1026773-66-9Relevant articles and documents
Enantioselective synthesis of cis-(2S,3R)- and trans-(2S,3S)- piperidinedicarboxylic acids using domino: Allylic acetate and Ireland-Claisen rearrangements and Michael addition as the key steps
Garrido, Narciso M.,Rosa Sanchez,Diez, David,Sanz, Francisca,Urones, Julio G.
, p. 872 - 880 (2011)
An enantioselective synthesis of (2S,3R)-piperidine-2,3-dicarboxylic acid and (2S,3S)-piperidine-2,3-dicarboxylic acid is described. This synthesis was mainly based on a δ-amino acid formation via a domino reaction: allylic acetate rearrangement, stereose