Synthetic Route of 102029-44-7, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone,introducing its new discovery.
Asymmetric biomimetic oxidations of phenols: Enantioselective synthesis of (+)- and (-)-dehydrodiconiferyl alcohol
Stereoselective bimolecular radical coupling reactions of phenylpropenoid phenols are described. Oppolzer’s camphor sultam 1 and Evans’s 2-oxazolidinone 2a-d derivatives of ferulic acid were prepared and oxidized to give dimeric benzofuran neolignan structures 11 in 40-50% overall yields. The chiral phenols were oxidized either enzymatically with hydrogen peroxide and horseradish peroxidase (HRP) or by silver oxide. The observed enantioselectivity after reductive cleavage of chiral auxiliaries gave the neolignan dehydrodiconiferyl alcohol 12 in 18-84% e.e.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 102029-44-7, and how the biochemistry of the body works.Synthetic Route of 102029-44-7
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H2004NO – PubChem