Rogers, Louis M.-A.; Rouden, Jacques; Lecomte, Ludovic; Lasne, Marie-Claire published the artcile< Enantioselective decarboxylation-reprotonation of an æµ?amino malonate derivative as a route to optically enriched cyclic æµ?amino acid>, Computed Properties of 112-63-0, the main research area is decarboxylation protonation cinchona alkaloid stereochem preparation amino acid.
Chiral tertiary amines have been examined as enantioselective decarboxylation-reprotonation reagents for the synthesis of æµ?amino acids via æµ?aminomalonates. N-Acetyl pipecolic acid Et ester (I), as a model compound, was obtained in good yield and 52% enantiomeric excess using a quinidine derived base.
Tetrahedron Letters published new progress about Amino acids Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Computed Properties of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics