777088-07-0Relevant academic research and scientific papers
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
(R)- or (S)-4-(3-hydroxy-4,4-dimethyl-2-oxopyrrolidin-1-yl)benzoic acid as a new chiral auxiliary for solid phase asymmetric Diels-Alder reactions
Akkari, Rhalid,Calmes, Monique,Escale, Francoise,Iapichella, Julien,Rolland, Marc,Martinez, Jean
, p. 2515 - 2525 (2007/10/03)
The synthesis of enantiopure (R)- and (S)-4-(3-hydroxy-4,4-dimethyl-2- oxopyrrolidin-1-yl)benzoic acid is described and the corresponding supported chiral acrylate derivative has been used as a dienophile in solid phase asymmetric Diels-Alder reactions wi
