Reference of 145589-03-3, 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. 145589-03-3, Name is (R)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one, molecular formula is C15H19NO3. In a Article，once mentioned of 145589-03-3
Via a Mannich reaction involving a dibenzyliminium species and the titanium enolates of Evans’ chiral acylated oxazolidinones the beta2-amino acids (R)- and (S)-Fmoc-beta2homovaline and (R)-Fmoc- beta2homoleucine are synthesized. These building blocks were used, in combination with commercially available alpha- and beta3-amino acids, for the synthesis of the cyclo- (alphabeta3alphabeta2alpha)2 peptide 2 and the cyclo-(alphabeta2alphabeta3alpha) 2 peptides 3-5. The peptides 2-5 were screened for their ability to inhibit a small panel of Gram-negative and Gram-positive bacterial strains.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 145589-03-3. In my other articles, you can also check out more blogs about 145589-03-3
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H2615NO – PubChem