Application of 790667-49-1, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 790667-49-1, Name is (S)-tert-Butyl 2-methyl-4-oxopiperidine-1-carboxylate, molecular formula is C11H19NO3. In a Article，once mentioned of 790667-49-1
We report the diastereoselective synthesis of novel spiropiperidine templates for use in SAR studies of beta-secretase (BACE) inhibitors and also as versatile ligands for other receptor types. The overall synthetic approach stems from chiral starting material benzyl (S)-2-methyl-4-oxopiperidine-1-carboxylate and employs an Overman rearrangement to control the stereochemistry at the quaternary center. This process is followed by a Grubbs metathesis to close a five-membered “top” ring to form an alpha,beta-unsaturated lactam or an alpha,beta-unsaturated sultam. We also demonstrate that this chemistry can accommodate additional substituents on the lactam/sultam ring and allows late stage sequential functionalization of the amine and amide nitrogens to rapidly produce diverse analogues.
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.Application of 790667-49-1, you can also check out more blogs about790667-49-1
Reference：
Piperidine – Wikipedia,
Piperidine | C5H15888N – PubChem