Simple exploration of 16251-45-9

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.Product Details of 16251-45-9, you can also check out more blogs about16251-45-9

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 16251-45-9. Introducing a new discovery about 16251-45-9, Name is (4S,5R)-4-Methyl-5-phenyloxazolidin-2-one

(R)-(+)-3-Amino-2-phenylpropanoic Acid: a Revised Absolute Configuration based on an Enantioselective Synthesis and an X-Ray Crystal Structure of the Salt with (1S)-(+)-Camphor-10-sulfonic Acid

Amidoalkylation of the lithium enolate of (4S,5R)-4-methyl-5-phenyl-3-(phenylacetyl)oxazolidin-2-one 5 by 1-(N-benzyloxycarbonylaminomethyl)benzotriazole 2c, followed by cleavage of the oxazolidinone chiral auxiliary and of the N-benzyloxycarbonyl group, gave (R)-(+)-3-amino-2-phenylpropanoic acid 1, the absolute configuration of which was determined by X-ray crystallography on the salt 8 with (1S)-(+)-camphor-10-sulfonic acid.

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.Product Details of 16251-45-9, you can also check out more blogs about16251-45-9

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H2157NO – PubChem