Application of 3190-70-3, 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.3190-70-3, Name is (S)-4-Isobutyloxazolidine-2,5-dione, molecular formula is C7H11NO3. In a article，once mentioned of 3190-70-3
The lithiated bis(lactim) ether 8a furnishes with aldehydes and ketones in good yields the addition products 11 with (3R) configuration.The asymmetric inductions at C-3 of 11 (d.e. values) amount to more than 95 percent with ketones, with aldehydes they are somewhat smaller.With unsymmetrical ketones or aldehydes C-3′ also becomes a chiral center.For the (3R)-major diastereomers the “second induction” at C-3′ varies from about 4 t about 87 percent (for benzaldehyde or isobutyraldehyde, respectively), preferably the (3R,3’S) epimers are formed. – Acid hydrolysis of 11 yields (besides methyl L-valinate) the (2R)-serine methyl esters 26.Their e.e. values correspond with the d.e. values of 11. – Dehydratation of 11 furnishes the “Hofmann olefins” 32 and/or the “Saytzeff olefins” 33 which can be transformed in various ways into optically active amino acids.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 3190-70-3
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H1523NO – PubChem