Proto, Stefano published the artcileModel Studies on the Synthesis of Madangamine Alkaloids. Assembly of the Macrocyclic Rings, Related Products of piperidines, the main research area is diastereoselective synthesis madangamine alkaloid macrocyclic ring reductive amination lactamization; ring closing metathesis macrocyclization synthesis madangamine alkaloid ring.
Using simplified model derivatives, the assembly of the macrocyclic rings of madangamines including the 13- and 14-membered D rings of madangamines C-E, the all-cis-triunsatd. 15-membered D ring of madangamine A, and the (Z,Z)-unsaturated 11-membered E ring common to madangamines A-E, has been studied.
Organic Letters published new progress about Diastereoselective synthesis. 106118-94-9 belongs to class piperidines, name is Methyl 2-oxopiperidine-3-carboxylate, and the molecular formula is C7H11NO3, Related Products of piperidines.
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem