Awesome Chemistry Experiments For (R)-4-Phenyl-3-propionyloxazolidin-2-one

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 160695-26-1. In my other articles, you can also check out more blogs about 160695-26-1

Electric Literature of 160695-26-1, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Article, and a compound is mentioned, 160695-26-1, (R)-4-Phenyl-3-propionyloxazolidin-2-one, introducing its new discovery.

(Matrix Presented) The highly stereoselective synthesis of beta-amino acids via the chiral 4-phenyloxazolidinone-controlled linear N-acyliminium ion reaction has been achieved by employing chiral N,O-acetal TMS ethers. In addition, the mechanism of the excellent stereochemical outcome has been elucidated. The oxazolidinone auxiliary plays a dual role in stereocontrol: the E/Z geometry control of the N-acyliminium ion induced by an initial stereoselective amide reduction, leading to the chiral N,O-acetal TMS ether, and face control of the nucleophile attack in the N-acyliminium ion reaction.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 160695-26-1. In my other articles, you can also check out more blogs about 160695-26-1

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H2251NO – PubChem