Application of 102029-44-7, 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.102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone, molecular formula is C10H11NO2. In a article，once mentioned of 102029-44-7
An asymmetric alkylation-ring-closing metathesis strategy was developed for the construction of alpha,alpha’-disubstituted medium ring ethers. The approach features an asymmetric alkylation of highly functionalized alpha-alkoxy acyl oxazolidinones followed by ring closure effected by Grubbs’ ruthenium catalyst. The relationship between diene conformation and the rate of ring- closure was examined.
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 102029-44-7
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H1774NO – PubChem