Enantiodiscrimination of several chiral molecules, i.e. S-(+)-(s) vs R-(-)-2-butanol (r) and S-(+)-(s) vs R-(-)-2-butylamine (r), is obtained by two-color resonance-enhanced two-photon ionization time-of-flight (2cR2PI-TOF) spectroscopy of their supersonically expanded complexes with a suitable chro
Surface enhanced enantiodifferentiation in reactions of chiral acetoacetates.
β Scribed by Georges Bram; Daniel Cabaret; Zoltan Welvart; Niall W.A. Geraghty; James Garvey
- Book ID
- 104216676
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 292 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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Utilizing the I\_-valine-based chiral lithioenamine (5) of ethyl acetoacetate (l), enantioface differentiating Michael reaction with alkylidenemalonates (2) gave, after decarboxylation, B-substituted g-keto esters (3) in a fair to good enantiomeric excess. Kinetic diastereoenrichment of the initial
Laser-induced fluorescence excitation spectroscopy in a supersonic expansion is used to evidence intermolecular chiral discrimination at the microscopic level. Measurements have been performed in (R)-(+)-and (S)-(-)-et-methyl-2-naphthalenemethanol (a naphthalene compound made chiral by the asymmetri