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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.Quality Control of (S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid, you can also check out more blogs about139009-66-8

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Quality Control of (S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid. Introducing a new discovery about 139009-66-8, Name is (S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid

A new method for the preparation of Xxx-Gly (E)-alkene dipeptide isosteres (EADIs), using LDA deprotonation followed by 1 N HCl quench, was explored. The method, named kinetic deconjugation, enabled the synthesis of Tyr-Gly, Gly-Gly, Ser-Gly, Pro-Gly, and Phe-Gly EADIs, as well as one Tyr-Gly trisubstituted alkene dipeptide isostere (TADI). Overall, this method, based on commercially available materials, leads to high yields, requires few synthetic steps and works on the gram scale in the synthesis of a wide variety of EADIs.

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.Quality Control of (S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid, you can also check out more blogs about139009-66-8

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H2382NO – PubChem