Discovery of (R)-4-Benzyl-2-oxazolidinone

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C10H11NO2, you can also check out more blogs about102029-44-7

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Computed Properties of C10H11NO2. Introducing a new discovery about 102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone

An access to chiral beta-benzyl-gamma-butyrolactones and its application to the synthesis of enantiopure (+)-secoisolariciresinol, (-)-secoisolariciresinol, and (-)-enterolactone

Both enantiomers of secoisolariciresinol and enantiopure (-)-enterolactone were synthesized through a highly stereoselective convergent synthesis. An Evans diastereoselective alkylation followed by a substrate-induced diastereoselective -alkylation of the newly formed optically active beta-benzyl-gamma- butyrolactone gave the beta-beta? linkage of the target skeleton. The (S,S)- and (R,R)-enantiomers of secoisolariciresinol and (-)-enterolactone were obtained in 12-14% (11 steps) and 20% (7 steps) overall yield, respectively. Georg Thieme Verlag Stuttgart New York.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C10H11NO2, you can also check out more blogs about102029-44-7

Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1712NO – PubChem