A new application about 57203-01-7

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of (S)-(Tetrahydrofuran-2-yl)methanol, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 57203-01-7, in my other articles.

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of (S)-(Tetrahydrofuran-2-yl)methanol, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 57203-01-7, Name is (S)-(Tetrahydrofuran-2-yl)methanol, molecular formula is C5H10O2

Enantioselective haloetherification by asymmetric opening of meso -halonium ions

A new approach to enantioselective haloetherification reactions via desymmetrization of in situ-generated meso-halonium ions is described. The combination of N-haloamides as a halogen source and sodium salts of chiral phosphoric acids as catalysts can be used for the cyclization of symmetrical ene-diol substrates, yielding the haloetherification products under practical conditions in enantioenriched form.(Figure Presented)

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of (S)-(Tetrahydrofuran-2-yl)methanol, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 57203-01-7, in my other articles.

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem