Synthetic Route of 173604-33-6, 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. 173604-33-6, Name is (R)-4-Benzhydryloxazolidin-2-one, molecular formula is C16H15NO2. In a Article，once mentioned of 173604-33-6
A detailed investigation of the effects of Lewis acid, temperature, and trapping efficiency of functionalized allylstannanes on diastereoselective radical allylation reactions of alpha-bromooxazolidinone imides 1 and 2 was conducted. Results indicate that despite the addition of Lewis acids, a bidentate chelated radical intermediate 21 may be accessible from only one diastereomer of starting material due to steric interactions in 20 that are not present in chelated intermediate 17. It is shown that application of the appropriate Lewis acid, increasing temperatures, and slower allylstannane traps all facilitate formation of 21. Thus highly stereoselective radical allylations (> 50:1, Tables 2 and 3) can be performed at room temperature as well as low temperatures.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 173604-33-6. In my other articles, you can also check out more blogs about 173604-33-6
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H2461NO – PubChem