206532-55-0Relevant academic research and scientific papers
A new divergent asymmetric synthesis of (+)- and (-)-ethosuximides and their anticonvulsant activities
Katoh, Takahiro,Nishide, Kiyoharu,Node, Manabu,Ogura, Hiroo
, p. 833 - 841 (2007/10/03)
Both enantiomers of ethosuximide were synthesized divergently from nitroolefin lactone [(-)-2a] or [(-)-2b], which was obtained by asymmetric nitroolefination of α-methyl-γ-butyrolactone with chiral nitro enamines derived from L-proline. Although anticonv
Synthesis of (+)- and (-)-ethosuximides utilizing asymmetric nitroolefination
Nishide, Kiyoharu,Katoh, Takahiro,Imazato, Hitoshi,Node, Manabu
, p. 839 - 845 (2007/10/03)
Both enantiomers of ethosuximide were synthesized from (S)-(-)- and (R)-(+)-2-methyl-2-[(E)-2-nitroethenyl]-γ-butyrolactones (1), which were obtained by asymmetric nitroolefination of α-methyl-γ-butyrolactone, via the lactone carboxylic acid (3).
