Archives for Chemistry Experiments of (S)-4-Hydroxydihydrofuran-2(3H)-one

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. SDS of cas: 7331-52-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 7331-52-4, in my other articles.

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, name: (S)-4-Hydroxydihydrofuran-2(3H)-one, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 7331-52-4, Name is (S)-4-Hydroxydihydrofuran-2(3H)-one, molecular formula is C4H6O3

A series of enantiomerically pure gamma-heteroatom substituted beta-hydroxy esters were synthesized with high enantioselectivities (up to 99.1% ee) by hydrogenation of gamma-heteroatom substituted beta-keto esters in the presence of Ru-(S)-SunPhos catalyst. These asymmetric hydrogenations provide key building blocks for a variety of naturally occurring and biologically active compounds.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. SDS of cas: 7331-52-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 7331-52-4, in my other articles.

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