One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Product Details of 122709-21-1, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 122709-21-1, Name is (S)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate, molecular formula is C13H24N2O5
Studies toward asymmetric synthesis of leiodelide A
An enantioselective route for oxazoline 4, a key fragment toward the asymmetric synthesis of leiodelide A, is described. We synthesized northern subunit 6 through a Julia-Lythgoe olefination and subsequent Sharpless asymmetric dihydroxylation. Moreover, a highly diastereoselective method using well-established Evans’ asymmetric aldol condensation was developed for preparation of southern fragment 5. The additional feature of this synthetic route is the formation of oxazoline 4 through DAST-promoted cyclization of the amidation product from subunits 5 and 6.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 122709-21-1, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 122709-21-1, in my other articles.
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2668NO – PubChem