2011
DOI: 10.1016/j.tetasy.2011.01.010
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Determination of the absolute configuration of the enantiomers of dihydroquinolines, isolated by chiral chromatography, by non empirical analysis of circular dichroism spectra and X-ray analysis

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“…[61] In compound 123 (Scheme 41), the exchange of the benzene ring connecting the acetal and ketenimine functions for a heterocyclic ring had pronounced consequences for the magnitudes of the energy barriers of the two mechanistic steps of the tandem cyclizations experienced by acetalic ketenimines. [61] In compound 123 (Scheme 41), the exchange of the benzene ring connecting the acetal and ketenimine functions for a heterocyclic ring had pronounced consequences for the magnitudes of the energy barriers of the two mechanistic steps of the tandem cyclizations experienced by acetalic ketenimines.…”
Section: 5-h Shiftsmentioning
confidence: 99%
“…[61] In compound 123 (Scheme 41), the exchange of the benzene ring connecting the acetal and ketenimine functions for a heterocyclic ring had pronounced consequences for the magnitudes of the energy barriers of the two mechanistic steps of the tandem cyclizations experienced by acetalic ketenimines. [61] In compound 123 (Scheme 41), the exchange of the benzene ring connecting the acetal and ketenimine functions for a heterocyclic ring had pronounced consequences for the magnitudes of the energy barriers of the two mechanistic steps of the tandem cyclizations experienced by acetalic ketenimines.…”
Section: 5-h Shiftsmentioning
confidence: 99%