Related Products of 43041-11-8, 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. 43041-11-8, Name is Methyl (R)-piperidine-2-carboxylate, molecular formula is C7H13NO2. In a Article，once mentioned of 43041-11-8
Available alpha-amino acids undergo arylation at their alpha position in an enantioselective manner on treatment with base of N?-aryl urea derivatives ligated to pseudoephedrine as a chiral auxiliary. In situ silylation and enolization induces diastereoselective migration of the N?-aryl group to the alpha position of the amino acid, followed by ring closure to a hydantoin with concomitant explulsion of the recyclable auxiliary. The hydrolysis of the hydantoin products provides derivatives of quaternary amino acids. The arylation avoids the use of heavy-metal additives, and is successful with a range of amino acids and with aryl rings of varying electronic character.
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.Reference of 43041-11-8, you can also check out more blogs about43041-11-8
Reference：
Piperidine – Wikipedia,
Piperidine | C5H7048N – PubChem