One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Quality Control of (R)-4-Benzyl-2-oxazolidinone, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone, molecular formula is C10H11NO2
Stereoselective syntheses of (+)-rhopaloic acid A and (-)-ent- and (¡À)-rac-rhopaloic acid A
Rhopaloic acid A (+)-1 and the related compounds (-)-ent-1 and (¡À)-rac-1 have been stereoselectively synthesized. The synthetic strategy consists of successive homologation of (2E,6E)-farnesol 7 and cyclization to form a tetrahydropyran ring, together with final introduction of an alpha-methylene group on the carboxylic moiety. The cyclization is carried out by intramolecular hetero-Michael addition leading to 2,5-disubstituted tetrahydropyrans. The stereochemistry can be rationalized by invoking a model of a chair-like transition state. The asymmetric synthesis is achieved by way of the Evans’ asymmetric alkylation procedure using (S)- or (R)-4-benzyloxazolidin-2-one as the chiral auxiliary. In the event, the configuration of natural rhopaloic acid A (+)-1 could be assigned as 2R,5S by comparison of the specific rotations of synthetic compounds with that of the natural product.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Quality Control of (R)-4-Benzyl-2-oxazolidinone, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 102029-44-7
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2043NO – PubChem