More research is needed about (R)-4-Benzyl-2-oxazolidinone

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 102029-44-7. In my other articles, you can also check out more blogs about 102029-44-7

Application of 102029-44-7, 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, 102029-44-7, (R)-4-Benzyl-2-oxazolidinone, introducing its new discovery.

A simple procedure for the asymmetric synthesis of lignans via chiral beta-benzyl-gamma-butyrolactones has been developed. The key benzylbutyrolactone intermediates were efficiently synthesized using a six-step procedure, starting from 3,4-(methylenedioxy)cinnamic acid. The key step in this sequence was a highly diastereoselective alkylation of an N-acyloxazolidinone enolate. The resulting beta-benzyl-gamma-butyrolactones were subsequently transformed into the benzylidene lignans gossypifan and savinin (hibalactone) via aldol condensation-dehydration reactions, and into the dibenzylbutyrolactone lignan 4?-demethylyalein, through alkylation. Oxidation of 4?-demethylyatein with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) afforded cis- and trans-benzylidenebenzylbutyrolactones, whereas oxidation with DDQ/TFA gave 4?-demethyl-deoxyisopodophyllotoxin.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 102029-44-7. In my other articles, you can also check out more blogs about 102029-44-7

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H1756NO – PubChem