamide, the ring closure can be realized either with retention (reflux in xylene with dibutyl tin dichloride – the Masamune protocol) or inversion (conversion into the mesylate and reflux with aqueous ethanolic NaOH) of the configuration at the chiral center in position 5.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 23364-44-5, you can also check out more blogs about23364-44-5
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI