New explortion of (S)-(Tetrahydrofuran-2-yl)methanol

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Product Details of 57203-01-7, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 57203-01-7

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Product Details of 57203-01-7, 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

C(sp3)-H bond functionalization has emerged as a robust tool enabling rapid construction of molecular complexity from simple building blocks, and the development of asymmetric versions of this reaction creates a powerful methodology to access enantiopure sp3-rich materials. Herein, we report the stereoselective functionalization of C(sp3)-H bonds of cyclic ethers employing a photochemically active diaryliodonium salt in combination with an anionic phase-transfer catalyst. The synthetic strategy outlined herein allows for regio- and stereochemical control in the alpha-C-H acetalization of furans and pyrans using alcohol nucleophiles, thus providing the ability to control the configuration at the stereogenic exocyclic acetal carbon.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Product Details of 57203-01-7, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 57203-01-7

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