Regioselective reduction of bipyridines was written by Plaquevent, Jean Christophe;Chichaoui, Ilhame. And the article was included in Tetrahedron Letters in 1993.Product Details of 31251-28-2 The following contents are mentioned in the article:
A method for the specific reduction of bipyridines through the use of the N-oxo derivatives is described. E.g., oxidation of 2,4′-bipyridine by m-chloroperbenzoic acid gave the N-oxo derivative, which was hydrogenated (H2, Pd) to give 38% piperidinylpyridine I. This study involved multiple reactions and reactants, such as 3-(Piperidin-3-yl)pyridine (cas: 31251-28-2Product Details of 31251-28-2).
3-(Piperidin-3-yl)pyridine (cas: 31251-28-2) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Piperidine derivatives are being utilized in different ways as anticancer, antiviral, antimalarial, antimicrobial, antifungal, antihypertension, analgesic, anti-inflammatory, anti-Alzheimer, antipsychotic and/or anticoagulant agents.Product Details of 31251-28-2
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem