1193752-89-4Relevant academic research and scientific papers
Enantioselective intramolecular Michael addition of nitronates onto conjugated esters: Access to cyclic γ-amino acids with up to three stereocenters
Nodes, William J.,Nutt, David R.,Chippindale, Ann M.,Cobb, Alexander J. A.
supporting information; experimental part, p. 16016 - 16017 (2010/02/16)
(Chemical Equation Presented) A highly stereoselective synthesis of conformationally constrained cyclic γ-amino acids has been devised. The key step involves an intramolecular cyclization of a nitronate onto a conjugated ester, promoted by a bifunctional
