76198-37-3Relevant articles and documents
Asymmetric Diels-Alder reaction using a new chiral β-nitroacrylate for enantiopure trans-β-norbornane amino acid preparation
Calmes, Monique,Escale, Francoise,Didierjean, Claude,Cazals, Guillaume,Martinez, Jean
, p. 2491 - 2496 (2008/03/13)
The main nitronorbornene adduct derived from the asymmetric Diels-Alder reaction of (S)-benzyl-4-(3-(3-nitroacryloyloxy)-4,4-dimethyl-2-oxopyrrolidin-1-yl)b enzoate (S)-1 and cyclopentadiene was isolated and transformed to afford the enantiopure bicyclic